- Review Article
- Open Access
Options on fibroid morcellation: a literature review
Gynecological Surgery volume 12, pages3–15(2015)
In laparoscopy, specimens have to be removed from the abdominal cavity. If the trocar opening or the vaginal outlet is insufficient to pass the specimen, the specimen needs to be reduced. The power morcellator is an instrument with a fast rotating cylindrical knife which aims to divide the tissue into smaller pieces or fragments. The Food and Drug Administration (FDA) issued a press release in April 2014 that discouraged the use of these power morcellators. This article has the objective to review the literature related to complications by power morcellation of uterine fibroids in laparoscopy and offer recommendations to laparoscopic surgeons in gynaecology. This project was initiated by the executive board of the European Society of Gynaecological Endoscopy. A steering committee on fibroid morcellation was installed and experienced ESGE members requested to chair an action group to address distinct clinical questions. Clinical questions were formulated with regards to the sarcoma risk in presumed uterine fibroids, diagnosis of sarcoma, complications of morcellation and future research. A literature review on the different subjects was conducted, systematic if appropriate and feasible. It was concluded that the true prevalence of uterine sarcoma in presumed fibroids is not known given the wide range of prevalences (0.45–0.014 %) from meta-analyses mainly based on retrospective trials. Age and certain imaging characteristics such as ‘lacunes’ suggesting necrosis and increased central vascularisation of the tumour are associated with a higher risk of uterine sarcoma, although the risks remain low. There is not enough evidence to estimate this risk in individual patients. Complications of morcellation are rare. Reported are direct morcellation injuries to vessels and bowel, the development of so-called parasitic fibroids requiring reintervention and the spread of sarcoma cells in the abdominal cavity, which may possibly or even likely upstaging the disease. Momentarily in-bag morcellation is investigated as it may possibly prevent morcellation complications. Because of lack of evidence, this literature review cannot give strong recommendations but offers only options which are condensed in a flow chart. Prospective data collection may clarify the issue on sarcoma risk in presumed fibroids and technology to extract tissue laparoscopically from the abdominal cavity should be perfected.
A uterine leiomyoma or myoma is a benign smooth muscle tumour of the myometrium and will be referred to in this article as fibroid. On April 17, 2014, the Food and Drug Administration (FDA) published a press release on the website where the use of laparoscopic power morcellation was ‘discouraged’ due to potential upstaging of uterine sarcoma . The motive to do so was the case history of a patient with a presumed fibroid who underwent a laparoscopic hysterectomy and morcellation of the uterus. The fibroid turned out to be a sarcoma and at reintervention spread of the sarcoma in the abdominal cavity was present. The FDA reported a risk of a uterine sarcoma in patients with presumed fibroids of 0.28 % meta-analysing the data of 18 studies. As some way of morcellation has been used for a long time by gynaecologic surgeons to extract tissue from the vagina or the endoscopic openings in order to enable vaginal or laparoscopic surgery, the professional community was shocked and representatives of many scientific societies published their opinions on the matter [2–9]. A common statement was the lack of solid scientific data to reach strong recommendations with regard to the counselling of patients with fibroids on the issue to choose laparoscopic surgery with its established benefits or for laparotomy to escape the small risks related to morcellation of the fibroid.
This review looks at morcellation complications in cases of presumed fibroids. Although intra-abdominal spread of endometrial cancer, adenomyosis and even trophoblastic tissue by morcellation of the uterus has been reported, these issues will not be addressed in this paper as those diagnoses are less unexpected by their clinical features.
To explore the available literature, the subject will be divided into clinical questions:
What is the risk of sarcoma in patients with a presumed fibroid
How to diagnose a uterine sarcoma and distinguish it from a fibroid
What are the complications of morcellation
How to prevent morcellation complications
What are the knowledge gaps
Recommendations on clinical management in patients with fibroids
The objective of this article is to formulate and grade statements and recommendations on fibroid morcellation based on the level of available evidence. The grading of articles and recommendations was performed according to Eccles et al.  (Table 1). As statements can be based on several articles, they are treated as recommendations.
What is the risk of sarcoma in patients with presumed fibroid(s)
Uterine fibroids are a common disorder with an estimated incidence of 20–40 % in women during their reproductive years [11, 12]. In contrast, leiomyosarcoma of the uterus is a rare entity with an annual incidence quoted at 0.64/100,000 women . According to a recently revised WHO classification of uterine sarcomas, the myometrial pure stromal sarcoma (leiomyoma, Smooth muscle Tumor of Unknown Potential [STUMP] and leiomyosarcoma) is to be distinguished from the endometrial stromal sarcoma (endometrial stromal nodule [ESN], the low-grade endometrial stromal sarcoma and the undifferentiated endometrial sarcoma). The carcinosarcoma or Mixed Müllerian Tumor (MMT) is classified as carcinoma. Excluding the MMT, leiomyosarcoma (LMS) accounts for 70 % and stromal sarcoma for 30 % of all uterine sarcomas . Uterine sarcomas consist 2–7 % of all uterine malignancies. Reliable figures for the incidence of STUMP and cellular fibroids are poorly documented. In one article from a single institution over a period of 36 years, there were 18 cases of STUMP and 72 cases of uterine leiomyosarcoma (none of which had a prior diagnosis of STUMP) in the hysterectomy specimens . All cases of STUMP were registered as disease free after 5 years with only conservative management. Sarcomas spread usually by blood or lymphatic vessels. Five-year survival ranges from 17 to 55 %. Survival of patients with a LMS is strongly associated with the number of mitoses per 10 high power fields (×100 magnification): 1–4, 98 %; 5–9, 42 %; ≥10, 15 %. A LMS embedded and confined to the uterus that is removed ‘en bloc’ is associated with a better survival up to 83 % .
Two authors (TI, KP) performed a systematic review of the literature on prevalence of uterine sarcoma in patients after uterus surgery, mostly because of presumed fibroids. Searches were performed of Pubmed and Embase using the MESH terms “Fibroids and Sarcoma and uterine neoplasms”, “Myomectomy and Complications”. Further papers were obtained from the reference lists of papers reviewed. Two further papers were submitted for inclusions which were unpublished manuscripts [16, 17] (Ind et al. 2014, personal communication). Only papers with over 500 subjects were included to address the issues of publication bias in smaller series. Further analysis using the terms above and cross referencing with published reviews reference lists on this subject, but with the exclusion of review articles, letters and case reports from the analysis, 12 papers are left where the data seemed reliable and acceptable to help answer the question [8, 16–26]. All evidence finally reviewed has been retrieved from observational single arm cohort studies and is therefore level III evidence. The recommendations are therefore graded as Grade C.
The overall risk of not previously presumed sarcomatous change in the uterus from all papers was 0.14 % (1 in 700). However, there were large differences between papers with figures varying from 0.49 % (1 in 204)  to 0.056 % (1 in 1,788) . On average, papers that looked at myomectomy specimens gave a lower risk of sarcomatous change of 0.08 % (1 in 1,306) compared to those that looked at hysterectomy specimens where the overall pooled risk was 0.15 % (1 in 650). The risk appears to be age related with one study demonstrating a lower risk in patients under 45 years of age (Ind et al. 2014, personal communication).
This meta-analysis, based largely on peer-reviewed articles and two submitted articles, shows a prevalence of 0.14 % which is lower than but within the range of similar literature reviews [1, 6]. In the current selection of studies, the small numbers (<500) were excluded. Recently presented data, submitted for publication, however show that including small trials brings the average reported prevalence of sarcoma down (Pritts E, 2014, personal communication).
Pritts et al. selected 131 articles with 29.877 patients operated for fibroids and found a sarcoma prevalence of 1:7,400 (0.014 %). They explain the large prevalence difference with the available literature by including more prospective trials (50 % half of which randomised trials) that lack the confounder of patient selection of retrospective trials. Also trials with smaller numbers were included increasing the power of the meta-analysis using Bayesian statistics to correct for small patient numbers. Although the large differences in prevalence undermine the credibility of all collected data on the prevalence of sarcoma in presumed fibroids, it is likely that the prevalence is much lower than recently reported. Prospective collection of multicentric data of contemporary patients may clarify the important issue of prevalence.
As the LMS has a similar clinical and diagnostic appearance to the leiomyoma in contrast to the endometrial stromal sarcoma, our interest is primarily to distinguish fibroids from LMS. The endometrial stromal sarcomas usually cause abnormal—non cyclic—uterine bleeding. But also LMS can present as a type 0—100 % protruding in the uterine cavity—causing abnormal uterine bleeding. In the current review, all kinds of sarcomatous changes were included in the meta-analysis, including STUMP’s. This may have blurred the prevalence results. In particular including studies with laparoscopic supracervical hysterectomies, sometimes without the presumption of fibroids, will result in a lower reported prevalence. A difference in prevalence between studies where fibroids intended to be morcellated and the older (pathology) studies where all uteri and fibroids served as a denominator in the prevalence rate has also been demonstrated .
Data on age and prevalence does not allow the estimation of an accurate risk of sarcoma in the individual patient scheduled for fibroid surgery but they may be taken into account to define a low and intermediate risk group of patients. The paradox remains that as presumed fibroids are less prevalent in postmenopause, the highest (absolute) number of sarcomas is found in the fourth decade, although the incidence is still extremely low . In one study, 18/21 sarcoma patients (86 %) were premenopausal . The statements of this section are in Table 2.
How to distinguish a fibroid from a sarcoma by diagnostic tests
Even if an accurate distinction between fibroids and sarcomas by preoperative diagnostic test is not possible, potential specific characteristics of both disorders would enable the clinician to better predict the presence of sarcoma in a presumed fibroid and counsel patients likewise. Uterine sarcomas are characterised by the common oncologic features such as growth, necrosis and increased vascularity. However, these characteristics occur also in fibroids.
Although the focus of this overview is on fibroid morcellation, the same may be applicable to other therapeutic options such as selective uterine artery embolisation, fibroid ablation, hysteroscopic resection or medical treatment.
In this section, the evidence is reviewed as to the predictive value of imaging and other diagnostic tests in differentiating between a (benign) fibroid and a LMS of the uterus.
One of the authors (TvdB) performed a systematic Medline search of the literature in order to map the different diagnostic tests and their characteristics. The following search terms were used: “uterine leiomyosarcoma” [all fields], “diagnosis” [all fields], “ultrasonography” [all fields], “LDH” [all fields] or “LDH isoenzymes” [all fields] and “markers” [all fields]. After including cross references, 37 articles were available for further consideration [22, 28–64].
Imaging (US, MRI)
There are no pathognomonic features predicting a LMS on any imaging technique [29, 30, 36]. Rapid increase in size (within 3 months) has been reported in case reports of LMS [48, 59] but is generally not distinctive as it may occur in fibroids as well . No growth—in 3 months—may be reassuring unless caused by GnRH [65, 66]. Not only can the uterine sarcoma be accompanied by fibroids responding to GnRH, but it may also be sensitive for estrogen deprivation itself due to its estrogen receptors. It has been reported in a group of 21 uterine sarcomas that all but one (95 %) was either solitary or in case of several myometrial lesions the largest . Another study with ultrasound compared eight LMS and three STUMPs with 225 fibroids and reported that LMSs were significantly larger than other uterine smooth muscle tumours . They were all solitary, and seven of eight lesions had a diameter ≥8 cm. Degenerative cystic changes were observed in four lesions, and increased peripheral and central vascularity was demonstrated in seven lesions. Sensitivity, specificity and positive predictive value of increased central and peripheral vascularity in the diagnosis of LMS were 100, 86 and 19 %, respectively. Combining other sonographic findings with marked central vascularity, the positive predictive value increased to 60 %, but sensitivity decreased to 75 %. 2D ultrasound Power Doppler (USPD) may be related to the nature of the tumour, with a peak systolic velocity having a sensitivity of 80 % for detecting sarcoma with a specificity of 97 %. No studies on sarcoma diagnosis have been published on vascular indices measured by 3D USPD.
Although LMS may have on ultrasound and MRI a similar appearance to fibroids [30, 36], a large >8 cm, solitary, oval-shaped, highly vascularised (peripheral and central) and irregular, heterogeneous myometrial tumour with central necrosis/degenerative cystic changes and absence of calcifications should raise the suspicion of a LMS [29, 30, 35, 41]. MR imaging is superior to CT scan to delineate the extent and to evaluate the tissue characteristics of the lesion . MRI, especially the T2-weighted sequences, may help evaluating tumour extension in the uterus  and in differentiating between a leiomyoma and a LMS [51, 54]. In a small series, contrast enhancement after administration of gadolinium (Gd)-DTPA was detected in all 10 LMS, but absent in 28 of 32 uterine degenerated leiomyoma patients .
Positron emission tomography has a place in the diagnostic armentarium of presumed fibroids. In PET scanning, a radionuclide (tracer) on a biologically active molecule is visualised. In imaging of fibroids, usually fluodeoxyglucose (FDG) is used, but also other molecules, such as deoxyfluorothymidine (FLT) or alphafluorobeta-estradiol (FES), have been reported. In general, the uptake of FDG in a fibroid is associated with the estrogen status, cellularity and the presence of malignancy . One retrospective study compares different imaging techniques in the case of suspected uterine sarcoma. Of the five sarcomata, all were detected by FDG PET, four by dynamic MRI and two by PowerDoppler ultrasound . FES may be more accurate in distinguishing LMS from fibroids than FDG, with an accuracy of respectively 93 and 81 % .
Serum markers (LDH and CA125)
In a prospective series of 227 patients, the total LDH and LDH isozyme type 3 were elevated in all 10 patients with LMS as compared with degenerated leiomyomas . Elevated CA125 have been reported in patients with LMS, especially in advanced-staged LMS [44, 59]. In a series of 42 consecutive LMS, the values of preoperative serum CA125 were significantly higher in the uterine LMS group than those in the uterine leiomyoma group. However, there was significant overlapping of preoperative serum CA125 between the uterine leiomyoma group and early-stage uterine LMS which limits the clinical use .
The role of endometrial sampling without abnormal uterine bleeding in the detection of uterine sarcoma is not yet elucidated . In a large series of 938 malignant tumours in hysterectomy specimens from a pathology laboratory, 142 specimens with sarcomas were found of which 72 (51 %) had endometrial sampling. In 62/72 (86 %), the sampling was positive for sarcoma. As preoperative abnormal uterine bleeding was not registered and analysed in this study, it is not clear which patients were selected for endometrial sampling. It may be assumed that abnormal uterine bleeding was the indication for endometrial sampling in sarcoma patients and not the presumed fibroid itself.
Also the role of image-guided needle biopsies is not completely clear. The predictive value of a negative biopsy might be expected to be low because of the large areas of necrosis, an excellent negative predictive value is reported using MRI-guided needle biopsies and Bell’s classification on histology  with a cut-off level of 2 . With this cut-off level, chosen not to miss malignancy, the sensitivity, specificity, positive and negative predictive values were 100, 98.6, 58 and 100.0 %, respectively. No data are found on the possible spread of sarcoma cells by multiple puncturing of the sarcoma. In breast cancer needle puncture, an increase of positive lymph nodes compared to breast tumours that were not punctured was found . On the other hand, incisional biopsy of melanoma has no apparent effect on tumour spread . Tulandi et al.  report on two cases of multiple transabdominal biopsies and frozen section before proceeding with morcellation.
Finally, it should be stressed that even the histological diagnosis of LMS on an intact hysterectomy specimen may be difficult because of locally differing diagnostic criteria [31, 38]. Statements on diagnosis of uterine sarcoma are listed in Table 3.
What are complications of morcellation?
A complication can be defined as an unintended and undesirable event following clinical management resulting in its adjustment or irreversible injury to the patient. Known complications are direct morcellation injuries where the activated morcellator injures intestines or blood vessels. Secondary to morcellation of fibroids, chips can implant on the peritoneum causing parasitic fibroids which may need further surgery. If a presumed fibroid appears to be a sarcoma (or other malignancy), any method of morcellation disrupts the integrity of the tumour, possibly upstaging the disease and affecting survival. In case of power morcellation, the centripetal forces of the cylindrical knife may add to the phenomenon of ‘seeding’ of tumour cells on the peritoneum. Finally, the fragmental state of the specimen due to morcellation may impair proper selection for histologic evaluation of that part of the tumour that is suspicious of malignancy. This might cause treatment delay. In this section, these complications will be discussed separately.
Direct morcellation injuries
In the field of gynaecology, the majority of symptomatic masses are represented by uterine fibroids. During operative laparoscopy, power morcellation is indispensable to remove large tissue fragments while the laparoscopy offers quicker recovery, less post-operative pain, fewer wound complications and less post-operative morbidity than open procedures. In addition, power morcellators shorten the time of surgery significantly. An ‘electrical cutting device for laparoscopic removal of tissue from the abdominal cavity’ was introduced by Steiner in 1993 . Similar instruments according to the Steiner principle have been commercialised since.
Despite the well-established advantages of power morcellation during laparoscopy, the use of power morcellators is not completely without concern. Milad  reviewed the FDA’s adverse event database “MAUDE” between 1992 and 2013, where injuries to the small/large bowel (31), large blood vessels (27), the kidney (3), ureter (3), bladder (1) and diaphragm (1) have been reported using power morcellation. In six cases, the accidents were fatal. This underlines that direct morcellation injuries are serious and, though underreported, extremely rare. It is recommended to maintain adequate distension and use morcellators with a nozzle to promote lateral pealing preventing the morcellator from coring the tissue and thereby losing the morcellator’s tip out of sight .
Traditionally, parasitic fibroids were thought to be pedunculated subserosal fibroids that were accidentally separated from the uterus and had become attached to another organ in the pelvis for their blood supply (3). The increasing number of case reports of parasitic fibroids after the use of laparoscopic morcellation has contributed to the development of an iatrogenic theory. It is thought that seeding of retained small tissue fragments after morcellation can lead to the development of parasitic fibroids in the peritoneal cavity . Most patients presented with symptoms such as abdominal or pelvic pain, dyspareunia, abdominal distension, urinary frequency and constipation. One of five patients is asymptomatic and the presence of a pelvic mass unexpectedly diagnosed during routine examination or another surgical procedure. Additional published cases indicated that although rare, parasitic fibroids can occur long after laparoscopic morcellation and are often asymptomatic or present with abdominal or pelvic pain. Little is known about the incidence and risk factors of this phenomenon.
To answer questions about the incidence, risk factors and other characteristics of parasitic fibroids, one of the authors (HP) conducted a systematic literature search the MEDLINE and Embase databases. The report of this systematic review will be submitted elsewhere.
The overall incidence of parasitic fibroids after laparoscopic surgery with the use of morcellation was reported to be between 0.12 and 0.9 % [75–77]. The reported incidence of parasitic myomas after laparoscopic myomectomy was 0.2–1.2 % [76, 78, 79].
With regards to the risk factors, gonadal steroids hormones are known to influence the growth of uterine fibroids. It is hypothesised that prolonged exposure to steroid hormones (e.g. hormonal replacement therapy) during postmenopause could be a risk factor for the development of parasitic fibroids. In case of parasitic fibroids, there is often more than one. Statements on parasitic fibroids are listed in Table 4.
‘Upstaging’ uterine sarcoma
Although reducing a uterine sarcoma with electromechanical power morcellation within the abdominal cavity is contrary to oncologic surgical principles, the question remains if sarcoma cells are more inclined to implant in the peritoneum after power morcellation then after ‘en bloc’ removal of the uterine specimen with sarcoma embedded and if survival is affected given the bad prognosis that the sarcoma already has. These two questions have been addressed in literature. Two case reports support the concept of upstaging by power morcellation [80, 81]. In the reported patients, reintervention showed seeding of sarcomatous tissue, which was not visible during initial surgery. These findings have been confirmed in larger studies where the percentage upstaging ranged from 15 to 64 % [18, 28, 82, 83].
Not only electromechanical power morcellation is associated with the risk of upstaging but also other ‘manipulations’ of the sarcomatous tumour, such as myomectomy by laparotomy, subtotal hysterectomy and hysteroscopic resection of submucous fibroids, may affect survival suggesting upstaging . The question as to whether seeding affects survival is also addressed by Seidman et al. . In four of seven patients with LMS who were extracted by power morcellation, seeding was visible during reintervention. Three patients died from the disease and one was alive with metastatic disease. Three patients with morcellated sarcoma without signs of seeding were alive without metastases.
Two studies by Park et al. [85, 86] compared the survival of patients with uterine sarcoma with (n = 48) and without morcellation (n = 58) during surgery and demonstrated a significant difference of survival in favour of the non-morcellated group (Table 5). Although confounding factors cannot be excluded in these retrospective trials, an effect in favour of the morcellation group would have been expected as clinical suspicion of sarcoma based on size and imaging texture could have resulted in a worse prognosis in the laparotomy group.
Recently, a literature review was published by Pritts et al.  where she critically appraised the studies that reported on upstaging of sarcoma by morcellation which she evaluated as ‘rather poor’. Although this weakens the alarming statements on upstaging, it does not prove the contrary (the innocence of open morcellation of sarcoma) and underlines the need for further studies. Statements on upstaging of uterine sarcoma by morcellation are listed in Table 6.
Missing the diagnosis of malignancy because of shredded material
Morcellated specimens are poorly amenable to pathologic examination because the morcellation abolishes many of the anatomic features that allow meaningful gross description, including the notions of orientation, dimension, adjacency, border and margin . This has been described in other uterine malignancies and could lead to delayed diagnosis or suboptimal staging, causing treatment delay [89, 90].
How to prevent morcellation complications
Given the scarcity of direct morcellation injuries, no clinical trials are available and all suggestions to prevent them may be considered as good practice points. With regards to preventing direct morcellation injuries, the options are listed in Table 7; regarding the development of parasitic fibroids, the options are mentioned in Table 8. The options to prevent upstaging of uterine sarcomas by power morcellation will be presented under the final options in Table 10.
The—on some issues—systematic literature search on which this review is based revealed some serious gaps in available knowledge. Due to the low prevalence of uterine sarcomas, most data on prevalence and risk factors are derived from case histories or retrospective trials with low numbers. Prospective data collection of patients after fibroid surgery on age, imaging and laboratory results and subsequent histology is needed to answer questions on individual risk estimation in order to enable the patient to give a well-considered consent prior to minimal invasive surgery.
The development of safer morcellation techniques in the abdominal cavity by technical innovation, including in-bag morcellation, is in its infancy. No doubt that safe in-bag morcellation of fibroids has the potential to avoid many of the reported morcellation complications, such as direct morcellation injuries, parasitic fibroids and the upstaging of morcellated sarcomas. However, not all risks are addressed such as spillage from the content of the bag in the abdomen especially if the bag is punctured to introduce a laparoscope in the bag for better visualisation of the morcellator’s tip. The in vitro results are promising. Cohen and Einarsson  demonstrated in-bag morcellation in an in vitro study, in which they successfully morcellated beef tongue specimens. In only 1 of the 13 trials did leakage of the bag occur. Washings of the container after retrieval of the specimen bag were negative for muscle cells, except for the open control and the trial with leakage of the retrieval bag. A small series of in-bag morcellation have been published with good results [92, 93]. Vaginal morcellation in a bag has been described also . Possible draw backs are the need for a sufficient vaginal entry and the fact that only hysterectomy specimens are suitable for this technique. Future studies must establish the role of vaginal in-bag morcellation.
In urology in-bag (‘contained’) morcellation has been performed in low-grade renal cell carcinoma (RCC). In a retrospective study, Wu et al.  evaluated in-bag morcellation in 188 patients with low-stage RCC. After a mean follow-up of 21 months, no difference in survival was demonstrated compared to open nephrectomy, although one port site metastases occurred. The safety and effectiveness in terms of survival was confirmed in another study . In low-grade renal cell carcinoma, laparoscopic approach combined with in-bag morcellation of the kidney appears to be safe and effective.
Port site metastases after morcellation are thought to be related to the laparoscopic approach itself and not to the morcellation technique as exteriorising the bag before morcellation is meant to prevent contact of the tumour with the abdominal wall. In a review on port site metastases, the in-bag morcellation technique is recommended to prevent port site metastases .
Two studies report on the techniques of containment. Parekh et al.  suggested that specimens should be morcellated in fluid-filled retrieval bags. In an in vitro study, five porcine kidneys were morcellated. No perforation or leakage occurred in the fluid-filled bags compared to one perforation in ‘dry’ morcellation. Also, morcellation time was shorter, when compared to the dry bags.
Meng et al.  suggested that washings of a specimen retrieval bag may help the pathological diagnosis after renal morcellation. In their prospective study, 22 consecutive washings were examined. In 9 of 13 patients with carcinoma, the cytological examination confirmed pathology and in three cases cytology provided additional information. In all nine benign cases, cytology was consistent with pathology.
The potential benefits and risks of in-bag morcellation should be further evaluated by clinical studies before it can be recommended in general practice. Furthermore, although in-bag morcellation appears to be very promising as a tool for the prevention of morcellation-related complications, further research is needed to improve the morcellation mechanism itself . The statements on knowledge gaps and potential technical innovations are listed in Table 9.
In the previous sections, the results of a literature search are shown to answer questions about fibroid morcellation in laparoscopy, related complications and what is needed to prevent them. It has not been the aim of this study to address morcellation of other structures such as uteri without presumed fibroids (e.g. some cases of LSH) or morcellation of ovarian masses.
As expected, the level of evidence is not sufficient to give recommendations. Therefore, it was decided to present options (Table 10), which are condensed in a flowchart to offer structure in the clinical management (Fig. 1). The flowchart can at best support the clinician to pursue safe and effective fibroid treatment but ‘reassuring’ does not exclude sarcoma and in ‘non-reassuring’ cases the diagnosis will likely be benign. Therefore, it cannot have the status of guideline.
The ‘additional characteristics’ in the flowchart for women over 40 years of age are based on the literature review in the previous sections. These characteristics have been associated with discrimination of sarcomas from fibroids but they lack thorough scientific evaluation. In the case of LDH, the predictive value is based on only one trial . We have to realise we are looking for a needle in a haystack indeed. This means that for each single ‘risk factor’, we can easily argue that it is of no importance. However, the association of several risk factors is probably more relevant than a single one. If more risk factors are present, it might be wise to be prudent, although the risk of sarcoma remains low.
Fibroid growth has been discussed among the authors at length and it was concluded that ‘growth’ or ‘rapid growth’ are not specifically associated with sarcoma but also with fibroids. On the other hand, a stable size during several months without administration of suppressing hormones (GnRH or Ullipristal) does make a sarcoma highly unlikely. Growth of the presumed fibroids during GnRH treatment or in menopause should raise suspicion about the nature of tumour.
The in-bag morcellation of presumed fibroids has the potential to prevent the rare morcellation-related complications typical of ‘open’ morcellation, such as direct morcellation injuries by distending the morcellation bag, the spread of fibroid chips, sarcoma or other malignant particles and cells in the abdominal cavity. More research is needed to improve the technique and on safety before in-bag morcellation can be recommended as a general tool in laparoscopic surgery.
We have chosen not to list all the literature on the benefits of laparoscopic surgery which are an important argument in the trade-off between laparoscopy with morcellation and laparotomy without. The vast amount of evidence in favour of laparoscopy is elegantly abstracted in the ‘second look’ article by Pitkin and Parker .
Taking needle biopsies before surgery would be an interesting option in case of intended fibroid surgery to rule out sarcoma; however, there are different opinions on the potential harmful effects of tumour manipulation and spread by needle biopsy [45, 69, 70]. Also representativeness of needle biopsies may be a yet unresolved drawback, given the necrotic areas in the sarcoma.
It is clear that there is much research to be done. At first, the issue on sarcoma risk in patients scheduled for fibroid morcellation should be clarified. The preliminary report of Pritts et al. (2014, personal communication) that includes more prospective trials and is based on sound statistics shows much lower prevalences (1:7,400) than previously reported in the meta-analyses based on retrospective trials (1:352) .
Secondly, more data must be collected to estimate the risk of sarcoma in individual patients with presumed fibroids, based on epidemiological data from the patient and diagnostic tests such as imaging.
Thirdly, technical innovation, such as in-bag morcellation, should enable safe morcellation of intra-abdominal specimens.
A corner stone in the doctor and patient relationship is the informed consent procedure. This means that the patient needs to be informed as completely as possible and based on the best available evidence in order to let her make the best choice of treatment tailored to her individual situation.
FDA (2014) FDA discourages use of laparoscopic power morcellation for removal of uterus or uterine fibroids. Food Drug Adm 17:4, Ref Type: Internet Communication
Goff BA (2014) SGO not soft on morcellation: risks and benefits must be weighed. Lancet Oncol 15(4):e148–e2045
Ankum WA (2014) Food and drug administration ontraadt gebruik van morcellator (redactioneel commentaar). Ned Tijdschr Obstet Gynaecol 127:216–219
Patient safety must be a priority in all aspects of care. Lancet Oncol 2014; 15(2):123–2045
WGE (2014) Morcelleren: reactie van Werkgroep Gynaecologische Endoscopie op FDA-advies; FDA ontraadt gebruik van morcellator. Ned Tijdschr Obstet Gynaecol 127:215
Knight J, Falcone T (2014) Tissue extraction by morcellation: a clinical dilemma. J Minim Invasive Gynecol 21(3):319–320
Kho KA, Nezhat CH (2014) Evaluating the risks of electric uterine morcellation. JAMA 311(19):905–906
Leung F, Terzibachian JJ (2012) Re: “The impact of tumor morcellation during surgery on the prognosis of patients with apparently early uterine leiomyosarcoma”. Gynecol Oncol 124(1):172–173
European Society of Gynaecological Endoscopy (ESGE). Statement on morcellation (of presumed fibroids appearing to be sarcomas). ESGE executive board. 2014. Ref Type: Internet Communication
Eccles M, Mason J (2001) How to develop cost-conscious guidelines. Health Technol Assess 5(16):1–69
Ryan GL, Syrop CH, Van Voorhis BJ (2005) Role, epidemiology, and natural history of benign uterine mass lesions. Clin Obstet Gynecol 48(2):312–324
Wallach EE, Vlahos NF (2004) Uterine myomas: an overview of development, clinical features, and management. Obstet Gynecol 104(2):393–406
Harlow BL, Weiss NS, Lofton S (1986) The epidemiology of sarcomas of the uterus. J Natl Cancer Inst 76(3):399–402
Lurain JR, Piver MS (1992) Uterine sarcomas: clinical features and management. In: Coppleson X, Monagham J, Morrow P, Tattersall M (eds) Gynecologic oncology. Chruchill Livingstone, London, pp 827–840
Ng JS, Han A, Chew SH, Low J (2010) A clinicopathologic study of uterine smooth muscle tumours of uncertain malignant potential (STUMP). Ann Acad Med Singap 39(8):625–628
Bojhar B, de Wilde RL, Tchartchian. (2014) Malignancy rate of 10,731 uteri morcellated during laparoscopic supracervical hysterectomy in 2013. (Personal Communication)
Ind TEJ, Rajab R, Manyonda I. (2014) Uterine sarcomas and myomectomy—a single institutions experience. (Unpublished Work)
Seidman MA, Oduyebo T, Muto MG, Crum CP, Nucci MR, Quade BJ (2012) Peritoneal dissemination complicating morcellation of uterine mesenchymal neoplasms. PLoS ONE 7(11):e50058
Rowland M, Lesnoch J, Edwards R, Richard S, Zom K, Sukumvanich P (2012) Occult uterine cancer in patients undergoing laparoscopic hysterectomy with morcellation. Gynecol Oncol 127(1):S29
Kamikabeya TS, Etchebehere RM, Nomelini RS, Murta EF (2010) Gynecological malignant neoplasias diagnosed after hysterectomy performed for leiomyoma in a university hospital. Eur J Gynaecol Oncol 31(6):651–653
Takamizawa S, Minakami H, Usui R, Noguchi S, Ohwada M, Suzuki M et al (1999) Risk of complications and uterine malignancies in women undergoing hysterectomy for presumed benign leiomyomas. Gynecol Obstet Investig 48(3):193–196
Parker WH, Fu YS, Berek JS (1994) Uterine sarcoma in patients operated on for presumed leiomyoma and rapidly growing leiomyoma. Obstet Gynecol 83:414–418
Leibsohn S, D′Ablaing G, Mishell DR Jr, Schlaerth JB (1990) Leiomyosarcoma in a series of hysterectomies performed for presumed uterine leiomyomas. Am J Obstet Gynecol 162:968–974, discus:968–974
Wright JD, Tergas AI, Burke WM, Cui RR, Ananth CV, Chen L et al. (2014) Uterine pathology in women undergoing minimally invasive hysterectomy using morcellation. JAMA 312(12):1253–1255
Paul GP, Naik SA, Madhu KN, Thomas T (2010) Complications of laparoscopic myomectomy: a single surgeon’s series of 1001 cases. Aust N Z J Obstet Gynaecol 50(4):385–390
Sizzi O, Rossetti A, Malzoni M, Minelli L, La GF, Soranna L et al (2007) Italian multicenter study on complications of laparoscopic myomectomy. J Minim Invasive Gynecol 14(4):453–462
Brolmann H, Hehenkamp WJK, Huirne JAF (2014) Heeft het myoom zijn onschuld verloren? Ned Tijdschr Obstet Gynaecol 127:322–325
Oduyebo T, Rauh-Hain AJ, Meserve EE, Seidman MA, Hinchcliff E, George S et al (2014) The value of re-exploration in patients with inadvertently morcellated uterine sarcoma. Gynecol Oncol 132(2):360–365
Amant F, Coosemans A, Debiec-Rychter M, Timmerman D, Vergote I (2009) Clinical management of uterine sarcomas. Lancet Oncol 10(12):1188–1198
Aviram R, Ochshorn Y, Markovitch O, Fishman A, Cohen I, Altaras MM et al (2005) Uterine sarcomas versus leiomyomas: gray-scale and Doppler sonographic findings. J Clin Ultrasound 33(1):10–13
Bell SW, Kempson RL, Hendrickson MR (1994) Problematic uterine smooth muscle neoplasms. A clinicopathologic study of 213 cases. Am J Surg Pathol 18(6):535–558
Cormio G, Loizzi V, Ceci O, Leone L, Selvaggi L, Bettocchi S (2014) Unsuspected diagnosis of uterine leiomyosarcoma after laparoscopic myomectomy. J Obstet Gynaecol. doi: 10.1016/j.jmig.2009.08.181
Dizon DS, Birrer MJ (2014) Advances in the diagnosis and treatment of uterine sarcomas. Discov Med 17(96):339–345
Evans HL, Chawla SP, Simpson C, Finn KP (1988) Smooth muscle neoplasms of the uterus other than ordinary leiomyoma. A study of 46 cases, with emphasis on diagnostic criteria and prognostic factors. Cancer 62(2239–2247):2239–2247
Exacoustos C, Romanini ME, Amadio A, Amoroso C, Szabolcs B, Zupi E et al (2007) Can gray-scale and color Doppler sonography differentiate between uterine leiomyosarcoma and leiomyoma? J Clin Ultrasound 35(8):449–457
Fukunishi H, Funaki K, Ikuma K, Kaji Y, Sugimura K, Kitazawa R et al (2007) Unsuspected uterine leiomyosarcoma: magnetic resonance imaging findings before and after focused ultrasound surgery. Int J Gynecol Cancer 17(3):724–728
Geyer H (1968) LDH isoenzymes in tumors of the human uterus. Klin Wochenschr 46(7):389–390
Giuntoli RL, Gostout BS, DiMarco CS, Metzinger DS, Keeney GL (2007) Diagnostic criteria for uterine smooth muscle tumors: leiomyoma variants associated with malignant behavior. J Reprod Med 52(11):1001–1010
Goto A, Takeuchi S, Sugimura K, Maruo T (2002) Usefulness of Gd-DTPA contrast-enhanced dynamic MRI and serum determination of LDH and its isozymes in the differential diagnosis of leiomyosarcoma from degenerated leiomyoma of the uterus. Int J Gynecol Cancer 12(4):354–361
Hadoux J, Morice P, Lhomme C, Duvillard P, Balleyguier C, Haie-Meder C et al (2013) Uterine leiomyosarcoma: epidemiology, pathology, biology, diagnosis, prognosis and treatment. Bull Cancer 100(9):903–915
Hata K, Hata T, Makihara K, Aoki S, Takamiya O, Kitao M et al (1990) Sonographic findings of uterine leiomyosarcoma. Gynecol Obstet Investig 30(4):242–245
Hata K, Hata T, Maruyama R, Hirai M (1997) Uterine sarcoma: can it be differentiated from uterine leiomyoma with Doppler ultrasonography? A preliminary report. Ultrasound Obstet Gynecol 9(2):101–104
Janus C, White M, Dottino P, Brodman M, Goodman H (1989) Uterine leiomyosarcoma–magnetic resonance imaging. Gynecol Oncol 32(1):79–81
Juang CM, Yen MS, Horng HC, Twu NF, Yu HC, Hsu WL (2006) Potential role of preoperative serum CA125 for the differential diagnosis between uterine leiomyoma and uterine leiomyosarcoma. Eur J Gynaecol Oncol 27(4):370–374
Kawamura N, Ichimura T, Ito F, Shibata S, Takahashi K, Tsujimura A et al (2002) Transcervical needle biopsy for the differential diagnosis between uterine sarcoma and leiomyoma. Cancer 94(6):1713–1720
Lusby K, Savannah KB, Demicco EG, Zhang Y, Ghadimi MP, Young ED et al (2013) Uterine leiomyosarcoma management, outcome, and associated molecular biomarkers: a single institution’s experience. Ann Surg Oncol 20(7):2364–2372
Melia P, Maestro C, Bruneton JN, Gasperoni A, Peyrottes I, Teissier E et al (1995) MRI of uterine leiomyosarcoma. Apropos of 2 cases. J Radiol 76(1):69–72
Milman D, Zalel Y, Biran H, Open M, Caspi B, Hagay Z et al (1998) Unsuspected uterine leiomyosarcoma discovered during treatment with a gonadotropin-releasing hormone analogue: a case report and literature review. Eur J Obstet Gynecol Reprod Biol 76(2):237–240
Murase E, Siegelman ES, Outwater EK, Perez-Jaffe LA, Tureck RW (1999) Uterine leiomyomas: histopathologic features, MR imaging findings, differential diagnosis, and treatment. Radiographics 19(5):1179–1197
Nappi L, Di Spiezio SA, Indraccolo U, Bettocchi S (2008) Hysteroscopic resection of uterine leiomyosarcoma: a case report and literature review. J Minim Invasive Gynecol 15(3):380–383
Pattani SJ, Kier R, Deal R, Luchansky E (1995) MRI of uterine leiomyosarcoma. Magn Reson Imaging 13(2):331–333
Posy HE, Elkas JC, Yemelyanova AV, Diaz-Montes TP, Bristow RE, Giuntoli RL (2009) Metastatic leiomyosarcoma diagnosed after uterine artery embolization. Eur J Gynaecol Oncol 30(2):199–202
Rauh-Hain JA, Oduyebo T, Diver EJ, Guseh SH, George S, Muto MG et al (2013) Uterine leiomyosarcoma: an updated series. Int J Gynecol Cancer 23(6):1036–1043
Takemori M, Nishimura R, Sugimura K (1992) Magnetic resonance imaging of uterine leiomyosarcoma. Arch Gynecol Obstet 251(4):215–218
Tulandi T, Ferenczy A (2014) Biopsy of uterine leiomyomata and frozen sections before laparoscopic morcellation. J Minim Invasive Gynecol 14:10
Ueda M, Otsuka M, Hatakenaka M, Torii Y (2000) Uterine endometrial stromal sarcoma located in uterine myometrium: MRI appearance. Eur Radiol 10(5):780–782
Ueda H, Togashi K, Konishi I, Kataoka ML, Koyama T, Fujiwara T et al (1999) Unusual appearances of uterine leiomyomas: MR imaging findings and their histopathologic backgrounds. Radiographics 19:S131–S145
Umesaki N, Tanaka T, Miyama M, Kawamura N, Ogita S, Kawabe J et al (2001) Positron emission tomography with (18) F-fluorodeoxyglucose of uterine sarcoma: a comparison with magnetic resonance imaging and power Doppler imaging. Gynecol Oncol 80(3):372–377
Vellanki VS, Rao M, Sunkavalli CB, Chinamotu RN, Kaja S (2010) A rare case of uterine leiomyosarcoma: a case report. J Med Case Rep 4:222. doi:10.1186/1752-1947-4-222-222-224
Widy-Kierska K, Roszkowski I (1969) LDH isoenzymes in patients with uterine tumors. Obstet Gynecol 33(2):173–176
Yanai H, Wani Y, Notohara K, Takada S, Yoshino T (2010) Uterine leiomyosarcoma arising in leiomyoma: clinicopathological study of four cases and literature review. Pathol Int 60(7):506–509
Zhang HJ, Zhan FH, Li YJ, Sun HR, Bai RJ, Gao S (2011) Fluorodeoxyglucose positron emission tomography/computed tomography and magnetic resonance imaging of uterine leiomyosarcomas: 2 cases report. Chin Med J (Engl) 124(14):2237–2240
Schwartz LB, Diamond MP, Schwartz PE (1993) Leiomyosarcomas: clinical presentation. Am J Obstet Gynecol 168:180–183
Schwartz LB, Diamond MP, Schwartz PE (1993) Leiomyosarcomas: clinical presentation. Am J Obstet Gynecol 168(1 Pt 1):180–183
Kawamura N, Iwanaga N, Hada S, Maeda K, Sumi T, Ishiko O et al (2001) Transient shrinkage of a uterine leiomyosarcoma treated with GnRH agonist for a presumed uterine leiomyoma: comparison of magnetic resonance imaging finding before and during GnRH agonist treatment. Oncol Rep 8(6):1255–1257
Wang PH, Lee WL, Chao HT, Shu LP, Kao HL, Wu CW et al (1999) Relationship between hormone receptor concentration and tumor shrinkage in uterine myoma after treatment with a GnRHa. Zhonghua Yi Xue Za Zhi (Tapei) 62(5):294–299
Yoshida Y, Kiyono Y, Tsujikawa T, Kurokawa T, Okazawa H, Kotsuji F (2011) Additional value of 16 alpha-[18F] fluoro-17 beta-oestradiol PET for differential diagnosis between uterine sarcoma and leiomyoma in patients with positive or equivocal findings on [18F] fluorodeoxyglucose PET. Eur J Nucl Med Mol Imaging 38(10):1824–1831
Bansal N, Herzog TJ, Burke W, Cohen CJ, Wright JD (2008) The utility of preoperative endometrial sampling for the detection of uterine sarcomas. Gynecol Oncol 110(1):43–48
Hansen NM, Ye X, Grube BJ, Giuliano AE (2004) Manipulation of the primary breast tumor and the incidence of sentinel node metastases from invasive breast cancer. Arch Surg 139(6):634–639
Martin RC, Scoggins CR, Ross MI, Reintgen DS, Noyes RD, Edwards MJ et al (2005) Is incisional biopsy of melanoma harmful? Am J Surg 190(6):913–917
Steiner RA, Wight E, Tadir Y, Haller U (1993) Electrical cutting device for laparoscopic removal of tissue from the abdominal cavity. Obstet Gynecol 81(3):471–474
Milad MP, Milad EA (2014) Laparoscopic morcellator-related complications. J Minim Invasive Gynecol 21(3):486–491
Milad MP, Sokol E (2003) Laparoscopic morcellator-related injuries. Am J Assoc Gynecol Laparosc 10(3):383–385
Nezhat C, Kho K (2010) Iatrogenic myomas: new class of myomas? J Minim Invasive Gynecol 17(5):544–550
Donnez O, Jadoul P, Squifflet J, Donnez J (2009) A series of 3190 laparoscopic hysterectomies for benign disease from 1990 to 2006: evaluation of complications compared with vaginal and abdominal procedures. BJOG 116(4):492–500
Cucinella G, Granese R, Calagna G, Somigliana E, Perino A (2011) Parasitic myomas after laparoscopic surgery: an emerging complication in the use of morcellator? Description of four cases. Fertil Steril 96(2):e90–e96
Leren V, Langebrekke A, Qvigstad E (2012) Parasitic leiomyomas after laparoscopic surgery with morcellation. Acta Obstet Gynecol Scand 91(10):1233–1236
Sinha R, Hegde A, Mahajan C, Dubey N, Sundaram M (2008) Laparoscopic myomectomy: do size, number, and location of the myomas form limiting factors for laparoscopic myomectomy? J Minim Invasive Gynecol 15(3):292–300
Ordulu Z, Dal CP, Chong WW, Choy KW, Lee C, Muto MG et al (2010) Disseminated peritoneal leiomyomatosis after laparoscopic supracervical hysterectomy with characteristic molecular cytogenetic findings of uterine leiomyoma. Genes Chromosom Cancer 49(12):1152–1160
Anupama R, Ahmad SZ, Kuriakose S, Vijaykumar DK, Pavithran K, Seethalekshmy NV (2011) Disseminated peritoneal leiomyosarcomas after laparoscopic “myomectomy” and morcellation. J Minim Invasive Gynecol 18(3):386–389
Della BC, Karini H (2010) Endometrial stromal sarcoma diagnosed after uterine morcellation in laparoscopic supracervical hysterectomy. J Minim Invasive Gynecol 17(6):791–793
Morice P, Rodriguez A, Rey A, Pautier P, Atallah D, Genestie C et al (2003) Prognostic value of initial surgical procedure for patients with uterine sarcoma: analysis of 123 patients. Eur J Gynaecol Oncol 24(3–4):237–240
Einstein MH, Barakat RR, Chi DS, Sonoda Y, Alektiar KM, Hensley ML et al (2008) Management of uterine malignancy found incidentally after supracervical hysterectomy or uterine morcellation for presumed benign disease. Int J Gynecol Cancer 18(5):1065–1070
Perri T, Korach J, Sadetzki S, Oberman B, Fridman E, Ben-Baruch G (2009) Uterine leiomyosarcoma: does the primary surgical procedure matter? Int J Gynecol Cancer 19(2):257–260
Park JY, Kim DY, Kim JH, Kim YM, Kim YT, Nam JH (2011) The impact of tumor morcellation during surgery on the outcomes of patients with apparently early low-grade endometrial stromal sarcoma of the uterus. Ann Surg Oncol 18(12):3453–3461
Park JY, Park SK, Kim DY, Kim JH, Kim YM, Kim YT et al (2011) The impact of tumor morcellation during surgery on the prognosis of patients with apparently early uterine leiomyosarcoma. Gynecol Oncol 122(2):255–259
Pritts E, Parker WH, Brow J, Olive DL (2014) Outcome of occult uterine leiomyosarcoma after surgery for presumed uterine fibroids: a systematic review. J Min Invasive Gynecol 22(1):26–33
Hagemann IS, Hagemann AR, LiVolsi VA, Montone KT, Chu CS (2011) Risk of occult malignancy in morcellated hysterectomy: a case series. Int J Gynecol Pathol 30(5):476–483
Rivard C, Salhadar A, Kenton K (2012) New challenges in detecting, grading, and staging endometrial cancer after uterine morcellation. J Minim Invasive Gynecol 19(3):313–316
Schneider A (1997) Recurrence of unclassifiable uterine cancer after modified laparoscopic hysterectomy with morcellation. Am J Obstet Gynecol 177(2):478–479
Cohen SL, Greenberg JA, Wang KC, Srouji SS, Gargiulo AR, Pozner CN et al (2014) Risk of leakage and tissue dissemination with various contained tissue extraction (CTE) techniques: an in vitro pilot study. J Minim Invasive Gynecol 14:10
Cohen SL, Einarsson JI, Wang KC, Brown D, Boruta D, Scheib SA et al (2014) Contained power morcellation within an insufflated isolation bag. Obstet Gynecol 124(3):491–497
Einarsson JI, Cohen SL, Fuchs N, Wang KC (2014) In bag morcellation (IBM). J Minim Invasive Gynecol 14:10
Favero G (2013) Tips and tricks for successful manual morcellation: a response to “vaginal morcellation: a new strategy for large gynecological malignant tumors extraction. A pilot study”. Gynecol Oncol 128(1):151
Wu SD, Lesani OA, Zhao LC, Johnston WK, Wolf JS Jr, Clayman RV et al (2009) A multi-institutional study on the safety and efficacy of specimen morcellation after laparoscopic radical nephrectomy for clinical stage T1 or T2 renal cell carcinoma. J Endourol 23(9):1513–1518
Barrett PH, Fentie DD, Taranger LA (1998) Laparoscopic radical nephrectomy with morcellation for renal cell carcinoma: the Saskatoon experience. Urology 52(1):23–28
Tsivian A, Sidi AA (2003) Port site metastases in urological laparoscopic surgery. J Urol 169(4):1213–1218
Parekh AR, Moran ME, Newkirk RE, Desai PJ, Calvano CJ (2000) Tissue removal utilizing steiner morcellator within a lapsac: effects of a fluid-filled environment. J Endourol 14(2):185–189
Meng MV, Koppie TM, Stoller ML (2003) Pathologic sampling of laparoscopically morcellated kidneys: a mathematical model. J Endourol 17(4):229–233
Arkenbout EA, van den Haak L, Driessen SR, Thurkow A.L., Jansen FW (2014) Assessing basic ‘physiology’ of the morcellation process and tissue spread: a time action analysis. J Minim Invasive Gynaecol. pii: S1553-4650(14)01448-4. doi: 10.1016/j.jmig.2014.10.009
Pitkin RM, Parker WH (2010) Operative laparoscopy: a second look after 18 years. Obstet Gynecol 115(5):890–891
We are grateful to the members of the ESGE steering committee on fibroid morcellation who are not in the author’s list for their critical comments: Andreas Thurkow, Bern Bojahr and Judith Huirne. Also thanks to Rhona O’Flaherty for the administrative support of this initiative.
Hans Brölmann-Protocol/manuscript writing/editing
Vasilis Tanos-Manuscript editing
Grigoris Grimbizis-Manuscript editing
Thomas Ind-Data collection and analysis, manuscript writing
Kevin Philips-Manuscript editing
Thierry van den Bosch-Data collection and analysis, manuscript writing
Samir Sawalhe-Data collection and analysis, manuscript writing
Lucas van den Haak-Data collection and analysis, manuscript writing
Frank-Willem Jansen-Data collection and analysis, manuscript writing
Johanna Pijnenburg-Data collection and analysis, manuscript writing
Florin-Andrei Taran-Data collection and analysis, manuscript writing
Sara Brucker-Data collection and analysis, manuscript writing
Arnaud Wattiez-Manuscript editing
Rudi Campo-Manuscript editing
Peter O’Donovan-Manuscript editing
Rudy-Leon de Wilde-Manuscript editing
Conflict of interest
Hans Brölmann, Vasilis Tanos, Grigoris Grimbizis, Thomas Ind, Kevin Philips, Thierry van den Bosch, Lucas van den Haak,Frank-Willem Jansen, Johanna Pijnenborg, Florin-Adrei Taran, Sara Brucker, Arnaud Wattiez, Rudi Campo, Peter O’Donovan and Rudy-Leon de Wilde declare that they have no conflict of interest with regards to the manuscript ‘options on fibroid morcellation; a literature review’. Samir Sawalhe is the designer of the Sawalhe II supercut morcellator manufactured by Storz.
Informed consent statement
This article does not contain any studies with human or animal subjects performed by the any of the authors.
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Brölmann, H., Tanos, V., Grimbizis, G. et al. Options on fibroid morcellation: a literature review. Gynecol Surg 12, 3–15 (2015). https://doi.org/10.1007/s10397-015-0878-4
- Leiomyoma uteri
- Endometrial stromal sarcoma
- Power morcellation