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Port-site metastasis after diagnostic laparoscopy for presumably benign ruptured ovarian cyst: disseminated intraperitoneal metastasis of a Krukenberg tumor

Abstract

The occurrence of port-site metastasis (PSM) has been reported largely after surgical laparoscopy for gastrointestinal and gynecological carcinomas, mainly ovarian and cervical neoplasia. We present an uncommon case of a port-site metastasis after diagnostic laparoscopy for presumably benign ruptured ovarian cyst, which turned out to be a disseminated intraperitoneal metastasis of a Krukenberg tumor. Although such tumors are rare, every surgeon should be aware of their incidence, especially in relation to the clinical presentation, the younger patient age and peritoneal metastasis of an unknown primary tumor. Since the risk related to PSM after laparoscopic surgery for malignancy still has to be determined, preventive measures should be encouraged when laparoscopy is carried out and intraoperatively ascites or peritoneal carcinosis is being diagnosed.

Introduction

Laparoscopic surgery has become a very popular and widespread operating technique in gynecological surgery, representing one of the most important surgical innovations in the past 20 years. Minimally invasive surgery has many advantages compared to conventional laparotomy, including better cosmetic wound, reduced postoperative pain, shorter hospitalization and rapid recovery [1]. Nowadays, the use of laparoscopy has even been advocated for oncological operations since patients have a lower morbidity and shorter hospital stays [2, 3, 4]. However, with the widespread popularity of this technique, a new possible complication has become evident: the port-site metastasis (PSM). Occurrence of PSM has largely been reported after surgical laparoscopy for colonic or ovarian carcinomas [3, 4]. The incidence of PSM following laparoscopic surgery is estimated between 0 and 21% [5]. Wexner and Cohen [6] estimated the incidence of PSM to be approximately 4%, with a range between 1.5 to 21%. These results raised concern, since they were higher compared to the incidence of wound metastases after conventional surgery (approximately 0.7%) of operated cases [7]. However, an incidence of trocar metastases occurring in 0.7–1.1% of the cases was recently reported, with a correspondence to the known incidence of 0.8–1.6% incision metastases in conventional tumor surgery [8]. Furthermore, in a recent review, an overall incidence of 0.71% for PSM occurrence has been suggested [4]. The overall incidence of PSM in gynecologic cancers was estimated at 2.3%, with the highest risk being in patients with recurrence of ovarian or primary peritoneal malignancies undergoing procedures in the presence of ascites [9].

We report an extremely rare case of intraperitoneal carcinoma with abdominal wall invasion on the trocar site following diagnostic laparoscopic surgery for presumably ruptured ovarian cyst. Subsequent staging procedures revealed a Krukenberg tumor. This is, to our knowledge, the first report of a PSM of a peritoneal metastatic Krukenberg carcinoma.

Case report

A 30-year-old woman presented to a gynecological emergency department with acute lower abdominal pain. The medical history was unremarkable. The patient did not complain of nausea, vomiting, changing bowel function or weight loss. Ultrasound was significant for intra-abdominal fluid without any abdominal or pelvic mass. A diagnostic laparoscopy was performed for a presumably ruptured benign ovarian cyst. During the operation, yellowish ascites were noted, which presented throughout the peritoneum. Additionally, metastatic foci of a primarily unknown cancer at the diaphragm were noted, consistent with a peritoneal carcinoma. Both ovaries appeared to be slightly enlarged in size and shape, but no biopsy could be performed. The patient was then admitted to the reporting institution for further evaluation and therapy. She presented to our department with an approximately 5×4×4-cm, hard, non-tender, mobile mass at the left lower abdominal region of the trocar incision, suggesting a port-site metastasis of a malignant tumor. A gynecological ultrasound revealed abdominal ascites with slightly enlarged ovaries. The cytological examination of the punctured abdominal ascites revealed highly suspicious neoplastic cancer cells, without any information about the primary tumor site. A subsequent CT scan revealed peritoneal carcinosis with ascites, enlarged paravasal lymph nodes and ovaries, right pleura effusion and a tumor on the ventral part at the greater curve of the stomach between the corpus and antrum. These results were consistent with a metastatic gastric cancer (Krukenberg tumor). A subsequent gastroscopy showed an approximately 10-cm, hard gastric tumor with no stenosis. Multiple biopsies revealed only a reflux esophagitis and a gastric Helicobacter pylori infection. Due to the highly suspicious tumor, a second gastroscopy was performed and multiple biopsies were taken. These biopsies showed a poorly differentiated tumor of unknown origin. Further immunohistochemical analysis revealed a negative steroid receptor status, suggesting a primary gastric cancer metastatic to the ovaries. After adequate mobilization, the patient was dismissed and referred for further palliative chemotherapeutic treatment.

Discussion

We presented for the first time a case of port-site metastasis after diagnostic laparoscopy for a presumably benign ruptured ovarian cyst. Intraoperatively, disseminated intraperitoneal metastasis of an unknown primary tumor was diagnosed, revealing a Krukenberg tumor after staging procedures. The patient presented with lower abdominal pain without nausea or vomiting. Although ultrasound scan demonstrated free fluid within the abdomen, the laparoscopy was performed with the presumabe diagnosis of a ruptured ovarian cyst. Intraoperatively, the ovaries seemed to be slightly enlarged, but with no obvious clinical signs of an ovarian tumor. The rapid appearance of PSM within a couple of days since primary laparoscopy was suspicious of an aggressive tumor type. However, the disseminated intraperitoneal metastasis was suggestive of an unknown primary tumor rather than metastatic ovarian cancer.

PSM in gynecologic oncological surgery was first reported in 1978 [10], occurring after laparoscopic surgery for endometrial, fallopian tube, ovarian and cervical cancer [3, 4, 11]. Meanwhile, PSM have been described after laparoscopic surgery for several gastrointestinal carcinomas, including the gall bladder [12], colon [4] and stomach [13, 14]. Metastatic neoplasms are by far the most common tumors encountered in the female peritoneum [15]. Most are associated with known primary tumor sites, such as the ovary, gastrointestinal tract or breast. In a large survey of over 118,000 laparoscopic procedures, mainly cholecystectomies, just 4 cases of PSM after diagnosing gastric cancer with peritoneal metastasis were described [14]. Gastric carcinomas have the disposition to metastasize to the ovaries, mainly through lymphatic vessels. The first documented case by Krukenberg [16] consists of a report of neoplastic metastases to the ovaries of well-defined histology from the gastrointestinal tract. Meanwhile, it is recognized that Krukenberg tumors are rare events, occurring predominantly in premenopausal women [17], with 93% of the cases originating from the stomach [18]. Unfortunately, the prognosis for such tumors is unfavorable, with an average 5-year survival of 12% [19].

Several mechanisms have been suggested to explain the genesis etiology of PSM (Table 1). The two mechanisms that have been studied most intensively are the aerosolization of tumor cells into exhaust gas during laparoscopy and the direct spread of free intraperitoneal tumor cells due to contact with the instruments and/or trocars [20]. Other potential mechanisms for the development of PSM include hematogenous spread, direct wound implantation, surgical technique, tumor manipulation, pneumoperitoneum, pressure, CO2 insufflation and an impairment of the immune response of the patient (for review, see [3, 4, 11]). However, the precise etiological mechanisms of PSM still are not fully elucidated. Understanding the mechanisms of tumor implantation at the port site might lead to the creation of preventive strategies. However, the etiology of tumor implantation at the port site is not yet fully understood. Since the risk related to PSM after laparoscopic surgery for malignancy still has to be determined, preventive measures should be encouraged when laparoscopy is carried out.

Table 1 Possible risk factors contributing to port-site metastasis

Different measures have been proposed by several authors, including sufficient technical preparation (adequate equipment and technique), avoidance of gas leakage and tumor manipulation, use of retrieval bags for specimens as well as povidone-iodine irrigation of the laparoscopic instruments, the trocars and the port-site wounds (Table 2; for review see [3, 4, 11, 21]).

Table 2 Possible prevention measurements of port-site metastases

In conclusion, we presented an uncommon case of a port-site metastasis after diagnostic laparoscopy for presumably benign ruptured ovarian cyst, which turned out to be a disseminated intraperitoneal metastasis of a Krukenberg tumor. Although such tumors are rare, every surgeon should be aware of their incidence, especially of its relation to the clinical presentation, the younger patient age and peritoneal metastasis of an unknown primary tumor. Additionally, one should consider Krukenberg tumors as a differential diagnosis if a peritoneal metastasis is present without obvious signs of ovarian cancer. Since the risk related to port-site metastases after laparoscopic surgery for malignancy has still to be determined, preventive measures should be encouraged when laparoscopy is carried out and ascites or peritoneal carcinosis is being diagnosed intraoperatively. However, the feasibility, medical consequences and cost-effectiveness of such preventive measures are still unclear.

References

  1. Rock JA, Warshaw JR (1994) The history and future of operative laparoscopy. Am J Obstet Gynecol 170:7–11

    Google Scholar 

  2. Spirtos NM, Schlaerth JB, Gross GM, Spirtos TW, Schlaerth AC, Ballon SC (1996) Cost and quality-of-life analyses of surgery for early endometrial cancer: laparotomy versus laparoscopy. Am J Obstet Gynecol 174:1795–1799

    Google Scholar 

  3. Wang PH, Yuan CC, Lin G, Ng HT, Chao HT (1999) Risk factors contributing to early occurrence of port site metastases of laparoscopic surgery for malignancy. Gynecol Oncol 72:38–44

    Google Scholar 

  4. Ziprin P, Ridgway PF, Peck DH, Darzi AW (2002) The theories and realities of port-site metastases: a critical appraisal. J Am Coll Surg 195:395–408

    Google Scholar 

  5. Reymond MA, Schneider C, Kastl S, Hohenberger W, Kockerling F (1998) The pathogenesis of port-site recurrences. J Gastrointest Surg 2:406–414

    Google Scholar 

  6. Wexner SD, Cohen SM (1995) Port site metastases after laparoscopic colorectal surgery for cure of malignancy. Br J Surg 82:295–298

    Google Scholar 

  7. Reilly WT, Nelson H, Schroeder G, Wieand HS, Bolton J, O’Connell MJ (1996) Wound recurrence following conventional treatment of colorectal cancer. A rare but perhaps underestimated problem. Dis Colon Rectum 39:200–207

    Google Scholar 

  8. Müller JM (1999) Videoendoskopische Chirurgie. Dtsch Ärztebl 96A:1779–1782

  9. Nagarsheth NP, Rahaman J, Cohen CJ, Gretz H, Nezhat F (2004) The incidence of port-site metastases in gynecologic cancers. JSLS 8:133–139

    Google Scholar 

  10. Dobronte Z, Wittmann T, Karacsony G (1978) Rapid development of malignant metastases in the abdominal wall after laparoscopy. Endoscopy 10:127–130

    Google Scholar 

  11. Ramirez PT, Wolf JK, Levenback C (2003) Laparoscopic port-site metastases: etiology and prevention. Gynecol Oncol 91:179–189

    Google Scholar 

  12. Lundberg O, Kristoffersson A (1990) Port site metastases from gallbladder cancer after laparoscopic cholecystectomy. Results of a Swedish survey and review of published reports. Eur J Surg 165:215–222

    Google Scholar 

  13. Cava A, Roman J, Gonzalez Quintela A, Martin F, Aramburo P (1990) Subcutaneous metastasis following laparoscopy in gastric adenocarcinoma. Eur J Surg Oncol 16:63–67

    Google Scholar 

  14. Paolucci V, Schaeff B, Schneider M, Gutt C (1999) Tumor seeding following laparoscopy: international survey. World J Surg 23:989–995

    Google Scholar 

  15. Fox H (1993) Primary neoplasia of the female peritoneum. Histopathology 23:103–110

    Google Scholar 

  16. Krukenberg F (1896) Veber des fibroma ovarii mucocellulare. Arch Gynecol 50:287–290

    Google Scholar 

  17. McGill FM, Ritter DB, Rickard CS, Kaleya RN, Wadler S, Greston WM, O’Hanlan KA (1999) Krukenberg tumors: can management be improved? Gynecol Obstet Invest 48:61–65

    Google Scholar 

  18. Hale RW (1968) Krukenberg tumor of the ovaries. A review of 81 records. Obstet Gynecol 32:221–225

    Google Scholar 

  19. Webb M, Decker D, Mussey E (1975) Cancer metastatic to the ovary. Obstet Gynecol 45:391–394

    Google Scholar 

  20. Hewett PJ, Thomas WM, King G, Eaton M (1996) Intraperitoneal cell movement during abdominal carbon dioxide insufflation and laparoscopy. An in vivo model. Dis Colon Rectum 39:S62–S66

    Google Scholar 

  21. Tjalma WA (2003) Laparoscopic surgery and port-site metastases: routine measurements to reduce the risk. Eur J Gynaecol Oncol 24:236

    Google Scholar 

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Mylonas, I., Lochmüller, EM., Greulich, T. et al. Port-site metastasis after diagnostic laparoscopy for presumably benign ruptured ovarian cyst: disseminated intraperitoneal metastasis of a Krukenberg tumor. Gynecol Surg 1, 267–269 (2004). https://doi.org/10.1007/s10397-004-0052-x

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