- Original Article
- Open Access
Symptomatic endometriosis developing several years after menopause in the absence of increased circulating estrogen concentrations: a systematic review and seven case reports
- Received: 23 September 2018
- Accepted: 10 January 2019
- Published: 15 February 2019
Abstract
Background
To review women with symptomatic and clinically progressive endometriosis after menopause in the absence of estrogen intake or excessive systemic endogenous production.
Design
Seven case reports and a systematic review of the literature from 1995 till February 2018.
Results
Only 7 case reports from the authors and 29 cases from the literature described women with either cystic ovarian or deep endometriosis. Severity, symptoms, and localization are highly variable. No case report describes symptomatic superficial typical lesions. In 22 of 36 women (61%), symptoms started more than 10 years after menopause.
Conclusions
Symptomatic and clinically progressive endometriosis after menopause in the absence of increased systemic estrogen concentrations or exogenous estrogen intake starts more than 10 years after menopause in the majority of women. This observation suggests that a genetic and/or epigenetic incident caused estrogen-independent progression, increased sensitivity to estrogens or increased local production of estrogens. This observation is important for understanding the pathophysiology of endometriosis, for the management of postmenopausal endometriosis, and for individualization of medical therapy of endometriosis since estrogen-independent endometriosis growth probably also occurs before menopause.
Keywords
- Endometriosis
- Pathophysiology of endometriosis
- Postmenopausal endometriosis
- Genetics
- Epigenetics
Introduction
Symptomatic endometriosis starting several years after menopause in women not taking hormone replacement therapy (HRT) is a rare condition. Case reports only describe women with increasing pain, ovarian masses, or intestinal symptoms suspicious of a cancer. This is consistent with Kempers’ [1] observations in 1960 on postmenopausal endometriosis. This was before estrogen assays, laparoscopy or ultrasound. Of all postmenopausal women operated for clinical symptoms between 1945 and 1958 in the Mayo clinic, endometriosis was found in 136 women, of whom 41 had symptoms compatible with endometriosis, 35 had an endometrioma, and 4 had progressive severe pain and/or bowel symptoms. The article in addition reported that in a control group of 50 hysterectomies, 8 atrophic endometriosis lesions were found.
Endometriosis is considered a hormonally responsive endometrium-like tissue where estrogens stimulate growth and progestins stop growth and eventually cause decidualization. It seems logical that after menopause endometriosis will become less active [2–4] since endometriosis is defined as (normal) endometrium-like tissue outside the uterus resulting from implantation of cells or endometrial fragments following retrograde menstruation [5]. However, the pathophysiology of endometriosis [6] is unclear and endometriosis may result from dislocation of basal endometrium [7] and metaplasia of peritoneal mesothelial cells [8] or of peritoneal or endometrial stem cells [9]. That endometriosis is phenotypically different from endometrium is according to the implantation/metaplasia theory, considered to be the consequence of the environmental factors in the peritoneal cavity, and of immunologic or of other predisposing factors.
The concept that endometriosis is a normal endometrium outside the uterus is not consistent with all clinical observations. The clinical, histologic, and immuno-cytochemical differences suggested that peritoneal, ovarian, and deep endometriosis are three different diseases [10]. The normal endometrium theory is not compatible with the clonal aspect of deep and cystic endometriosis [6]. Therefore, the endometriotic disease theory (EDT) [6, 11] and recently the genetic–epigenetic theory [12] suggest that the endometriotic cells are cells with a series of genetic or epigenetic transformations with epigenetic defined as “heritable changes in gene function that do not involve changes in the DNA sequence.” These changes can occur in either mature adult or neonatal endometrium [13] following retrograde menstruation, or in stem/progenitor cells from the endometrium [13] or from the peritoneal cavity or even in bone marrow cells [14–16]. The specific combination of genetic and epigenetic incidents will determine the development into typical, cystic, or deep endometriosis. Subtle lesions are considered a mixture of implanted normal endometrium and of early endometriosis which after additional genetic and/or epigenetic incidents can develop into more severe lesions.
Stimulated by the observation of two women with progressively increasing symptoms of endometriosis after menopause in the absence of increased estrogen secretion or intake, we decided to perform a systematic review of symptomatic postmenopausal endometriosis in the absence of increased systematic endogenous estrogen production or estrogen intake. The aim was to establish its prevalence and clinical presentation.
Materials and methods
Case reports and systematic review
Women with progressive endometriosis after menopause in the absence of estrogens
Patient | Age | Menopause | BMI, kg/m2 | Previous surgery | Medication | Indication for diagnosis | Final diagnosis | Comorbidities | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Age | Age | Type | Endo | Type | Months | Pain type | Pain increasing | Finding | E2, pg/ml | CA125, U/mL | CT | MRI | US | Surgery | |||||
Case report 1 | 72 | 54 | Spt | 65 | 4 | 0 | 0 | 3 | 1 | 1 | – | – | – | 3 | 3 | Diverticulitis | |||
Case report 2 | 64 | 51 | Surg | 37 | 51 | 2 | 3 | 0 | 3 | 1 | 1 + 2 + 3 | – | – | – | 3 | 3 | 3 | Diabetes, hypertension, obesity | |
Case report 3 | 62 | 45 | Spt | 31 | 57 | 3 | 1 | 3 | 3 | 1 | 1 + 3 | – | – | – | 3 | 3 | – | Hypertension, obesity | |
Case report 4 | 43 | 36 | Spt | 24 | 36 | 2 | 3 | 0 | 3 | 1 | 1 | – | – | – | 0 | 0 | 3 + 4 | ||
Case report 5 | 37 | 32 | Spt | 27 | 32 | 4 | 3 | 1 | 6 | 3 | 1 | 1 | – | – | – | 3 | 3 | – | Adenomyosis |
Case report 6 | 52 | 48 | Spt | – | 50 | 1 | 5 | 0 | – | 1 | 1 | – | – | – | – | 2 | 2 | ||
Case report 7 | 67 | 52 | Spt | 32 | No | 0 | – | 1 + 3 | – | – | – | 3 | 3 | 3 | Diverticulitis | ||||
Maeda [27] | 65 | *50* | Spt | – | 34 | 1 | 0 | 1 | 6 | – | – | 4 | < 10 | – | 6 | 6 | – | 3 | |
Manero [28] | 62 | 47 | Spt | – | No | 0 | – | – | 1 | – | 0 | – | – | 2 | 2 | ||||
Matsushima [29] | 56 | 50 | Spt | 31 | No | 0 | – | 1 | 3 | 12.6 | 48 | – | 6 | 6 | 2 | ||||
Rose e Silva 1 [30] | 62 | 48 | Spt | – | – | 0 | – | – | 1 | – | 8 | – | – | 2 | 2 | ||||
Rose e Silva 1 [30] | 78 | 58 | Spt | – | 58 | 1 | 0 | 0 | – | – | 0 | – | 6 | 6 | – | 6 | 5 | ||
Rose e Silva 1 [30] | 54 | 48 | Spt | – | – | 0 | – | – | 1 | – | 30 | – | – | 3 | 3 | Hypertension | |||
Medina [31] | 74 | 54 | Spt | 29 | No | 0 | 1 | 1 | – | 0 | – | – | 6 | 3 | |||||
Bellina [32] | 54 | 47 | Surg | – | 47 | 1 | 0 | 0 | – | – | 5 | 25 | – | – | – | 6 | 2 | ||
Izuishi [33] | 54 | 52 | Spt | – | No | 0 | – | – | 1 | – | Normal | 6 | – | – | 3 | ||||
Popoutchi [34] | 74 | 52 | Spt | – | 71 | 2 | 0 | 0 | – | – | 3 | – | – | 6 | – | – | 3 | Obesity | |
Torres-Rincón [35] | 49 | *50* | – | – | No | – | – | 5 | – | – | – | – | – | – | |||||
Deval [36] | 69 | *50* | Spt | 32 | No | 0 | 1 | 1 | 1 + 3 | – | 0 | – | 6 | 6 | 3 | ||||
Bidarmaghz [37] | 63 | 49 | Spt | – | No | 0 | 5 | – | – | 6 | – | – | 3 | ||||||
Gudla [38] | 63 | 48 | Surg | – | 48 | 2 | 0 | 0 | – | 1 | 5 | – | 19 | 6 | – | – | 3 | ||
Bailey [39] | 53 | 45 | Surg | 37 | 45 | 2 | 3 | 0 | – | – | 0 | 16 | – | 6 | 6 | – | 3 | Hypertension, obesity | |
Khong [40] | 62 | 50 | Surg | – | 50 | 2 | 2 + 5 | 0 | – | – | 4 | – | – | – | – | 3 | 3 | Hypertension | |
Zhuang [41] | 62 | *50* | Spt | – | No | 0 | 4 | – | – | 6 | – | – | 3 | ||||||
Rabinerson [42] | 58 | 52 | Spt | – | 43 | 4 | 0 | 0 | 3 | – | 15 | – | – | 3 | 3 | ||||
Jakhmola [43] | 50 | *48* | Spt | – | No | 0 | 2 | 1 | 1 | – | – | 6 | – | – | 4 | ||||
Bhat [44] | 50 | *48* | Surg | – | ? | 2 | 3 | 0 | 1 | 1 | 0 | – | 596 | 3 | – | – | 3 | ||
Suchonska [45] | 84 | 50 | Spt | – | No | 0 | 4 | – | 6 | – | 6 | 3 | Hypertension | ||||||
Agarwal Sharma [46] | 69 | *50* | Spt | – | No | 0 | – | – | 5 | – | 120 | 6 | – | 6 | 2 | ||||
Mohamed [47] | 60 | *50* | Spt | – | No | 0 | 1 | 1 | 5 | – | 0 | 6 | – | – | 3 | ||||
Plodeck [48] | 72 | *50* | Spt | – | ? | 1 | 0 | 0 | 2 | 1 | 5 | – | 0 | 6 | – | – | 3 | Hypertension | |
Flyckt [49] | 59 | 43 | Surg | 33 | 43 | 2 | 0 | 1 + 2 | 4 | – | – | 1 | 19 | – | 6 | – | – | – | |
Cameron [50] | 66 | 50 | Surg | 50 | 2 | 0 | 2 | 9 | 0 | – | – | 6 | – | – | 5 | ||||
Sasson [51] | 61 | 45 | Spt | 38 | 59 | 4 | 4 | 2 | 3 | – | 1 | 5 | 39 | 7 | 5 | – | 5 | 5 | |
Jaegle [52] | 62 | *50* | Spt | 41 | No | 3 | 43 | 4 | – | 38 | 6 | – | 6 | 4 | Hypertension, diabetes 2, obesity | ||||
Bese [53] | 74 | 50 | Spt | 30 | 61 | 5 | 3 | 3 + 5 | 24 | – | 0 | – | 64 | 6 | – | – | 3 + 6 | ||
The quality of evidence described in these case reports [17] is high since the descriptions have comprehensive details written by clinicians noting the uncommon finding during surgery in postmenopausal women of severe endometriosis in the absence of increased circulating estrogen concentrations. However, the reports obviously carry a publication bias, since only women with symptoms sufficiently severe to perform surgery and in whom severe endometriosis was found were published. This review does not draw conclusions on the prevalence of symptomatic endometriosis after menopause, which is likely much higher. We know that unexpected endometriosis is frequent in women undergoing surgery after menopause [1].
We asked our colleagues (see the “Acknowledgments” section) with a known interest and a large experience of severe endometriosis surgery to retrieve all women in whom they had performed surgery for postmenopausal endometriosis without increased estrogen production or estrogen intake. This resulted in five additional cases and in a few cases of whom the records could not be retrieved.
Types of endometriosis: definitions used
Endometriosis, defined as “endometrial-like glands and stroma outside the uterus,” can present as small microscopical lesions and macroscopically as subtle, typical, cystic, and deep lesions. Although the case reports of postmenopausal lesions described in this manuscript are limited to cystic ovarian endometriosis and larger nodules of deep endometriosis, the definitions used in this manuscript are as follows. Typical lesions are superficial (less than 5 mm) “powder burn” black dots in a fibrotic area. Subtle lesions are non-colored superficial lesions [18]. A discussion of the exact depth of subtle lesions, of their clinical significance [19], of the histological confirmation of biopsies [20], of Müllerianosis [21], and of the significance of larger areas with subtle lesions is beyond the scope of this article. Cystic endometrioses are the (larger) chocolate cysts of the ovary but not the smaller (3–6 mm) cysts under the peritoneum or close to the vagina in deep endometriosis. Deep endometriosis is defined as endometriosis deeper than 5 mm under the peritoneal surface [22]. A discussion of the limitations of depth to define deep endometriosis [12] is beyond the scope of this manuscript.
Results
Case reports of postmenopausal endometriosis in women without estrogen intake or signs of endogenous estrogen production
Only seven case reports could be collected, and ten surgeons did not remember having seen such cases.
Case 1 (FA)
A 72-year-old woman with spontaneous menopause at age 54 was referred for increasing pelvic pain. She had her menarche at 11 years and did not have antecedents of dysmenorrhea, dyspareunia, dysuria, dyschezia, endometriosis, nor infertility. Her medical, surgical, and gynecological history was uneventful except a diverticulitis and a volvulus 6 years before. She had never taken hormone replacement therapy (HRT), and the vaginal epithelium was atrophic. The gynecological exam and a transvaginal ultrasound confirmed a normal uterus and ovaries. However, it also showed a 1-cm arciform thickening at the insertion of the right uterosacral ligament and a 24-mm nodule at 11 cm from the anus, on the recto-sigmoid, infiltrating the muscularis and affecting 15% of the circumference of the bowel. In the absence of other signs of malignancy, a laparoscopy was performed with a total hysterectomy, bilateral salpingo-oophorectomy, a segmental resection of the bowel, and a resection of the retro-cervical and right pararectal nodule. The pathology revealed active endometriotic glands and stroma in the retro-cervical and right pararectal nodules. The bowel lesion had fibrosis secondary to diverticulitis. Recovery was uneventful, and she was discharged on day 5. After 4 weeks, she returned to her normal activities and is pain free.
Case 2 (FA)
A 64-year-old woman with spontaneous menopause at age 50 was referred for increasing pelvic pain, dyspareunia, dyschezia, and repetitive constipation which had started some 5 years ago. She was a G3 P1 A2 with menarche at 11 years of age and a BMI of 37. At age 51, she had been operated for abdominal pain, nausea, and a large endometriotic mass close to the left kidney with signs of renal failure. An abdominal total hysterectomy with bilateral salpingo-oophorectomy and left nephrectomy had confirmed the diagnosis of endometriosis. She never had taken HRT, and the vaginal epithelium was atrophic. Clinical exam revealed a large painful nodule. MRI showed two nodules: one large nodule in the pouch of Douglas, invading the vaginal cuff and left parametrium and extending up to the hypogastric plexus and the left sacral nerves (S3 and S4); another nodule of 37 × 32 × 14 mm was seen in the rectum at 7.9 cm from the anal border, infiltrating the muscularis and submucosa. Transvaginal ultrasound examination confirmed a 35 × 28 × 23 mm nodule in the vaginal cuff and a 41 × 10 × 19 mm nodule in the recto-sigmoid, compromising 50% of the circumference, infiltrating the muscularis and submucosa at 9 cm from the anal border. A laparoscopic segmental bowel resection and resection of the deep endometriosis nodule invading the pelvic floor, the sacral nerves, and the left sciatic nerve confirmed the diagnosis of endometriosis. Postoperative recovery was uneventful, and she was discharged on day 5 and is pain free for 5 months.
Case 3 (FA)
A 62-year-old woman with spontaneous menopause at age 45 was seen for increasing severe pelvic pain (10/10) and rectal pain with tenesmus. She was a P3G3 with menarche at age 13, a BMI of 31, and hypertension. She had not taken HRT since menopause, and the vagina was atrophic. Four years before, she had undergone a recto-sigmoidectomy with resection of an endometriosis nodule from the right uterosacral ligament and rectovaginal septum. Not responding to treatment with GnRha after surgery, she returned in 2017. At MRI, a retro-cervical nodule infiltrating the apical portion of the vagina and a nodule (17 × 06 mm) in the sigmoid were found. Ultrasonography confirmed the rectovaginal (15 × 4 mm) and the recto-sigmoid nodule (17 × 7 × 3 mm), compromising 25% of the circumference and infiltrating the muscularis. She is planned for surgery.
Case 4 (AU)
A 43-year-old woman with surgical menopause at age 36 visited for increasing severe pain symptoms for 2 years. She was a P2G2 with menarche at 11 years and a BMI of 24. She had undergone a hysterectomy at age 34 for pain and a bilateral adnexectomy at age 36 for pain and endometriosis, after which she was pain free for 5 years. She had not taken HRT postoperatively, and her vagina was atrophic. The gynecological examination, MRI, and ultrasound were negative. A diagnostic laparoscopy revealed a large pelvic endometriosis plaque (5 × 4 cm) with small cystic spots (3–5 mm) in the pouch of Douglas and a deep endometriosis (1 × 1 cm) nodule around the right ureter, all of which were removed during the procedure. Pathology confirmed the diagnosis of endometriosis. The postoperative recovery was uneventful, and she is pain free for 1 year.
Case 5 (AU)
A 37-year-old woman with spontaneous menopause at age 32 visited for increasing pain symptoms for 1 year. She was a P0G0 with a menarche at age 9 and a BMI of 27. At 23 years of age, she had undergone an adnexectomy for pain, and at age 27, we removed a rectovaginal deep endometriosis nodule extending around the left ureter (3 × 2 × 2 cm) and a cystic ovarian endometriosis from the remaining ovary. At age 32, a hysterectomy without ovariectomy was performed. Postoperatively, she became menopausal with increased FSH concentrations and a 17b-estradiol concentration of 80 pgr/ml, which is insufficient for endometrial proliferation. Following hysterectomy, she was pain free for 4 years, after which she had progressively increasing pelvic pain on no hormonal therapy. Her clinical examination, MRI, and ultrasound demonstrated a 4 × 4 cm deep endometriosis nodule of the cecum. In order to avoid a fourth surgical intervention, she was treated with GnRha without success. We plan to try an aromatase inhibitor.
Case 6 (LA)
A 52-year-old woman with spontaneous menopause at age 48 visited for increasing pain symptoms for 1 year. She was a P3G8. At age 50, she had undergone a total laparoscopic hysterectomy because of pain and an adenomyotic uterus. She had not taken HRT, and clinical examination demonstrated vaginal atrophy. A large cystic ovarian endometriosis was diagnosed. The pathology of the excised cyst confirmed the endometriosis. The postoperative recovery was uneventful, and she now is pain free for 4 months.
Case 7 (MM)
A 67-year-old woman with spontaneous menopause at age 52 was referred because of chronic pelvic pain, dyschezia, dyspareunia intermittent diarrhea since several years, and a suspicion of vaginal fornix endometriosis. She was a P0G0 with menarche at 12 years, a BMI of 32, and a history of sigmoid diverticulosis. She had not been taking HRT since menopause. The clinical examination revealed a vaginally visible retro-cervical nodule extending to the left parametrium. By ultrasonography, this nodule (18 × 11 × 29 mm) was confirmed together with another nodule (16 × 5 × 12 mm) at 8-cm distance from the anal verge. In addition to adenomyosis, a thickened endometrial layer suggestive for a polypoid hyperplasia, normal ovaries, and severe adnexal adhesions were found. MRI confirmed the retro-para-cervical nodule. After confirmation of endometrial hyperplasia without atypia on endometrial biopsy, a laparoscopic adhesiolysis, total hysterectomy, bilateral salpingo-oophorectomy, ureterolysis with resection of the retro-para-cervical and vaginal bowel nodule, and shaving of a small rectal nodule were performed. Adenomyosis and deep infiltrating endometriosis were confirmed at histopathologic evaluation. The postoperative recovery was uneventful, and she was discharged on day 2. She is pain free for 2 years without signs of recurrence both clinically and at US.
A systematic review of clinically progressive postmenopausal endometriosis without estrogen intake or increased production
Women with progressive and symptomatic endometriosis after menopause (this series) and women operated after menopause in whom endometriosis was found (Kempers). The frequency distribution of the years after menopause and/or the age of the women is indicated
Our review found 29 women (Table 1) with progressively increasing symptoms after menopause in whom endometriosis was diagnosed in the absence of HRT intake or an increased endogenous estrogen production. The symptoms are variable and comprise increasing pain with urinary symptoms [26], an asymptomatic cystic ovarian endometrioma or a cystic ovarian endometrioma with pain [27–31], a small bowel obstruction [32, 33], a rectovaginal deep endometriosis [29, 34], a sigmoid deep endometriosis [35], even a sigmoid obstruction more than 10 years after menopause [36], a deep endometriosis with progressive hydronefrosis [37], with renal failure [38] and with severe hypertension [39], urinary bleeding with an hydronephrosis and a polypoid intra-ureteral lesion [40], a vaginal endometriotic cyst [41], a lesion mimicking a bowel tumor [42], or an abdominal hemorrhage [43]. Some women were preoperatively suspected to have a cancer either an adenocarcinoma [44] or a disseminated ovarian cancer although during surgery only superficial endometriosis lesions together with bilaterally large endometriomas were found [45]. Even endometriosis suspicious of a gastric cancer [46] or of a pancreatic tumor in a 69-year-old woman [47], endometriosis with inferior vena cava involvement [48], and endometriosis in the abdominal wall were described. A nodular wall endometriosis developed in a woman without ovarian function treated with an aromatase inhibitor for breast cancer [49]. A new cystic endometrioma in the wall appeared spontaneously after the excision of two previous cysts. Plasma concentrations of 17b-estradiol were low (20–40 pg/ml); cyst fluid concentrations were 80 pg/ml returning to normal after GnRha treatment [50]. A series of reports describe progressive endometriosis in women taking tamoxifen [51–54].
Figure 1 illustrates that a majority of women were over 60 years old and more than 10 years after menopause.
The treatment of symptomatic postmenopausal endometriosis seems to be surgical excision. If this cannot be performed, a treatment with aromatase inhibitors was suggested [55].
Discussion
The article of Kempers [1] and the three reviews on endometriosis found in women undergoing surgery after menopause [23–25] describe postmenopausal women who did not take HRT. It is not surprising that the prevalence decreases with age (Fig. 1) since the age of menopause is variable and since ovarian activity can be intermittently increased in the first years after menopause. Unfortunately, the number of years since menopause is not always available. In addition, it is difficult to know whether the indication for surgery had been endometriosis, whether pain was caused by endometriosis, or whether endometriosis was a plausible explanation after surgery. They remain, however, remarkable documents with a detailed description of the clinical importance of endometriosis in women undergoing surgery after menopause [1]. The importance of postmenopausal endometriosis is also emphasized in this review of contemporary articles. Endometriosis was considered to be the cause of postmenopausal surgery in 13 women out of 516 surgeries by Scott and Te Linde [56] and in 37 out of 1000 by Henriksen [57]. To interpret these data collected more than 60 years ago, we should remember that this was before the introduction of hormone replacement therapy, estrogen assays, or ultrasound and with little knowledge of endocrinology such as peripheral conversion to estrogens and the intermittent and variable ovarian activity during the first years after menopause. This explains Kempers’ conclusion that these women must have had estrogen production somewhere. He also clearly demonstrates that most women were young and (probably) early after menopause. Differences in life expectancy cannot explain the differences between the data in the Kempers’ article and in this article since life expectancy after menopause was estimated to be 27 years in 1955 and 33 years today [58].
Our series describe women with progressive symptoms after menopause in whom endometriosis was diagnosed in the absence of estrogen intake or increased endogenous production. This is a rare condition, limited to case reports. Notwithstanding all limitations imposed by a recall bias, this also seems to be a rare condition when asking surgeons with a large experience in endometriosis surgery. The biphasic frequency distribution of age and years after menopause moreover suggests two different endometriosis populations. The high incidence of endometriosis in women younger than 55 years old or early after menopause and decreasing thereafter is compatible with an estrogen-responsive tissue. The second group after 60 years or more than 10 years after menopause can only be explained by circulating estrogen-independent progression of endometriosis or a change in estrogen sensitivity or local production of estrogens. In more than half of the women, symptoms started more than 10 years after menopause. That women clearly remember when symptoms started moreover suggests that the progression of these endometriosis lesions started abruptly at a specific point in time after menopause. This observation in postmenopausal women can be explained by the occurrence of a new genetic or epigenetic incident as postulated by the genetic–epigenetic theory to be the pathophysiology of endometriosis [12]. That such an incident is more likely to occur in women with a predisposition and with previous genetic–epigenetic incidents is supported by the observation that most of these women had been diagnosed with endometriosis before menopause. This genetic–epigenetic instability also is fully compatible with the rare occurrences of malignant transformation of endometriosis after menopause [59].
It is surprising that all reports of clinically progressive postmenopausal endometriosis lesions were either cystic ovarian endometriosis or deep endometriosis, without a single case report of clinically progressive superficial endometriosis. This contrasts with the high prevalence of typical lesions in premenopausal women who undergo a diagnostic laparoscopy for chronic pain. It is unclear, whether these women have less severe pain, and thus is not reported. The absence of reports thus can be a publication bias. An alternative explanation could be that after menopause typical lesions no longer cause pain. Only deep and cystic ovarian endometriosis seem to carry the risk that additional genetic or epigenetic incidents cause them to start proliferation in the absence of increased circulating estrogens.
Our series permits the conclusion that (some) cystic or deep endometriosis lesions can progress notwithstanding the low postmenopausal estrogen concentrations which are insufficient to stimulate the endometrium or to lubricate the vagina. Conversion of precursor steroids to estrogens in peripheral tissue, especially fat, might have played a role in some cases, as in the seventh case report with endometrial hyperplasia and obesity. In most cases, however, peripheral conversion as a cause of endometriosis progression is unlikely considering the absence of endometrial stimulation and the onset of symptoms many years after menopause in non-obese women. An alternative explanation could be a local estrogen production within the endometriosis lesions. Aromatase activity with local estrogen production and/or progesterone resistance in endometriosis lesions of young women are well known, although not yet described in postmenopausal endometriosis. The mechanism and pathways for this aromatase activity and local estrogen production and lack of apoptosis are moreover increasingly viewed as the result of genetic and/or epigenetic incidents or genetic polymorphism [2, 60–62]. The case report of the wall endometrioma in a postmenopausal woman [50] confirms aromatase activity because of the increased, although still below 100 pg/ml, estrogen concentration in the cyst fluid.
These endometriosis lesions with progressive symptoms and starting often more than 10 years after menopause strongly suggest heterogeneity of cystic and deep endometriosis. Indeed, most cystic and deep endometriosis lesions are stimulated by estrogens and growth will be inhibited by progestins. This is moreover indirectly confirmed by the many reports of endometriosis in postmenopausal women taking hormone replacement therapy. However, some lesions grow in the absence of increased estrogen concentrations in plasma. The frequency of these circulating estrogen-independent lesions before menopause is unknown since they will only be diagnosed after menopause. This heterogeneity in cystic and deep endometriosis moreover is consistent with clinical observations during surgery. Heterogeneity of endometriosis lesions is also consistent with the variable response to medical therapy. Whereas the response of the endometrium to estrogens and progestins is predictable, pain relief of endometriosis by medical therapy is much more variable. The occasional progression of deep endometriosis [63] or the severe bleedings [64] during pregnancy also supports heterogeneity of lesions.
These rare symptomatic and progressive cases of endometriosis after menopause, starting more than 10 years after menopause, and the heterogeneity of cystic and deep endometriosis lesions and the heterogeneity in aromatase activity and progesterone resistance in endometriosis lesions can be explained with the genetic–epigenetic theory [6, 12], postulating a cumulative series of genetic or epigenetic incidents in the pathophysiology of endometriosis. Predisposition or susceptibility of endometriosis is considered to be caused by genetic and epigenetic incidents transmitted at birth. The transmitted incidents are insufficient to express the disease, but a woman with more severe transmitted incidents is at higher risk to develop the disease when additional incidents occur later. The many differences in the endometrium of women with and without endometriosis can be considered as the expression of these incidents transmitted at birth. The variable genetic and/or epigenetic incidents can explain that endometriosis is heterogeneous. It also can explain that the growth of endometriosis can occur notwithstanding low circulating estrogen concentrations as evidenced by this series and by endometriosis in a man [65] not taking estrogens (the other six reported cases of endometriosis were in men who had been taking estrogens for prostate cancer [66]). The onset of these progressive and symptomatic lesions more than 10 years after menopause suggests that new or additional incidents did occur. This poly-genetic and poly-epigenetic concept of pathophysiology of endometriotic disease also is fully compatible with recent histochemical profiling of endometriosis [67] and the induction of epigenetic changes in endometriosis [68].
Already in 1960 [1], Kempers described a series of women with active adenomyosis after menopause. Although the relationship between adenomyosis and endometriosis remains unclear, a similar pathogenesis of a combination of a series of genetic and/or epigenetic incidents can be postulated [69].
In conclusion, postmenopausal endometriosis progressing in the absence of estrogen intake or of a systemic increased production is an argument for the genetic–epigenetic theory to explain the pathophysiology of endometriosis. These lesions thus should be considered a benign tumor and no longer as normal endometrium or as “normal” metaplastic cells with an abnormal behavior because of the environment or of the immunology. The direct clinical consequences of endometriosis progressing after menopause in the absence of increased estrogen concentrations are the heterogeneity of endometriosis lesions with a variable reaction during pregnancy and a variable response to medical therapy. Since this circulating estrogen-independent growth probably also occurs before menopause, women with medical therapy need an individual follow-up and therapy should be reconsidered when lesions grow. After menopause, it is important to recognize these lesions as different from a cancer.
Conclusions
Postmenopausal endometriosis can start to progress more than 10 years after menopause in the absence of estrogen intake or of a systemic increased production. This suggests that an acute genetic or epigenetic incident happened. The exact mechanism is not known, and it is unclear whether the growth of these lesions is estrogen independent or the consequence or an altered estrogen sensitivity or of an altered estrogen production within the lesion. It is unclear whether these are new lesions or a change in existing lesions. This observation can be explained by the genetic–epigenetic theory which considers the pathophysiology of endometriosis as a cumulative series of genetic or epigenetic incidents. That the specific set of incidents is specific for each lesion can explain the heterogeneity of endometriosis lesions. After menopause, only incidents which stimulate growth in the absence of increased circulating estrogens will become clinically symptomatic. These lesions thus should be considered a benign tumor and not as “normal” metaplastic cells with an abnormal behavior because of the environment or of the immunology.
Declarations
Acknowledgements
We thank Mauricio Abrao (Sao Paulo), Jacques Donnez (Belgium), Victor Gomel (Canada), Jörg Keckstein (Austria), Ceana and Camran Nezhat (USA), Antonio Setubal (Lisbon), Charles Koh (USA), Harry Reich and Assia Stepanian (USA) Arnaud Wattiez (Dubai) and Errico Zupi (Italy). Unfortunately they could not retrieve additional case reports.
Funding
No funding
Availability of data and materials
Records of case reports are available with the authors as indicated
Authors’ contributions
FAA, PK, and AU contributed to the conception and design of the study. FAA, PA, and PK contributed to the acquisition of the data. All authors contributed to the drafting and revision and final approval of the manuscript.
Ethics approval and consent to participate
Not applicable
Consent for publication
All authors agreed for publication
Competing interests
The authors declare that they have no competing interests.
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