Clear cell carcinoma of the pelvic side wall arising from endometriosis

A 63 year-old (gravida 1, para 1) woman initially presented with a suspected left inguinal hernia in May 2017; The patient's medical history was significant for hypertension and hypercholesterolemia. The initial herniorrhaphy was performed by a general surgeon who aborted the procedure when he ascertained that the condition was not an inguinal hernia but instead, a malignant condition. During the attempt at intraoperative repair, a necrotic, cancerous mass was encountered. Following a review of histologic and imaging data, the lesion was presumed to be ovarian cancer. The patient's preoperative CA-125 was 470 U/mL; she then commenced with neoadjuvant intravenous chemotherapy encompassing paclitaxel (80 mg/m 2 ) on days 1, 8, and 15 of a 21-day cycle and carboplatin (AUC 6) on day 1. After the completion of two cycles of chemotherapy, the patient was taken to the Operating Room and underwent an exploratory laparotomy, total abdominal hysterectomy and bilateral salpingo-oophorectomy, total omentectomy, bilateral pelvic lymph node dissection, bilateral inguinal lymph node dissection, radical dissection of the left inguinal ligament with radical tumor debulking and mesh reconstruction. During an examination of the abdomen and pelvis, a 12 × 10 cm cystic and solid left inguinal mass was identified, which extended through the femoral canal into the abdominal cavity ( Fig. 1 ). The entire neoplasm was retroperitoneal, with visible, gross tumor at the distal iliac vessels and in the medial left inguinal space. There was evidence of both left pelvic and inguinal lymphadenopathy; furthermore, a pathologically, enlarged right inguinal lymph node, measuring approximately 4 cm, was noted with an absence of pathologic right pelvic and peri-aortic adenopathy. Fig. 1 Large complex solid and cystic mass that is arising from the left hemipelvic sidewall, and extending to the inguinal region and skin surface. Fig. 1 Large complex solid and cystic mass that is arising from the left hemipelvic sidewall, and extending to the inguinal region and skin surface. The patient's appendix, small and large bowel were all palpably normal. There was no visible evidence of endometriosis on the uterus or ovaries. The left ovary was normal and adjacent to the large retroperitoneal pelvic and inguinal mass. The disease was noted to be densely adherent to the external iliac vessels and fixed to the surrounding tissue, with minimal mobility. An incision was made over the left groin and approximately 300 mL of dark bloody fluid was aspirated; thereafter, a large, solid and cystic mass in the medial groin incision was visualized. The lesion was dissected, mobilized externally and ultimately delivered through the femoral canal into the abdomen. The remaining tumor and enlarged lymph nodes within the medial inguinal space were also excised. A left pelvic lymph node dissection, resection of proximal lymphatic tissue and removal of obturator nodes were also performed; this procedure was repeated on the contralateral side. Subsequently, a biologic mesh was inserted into the left pelvis, which was secured with 2–0 Vicryl and Tisseel. The right groin mass was completely excised; The patient tolerated the procedure well and was admitted to the Recovery Room in stable condition. The final pathology revealed Stage IVB clear cell carcinoma arising from endometriosis with a synchronous but apparently unrelated stage IA endometrial adenocarcinoma ( Fig. 2 a–d). There were also 5 pelvic lymph nodes positive for malignancy. The disease was confined to the retroperitoneal/inguinal mass, bilateral inguinal nodes, and left pelvic lymph nodes. The uterus, cervix, tubes, ovaries, and right pelvic nodes were normal. Following a molecular biomarker evaluation, her tumor was determined to be MSI stable, effectively precluding Lynch syndrome. Postoperatively, the patient was slated for radiotherapy and completion of her chemotherapy regimen. Fig. 2 a) Representative histologic section of endometrial lesion showing FIGO grade 1 endometrioid-type adenocarcinoma with abundant squamous morules (H&E; 40×); b) Focus of endometriosis associated with pelvic side wall lesion (H&E; 40×); c) Area of presumed endometriosis with hemosiderin deposition in association with clear cell carcinoma (arrows; H&E; 40×); d) High-power view of clear cell carcinoma (pelvic side wall lesion) with variable eosinophilic cytoplasm (eosinophilic variant of clear cell carcinoma) (H&E; 400×). Fig. 2 a) Representative histologic section of endometrial lesion showing FIGO grade 1 endometrioid-type adenocarcinoma with abundant squamous morules (H&E; 40×); b) Focus of endometriosis associated with pelvic side wall lesion (H&E; 40×); c) Area of presumed endometriosis with hemosiderin deposition in association with clear cell carcinoma (arrows; H&E; 40×); d) High-power view of clear cell carcinoma (pelvic side wall lesion) with variable eosinophilic cytoplasm (eosinophilic variant of clear cell carcinoma) (H&E; 400×).

All authors deny any conflict of interest associated with this manuscript.

Endometriosis undergoing malignant transformation is an extremely unusual finding. Sampson attributed this process to the disease's proximity to the neoplasm, exclusion of an additional primary site of malignancy, and the histologic appearance of endometrial stroma contiguous with epithelial glands ( Debus & Schuhmacher, 2001 ; Sampson, 1925 ). Additionally, prolonged exposure to unopposed estrogen has been implicated ( Agarwal & Subramanian, 2010 ; Debus & Schuhmacher, 2001 ). When endometriosis transitions to a malignant pathology, the ovary is commonly involved ( Agarwal & Subramanian, 2010 ). Conversely, abdominal wall carcinoma arising from endometriosis is exceedingly uncommon, with only 27 cases documented since 2014 ( Taburiaux et al., 2015 ). Carcinoma of the pelvic side wall originating from endometriosis is seemingly more atypical, as we were only able to identify two patients in the literature with this condition ( Leiserowitz et al., 2003 ). In the current study, we review the history of a woman diagnosed with clear cell carcinoma of the pelvic side wall with metastatic involvement of the medial groin, stemming from endometriosis. Endometriosis has been identified as a precursor of clear cell carcinoma, which presumably accounts for the higher incidence of this histologic subtype ( Taburiaux et al., 2015 ). The precipitant of the neoplastic event in the current study remains idiopathic, although one may conjecture that genetics, immunological or hormonal factors were contributing factors ( Marques et al., 2017 ). We can ultimately preclude the influence of estrogen therapy since the patient did not have a history of taking this medication. The clinical management of clear cell carcinoma of the pelvic side wall is indeterminate. Surgical treatment has reportedly been comprised of local resection, total abdominal hysterectomy or salpingo-oophorectomy ( Ijichi et al., 2014 ). In addition to definitive surgery, a regimen of carboplatin and paclitaxel has been considered effective at treating this malignancy ( Marques et al., 2017 ). Radiotherapy has also been reportedly beneficial in combination with platinum-based therapy for the treatment of endometriosis related cases of malignant transformation ( Mihailovici et al., 2017 ); moreover, radiotherapy is potentially indicated when addressing metastatic disease ( Macrie et al., 2014 ). Unfortunately, once a patient exhibits disease recurrence, secondary treatment is ostensibly ineffective ( Ijichi et al., 2014 ). When oncology physicians encounter primary and metastatic lesions in very unusual locations, they should consider the potential for malignant endometriosis in the differential diagnosis, especially in patients who have a history of endometriosis, underwent gynecologic surgery or were previously treated with hormone replacement therapy. Despite the remote incidence of pelvic side wall carcinoma arising from endometriosis, we recommend further study evaluating the optimal method in which to diagnose and manage this complicated disease.

Endometriosis is characterized by the presence of ectopic endometrial tissue. The condition, albeit benign, is often painful and a source of infertility in nearly 10–15% of reproductive-aged women ( Kavoussi et al., 2016 ). Endometriosis originates from metaplasia of the coelomic epithelium and has the potential to infiltrate distant areas via hematogenous and lymphatic dissemination ( Su et al., 2004 ). Endometriosis has been identified in the ovaries, pelvis, cervix, labia and vagina ( Agarwal & Subramanian, 2010 ); alternatively, uncommon implantation sites include the lung, bladder and within abdominal surgery scars ( Acién & Velasco, 2013 ; Bodner et al., 2003 ). In very rare cases, the disease undergoes malignant transformation, with documented rates approximating 0.3% to 1.0% ( Matter et al., 2003 ; Debus & Schuhmacher, 2001 ). When this neoplastic process arises, the disease typically is comprised of endometrioid or clear cell histology ( Ruiz et al., 2015 ; Bats et al., 2008 ). Endometriosis has been described in patients with a history of gynecologic surgery, namely following a caesarean section ( Horton et al., 2008 ). Nevertheless, it is quite unusual to encounter a carcinoma originating from endometriosis in the abdominal wall ( Marques et al., 2017 ; Taburiaux et al., 2015 ), let alone the pelvic side wall. Herein, we review a patient with clear cell carcinoma of the pelvic side wall, stemming from endometriosis.