A Rare Presentation of Polypoid Endometriosis of the Douglas Pouch: Case Report

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A case report describes a 46-year-old woman whose MRI revealed a mass suspicious for malignancy but was histologically diagnosed as a rare polypoid endometriosis lesion of the Douglas pouch.

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This case report describes a 46-year-old woman referred for MRI due to menometrorrhagia, in whom a solid 40 mm pelvic lesion near the uterus was incidentally discovered; the workup used MRI (including diffusion and dynamic contrast enhancement), follow-up ultrasound, and staging CT. Despite imaging features that suggested benign hemorrhagic content and no malignant signs (no lymphadenopathy, no diffusion restriction, and no concerning enhancement pattern), the lesion was suspected preoperatively to be an ovarian Granulosa cell tumor, leading to extensive surgery (hysterectomy and left salpingo-oophorectomy). Histopathology identified a benign polypoid endometriosis nodule arising from the Douglas pouch with endometrial glands and CD10-positive stromal component, and the report notes that MRI characteristics for polypoid endometriosis are not fully defined, limiting preoperative diagnosis. This paper is centrally about endometriosis — it documents a rare case of polypoid endometriosis in the Douglas pouch with associated adenomyosis findings.

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Abstract

A case is reported of a 46-year-old woman referred to a magnetic resonance imaging (MRI) for menometrorrhagia. MRI revealed a mass lesion lateral to the uterus fundus, suspicious of an ovarian granulosa cell tumor. Extensive surgery was performed. Histological examination revealed a polypoid endometriosis lesion arising from the Douglas pouch. Teaching point: Polypoid endometriosis is a rare benign entity with a challenging differential diagnosis from malignancy. Specific MRI features can contribute to the diagnosis and thus avoid excessive surgical resection.
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Introduction

Polypoid endometriosis is a rare variant of endometriosis first described in 1980 [1] and refers either to lesions that histologically look like endometrial polyps or to lesions that are histologically similar to endometriosis but with an exophytic growth [2]. These nodular lesions may occur at either surface of the ovary, digestive tract, uterine serosa, bladder, ureter, or pelvis peritoneum. We report a case of a polypoid endometriosis nodule arising from the Douglas pouch incidentally discovered on magnetic resonance imaging (MRI). Case report A 46-year-old female was referred for an MRI for menometrorrhagia. Her medical past history and pelvic examination were unremarkable. She had been using oral contraceptives for years. MRI (1.5T) showed a solid lesion left to the uterus, measuring 40 mm, with homogeneous intermediate T2-signal intensity similar to endometrium and hyperintense T1 spots after fat suppression, consistent with hemorrhagic content (Figure 1). This lesion seemed to be distinct from the left ovary and, no pedicle attached it to the uterus. No peritoneal carcinosis nodule and no lymphadenopathy were associated. The lesion showed no diffusion restriction (ADC 1.4) and progressive enhancement (type 1 curve compared with that of uterine myometrium), similar to that of endometrium (Figure 1). It was associated with thickening of the junctional zone, consistent with diffuse adenomyosis. In this context of adenomyosis associated with a solid homogeneous mass that presented hemorrhagic changes, the lesion was suspected to be an ovarian Granulosa cell tumor. Transvaginal ultrasound performed after MRI demonstrated that the lesion was mobilized when moving the ovary. The mass was diffusely hyperechoic, with the presence of a few bright spots that could correspond to microcysts (Figure 2). The staging computed tomography (CT) scan was negative and showed spontaneously dense spots in the mass on unenhanced scans, consistent with hemorrhagic changes (Figure 3). After clinical case discussion, the patient underwent extensive surgery (hysterectomy and left salpingo-oophorectomy) on the hypothesis of a malignant ovary tumor. A nodular lesion arising from the Douglas pouch was found, bleeding upon contact. There was no lesion arising from the ovary, fallopian tube, or uterus (Figure 4). Histopathological examination revealed a benign polypoid endometriosis nodule characterized by dilated endometrial glands with some cystic areas and a stromal component positive to CD10 in immunohistochemistry demonstrating its endometrial origin (Figure 5).

Discussion

Polypoid endometriosis is a benign and distinctive form of pelvic endometriosis not well known as it is rather uncommon. Only a limited cohorts are reported in the literature studying its histopathological and clinical aspects [2]. The differential diagnosis of malignancy is raised [3,4] as it can mimic ovarian tumors with peritoneal dissemination imaging and surgery. MRI features are not fully defined, rendering preoperative diagnosis difficult, especially in the absence of a known history of endometriosis. MRI characteristics found in the literature include polypoid lesions either single or multiple, often appearing hyperintense on T2-weighted sequences due to cystic glands dilatation [4 - 6]. Another MRI feature frequently reported is the presence of foci of hyperintensity on T1-fat suppressed sequences reflecting hemorrhage [7] and a peripheral T2 black rim sign demonstrating fibrous tissue surrounding the lesion [8]. No additional signs of malignancy are seen: no lymphadenopathy, high apparent diffusion coefficient (ADC) values on diffusion weighted imaging (DWI) and moderate enhancement on dynamic contrast enhanced-MRI (DCE-MRI). Coexisting adenomyosis is found to be frequent [8]. Interestingly, polypoid endometriosis commonly affects peri- to postmenopausal women, while traditional endometriosis predominates in premenopausal women. The present case is unique with regards to the completeness of its multimodality exploration. In conclusion, the definition of MRI-specific characteristics could help to evoke the benignity of the lesion and prevent overtreatment, especially in women of childbearing age.

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