Synchronous Bilateral Ovarian Mesonephric-like Adenocarcinomas with Separate Origins from High-Grade Mullerian Adenosarcoma and Endometriosis: Report of a Rare Case.

IF 1.6 4区 医学 Q3 OBSTETRICS & GYNECOLOGY
Zitong Zhao, Ravichandran Nadarajah, Inny Busmanis
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Abstract

Mesonephric-like adenocarcinoma (MLA) of the ovary is a recently recognized, rare malignancy with aggressive clinical behavior, and is thought to originate from Mullerian epithelium with mesonephric transdifferentiation. Emerging evidence suggests that MLA may be classified as an endometriosis-associated neoplasm. The presence of a sarcomatous component within MLA is extremely rare, with common differential diagnoses including the spindle cell component of MLA, carcinosarcoma, as well as mixed Mullerian adenocarcinoma and adenosarcoma. Herein, we report a 58-year-old Chinese woman with bilateral ovarian solid-cystic masses. The left ovarian mass comprised a biphasic tumor with a predominantly high-grade sarcomatous component displaying heterologous mesenchymal differentiation, including liposarcoma, rhabdomyosarcoma and chondrosarcoma-like areas, with a null-type p53 expression. The epithelial component ranged from a bland appearance in areas diagnostic of adenosarcoma to a clearly invasive carcinoma, both with mesonephric-like phenotype, being negative for estrogen receptor, progesterone receptor, and Wilms' tumor 1, variably positive for paired box gene 8, GATA binding protein 3, and thyroid transcription factor 1, with a wild-type p53 expression. The differing p53 expression between the epithelial and sarcomatous elements mitigated against a diagnosis of carcinosarcoma. The right ovarian mass showed endometriosis with focal direct evidence of the development of malignancy within a benign endometriotic cyst, exhibiting the identical immunoprofile of MLA but originating as another malignancy. To the best of our knowledge, this case represents the first reported case of synchronous bilateral ovarian MLAs with separate origins, from high-grade Mullerian adenosarcoma and endometriosis respectively, which broadens the morphologic spectrum of MLA and provides further evidence supporting the Mullerian origin theory.

高级别穆勒管腺肉瘤和子宫内膜异位症不同来源的同步性双侧卵巢中肾样腺癌:一例罕见病例报告。
卵巢中肾样腺癌(MLA)是一种最近发现的罕见恶性肿瘤,具有侵袭性临床行为,被认为起源于中肾转分化的穆勒管上皮。新出现的证据表明MLA可能被归类为子宫内膜异位症相关肿瘤。MLA中存在肉瘤成分的情况极为罕见,常见的鉴别诊断包括MLA的梭形细胞成分、癌肉瘤以及混合型穆勒腺癌和腺肉瘤。在此,我们报告一位58岁的中国女性双侧卵巢实性囊性肿块。左侧卵巢肿块包括一个双相肿瘤,主要为高级肉瘤成分,显示异源间充质分化,包括脂肪肉瘤、横纹肌肉瘤和软骨肉瘤样区域,p53表达为无效型。上皮成分从腺肉瘤诊断区域的平淡外观到明显的浸润性癌,均具有中肾样表型,雌激素受体、孕激素受体和威尔姆斯肿瘤1呈阴性,配对盒基因8、GATA结合蛋白3和甲状腺转录因子1呈可变阳性,野生型p53表达。上皮细胞和肉瘤细胞之间p53表达的差异减轻了癌肉瘤的诊断。右侧卵巢肿块显示子宫内膜异位症,有灶性直接证据表明良性子宫内膜异位囊肿内发生了恶性肿瘤,表现出与MLA相同的免疫特征,但起源于另一种恶性肿瘤。据我们所知,该病例代表了第一例报告的同步性双侧卵巢MLA,分别来自高级穆勒氏腺肉瘤和子宫内膜异位症,这拓宽了MLA的形态学范围,并为支持穆勒氏起源理论提供了进一步的证据。
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来源期刊
CiteScore
3.90
自引率
12.50%
发文量
154
审稿时长
6-12 weeks
期刊介绍: International Journal of Gynecological Pathology is the official journal of the International Society of Gynecological Pathologists (ISGyP), and provides complete and timely coverage of advances in the understanding and management of gynecological disease. Emphasis is placed on investigations in the field of anatomic pathology. Articles devoted to experimental or animal pathology clearly relevant to an understanding of human disease are published, as are pathological and clinicopathological studies and individual case reports that offer new insights.
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