孕妇卵巢微囊性间质瘤,以奇异核为主。

IF 0.7 Q4 PATHOLOGY Case Reports in Pathology Pub Date : 2022-01-01 DOI:10.1155/2022/8457901
Tip Pongsuvareeyakul, Chalita Kingnate, Kornkanok Sukpan, Surapan Khunamornpong
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摘要

微囊性间质瘤(MST)是卵巢性索间质瘤中罕见的纯间质肿瘤。它的特征是明显的微囊状外观,肿瘤细胞温和。虽然大多数MST的病理诊断可以基于典型的组织形态学,但由于病理学家对MST的组织学谱不熟悉,以及MST对抑制素和calretinin(常用的性索间质标志物)的阴性,形态学变化的病例可能会给诊断带来挑战。MST与黏液上皮肿瘤共存极为罕见。我们提出的第一个病例,据我们所知,卵巢MST与主要奇异核共存粘液囊腺瘤的孕妇。本病例的组织形态学对诊断提出了挑战,并提出了多种卵巢恶性肿瘤包括非肿瘤性病变的鉴别诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Microcystic Stromal Tumor with Predominant Bizarre Nuclei of Ovary in a Pregnant Woman.

Microcystic stromal tumor (MST) is a rare type of pure stromal tumor in the category of ovarian sex cord-stromal tumors. It is characterized by a distinctive microcystic appearance with bland tumor cells. Although the pathological diagnosis can be straightforward based on the typical histomorphology in most MSTs, the cases with morphologic variation can pose a diagnostic challenge due to unfamiliarity of pathologists with the histologic spectrum of MST and its negativity for inhibin and calretinin, the commonly used sex cord-stromal markers. The coexistence between MST and mucinous epithelial tumor is extremely rare. We present the first case, to our knowledge, of ovarian MST with predominant bizarre nuclei coexisting with mucinous cystadenoma in a pregnant woman. The histomorphology in this case presents a diagnostic challenge and raises differential diagnosis for a wide variety of ovarian malignant neoplasms including nonneoplastic lesions.

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审稿时长
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