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囊性成熟性畸胎瘤和表皮样囊肿合并颗粒细胞瘤:一种罕见的卵巢情况。两例病例报告并文献复习

Cystic mature teratoma and epidermoid cyst associated with granulosa cell tumour: a rare ovarian scenario. Two case reports and review of the literature.

作者信息

Giunta P, Patriarca C, Crepaldi E

机构信息

Pathology Unit, Melegnano Hospital, Italy.

出版信息

Pathologica. 2008 Dec;100(6):485-8.

Abstract

We describe two cases of association between an ovarian granulosa cell tumour and a cystic mature teratoma and an epidermoid cyst. These are very rare combinations that might lead to incorrect diagnostic interpretation, since the simultaneous presence, on routine gross and microscopic examination, of a cystic squamous lesion, intimately connected with (case 1), or contralateral to (case 2) a solid, histologically trabecular or microfollicular tumour, might suggest a diagnosis of a carcinoid tumour in a mature cystic teratoma. The differential diagnostic problems and a review of the literature are presented.

摘要

我们描述了两例卵巢颗粒细胞瘤与囊性成熟畸胎瘤及表皮样囊肿相关联的病例。这些是非常罕见的组合,可能导致错误的诊断解读,因为在常规大体和显微镜检查中,同时存在一个与实性、组织学呈小梁状或微滤泡状肿瘤紧密相连(病例1)或对侧(病例2)的囊性鳞状病变,可能提示成熟囊性畸胎瘤中类癌肿瘤的诊断。本文介绍了鉴别诊断问题并对文献进行了综述。

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