双侧青少年颗粒细胞瘤伴发骨内生软骨瘤

Bilateral juvenile granulosa cell tumours associated with skeletal enchondromas.

作者信息

Pounder D J, Iyer P V, Davy M L

出版信息

Aust N Z J Obstet Gynaecol. 1985 May;25(2):123-6. doi: 10.1111/j.1479-828x.1985.tb00624.x.

DOI:10.1111/j.1479-828x.1985.tb00624.x

Abstract

Asynchronous bilateral granulosa cell tumours of the ovary occurred in a patient with enchondromas. The first tumour, presenting at age 15, was misdiagnosed initially as an androblastoma. The second tumour presented 7 years and 3 pregnancies later. The possible therapeutic and pathogenetic implications of these observations are discussed.

摘要

一名患有内生软骨瘤的患者发生了卵巢异步双侧颗粒细胞瘤。第一个肿瘤在患者15岁时出现，最初被误诊为成男性细胞瘤。第二个肿瘤在7年后以及3次妊娠后出现。本文讨论了这些观察结果可能的治疗和发病机制意义。