Autoimmune oophoritis: Clinical presentation of an unusual clinical entity

M. Varras, A. Anastasiadis, J. Panelos, E. Balassi, A. Demou, C. Akrivis
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引用次数: 1

Abstract

Introduction Autoimmune oophoritis is a rare condition , which provokes ovarian failure with either primary amenorrhea or secondary amenorrhea and a subsequent loss of fertility and ovarian hormonal function. The purpose of this report is to document the clinical findings from two patients with aut-oimmune oophoritis. Cases report Two cases of autoimmune oophorit-is are presented whose histopathol-ogical findings were consistent with international literature. Both cases were histopathologically characteri-sed by lymphocytic and plasmacytic inflammatory infiltrations around the cystic follicles. The inflammation was located both in the theca and gr-anular layers. Conclusion Patients with autoimmune oophorit-is should be recognised by the histo-pathology of the ovarian biopsies as they are at an increased risk of developing other autoimmune disorders.
自身免疫性卵巢炎:一种不寻常临床实体的临床表现
自身免疫性卵巢炎是一种罕见的疾病,它引起卵巢功能衰竭,伴有原发性闭经或继发性闭经,随后丧失生育能力和卵巢激素功能。本报告的目的是记录两例自身免疫性卵巢炎的临床表现。报告两例自身免疫性卵巢囊肿,其组织病理学结果与国际文献一致。两例患者的组织病理学特征均为囊泡周围淋巴细胞和浆细胞性炎症浸润。炎症位于鞘膜层和环膜层。结论自身免疫性卵巢囊肿患者发生其他自身免疫性疾病的风险增加,应通过卵巢活检的组织病理学来识别。
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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