肉芽肿病合并多血管炎以多种乳房病变为首发症状1例:基于病例的回顾。

Case Reports in Rheumatology Pub Date : 2021-08-20 eCollection Date: 2021-01-01 DOI:10.1155/2021/4416072
Masatoshi Kawataka, Toshiki Kido, Reina Tsuda, Takafumi Onose, Ryoko Asano, Miho Yamazaki, Naonori Sugishita, Hiroyuki Hounoki, Toshiko Kakiuchi, Koichiro Shinoda, Kazuyuki Tobe
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引用次数: 1

摘要

一名44岁女性以乳头脓液样分泌物就诊于我院,诊断为巩膜炎。她的乳房发现皮下硬化和溃疡。她被诊断为肉芽肿病合并多血管炎(GPA),考虑到硬膜炎、鼻窦炎、皮肤肉芽肿形成和抗蛋白酶3-抗中性粒细胞胞浆抗体,并成功治疗糖皮质激素。15个月后,她出现肺实变和右乳房结节。乳腺结节活检显示肉芽肿性血管炎,她接受了利妥昔单抗治疗。虽然累及乳腺的GPA是罕见的,单侧乳腺肿块是典型的临床特征;因此,在这种情况下应该考虑GPA。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A Case of Granulomatosis with Polyangiitis with Various Breast Lesions as the Initial Symptoms: A Case-Based Review.

A Case of Granulomatosis with Polyangiitis with Various Breast Lesions as the Initial Symptoms: A Case-Based Review.

A Case of Granulomatosis with Polyangiitis with Various Breast Lesions as the Initial Symptoms: A Case-Based Review.

A Case of Granulomatosis with Polyangiitis with Various Breast Lesions as the Initial Symptoms: A Case-Based Review.

A 44-year-old woman presenting with pus-like discharge from the nipples visited our hospital for scleritis. Subcutaneous induration and ulceration were found on her breast. She was diagnosed with granulomatosis with polyangiitis (GPA) considering scleritis, sinusitis, cutaneous granuloma formation, and antiproteinase 3-antineutrophil cytoplasmic antibodies and was successfully treated with glucocorticoids. Fifteen months later, she developed pulmonary consolidation and a right breast nodule. Biopsies of the breast nodule showed granulomatous vasculitis, and she was treated with rituximab. While breast involvement in GPA is rare, unilateral breast mass is a typical clinical feature; thus, GPA should be considered in such cases.

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