罕见的疤痕结节病:皮肤伪装者

R. Gomes, R. Hasan, Athai Majumder, Kazi Tamanna Akter
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引用次数: 0

摘要

结节性肉芽肿浸润于旧的皮肤疤痕是结节病不常见的皮肤表现之一。在这里我们报告的情况下,32岁的女性谁提出了肿胀和刺激在9个月阑尾切除术疤痕。切口瘢痕活检显示非干酪化肉芽肿。询问时,她有炎性多关节炎及持续干咳两个月。高分辨率CT (HRCT)显示右侧气管旁,肺门旁,主动脉旁和隆突下淋巴结病变,双肺野均有肺结节密度。纵隔淋巴结FNAC显示非干酪样肉芽肿与结节病一致。使用一个疗程的口服类固醇、羟氯喹和甲氨蝶呤,皮肤炎症得以成功消退。瘢痕结节病的发病率是罕见的,因此不是很清楚。然而,先前存在的疤痕的炎症改变可能是疾病发病的重要指标。中南大学学报(自然科学版);10 (2): 122 - 125
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rare Scar Sarcoidosis: A Dermatologic Masquerader
Infiltration of sarcoid granuloma in old cutaneous scars is one of the uncommon cutaneous manifestations of sarcoidosis. Here we report the case of a 32-year-old female who presented with swelling and irritation in a 9-month-old appendicectomy scar. An incisional scar biopsy was done and it revealed non-caseating granuloma. On query she had inflammatory polyarthritis and persistent dry cough for last two months. High resolution CT (HRCT) revealed right paratracheal, both hilar, paraaortic, and subcarinal lymphadenopathy with pulmonary nodular densities in both lung fields. FNAC from mediastinal node revealed non-caseating granuloma consistent with sarcoidosis. Successful regression of cutaneous inflammation was achieved using a course of oral steroids, hydroxychloroquine and methotrexate. The incidence of scar sarcoidosis is rare and therefore not well-understood. However, inflammatory alterations in preexisting scars may be important indicators of disease onset. J Enam Med Col 2020; 10(2): 122-125
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