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一名患有奈梅亨断裂综合征儿童的慢性非感染性坏死性肉芽肿

Chronic noninfectious necrotizing granulomas in a child with Nijmegen breakage syndrome.

作者信息

Vogel Curt A, Stratman Erik J, Reck Samuel J, Lund Jared J

机构信息

University of Wisconsin, Madison, Wisconsin, USA.

出版信息

Pediatr Dermatol. 2010 May-Jun;27(3):285-9. doi: 10.1111/j.1525-1470.2010.01140.x.

Abstract

Nijmegen breakage syndrome (NBS) is a chromosomal breakage disorder with characteristic physical features, chromosomal instability, and combined immunodeficiency. It is closely related to other chromosomal breakage disorders like ataxia telangiectasia. Noninfectious granulomatous inflammation refractory to treatment is a relatively common feature in ataxia telangiectasia. Herein we report a patient with NBS who developed chronic refractory necrotizing granulomatous ulcerations and review the pathophysiology of NBS and noninfectious granulomas in primary immunodeficiency syndromes.

摘要

尼曼-匹克氏病(NBS)是一种染色体断裂疾病,具有特征性的身体特征、染色体不稳定性和联合免疫缺陷。它与其他染色体断裂疾病如共济失调毛细血管扩张症密切相关。对治疗难治的非感染性肉芽肿性炎症是共济失调毛细血管扩张症中相对常见的特征。在此,我们报告一名患有NBS的患者,其出现了慢性难治性坏死性肉芽肿性溃疡,并回顾了NBS和原发性免疫缺陷综合征中非感染性肉芽肿的病理生理学。

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