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模仿朗格汉斯细胞组织细胞增多症的干扰素-γ受体缺陷

Interferon-gamma receptor deficiency mimicking Langerhans' cell histiocytosis.

作者信息

Edgar J D, Smyth A E, Pritchard J, Lammas D, Jouanguy E, Hague R, Novelli V, Dempsey S, Sweeney L, Taggart A J, O'hara D, Casanova J L, Kumararatne D S

机构信息

Regional Immunology Service, The Royal Hospitals, Belfast, N Ireland, United Kingdom.

出版信息

J Pediatr. 2001 Oct;139(4):600-3. doi: 10.1067/mpd.2001.117068.

DOI:10.1067/mpd.2001.117068
PMID:11598613
Abstract

Two patients who were initially given a diagnosis of Langerhans' cell histiocytosis on the basis of the clinical, radiologic, and biopsy findings had mycobacterial infection subsequently identified. The correct diagnosis of dominant partial interferon-gamma receptor deficiency was established.

摘要

两名患者最初根据临床、放射学和活检结果被诊断为朗格汉斯细胞组织细胞增多症，随后被确定为分枝杆菌感染。最终确立了主要的部分干扰素-γ受体缺陷的正确诊断。

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