Langerhans cell histiocytosis with hypogonadotrophic hypogonadism

被引：0
|
作者：
Ong, C. W. M. [1 ]
Chua, L. S. [1 ]
Ng, A. [1 ]
Low, S. Y. [1 ]
机构：
[1] Natl Univ Singapore Hosp, Div Infect Dis, Dept Med, Singapore 119074, Singapore
来源：
SINGAPORE MEDICAL JOURNAL | 2009年 / 50卷 / 05期
关键词：
diabetes insipidus; hypogonadotrophic hypogonadism; interstitial lung disease; Langerhans cell histiocytosis; PULMONARY HISTIOCYTOSIS; LUNG; DIAGNOSIS;
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
Langerhans cell histiocytosis (LCH) is a rare disease characterised by monoclonal proliferation and infiltration of organs by large mononuclear cells. Organs commonly involved include the lungs and pituitary gland. However, the disease association with hypogonadotrophic hypogonadism has not been reported in the literature, to our knowledge. We report a 26-year-old Chinese man with LCH, recurrent pneumothoraces, diabetes insipidus and hypogonadotrophic hypogonadism. The clinical features and management of the disease are reviewed.
引用
收藏
页码：E185 / E188
页数：4
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