IDIOPATHIC PULMONARY HEMOSIDEROSIS - REPORT OF 2 CASES AND REVIEW OF THE LITERATURE

被引:25
作者
BAILEY, P
GRODEN, BM
机构
[1] Department of General Medicine, Ballochmyle Hospital, Mauchline
关键词
D O I
10.1136/pgmj.55.642.266
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Idiopathic pulmonary haemosiderosis (IPH) is a rare disorder affecting mainly children and adolescents, and is usually fatal. However, there is increasing evidence that the aetiology of this condition is immunological, and that immunosuppressives may prolong remission. Two cases are reported, one of which has the atypical feature of a malabsorption syndrome. This has not been previously reported. The literature is reviewed and current ideas on the postulated immunological basis to IPH are discussed. © 1979 The Fellowship of Postgraduate Medicine.
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页码:266 / 272
页数:7
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