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Idiopathic Pulmonary Hemosiderosis 1례

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Alternative Title
A Case of Idiopathic Pulmonary Hemosiderosis
Abstract
Idiopathic pulmonary hemosiderosis(IPH) is a relatively rare disease of unknown etiology characterized pathologically by recurrences of intraalveolar pulmonary hemorrhage.

Clinical features include hemoptysis, iron deficiency anemia and pulmonary parenchymal infiltrations on chest radiograph. Hemosiderin-laden macrophages are demonstrated by examination of sputum or lung biopsy specimens.

We diagnosed IPH by lung biopsy in 9 year-old girl who had had recurrent hemoptysis, iron deficiency anemia and diffuse pulmonary infiltrates on chest radiograph and report this case with brief literature review.
Idiopathic pulmonary hemosiderosis(IPH) is a relatively rare disease of unknown etiology characterized pathologically by recurrences of intraalveolar pulmonary hemorrhage.

Clinical features include hemoptysis, iron deficiency anemia and pulmonary parenchymal infiltrations on chest radiograph. Hemosiderin-laden macrophages are demonstrated by examination of sputum or lung biopsy specimens.

We diagnosed IPH by lung biopsy in 9 year-old girl who had had recurrent hemoptysis, iron deficiency anemia and diffuse pulmonary infiltrates on chest radiograph and report this case with brief literature review.
Author(s)
심정연홍수종김영휘문형남홍창의공경엽
Issued Date
1993
Type
Research Laboratory
URI
https://oak.ulsan.ac.kr/handle/2021.oak/5353
http://ulsan.dcollection.net/jsp/common/DcLoOrgPer.jsp?sItemId=000002025370
Alternative Author(s)
Shim, Jung YeonHong, Soo JongKim, Young WheeMoon, Hyung NamHong, Chang YeeGong, Gyeong Yeob
Publisher
울산의대학술지
Language
kor
Rights
울산대학교 저작물은 저작권에 의해 보호받습니다.
Citation Volume
2
Citation Number
2
Citation Start Page
149
Citation End Page
155
Appears in Collections:
Research Laboratory > The ULSAN university medical journal
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