| A case of interstitial pulmonary fibrosis. |
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Hak Won Kim1, Ho Joon Im1, In Joon Seol1, Ha Baik Lee1, Hahng Lee1, Seok Chol Jeon2, Moon Hyang Park3 |
1Department of Pediatrics, Hanyang University, College of Medicine, Seoul, Korea
2Department of Diagnostic Radiology, Hanyang University, College of Medicine, Seoul, Korea
3Department of Pathology, Hanyang University, College of Medicine, Seoul, Korea |
| 소아에서의 간질성 폐 섬유증 1례* |
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김학원1, 임호준1, 설인준1, 이하백1, 이항1, 전석철2, 박문향3 |
1한양대학교 의과대학 소아과학교실
2한양대학교 의과대학 진단방사선과학교실
3한양대학교 의과대학 조직병리학교실 |
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Received: 17 August 1990 • Accepted: 2 November 1990 |
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| Abstract |
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Interstitial pulmonary fibrosis is a rare, diffuse lug disease which has a tendency to destroy the lung
architectures by consequent healing with progressively severe fibrosis.
We report with a brief review of literature, one case of a 7-year old female with the typical pictures
of interstitial pulmonary fibrosis, histologically on open lung biopsy, and clinically presenting with
chronic respiratory difficulty but without definite symptoms relared to collagen diseases in spite of
positive antinuclear antibody and positive rheumatoid factor |
| Key Words:
Interstital Pulmonary Fibrosis |
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