Idiopathic pulmonary hemosiderosis.

Authors

  • M Pinto Departamento de Medicina, Hospital Geral de Santo António, Porto.
  • J Correia
  • I Leal
  • A Reis
  • B Leão
  • S de Carvalho
  • C S Sousa

DOI:

https://doi.org/10.20344/amp.2540

Abstract

We report a case of a 23 year-old man admitted to hospital with cough, fever and recurrent episodes of haemoptysis. Laboratory findings, which included a pulmonary biopsy, established the diagnosis of Idiophatic Pulmonary Hemosiderosis (IPH). Despite a number of morphologic, immunologic and ultrastructural studies, the etiology and pathogenesis of this disease remain indetermined. To diagnose an IPH all the other causes of pulmonary hemorrhage must be excluded. This is a rare disease, even more rare in adults. Based on these facts the authors publish this article, which includes the case report and a literature review.

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How to Cite

1.
Pinto M, Correia J, Leal I, Reis A, Leão B, de Carvalho S, Sousa CS. Idiopathic pulmonary hemosiderosis. Acta Med Port [Internet]. 1996 Jan. 31 [cited 2024 Nov. 23];9(1):41-4. Available from: https://actamedicaportuguesa.com/revista/index.php/amp/article/view/2540

Issue

Section

Arquivo Histórico