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Idiopathic pulmonary hemosiderosis in an adult patient responded well to corticosteroid therapy.
- Source :
-
Tuberkuloz ve toraks [Tuberk Toraks] 2007; Vol. 55 (1), pp. 77-82. - Publication Year :
- 2007
-
Abstract
- Idiopathic pulmonary hemosiderosis (IPH) is a very rare disorder of unknown etiology characterized by recurrent or chronic hemorrhage and accumulation of hemosiderin in the lung parenchyma. It is most common in children but can occur in adults. Clinical manifestations of the disease include iron deficiency anemia without any known cause, pulmonary symptoms such as hemoptysis, dyspnea and cough, and parenchymal lesions on chest X-ray. The clinical course of the disease may vary from patient to patient however, in general, the prognosis of the disease is worse. Treatment is symptomatic and supportive. Corticosteroids and other immune suppressive agents were used for the therapy of IPH. Since it is seen rarely in adults and the clinical course of the disease vary from patient to patient we presented an adult male patient with IPH responded well to steroid therapy clinically and radiologically.
- Subjects :
- Adult
Biopsy, Needle
Bronchoscopy
Diagnosis, Differential
Glucocorticoids administration & dosage
Hemosiderosis blood
Hemosiderosis diagnostic imaging
Hemosiderosis pathology
Humans
Lung Diseases blood
Lung Diseases diagnostic imaging
Lung Diseases pathology
Male
Prednisolone administration & dosage
Tomography, X-Ray Computed
Glucocorticoids therapeutic use
Hemosiderosis diagnosis
Hemosiderosis drug therapy
Lung Diseases diagnosis
Lung Diseases drug therapy
Prednisolone therapeutic use
Subjects
Details
- Language :
- English
- ISSN :
- 0494-1373
- Volume :
- 55
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Tuberkuloz ve toraks
- Publication Type :
- Academic Journal
- Accession number :
- 17401798