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A Case of Pulmonary Hemosiderosis that was Dissolved by an Oral Prednisolone and the Milk Avoidance
Author(s) -
Mi Suk Kim,
Ju Kyung Lee,
Jun Song,
Young Yull Koh,
Woo Sun Kim,
Young Hun Choi,
Dong In Suh
Publication year - 2012
Publication title -
pediatric allergy and respiratory disease
Language(s) - English
Resource type - Journals
ISSN - 1225-679X
DOI - 10.7581/pard.2012.22.4.422
Subject(s) - medicine , prednisolone , bronchoalveolar lavage , hemosiderosis , pneumonia , tachypnea , gastroenterology , dermatology , anesthesia , surgery , lung , tachycardia
A 29-month-old boy presented with fever, dyspnea, and paleness. He was initially diagnosed with pneumonia and severe sepsis. Although he was treated with intravenous antibiotics and high dose methylprednisolone, dyspnea and paleness recurred two times. Under suspicion of pulmonary hemosiderosis, we performed video-assisted thoracoscopic lung biopsy and bronchoalveolar lavage on him and found hemosiderin-laden macrophages in both specimens. Despite thorough history and laboratory examination, we could not find any pathologic or serologic evidence for primary and secondary causes of pulmonary hemosiderosis except for one that indicating Heiner s syndrome. ’ After taking oral prednisolone he showed improvement of anemia and dyspnea, which was maintained by milk avoidance. Based on the history and the existence of immunoglobulin G antibodies against milk components, we are considering it as the case of Heiner s syndrome. ’ [Pediatr Allergy Respir Dis(Korea) 2012;22:422-427]

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