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Infantile histiocytosis X: Case reoprt
Tanaffos. 2002; 1 (3): 57-61
in English | IMEMR | ID: emr-61060
ABSTRACT
Langerhans cell histiocytosis [LCH] is a disease of unknown etiology that presents in three forms Letterer- Siwe disease, Hand-Schuller-Christian disease, and Eosinophilic Granuloma. It is a multifocal disease that usually affects several organs and unifocal forms are rare. Pulmonary involvement occurs in approximately 40% of cases and almost always in young adults. Lungs are rarely affected in infant patients. This report presents a 15-month-old male infant that was admitted for cyanosis and respiratory distress. Diagnostic work up revealed a primary pulmonary histiocytosis and the treatment made a significant improvement of signs and symptoms by the time of discharge
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Index: IMEMR (Eastern Mediterranean) Main subject: Histiocytosis, Langerhans-Cell / Infant Limits: Humans / Male Language: English Journal: Tanaffos Year: 2002

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Index: IMEMR (Eastern Mediterranean) Main subject: Histiocytosis, Langerhans-Cell / Infant Limits: Humans / Male Language: English Journal: Tanaffos Year: 2002