Unusual presentation: Pulmonary hemosiderosis with celiac disease and retinitis pigmentosa in a child

Idiopathic pulmonary hemosiderosis (IPH) is a rare disease characterized by anemia, hemoptysis and recurrent alveolar hemorrhage. The combination of IPH and celiac disease (CD) is extremely rare. We report a 9‐year‐old boy with Lane‐Hamilton syndrome, co‐occurrence of pulmonary hemosiderosis with CD...

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Veröffentlicht in:	Pediatric pulmonology 2011-08, Vol.46 (8), p.820-823
Hauptverfasser:	Keskin, Ozlem, Keskin, Mehmet, Guler, Elif, Tutar, Ediz, Saygili, Oguzhan, Kucukosmanoglu, Ercan, Kor, Yilmaz, Celik, Haydar, Coskun, Enes
Format:	Artikel
Sprache:	eng
Schlagworte:	Biological and medical sciences celiac disease Celiac Disease - diagnosis Celiac Disease - diet therapy Child Dietary Supplements Gastroenterology. Liver. Pancreas. Abdomen General aspects Gliadin - adverse effects Hemosiderosis - diagnosis Hemosiderosis - diet therapy Hemosiderosis, Pulmonary Humans Iron - therapeutic use Lung Diseases - diagnosis Lung Diseases - diet therapy Male Medical sciences Metabolic diseases Metals (hemochromatosis...) Other diseases. Semiology Other metabolic disorders Pneumology pulmonary hemosiderosis retinitis pigmentosa Retinitis Pigmentosa - diagnosis Retinitis Pigmentosa - diet therapy Stomach. Duodenum. Small intestine. Colon. Rectum. Anus
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Zusammenfassung:	Idiopathic pulmonary hemosiderosis (IPH) is a rare disease characterized by anemia, hemoptysis and recurrent alveolar hemorrhage. The combination of IPH and celiac disease (CD) is extremely rare. We report a 9‐year‐old boy with Lane‐Hamilton syndrome, co‐occurrence of pulmonary hemosiderosis with CD. This presentation is unique presentation because he has also retinal pigmentation. Pediatr. Pulmonol. 2011; 46:820–823. © 2011 Wiley‐Liss, Inc.
ISSN:	8755-6863 1099-0496
DOI:	10.1002/ppul.21420