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ASSOCIATION OF PULMONARY HEMOSIDEROSIS AND CELIAC DISEASE

dc.contributor.authorDogan, Murat
dc.contributor.authorBektas, Mehmet Selcuk
dc.contributor.authorDogan, Sekibe Zehra
dc.contributor.authorAktar, Fesih
dc.contributor.authorCesur, Yaşar
dc.contributor.institutionauthorCESUR, YAŞAR
dc.date.accessioned2020-10-29T14:57:51Z
dc.date.available2020-10-29T14:57:51Z
dc.date.issued2011-05-01T00:00:00Z
dc.description.abstractIdiopathic pulmonary hemosiderosis (IPH) is a rare disease of unknown autoimmune etiology mainly affecting children and adolescents. We report the case of an 6-years-old boy with cough and tiredness. There were no gastrointestinal symptoms were not determined. Body weight and height were in normal percentiles. Physical examination revealed cutaneous and mucosal pallor, due to severe anemia (hemoglobin 3 g/dL). Infiltrations were seen at the chest X-rays at both lungs, but markedly at left lung. In sputum examinations, hemosiderin-laden macrophages were seen. The diagnosis of IPH was made. The association of IPH and Celiac disease (CD) is well known. Searching associated CD was performed and then confirmed by biological and histological examinations. A gluten-free diet was initiated. Evolution was favorable. Searching for CD in IPH should be done, even in the absence of gastrointestinal symptoms.
dc.identifier.citationDogan M., Bektas M. S. , Dogan S. Z. , Aktar F., Cesur Y., -ASSOCIATION OF PULMONARY HEMOSIDEROSIS AND CELIAC DISEASE-, NOBEL MEDICUS, cilt.7, ss.103-105, 2011
dc.identifier.doi10.1002/ppul.21357
dc.identifier.scopus79951777973
dc.identifier.urihttp://hdl.handle.net/20.500.12645/25528
dc.identifier.wosWOS:000293818000020
dc.titleASSOCIATION OF PULMONARY HEMOSIDEROSIS AND CELIAC DISEASE
dc.typeArticle
dspace.entity.typePublication
local.avesis.id31fa45fe-f05f-4d76-8922-c41292b81d21
local.publication.isinternational1
relation.isAuthorOfPublicationddd881a5-c7cb-41e5-b4e1-0693a98a0d29
relation.isAuthorOfPublication.latestForDiscoveryddd881a5-c7cb-41e5-b4e1-0693a98a0d29
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