Familial hemophagocytic lymphohistiocytosis in two brothers
Familial hemophagocytic lymphohistiocytosis is a disorder which presents with fever, pancytopenia, liver dysfunction and also an increase in non-malignant histiocytes with prominent hemophagocytosis in various organs. It is usually difficult to distinguish from other hemophagocytic syndrome in the a...
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Malaysian Medical Association
2004
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Online Access: | http://eprints.um.edu.my/24581/1/Familial_Hemophagocytic_Lymphohistiocytosis.pdf http://eprints.um.edu.my/24581/ http://www.e-mjm.org/2004/v59n1/Familial_Hemophagocytic_Lymphohistiocytosis.pdf |
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my.um.eprints.245812021-03-12T07:22:25Z http://eprints.um.edu.my/24581/ Familial hemophagocytic lymphohistiocytosis in two brothers Gan, Gin Gin Eow, Geok Im Teh, A. Ng, S.C. Sangkar, J.V. R Medicine Familial hemophagocytic lymphohistiocytosis is a disorder which presents with fever, pancytopenia, liver dysfunction and also an increase in non-malignant histiocytes with prominent hemophagocytosis in various organs. It is usually difficult to distinguish from other hemophagocytic syndrome in the absence of family history. It rarely manifests in adults. Chemotherapy is usually indicated. Here, we report the occurrence of this disorder in two brothers in their twenties. Malaysian Medical Association 2004 Article PeerReviewed text en http://eprints.um.edu.my/24581/1/Familial_Hemophagocytic_Lymphohistiocytosis.pdf Gan, Gin Gin and Eow, Geok Im and Teh, A. and Ng, S.C. and Sangkar, J.V. (2004) Familial hemophagocytic lymphohistiocytosis in two brothers. Medical Journal of Malaysia, 59 (1). pp. 100-102. ISSN 0300-5283 http://www.e-mjm.org/2004/v59n1/Familial_Hemophagocytic_Lymphohistiocytosis.pdf |
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R Medicine Gan, Gin Gin Eow, Geok Im Teh, A. Ng, S.C. Sangkar, J.V. Familial hemophagocytic lymphohistiocytosis in two brothers |
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Familial hemophagocytic lymphohistiocytosis is a disorder which presents with fever, pancytopenia, liver dysfunction and also an increase in non-malignant histiocytes with prominent hemophagocytosis in various organs. It is usually difficult to distinguish from other hemophagocytic syndrome in the absence of family history. It rarely manifests in adults. Chemotherapy is usually indicated. Here, we report the occurrence of this disorder in two brothers in their twenties. |
format |
Article |
author |
Gan, Gin Gin Eow, Geok Im Teh, A. Ng, S.C. Sangkar, J.V. |
author_facet |
Gan, Gin Gin Eow, Geok Im Teh, A. Ng, S.C. Sangkar, J.V. |
author_sort |
Gan, Gin Gin |
title |
Familial hemophagocytic lymphohistiocytosis in two brothers |
title_short |
Familial hemophagocytic lymphohistiocytosis in two brothers |
title_full |
Familial hemophagocytic lymphohistiocytosis in two brothers |
title_fullStr |
Familial hemophagocytic lymphohistiocytosis in two brothers |
title_full_unstemmed |
Familial hemophagocytic lymphohistiocytosis in two brothers |
title_sort |
familial hemophagocytic lymphohistiocytosis in two brothers |
publisher |
Malaysian Medical Association |
publishDate |
2004 |
url |
http://eprints.um.edu.my/24581/1/Familial_Hemophagocytic_Lymphohistiocytosis.pdf http://eprints.um.edu.my/24581/ http://www.e-mjm.org/2004/v59n1/Familial_Hemophagocytic_Lymphohistiocytosis.pdf |
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