Title of article
Autoimmune Lymphoproliferative Syndrome Misdiagnosed as Hemophagocytic Lymphohistiocytosis; A Case Report
Author/Authors
Abolghasemi, H baqiyatallah university of medical sciences - Department of Pediatrics, ايران , Shahverdi, E baqiyatallah university of medical sciences - Students’ Research Committee (SRC), ايران , Dolatimehr, F baqiyatallah university of medical sciences - Students’ Research Committee (SRC), ايران , Mehdi Oghli, R baqiyatallah university of medical sciences - Students’ Research Committee (SRC), ايران
From page
198
To page
200
Abstract
p Autoimmune lymphoproliferative Syndrome (ALPS) is a rare inherited disorder of apoptosis. It usually presents with chronic lymphadenopathy, splenomegaly, and symptomatic cytopenia in a child. Herein, we report a 14-year-old boy with symptoms misdiagnosed as hemophagocytic lymphohistiocytosis who was treated before ALPS was diagnosed for the patient. This case should alert pediatricians to consider ALPS in differential diagnosis of a child with lymphadenopathy, splenomegaly, and cytopenia. /p
Keywords
Autoimmune lymphoproliferative , syndrome , Hemophagocytic lymphohistiocytosis , Cytopenia , Splenomegaly , Lymphadenopathy
Journal title
Iranian Journal of Blood and Cancer (IJBC)
Journal title
Iranian Journal of Blood and Cancer (IJBC)
Record number
2669230
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