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Autoimmune Lymphoproliferative Syndrome Misdiagnosed as Hemophagocytic Lymphohistiocytosis; A Case Report
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نویسنده
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Abolghasemi H ,Shahverdi E ,Dolatimehr F ,Mehdi Oghli R
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منبع
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iranian journal of blood and cancer - 2015 - دوره : 7 - شماره : 4 - صفحه:198 -200
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چکیده
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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.
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کلیدواژه
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Autoimmune lymphoproliferative ,syndrome ,Hemophagocytic lymphohistiocytosis ,Cytopenia ,Splenomegaly ,Lymphadenopathy
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آدرس
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baqiyatallah university of medical sciences, Department of Pediatrics, ایران, baqiyatallah university of medical sciences, Students’ Research Committee (SRC), ایران, baqiyatallah university of medical sciences, Students’ Research Committee (SRC), ایران, baqiyatallah university of medical sciences, Students’ Research Committee (SRC), ایران
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Authors
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