Author/Authors
SUMNU, Abdullah istanbul Üniversitesi - istanbul Tıp Fakültesi - iç Hastalıkları Anabilim Dalı, Hematoloji Bilim Dalı, turkey , NALÇACI, Meliha istanbul Üniversitesi - istanbul Tıp Fakültesi - iç Hastalıkları Anabilim Dalı, Hematoloji Bilim Dalı, turkey
Title Of Article
FAMILIAL POLYCYTHEMIA IN TWO BROTHERS
شماره ركورد
25879
Abstract
Familial polycythemia (FP), namely primary familial congenital polycythemia is a rare automosal dominant disorder. FP is characterized by isolated erythrocytosis without evolution into leukemia or other myeloproliferative disorders, absence of splenomegaly, normal white blood cell and platelet counts, low plasma erythropoietin levels and hypersensitivity of erythroid progenitors to exogenous erythropoietin in vitro. We report here two brothers referred to our Hematology Department one of them was 22 years old the and other was 17. They had erytrocytosis and no other pathological findings. After excluding other diseases presenting with polycythemia we diagnosed familial polycythemia. We continue to treat with flebotomy when they are symptomatic.
From Page
31
NaturalLanguageKeyword
Familial polycythemia , two brothers , case reports
JournalTitle
Journal Of Istanbul Faculty Of Medicine
To Page
32
JournalTitle
Journal Of Istanbul Faculty Of Medicine
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