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Clinical presentation of a patient with congenital polycythemia
Tomislav F Hajnzić1, Renata Vrsalović, Marina Mataija
1Department of Pediatrics, Hematology Oncology Unit, University Hospital "Sestre Milosrdnice", Zagreb, Croatia. tomislav-franjo.hajnzic@zg.htnet.hr
Abstract:
The authors describe a 19 year old male with an isolated but absolute erythrocytosis with iron deficiency without evidence for polycythemia vera as well as another causes of erythrocytosis. The polycythemia was due to a recently described von Hippel-Lindau (VHL) mutation. By stopping iron therapy there was no more requirements for phlebotomy in this patient.
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