| Literature DB >> 26370868 |
Yoshiyasu Kono1, Akinobu Takaki, Hideo Gobara, Ken-Ichi Matsuoka, Masato Nishino, Hiroyuki Okada, Kazuhide Yamamoto.
Abstract
Polycythemia vera (PV) is a chronic myeloproliferative neoplasm that leads to hyperviscosity and the risk of thrombosis. We encountered the case of a young male Filipino patient diagnosed with PV after the rupture of esophageal varices. The complete blood cell count showed a slight increase in white blood cells. An abdominal computed tomography scan disclosed splenomegaly and occlusion of the portal vein and collateral vessels. A blood examination demonstrated an increase in all three blood cell lines within three months. Based on the presence of severe hypercellularity of the bone marrow and positivity for the JAK2V617F mutation, we finally diagnosed the patient with PV.Entities:
Mesh:
Substances:
Year: 2015 PMID: 26370868 DOI: 10.2169/internalmedicine.54.4687
Source DB: PubMed Journal: Intern Med ISSN: 0918-2918 Impact factor: 1.271