Polycythemia vera diagnosed after esophageal variceal rupture

Yoshiyasu Kono, Akinobu Takaki, Hideo Gobara, Ken Ichi Matsuoka, Masato Nishino, Hiroyuki Okada, Kazuhide Yamamoto

Research output: Contribution to journalArticlepeer-review

2 Citations (Scopus)


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.

Original languageEnglish
Pages (from-to)2395-2399
Number of pages5
JournalInternal Medicine
Issue number18
Publication statusPublished - Sept 15 2015


  • Esophagogastric varices
  • Polycythemia vera (PV)
  • Portal hypertension
  • Thrombosis

ASJC Scopus subject areas

  • Internal Medicine


Dive into the research topics of 'Polycythemia vera diagnosed after esophageal variceal rupture'. Together they form a unique fingerprint.

Cite this