| Literature DB >> 7677590 |
Abstract
In an autopsied female primary polycythemia was definitely diagnosed only after histological examination. A classical form of Vaquez-Osler disease was characterized by pronounced normo-, granulo- and megakaryocyte hyperplasia of the bone marrow, spleen and liver myelosis with an admixture of atypical megakaryocytes and splenomegaly. There was a complication in the form of two coronary arteries thrombosis. Lethal outcome resulted from myocardial infarction.Entities:
Mesh:
Year: 1995 PMID: 7677590
Source DB: PubMed Journal: Arkh Patol ISSN: 0004-1955