A Rare Cause Of Polycythemia: Idiopathic Pulmonary Arterial Hypertension

ASİYE KANBAY, HAKAN BÜYÜKOĞLAN, NEZİHE ÖZDOĞAN, FATMA SEMA OYMAK, MEHMET GÜNGÖR KAYA, İNCİ GÜLMEZ, RAMAZAN DEMİR

  • Year : 2011
  • Vol : 27
  • Issue : 3
  •  Page : 177-178
Idiopathic pulmonary arterial hypertension (IPAH) with an incidence of 1-2/million per-year. IPAH is a term used to define a variety of progressive conditions that have in common, increased pulmonary vascular resistance leading to right heart failure and death. Pulmonary arterial hypertension is presented with cyanosis, polyctemia and right heart failure. Increased prevelance of mortality is due to progression and late diagnosis of the disease. We present this case to alert physicians to keep in mind rare but serious disease IPAH in the differential diagnosis of polyctemia.
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Description : None of the authors, any product mentioned in this article, does not have a material interest in the device or drug. Research, not supported by any external organization. grant full access to the primary data and, if requested by the magazine they agree to allow the examination of data.
A Rare Cause Of Polycythemia: Idiopathic Pulmonary Arterial Hypertension
, Vol. 27 (3)
Received : 06.07.2010, Accepted : 06.07.2010, Published Online : 13.08.2018
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ISSN:1017-6616;
E-ISSN:2149-8059;