Pulmonary capillary hemangiomatosis with severe pulmonary hypertension

Koji Ito, Toshihiro Ichiki, Keiji Ohi, Kensuke Egashira, Mituhiko Ohta, Kenichi Taguchi, Akira Takeshita

研究成果: ジャーナルへの寄稿記事

23 引用 (Scopus)

抜粋

Pulmonary capillary hemangiomatosis (PCH) is a rare idiopathic lung disorder that occurs in young patients and leads to pulmonary hypertension (PH). It is difficult to diagnosis in the early stage and is often mistaken for primary PH; in almost all cases of PCH, the correct diagnosis is not made until autopsy. In the present case of PCH, the patient had severe pulmonary hypertension and died of respiratory failure. Pathologically, PCH is characterized by proliferation of benign thin-walled capillary sized blood vessels in the lung parenchyma.

元の言語英語
ページ(範囲)793-795
ページ数3
ジャーナルCirculation Journal
67
発行部数9
DOI
出版物ステータス出版済み - 9 1 2003

    フィンガープリント

All Science Journal Classification (ASJC) codes

  • Cardiology and Cardiovascular Medicine

これを引用

Ito, K., Ichiki, T., Ohi, K., Egashira, K., Ohta, M., Taguchi, K., & Takeshita, A. (2003). Pulmonary capillary hemangiomatosis with severe pulmonary hypertension. Circulation Journal, 67(9), 793-795. https://doi.org/10.1253/circj.67.793