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学術誌査読

    24 被引用数 (Scopus)

    抄録

    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.

    本文言語英語
    ページ(範囲)793-795
    ページ数3
    ジャーナルCirculation Journal
    67
    9
    DOI
    出版ステータス出版済み - 9月 1 2003

    !!!All Science Journal Classification (ASJC) codes

    • 循環器および心血管医学

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