Pulmonary Capillary Hemangiomatosis With Severe Pulmonary Hypertension
-
- Ito Koji
- Departments of Cardiovascular Medicine
-
- Ichiki Toshihiro
- Departments of Cardiovascular Medicine
-
- Ohi Keiji
- Departments of Cardiovascular Medicine
-
- Egashira Kensuke
- Departments of Cardiovascular Medicine
-
- Ohta Mituhiko
- Departments of Cardiovascular Medicine
-
- Taguchi Kenichi
- Anatomical Pathology, Kyushu University Graduate School of Medical Sciences
-
- Takeshita Akira
- Departments of Cardiovascular Medicine
この論文をさがす
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. (Circ J 2003; 67: 793 - 795)<br>
収録刊行物
-
- Circulation Journal
-
Circulation Journal 67 (9), 793-795, 2003
一般社団法人 日本循環器学会
- Tweet
詳細情報 詳細情報について
-
- CRID
- 1390282680080411648
-
- NII論文ID
- 110002666404
-
- NII書誌ID
- AA11591968
-
- COI
- 1:STN:280:DC%2BD3svgtVKmsg%3D%3D
-
- ISSN
- 13474820
- 13469843
-
- PubMed
- 12939557
-
- 本文言語コード
- en
-
- データソース種別
-
- JaLC
- Crossref
- PubMed
- CiNii Articles
-
- 抄録ライセンスフラグ
- 使用不可