Salazar A, Mañá J, Sala J, Landoni B R, Manresa F
Department of Internal Medicine, Bellvitge Hospital, University of Barcelona, Spain.
Respiration. 1994;61(2):117-9. doi: 10.1159/000196320.
A case is reported of a 48-year-old man previously diagnosed as having mitral valvular disease, who was admitted for evaluation of chronic cor pulmonale. Seven years before admission, an intraoperative liver biopsy had shown multiple noncaseating granulomas. The further course was characterized by progressive chronic intrahepatic cholestasis and portal hypertension. Right heart catheterization revealed a mean pulmonary artery pressure of 43 mm Hg and a normal wedge pressure (5 mm Hg). A perfusion lung scan was normal. Open lung biopsy demonstrated noncaseating granulomas and extensive pulmonary fibrosis. To our knowledge, only one case of sarcoidosis with combined portal and pulmonary hypertension has previously been described.
报告了一例48岁男性病例,该患者此前被诊断患有二尖瓣疾病,因慢性肺源性心脏病评估入院。入院前七年,术中肝脏活检显示多个非干酪样肉芽肿。后续病程的特征为进行性慢性肝内胆汁淤积和门静脉高压。右心导管检查显示平均肺动脉压为43 mmHg,楔压正常(5 mmHg)。肺灌注扫描正常。开胸肺活检显示非干酪样肉芽肿和广泛的肺纤维化。据我们所知,此前仅描述过一例合并门静脉和肺动脉高压的结节病病例。