Pietra G G, Edwards W D, Kay J M, Rich S, Kernis J, Schloo B, Ayres S M, Bergofsky E H, Brundage B H, Detre K M
Division of Lung Diseases, National Heart, Lung, and Blood Institute, Bethesda, Maryland.
Circulation. 1989 Nov;80(5):1198-206. doi: 10.1161/01.cir.80.5.1198.
Qualitative and quantitative studies were performed on pulmonary blood vessels in lung tissue obtained by biopsy, pneumonectomy, or autopsy from 58 patients in the Registry of Primary Pulmonary Hypertension sponsored by the Heart, Lung, and Blood Institute of the National Institutes of Health. In 49 patients (84%), the hypertensive vascular disease involved predominantly or exclusively muscular pulmonary arteries and arterioles. In each of these 49 patients, pulmonary artery medial hypertrophy was observed, and in 48 patients, it was also associated with intimal or luminal lesions. On the basis of the predominant histopathologic features, 25 of the 48 patients were classified as having pulmonary arteriopathy with plexiform lesions characterized by a combination of concentric laminar intimal fibrosis, eccentric intimal fibrosis, and plexiform lesions; in nine of these 25, recanalized thrombi were also present. Pulmonary arteriopathy with thrombotic lesions, defined by the presence of both eccentric intimal fibrosis and recanalized thrombi but without plexiform lesions, was observed in 19 patients. Intimal fibrosis, either concentric or eccentric, without plexiform or thrombotic lesions was found in four patients. Among the remaining nine patients in the Registry, pulmonary veno-occlusive disease was present in seven and chronic pulmonary venous hypertension in one. Pulmonary blood vessels were microscopically normal in a lung biopsy specimen from another patient. In general, patients with plexiform lesions and those with veno-occlusive disease had a much poorer prognosis than patients with thrombotic lesions. The present study shows the existence of several distinct histopathologic patterns of pulmonary vascular disease in individuals with primary pulmonary hypertension diagnosed by standardized clinical and laboratory criteria.
对美国国立卫生研究院心肺血液研究所发起的原发性肺动脉高压登记处58例患者经活检、肺切除术或尸检获得的肺组织中的肺血管进行了定性和定量研究。49例患者(84%)的高血压性血管疾病主要或仅累及肌性肺动脉和小动脉。在这49例患者中,均观察到肺动脉中层肥厚,48例还伴有内膜或管腔病变。根据主要组织病理学特征,48例患者中的25例被归类为具有丛状病变的肺动脉病,其特征为同心层状内膜纤维化、偏心内膜纤维化和丛状病变的组合;这25例中的9例还存在再通血栓。19例患者观察到具有血栓性病变的肺动脉病,其定义为存在偏心内膜纤维化和再通血栓但无丛状病变。4例患者发现有同心或偏心的内膜纤维化,但无丛状或血栓性病变。在登记处其余9例患者中,7例存在肺静脉闭塞性疾病,1例存在慢性肺静脉高压。另一例患者的肺活检标本中肺血管在显微镜下正常。一般来说,有丛状病变的患者和有肺静脉闭塞性疾病的患者的预后比有血栓性病变的患者差得多。本研究表明,在通过标准化临床和实验室标准诊断为原发性肺动脉高压的个体中存在几种不同的肺血管疾病组织病理学模式。