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肺静脉闭塞性疾病作为混合性结缔组织病患者肺动脉高压的主要病因

Pulmonary veno-occlusive disease as a primary cause of pulmonary hypertension in a patient with mixed connective tissue disease.

作者信息

Zhang Lizhi, Visscher Daniel, Rihal Charanjit, Aubry Marie-Christine

机构信息

Department of Pathology, Mayo Clinic College of Medicine, 200 First Street SW, Rochester, MN 55905, USA.

出版信息

Rheumatol Int. 2007 Oct;27(12):1163-5. doi: 10.1007/s00296-007-0362-1. Epub 2007 May 23.

Abstract

Mixed connective tissue disease (MCTD) is a systemic disease seen in a group of patients with overlapping clinical features of lupus, scleroderma, polymyositis, and rheumatoid arthritis. A defining feature of MCTD is the presence of antibodies against the U1-ribonucleoprotein (U1-RNP) complex. Pulmonary hypertension is the major cause of death in MCTD. We report an autopsy case of MCTD with pulmonary hypertension. The U1-RNP antibody of this patient was 171.9 U (normal < 25.0 U). The immediate cause of death was attributed to acute pulmonary embolism at left lower lobe. A severe vasculopathy characterized by fibrotic occlusion of small veins and venules, associated with prominent capillary congestion, was consistent with pulmonary veno-occlusive disease (PVOD). This is the first case reported in which PVOD is the primary cause of pulmonary hypertension in MCTD.

摘要

混合性结缔组织病(MCTD)是一种系统性疾病,见于一组具有狼疮、硬皮病、多发性肌炎和类风湿关节炎重叠临床特征的患者。MCTD的一个决定性特征是存在针对U1核糖核蛋白(U1-RNP)复合物的抗体。肺动脉高压是MCTD的主要死亡原因。我们报告一例伴有肺动脉高压的MCTD尸检病例。该患者的U1-RNP抗体为171.9 U(正常<25.0 U)。直接死因归因于左下叶急性肺栓塞。以小静脉和微静脉纤维性闭塞为特征的严重血管病变,伴有明显的毛细血管充血,符合肺静脉闭塞病(PVOD)。这是首例报道的以PVOD作为MCTD肺动脉高压主要原因的病例。

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