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[肺动脉肿瘤性血栓形成所致的肺动脉高压]

[Pulmonary arterial hypertension caused by neoplastic thrombosis of the pulmonary artery].

作者信息

Beaufils P, Cywiner-Golenzer C, Perrault M A, Rymer R, Slama R

出版信息

Arch Mal Coeur Vaiss. 1978 Jul;71(7):816-22.

PMID:102282
Abstract

Neoplastic thrombosis of the pulmonary artery is a rare and little known cause of pulmonary arterial hypertension. The clinical picture is one of acute respiratory failure and progressive right ventricular failure caused by pre-capillary pulmonary hypertension. In the living patient there is no way of distinguishing this condition from that of subacute cor pulmonale due to embolism, especially as the primary tumour is not always found either because it is too small or because it has already regressed by the time it has metastasised. The diagnosis usually rests on histological examination of the lungs, and two pathological types can be distinguished: carcinomatous lymphangitis with secondary invasion and thrombosis of the pulmonary arterioles on the one hand, and the neoplastic arterial emboli of a chorio-epithelioma on the other.

摘要

肺动脉肿瘤性血栓形成是一种罕见且鲜为人知的肺动脉高压病因。临床表现为急性呼吸衰竭和由毛细血管前肺动脉高压引起的进行性右心衰竭。在活体患者中,无法将这种情况与因栓塞导致的亚急性肺心病相区分,特别是由于原发性肿瘤并不总是能被发现,要么是因为它太小,要么是因为在转移时它已经消退了。诊断通常依靠肺组织学检查,可区分出两种病理类型:一方面是癌性淋巴管炎伴肺动脉小分支的继发性侵犯和血栓形成,另一方面是绒毛膜上皮癌的肿瘤性动脉栓子。

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