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一例罕见的脾脏囊性淋巴管瘤病例。

An unusual case of cystic lymphangiomatosis of the spleen.

作者信息

Spapen H D, Reynaert H, Debeuckelaere S, Achten E, Somers G

机构信息

Department of Internal Medicine, Vrije Universiteit, Brussels, Belgium.

出版信息

Neth J Med. 1990 Aug;37(1-2):24-6.

PMID:2215829
Abstract

Isolated lymphangiomatosis of the spleen is rare. When present, it is usually considered to be accompanied by splenomegaly. We describe a case of cystic lymphangiomatosis in a patient with a normal-sized spleen. While ultrasound, angiography and computed tomography are considered to complement each other in reaching a preoperative diagnosis of splenic lymphangiomatosis, in the present case, magnetic resonance imaging proved to be an additional helpful non-invasive diagnostic method.

摘要

脾脏孤立性淋巴管瘤病较为罕见。一旦出现,通常被认为伴有脾肿大。我们描述了一例脾脏大小正常的患者的囊性淋巴管瘤病。虽然超声、血管造影和计算机断层扫描在脾淋巴管瘤病的术前诊断中被认为是相辅相成的,但在本病例中,磁共振成像被证明是一种额外有用的非侵入性诊断方法。

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