Suppr超能文献

[脊髓内血管母细胞瘤。关于最近一组20例病例]

[Intraspinal hemangioblastoma. Apropos of a recent series of 20 cases].

作者信息

Emery E, Hurth M, Lacroix-Jousselin C, David P, Richard S

机构信息

Service de Neurochirurgie, Hôpital Bicêtre, Paris.

出版信息

Neurochirurgie. 1994;40(3):165-73.

PMID:7723923
Abstract

This report deals with a series of 20 patients admitted for a spinal hemangioblastoma between 1970 and 1993, 18 of whom between 1978 and 1993. There are 8 men and 12 women and the onset of spinal symptoms is before the age of 50 years for 76% of the patients. Nineteen patients have an intra-dural tumor (extramedullary 15.5%, intramedullary 75% with 62.5% close to the dorsal surface, 37.5% partly out, none totally enclosed with spinal cord) and only one patient has an extra-dural tumor. Cysts are present in 70% of our cases. Two cases have been revealed by an hemorrhagic syndrome. Ten cases belong to a von Hippel-Lindau (vHL) disease. Nineteen patients were operated on, one patient died. Total resection of the tumor was performed in 17. Symptoms improved postoperatively in 8 patients, were inchanged in 6, and worsened temporary in 4. MRI with gadolinium is the best procedure for both the diagnosis and the follow-up. After surgery, the prognosis is very good for sporadic cases with a single spinal lesion whereas it is very poor in case of vHl disease. For these patients (50% of our cases), half of them died because of the evolution of multifocal lesions even if they were operated on several times. Thus, each patient should have a precise check-up (SNC and visceral lesions). The gene causing vHL disease located on the short arm of the chromosome 3 has just been characterized. This will help to elaborate a presymptomatic diagnosis and a better screening of the patients with the hope of a specific treatment.

摘要

本报告涉及1970年至1993年间收治的20例脊髓血管母细胞瘤患者,其中18例在1978年至1993年间。患者中有8名男性和12名女性,76%的患者脊髓症状出现在50岁之前。19例患者患有硬膜内肿瘤(髓外15.5%,髓内75%,其中62.5%靠近背侧表面,37.5%部分突出,无完全包绕脊髓者),仅1例患者患有硬膜外肿瘤。70%的病例存在囊肿。2例由出血综合征发现。10例属于冯·希佩尔-林道(vHL)病。19例患者接受了手术,1例死亡。17例患者进行了肿瘤全切。术后8例患者症状改善,6例不变,4例暂时恶化。钆增强MRI是诊断和随访的最佳方法。手术后,单发脊髓病变的散发病例预后非常好,而vHL病患者预后很差。对于这些患者(占我们病例的50%),即使多次手术,其中一半仍因多灶性病变进展而死亡。因此,每位患者都应进行精确检查(神经系统和内脏病变)。位于3号染色体短臂上导致vHL病的基因刚刚被鉴定。这将有助于开展症状前诊断和更好地筛查患者,有望进行特异性治疗。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验