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巨大血管瘤性骨质溶解症(戈勒姆-斯托特综合征)的放射治疗

Radiotherapy in massive angiomatous osteolysis (Gorham-Stout's syndrome).

作者信息

Bek V, Haicl Z, Kolár J, Bednár B

出版信息

Strahlentherapie. 1981 Dec;157(12):813-8.

PMID:7330910
Abstract

The cases of two young men with the Gorham-Stout's syndrome of massive angiomatous osteolysis are presented. Attempted surgical removal of the pathological angiomatous tissue proved unsuccessful. Telegammatherapy with each patient receiving total focal dose of 40.0 Gy fractionated over a period of 4 weeks resulted in speedy and complete arrest of osteolysis, and in partial recalcification of the bone tissue destroyed. In one patient the favourable condition has been lasting for 9 years, in the other for 8 months from the end of the course of radiotherapy. The authors discuss the cause of a central fracture of the first patient's left acetabulum which was noted 5 years after the radiotherapy. Proceeding from their experience so far, the authors describe radiotherapy in the Gorham-Stout's syndrome as a method of choice, and give a list of the therapeutical principles.

摘要

本文介绍了两例患有巨大血管瘤性骨质溶解的戈勒姆-斯托特综合征的年轻男性病例。试图手术切除病理性血管瘤组织未获成功。对每位患者进行为期4周的分次照射,总局部剂量为40.0 Gy的远距γ射线治疗,导致骨质溶解迅速完全停止,且部分被破坏的骨组织重新钙化。放疗结束后,一名患者的良好状况持续了9年,另一名患者持续了8个月。作者讨论了第一名患者放疗5年后出现的左髋臼中央骨折的原因。基于目前的经验,作者将戈勒姆-斯托特综合征的放疗描述为一种首选治疗方法,并给出了治疗原则清单。

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