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地中海贫血中的骨髓异位。

The marrow heterotopia in thalassemia.

作者信息

Papavasiliou C, Gouliamos A, Andreou J

出版信息

Eur J Radiol. 1986 May;6(2):92-6.

PMID:3720753
Abstract

The subject of marrow heterotopia has been reviewed on the basis of 15 cases suffering from thalassemia. Other cases reported in the literature were also reviewed. Using conventional radiography, scintigraphy, computerized tomography and myelography, 17% of the cases admitted into the hospital with the diagnosis of Thalassemia, were found to have macroscopic masses of marrow heterotopia. The most common site of development of these masses was the costovertebral gutter, followed by the anterior end of the ribs and the extradural space of the spinal canal. In one case, masses were located in the maxillary antra. The clinical implications, the pathogenesis of the masses and the differential diagnosis from other tumour-like entities are discussed. Three patients presented with symptoms and signs of spinal cord compression. All three patients were treated satisfactorily with small doses of radiotherapy.

摘要

基于15例地中海贫血患者,对骨髓异位的主题进行了综述。同时也对文献中报道的其他病例进行了回顾。通过传统放射学、闪烁扫描、计算机断层扫描和脊髓造影检查发现,在因地中海贫血入院的患者中,17%存在肉眼可见的骨髓异位肿块。这些肿块最常见的发生部位是肋椎沟,其次是肋骨前端和椎管硬膜外间隙。有1例肿块位于上颌窦。文中讨论了这些肿块的临床意义、发病机制以及与其他肿瘤样病变的鉴别诊断。3例患者出现脊髓受压的症状和体征。所有3例患者均通过小剂量放疗得到了满意的治疗效果。

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