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胸腺肿瘤。88例手术病例回顾。

Tumours of the thymus. A review of 88 operation cases.

作者信息

Sellors T H, Thackray A C, Thomson A D

出版信息

Thorax. 1967 May;22(3):193-220. doi: 10.1136/thx.22.3.193.

Abstract

Eighty-eight cases of thymoma are discussed with the object of trying to co-ordinate the histological and clinical features. The pathological specimens were in all cases obtained at operation. The pathology classification introduced by Thomson and Thackray in 1957 has been found to correspond adequately with the clinical pattern. The most common groups of tumours are basically epithelial and can be separated into five or six subdivisions, each of which has a separate pattern of behaviour. Lymphoid and teratomatous tumours also occur, but there were only two examples in this series. Clinically, separation of patients who suffered from myasthenia (38) and those who did not (50) affords the first main grouping. The majority of patients who had myasthenia gravis had tumours classified as epidermoid (19) and lymphoepithelial (14), the former with a more malignant appearance and behaviour than the latter. Removal of the tumour with or without radiation gave considerable and sometimes complete relief from myasthenic symptoms. Non-myasthenic thymoma (50) was usually discovered as a result of pressure signs or in the course of routine radiography. Spindle or oval celled tumours followed a benign pattern whereas undifferentiated thymoma was in every sense malignant, as also were teratomatous growths. Granulomatous or Hodgkin-like thymomas were of special interest and had an unpredictable course, some patients surviving many years after what was regarded as inadequate treatment. The place of radiotherapy as a pre- or post-operative agent complementary to surgery is discussed.

摘要

本文讨论了88例胸腺瘤病例,旨在协调组织学和临床特征。所有病例的病理标本均在手术中获取。1957年汤姆森和萨克雷提出的病理分类已被发现与临床模式充分对应。最常见的肿瘤类型基本为上皮性,可分为五六个亚类,每个亚类都有各自独特的行为模式。也会出现淋巴样和畸胎瘤样肿瘤,但本系列中仅有两例。临床上,首先可将患有重症肌无力的患者(38例)和未患重症肌无力的患者(50例)区分开来。大多数重症肌无力患者的肿瘤分类为表皮样(19例)和淋巴上皮样(14例),前者的外观和行为比后者更具恶性。切除肿瘤并辅以或不辅以放疗,可使重症肌无力症状得到显著缓解,有时甚至完全缓解。非重症肌无力性胸腺瘤(50例)通常是由于压迫症状或在常规放射检查过程中被发现。梭形或椭圆形细胞肿瘤呈良性模式,而未分化胸腺瘤无论从哪方面看都是恶性的,畸胎瘤样生长也是如此。肉芽肿性或霍奇金样胸腺瘤特别值得关注,其病程难以预测,一些患者在被认为治疗不充分的情况下仍存活多年。本文还讨论了放疗作为手术前或手术后辅助手术的治疗手段的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbd4/471606/d3c3a8a91a17/thorax00093-0003-a.jpg

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