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伴有原发性涎腺淋巴瘤的家族性干燥综合征

Familial Sjögren's syndrome with associated primary salivary gland lymphoma.

作者信息

Lichtenfeld J L, Kirschner R H, Wiernik P H

出版信息

Am J Med. 1976 Feb;60(2):286-92. doi: 10.1016/0002-9343(76)90439-3.

Abstract

Primary salivary gland lymphoma has been rarely documented in patients with or without Sjögren's syndrome. The association of disseminated lymphoreticular neoplasms with Sjögren's syndrome has been recognized, and the malignancy is usually widespread at the time of diagnosis. Familial occurrence of Sjögren's syndrome is likewise infrequently observed. In the present report we describe a patient with Sjögren's syndrome in whom a primary parotid gland lymphoma subsequently developed. In addition to the propositus, two of four siblings had definite evidence of Sjögren's syndrome and a third had several abnormal studies commonly associated with the disease. This observation suggests that genetic influence alone or in conjunction with other factors may facilitate the development of Sjögren's syndrome.

摘要

原发性涎腺淋巴瘤在患有或未患有干燥综合征的患者中均鲜有记载。已认识到弥漫性淋巴网状肿瘤与干燥综合征有关,并且在诊断时恶性肿瘤通常已广泛扩散。干燥综合征的家族性发病同样很少见。在本报告中,我们描述了一名患有干燥综合征的患者,该患者随后发生了原发性腮腺淋巴瘤。除了先证者外,四个兄弟姐妹中有两个有明确的干燥综合征证据,第三个有几项与该疾病相关的异常检查结果。这一观察结果表明,单独的遗传影响或与其他因素共同作用可能会促进干燥综合征的发生。

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