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原发性干燥综合征初发表现为下颌下黏膜相关淋巴组织淋巴瘤:一例报告

Primary Sjögren's syndrome initially presenting as submandibular mucosa-associated lymphoid tissue lymphoma: A case report.

作者信息

Chen Liang-Yu, Tsai Ming-Hsui, Tsai Li-Tai, Lu Hsin-Man, Jan Chia-Ing

机构信息

Department of Otolaryngology - Head and Neck Surgery, China Medical University and Hospital, Taichung 40402, Taiwan, R.O.C.

Department of Otolaryngology - Head and Neck Surgery, China Medical University and Hospital, Taichung 40402, Taiwan, R.O.C.; Graduate Institute of Clinical Medical Science, China Medical University, Taichung 40402, R.O.C.

出版信息

Oncol Lett. 2016 Feb;11(2):921-924. doi: 10.3892/ol.2015.3980. Epub 2015 Nov 30.

Abstract

The present study reports the case of a 24-year-old female affected with primary Sjögren's syndrome (pSS), who presented with mucosa-associated lymphoid tissue (MALT) lymphoma of the submandibular gland. Reports of such cases, particularly in young patients, are very rare. The patient, who presented no oral or ocular symptoms prior to the development of the mass, underwent surgical ablation of the gland, and MALT lymphoma was diagnosed by histopathology. Since MALT lymphoma in the submandibular gland is rarely observed in otherwise healthy young females, a rheumatologist and an oncologist were consulted. Following a number of immunological tests, the results of the Schirmer's and Saxon tests were negative. However, the antinuclear antibody test revealed a speckled appearance, and there was also strong positivity for the serological markers of Sjögren's syndrome. Consequently, pSS was diagnosed, despite the fact that the patient did not fulfill all the diagnostic criteria for the disease. Therefore, MALT lymphoma in a single salivary gland should be used as a differential diagnosis for Sjögren's syndrome in young asymptomatic patients. Additionally, a multidisciplinary team is required for the treatment and management of these patients.

摘要

本研究报告了一例24岁患有原发性干燥综合征(pSS)的女性病例,该患者表现为下颌下腺黏膜相关淋巴组织(MALT)淋巴瘤。此类病例的报告,尤其是在年轻患者中,非常罕见。该患者在肿物出现之前没有口腔或眼部症状,接受了腺体的手术切除,通过组织病理学诊断为MALT淋巴瘤。由于在其他方面健康的年轻女性中很少观察到下颌下腺的MALT淋巴瘤,因此咨询了风湿病学家和肿瘤学家。经过多项免疫学检查,施密特试验和萨克森试验结果均为阴性。然而,抗核抗体试验显示为斑点状外观,干燥综合征的血清学标志物也呈强阳性。因此,尽管该患者未满足该疾病的所有诊断标准,但仍诊断为pSS。所以,单个唾液腺的MALT淋巴瘤应用于对年轻无症状患者的干燥综合征进行鉴别诊断。此外,这些患者的治疗和管理需要一个多学科团队。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3da/4734050/85d792c7fc63/ol-11-02-0921-g00.jpg

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