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在干燥综合征诊断之前诊断出的伴有多房性胸腺囊肿的胸腺淋巴样增生。

Thymic lymphoid hyperplasia with multilocular thymic cysts diagnosed before the Sjögren syndrome diagnosis.

作者信息

Minato Hiroshi, Kinoshita Eriko, Nakada Satoko, Nojima Takayuki, Tanaka Makoto, Usuda Katsuo, Sagawa Motoyasu, Iwao Haruka, Tanaka Masao, Doai Mariko, Takahashi Tomoko, Shibata Naoko

机构信息

Department of Pathology and Laboratory Medicine, Kanazawa Medical University, 1-1 Daigaku, Uchinada, Kahoku, Ishikawa, 9200293, Japan.

Department of Thoracic Surgery, Kanazawa Medical University, Uchinada, Ishikawa, Japan.

出版信息

Diagn Pathol. 2015 Jul 16;10:103. doi: 10.1186/s13000-015-0332-y.

Abstract

BACKGROUND

Thymic lymphoid hyperplasia is often present with myasthenia gravis as well as other autoimmune diseases such as systemic lupus erythematosus and rheumatoid arthritis. Of the 4 cases of thymic lymphoid hyperplasia associated with Sjögren syndrome that have been reported, no case with a thymic lesion diagnosis that led to the diagnosis of Sjögren syndrome has been reported. We herein report a case of thymic lymphoid hyperplasia with multilocular thymic cysts, diagnosed before Sjögren syndrome.

CASE PRESENTATION

A 37-year-old Japanese woman had an approximate 5-cm anterior mediastinal mass detected by chest imaging. The resected lesion revealed multilocular thymic cysts that were filled with colloid-like material. Histology showed lymph follicular hyperplasia with many epithelial cysts. The epithelium consisted of thymic medullary epithelium, and no epithelial proliferation was seen in the lymphoid tissue. Lymphocytes were composed of an organized mixed population of mature T and B cells without significant atypia. The infiltrated B cells did not reveal light chain restriction or immunoglobulin heavy chain gene rearrangement. After the pathological diagnosis of thymic lesion, tests for the presence of autoantibodies were positive for antinuclear antibodies, rheumatic factor, and anti-SSA/Ro antibodies. The Schirmer's, chewing gum, and Saxon tests showed decreased salivary and lacrimal secretion. Lip biopsy showed focal lymphocytic sialadenitis. The signs and symptoms of Sjögren syndrome had not resolved, without aggravation, 1 year after the thymectomy.

CONCLUSION

When a case with thymic lymphoid hyperplasia without myasthenia gravis is encountered, it is essential to consider the presence of another autoimmune disease including Sjögren syndrome.

摘要

背景

胸腺淋巴样增生常与重症肌无力以及其他自身免疫性疾病如系统性红斑狼疮和类风湿关节炎同时出现。在已报道的4例与干燥综合征相关的胸腺淋巴样增生病例中,尚无因胸腺病变诊断而导致干燥综合征确诊的病例报道。我们在此报告1例在干燥综合征确诊前诊断为多房性胸腺囊肿伴胸腺淋巴样增生的病例。

病例介绍

一名37岁日本女性经胸部影像学检查发现前纵隔有一约5 cm肿物。切除的病变显示为多房性胸腺囊肿,内充满胶样物质。组织学检查显示淋巴滤泡增生伴许多上皮囊肿。上皮由胸腺髓质上皮组成,淋巴组织未见上皮增生。淋巴细胞由成熟T细胞和B细胞组成的有序混合群体构成,无明显异型性。浸润的B细胞未显示轻链限制或免疫球蛋白重链基因重排。胸腺病变病理诊断后,自身抗体检测抗核抗体、类风湿因子和抗SSA/Ro抗体均呈阳性。施默试验、咀嚼口香糖试验和撒克逊试验显示唾液和泪液分泌减少。唇活检显示局灶性淋巴细胞性涎腺炎。胸腺切除术后1年,干燥综合征的体征和症状未缓解,也未加重。

结论

当遇到无重症肌无力的胸腺淋巴样增生病例时,必须考虑包括干燥综合征在内的其他自身免疫性疾病的存在。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61bb/4502560/8a34c153b296/13000_2015_332_Fig1_HTML.jpg

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