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腮腺黏膜相关组织低度淋巴瘤:一例应用流式细胞术免疫表型分析的细针穿刺细胞学诊断病例报告

Low-grade lymphoma of mucosa-associated tissue in the parotid gland: a case report of fine-needle aspiration cytology diagnosis using flow cytometric immunophenotyping.

作者信息

Cha I, Long S R, Ljung B M, Miller T R

机构信息

Department of Cytopathology, University of California, San Francisco 94143, USA.

出版信息

Diagn Cytopathol. 1997 Apr;16(4):345-9. doi: 10.1002/(sici)1097-0339(199704)16:4<345::aid-dc8>3.0.co;2-c.

Abstract

A 66-year-old woman with Sjögren's syndrome for 7 years presented with an enlarged right parotid gland. The left parotid gland, which showed myoepithelial sialadenitis (MESA), had been resected 4 years earlier. A fine-needle aspiration (FNA) biopsy of the right parotid gland was performed. Examination of the smears revealed cells of intermediate size with a round-to-irregular nuclear outline and distinct pale cytoplasm intermixed with small mature round lymphocytes. The chromatin was slightly paler and less clumped than in small mature lymphocytes. A small inconspicuous nucleolus was seen in most of the cells. Flow cytometry immunophenotyping performed on the FNA biopsy material showed a monoclonal population of B cells with kappa light chain restriction. The cytomorphology coupled with the immunophenotyping study in this clinical context suggested the diagnosis of low-grade B-cell lymphoma of mucosa-associated lymphoid tissue (MALT). Extensive staging work-up revealed no evidence of disseminated disease. The right parotid gland was surgically excised. Histology and gene rearrangement studies confirmed the cytologic diagnosis. To our knowledge, this is the first description of a low-grade lymphoma of MALT in a salivary gland to be diagnosed by FNA.

摘要

一名患有干燥综合征7年的66岁女性,出现右侧腮腺肿大。4年前已切除显示为肌上皮涎腺炎(MESA)的左侧腮腺。对右侧腮腺进行了细针穿刺(FNA)活检。涂片检查发现中等大小的细胞,核轮廓圆形至不规则,胞质淡染明显,与小的成熟圆形淋巴细胞混合。其染色质比小的成熟淋巴细胞略淡且聚集程度较低。大多数细胞可见一个小的不明显核仁。对FNA活检材料进行的流式细胞术免疫表型分析显示,B细胞单克隆群体存在κ轻链限制。在此临床背景下,细胞形态学与免疫表型研究提示诊断为黏膜相关淋巴组织(MALT)低度B细胞淋巴瘤。广泛的分期检查未发现播散性疾病的证据。右侧腮腺被手术切除。组织学和基因重排研究证实了细胞学诊断。据我们所知,这是首例通过FNA诊断的涎腺MALT低度淋巴瘤的描述。

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