[Clinical and cytological characteristics of primary thyroid lymphoma: a fine needle aspiration study of 10 cases].

Q3 Medicine
L Chen, Z Y Liu, J S Zhang
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引用次数: 0

Abstract

Objective: To evaluate the cytological features of primary thyroid lymphoma diagnosed by fine needle aspiration (FNA), using histology as the gold standard. Methods: FNA samples from the 10 cases of primary thyroid lymphoma diagnosed between October 2016 and November 2024 at the Department of Pathology, Beijing Hospital were analyzed. Clinical data were retrospectively reviewed. The smears, cell block slides, immunochemical and histological findings were examined. Results: Among the 10 patients, there were 2 males and 8 females. The median age was 72 (range, 70 to 76) years. Six patients showed rapid enlargement of new or existing tumors within a short period of time (1-2 months). The median diameter of the lesions was 5.0 (range, 4.5 to 5.3) cm. Thyroid FNA samples showed diffuse dysplastic lymphocytoid cells. Diffuse large B-cell lymphoma (DLBCL) was composed of highly consistent and dysplastic lymphocytoid cells with significant nuclear enlargement, obvious nucleoli, frequent mitoses and karyorrhexis, while indolent lymphomas were composed of mixed and mild atypical lymphocytoid cells with various cell sizes, small nucleoli, infrequent mitosis and karyorrhexis. A small number of thyroid follicular cells with eosinophilic alteration were also present. Immunochemistry on smear indicated a predominant B-cell population with Ki-67 index of 5% to 90%. All patients underwent core needle biopsy or resection except one case that only had cell block preparation. The final pathological diagnoses included 5 cases of DLBCL, 3 cases of extranodal marginal zone lymphoma of mucosa associated lymphoid tissue, 1 case of follicular lymphoma (grade 3b) with transformation of diffuse large B-cell lymphoma, and 1 case of chronic lymphocytic leukemia/small lymphocytic lymphoma with concurrent thyroid papillary carcinoma. Six patients had concurrent Hashimoto's thyroiditis. Conclusions: Primary thyroid lymphoma is rare, almost all of them are B-cell origin, and it often presents with rapid enlargement of neck masses. Aggressive lymphoma has prominent cell atypia and can be diagnosed by FNA. For indolent lymphoma, although the cell atypia is mild, there are still cytological characteristics of lymphoma. Therefore, FNA can be used to diagnose hematopoietic and lymphoid malignancies when combined with thyroid diffuse lesion on imaging and the clinical history of rapid growth in a short period of time. An accurate classification generally requires biopsy and molecular clonality examination.

原发性甲状腺淋巴瘤的临床及细胞学特征:细针穿刺10例研究。
目的:探讨细针穿刺(FNA)诊断原发性甲状腺淋巴瘤的细胞学特征,以组织学为金标准。方法:对2016年10月至2024年11月北京医院病理科诊断的10例原发性甲状腺淋巴瘤患者的FNA样本进行分析。回顾性分析临床资料。涂片、细胞块切片、免疫化学和组织学检查。结果:10例患者中男性2例,女性8例。中位年龄为72岁(70 - 76岁)。6例患者在短时间内(1-2个月)出现新发或已有肿瘤迅速扩大。病灶的中位直径为5.0(范围为4.5 - 5.3)cm。甲状腺FNA样品显示弥漫性发育不良的淋巴细胞样细胞。弥漫性大b细胞淋巴瘤(DLBCL)由高度一致和发育不良的淋巴细胞组成,细胞核明显增大,核仁明显,有丝分裂和核分裂频繁;惰性淋巴瘤由混合和轻度不典型淋巴细胞组成,细胞大小不一,核仁小,有丝分裂和核分裂少见。少量嗜酸性改变的甲状腺滤泡细胞也可见。免疫化学涂片示以b细胞群为主,Ki-67指数为5% ~ 90%。除1例仅行细胞阻滞准备外,所有患者均行核心针活检或切除。最终病理诊断为DLBCL 5例,粘膜相关淋巴组织结外边缘区淋巴瘤3例,滤泡性淋巴瘤(3b级)伴弥漫性大b细胞淋巴瘤转化1例,慢性淋巴细胞白血病/小淋巴细胞淋巴瘤合并甲状腺乳头状癌1例。6例患者并发桥本甲状腺炎。结论:原发性甲状腺淋巴瘤罕见,几乎全部为b细胞源性淋巴瘤,常表现为颈部肿物迅速增大。侵袭性淋巴瘤具有突出的细胞异型性,可通过FNA诊断。对于惰性淋巴瘤,虽然细胞异型性轻微,但仍有淋巴瘤的细胞学特征。因此,结合影像学上甲状腺弥漫性病变和短时间内快速生长的临床病史,FNA可用于诊断造血和淋巴系统恶性肿瘤。准确的分类通常需要活检和分子克隆检查。
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来源期刊
中华病理学杂志
中华病理学杂志 Medicine-Medicine (all)
CiteScore
1.00
自引率
0.00%
发文量
10377
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