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[滤泡性树突状细胞肉瘤的临床病理研究]

[Clinicopathological study on the follicular dendritic cell sarcoma].

作者信息

Zhang Shu-hong, Zhou Xiao-ge, Zheng Yuan-yuan, Zhang Yan-ning, Wang Peng, Xie Jian-lan, Jin Yan, Zheng Xiao-dan

机构信息

Department of Pathology, Beijing Friendship Hospital, Capital University of Medical Sciences, China.

出版信息

Zhonghua Zhong Liu Za Zhi. 2010 Feb;32(2):123-7.

Abstract

OBJECTIVE

To investigate the clinicopathologic features and differential diagnostic methods for follicular dendritic cell sarcoma.

METHODS

Histological and immunohistochemical examinations and EBER in situ hybridization were used to investigate the pathological features of 5 cases of follicular dendritic cell sarcoma, and related literature was reviewed.

RESULTS

There were 3 males and 2 females with a median age of 54 years (range, 28 - 75 years). The location of lesions included lymph node (2 cases), tonsil (1 case), stomach (1 case), and liver (1 case). The growth patterns were fascicular or whorls and/or diffuse. The neoplastic cells were spindle or ovoid in shape with indistinct border and slightly eosinophilic cytoplasm. The nuclei were round, oval or spindle in shape with small distinct nucleoli. Warthin-Finkeldey-like multinucleated giant cells were detected in two cases. Mitotic figures were found in 1-22/10 HPF. Immunohistochemical staining showed that CD21 and CD23 (3 of 5), CD35 (4 of 5), D2-40 (4 of 4), and CXCL13 (3 of 4) were positive in neoplastic cells. EBER was detected in one of five cases by in situ hybridization. Four cases were followed-up for 6 approximately 25 months and no recurrence or death was observed yet.

CONCLUSION

Follicular dendritic cell sarcoma is an extremely rare and should be considered as a moderately malignant tumor, and may present histological polymorphism with certain distinctive features. Immunohistochemistry is necessary in differential diagnosis to distinguish from other tumors.

摘要

目的

探讨滤泡树突状细胞肉瘤的临床病理特征及鉴别诊断方法。

方法

采用组织学、免疫组化检查及EBER原位杂交技术,对5例滤泡树突状细胞肉瘤的病理特征进行研究,并复习相关文献。

结果

5例患者中男性3例,女性2例,中位年龄54岁(范围28 - 75岁)。病变部位包括淋巴结(2例)、扁桃体(1例)、胃(1例)和肝(1例)。生长方式为束状或漩涡状和/或弥漫性。肿瘤细胞呈梭形或卵圆形,边界不清,胞质轻度嗜酸性。细胞核呈圆形、椭圆形或梭形,核仁小而明显。2例检测到Warthin-Finkeldey样多核巨细胞。每10个高倍视野中可见1 - 22个核分裂象。免疫组化染色显示肿瘤细胞中CD21和CD23(5例中的3例)、CD35(5例中的4例)、D2-40(4例中的4例)及CXCL13(4例中的3例)呈阳性。原位杂交检测5例中有1例EBER阳性。4例随访6至25个月,未见复发或死亡。

结论

滤泡树突状细胞肉瘤极为罕见,应被视为中度恶性肿瘤,可能呈现具有某些独特特征的组织学多态性。免疫组化在鉴别诊断中是必要的,以与其他肿瘤相区分。

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