与Castleman病相关的咽旁间隙滤泡树突状细胞肉瘤。

IF 2.5 4区 医学 Q2 PATHOLOGY
Shunsuke Koga, Du Wei, Gabriel C Caponetti, Kumarasen Cooper
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引用次数: 0

摘要

滤泡树突状细胞肉瘤(FDCS)是一种罕见的源自滤泡树突状细胞的恶性肿瘤。它偶尔与单中心Castleman病(UCD)有关,特别是透明血管(HV)变异(HV-UCD)。我们报告一位56岁女性,在HV-UCD的背景下,在咽旁间隙出现FDCS。患者表现为无痛性右颈部肿块和广泛的颈部淋巴结病,无全身症状。手术切除咽旁肿物后发现淋巴结内FDCS伴HV-UCD特征。免疫组织化学证实了病变细胞的滤泡树突状细胞谱系,CD21和CD23阳性。随后从2A、2B、3和4层淋巴结进行清扫,显示出没有FDCS残留的HV-UCD特征。该病例突出了FDCS所代表的诊断挑战,特别是当发生在异常位置时。虽然完全手术切除仍然是标准的治疗方法,但长期随访是必要的,以监测复发或转移。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Follicular Dendritic Cell Sarcoma of the Parapharyngeal Space Arising in Association With Castleman Disease.

Follicular dendritic cell sarcoma (FDCS) is a rare malignant neoplasm of follicular dendritic cell origin. It is occasionally associated with unicentric Castleman disease (UCD), particularly the hyaline-vascular (HV) variant (HV-UCD). We report a 56-year-old woman with FDCS arising in the parapharyngeal space in the background of HV-UCD. The patient presented with a painless right neck mass and extensive cervical lymphadenopathy without systemic symptoms. Surgical resection of the parapharyngeal mass revealed FDCS in the lymph nodes with features of HV-UCD. Immunohistochemistry confirmed the follicular dendritic cell lineage of the lesional cells, with positivity for CD21 and CD23. Subsequent lymph node dissection from levels 2A, 2B, 3, and 4 showed features of HV-UCD without residual FDCS. This case highlights the diagnostic challenge FDCS represents, particularly when arising in an unusual location. While complete surgical excision remains the standard of care, long-term follow-up is necessary to monitor for recurrence or metastasis.

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来源期刊
Pathology International
Pathology International 医学-病理学
CiteScore
4.50
自引率
4.50%
发文量
102
审稿时长
12 months
期刊介绍: Pathology International is the official English journal of the Japanese Society of Pathology, publishing articles of excellence in human and experimental pathology. The Journal focuses on the morphological study of the disease process and/or mechanisms. For human pathology, morphological investigation receives priority but manuscripts describing the result of any ancillary methods (cellular, chemical, immunological and molecular biological) that complement the morphology are accepted. Manuscript on experimental pathology that approach pathologenesis or mechanisms of disease processes are expected to report on the data obtained from models using cellular, biochemical, molecular biological, animal, immunological or other methods in conjunction with morphology. Manuscripts that report data on laboratory medicine (clinical pathology) without significant morphological contribution are not accepted.
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