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头颈部结外滤泡树突状细胞肉瘤:三例新病例并文献复习

Extranodal follicular dendritic cell sarcoma of the head and neck region: three new cases, with a review of the literature.

作者信息

Biddle David A, Ro Jae Y, Yoon Gil S, Yong Yap-Whang H, Ayala Alberto G, Ordonez Nelson G, Ro Jungsil

机构信息

Department of Pathology, The University of Texas M. D. Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, TX 77030, USA.

出版信息

Mod Pathol. 2002 Jan;15(1):50-8. doi: 10.1038/modpathol.3880489.

Abstract

Extranodal follicular dendritic cell (FDC) sarcoma of the head and neck region is uncommon, with 16 well-documented cases previously reported (four in the tonsil, four in the pharynx, two in the palate, five in the soft tissue, and one in the thyroid). We here report an additional three cases of extranodal FDC sarcoma in the tonsil (two cases) and pharynx (one case). In these new cases, the neoplastic cells were arranged in diffuse, fascicular, and vaguely whorled growth patterns. A background lymphocytic infiltrate was sprinkled throughout the neoplasms, with focal prominent perivascular cuffing. Scattered multinucleated giant cells were present. Immunohistochemically, tumor cells were strongly and diffusely positive for follicular dendritic cell markers CD21 and CD35. Tumor cells were diffusely positive for fascin and negative for leukocyte common antigen, S-100 protein, cytokeratin, and Epstein-Barr virus (EBV) latent membrane protein-1 (EBV-LMP). EBV was also not detected in the tumor cells by in situ hybridization for EBV-encoded RNAs. FDC sarcomas are probably an underrecognized neoplasm, especially when they occur in extranodal sites in the head and neck region. Two of the three new cases we report were initially misdiagnosed, and five cases of extranodal FDC sarcoma in the head and neck region reported in the recent literature were initially misdiagnosed. Our aim is to complement the current understanding of this neoplasm and alert pathologists to this rare entity in this region to avoid misdiagnosis. Recognition of extranodal FDC sarcoma requires a high index of suspicion, but this tumor has numerous distinctive histological features that should bring the neoplasm into the differential diagnosis. Confirmatory immunohistochemical staining with follicular dendritic cell markers such as CD21 and/or CD35 is essential for the diagnosis. Correct characterization of this neoplasm is imperative given its potential for recurrence and metastasis.

摘要

头颈部结外滤泡树突状细胞(FDC)肉瘤较为罕见,此前有16例详细记录的病例报道(4例位于扁桃体,4例位于咽部,2例位于腭部,5例位于软组织,1例位于甲状腺)。我们在此报告另外3例结外FDC肉瘤,其中2例位于扁桃体,1例位于咽部。在这些新病例中,肿瘤细胞呈弥漫性、束状和模糊的漩涡状生长模式。肿瘤内散在淋巴细胞浸润,局部血管周围套叠明显。可见散在的多核巨细胞。免疫组化显示,肿瘤细胞对滤泡树突状细胞标志物CD21和CD35呈强弥漫性阳性。肿瘤细胞对fascin呈弥漫性阳性,对白血细胞共同抗原、S-100蛋白、细胞角蛋白和爱泼斯坦-巴尔病毒(EBV)潜伏膜蛋白-1(EBV-LMP)呈阴性。通过原位杂交检测EBV编码RNA,肿瘤细胞中也未检测到EBV。FDC肉瘤可能是一种未被充分认识的肿瘤,尤其是当它们发生在头颈部的结外部位时。我们报告的3例新病例中有2例最初被误诊,近期文献报道的5例头颈部结外FDC肉瘤最初也被误诊。我们的目的是补充目前对该肿瘤的认识,并提醒病理学家注意该区域的这种罕见实体,以避免误诊。识别结外FDC肉瘤需要高度的怀疑指数,但这种肿瘤有许多独特的组织学特征,应将其纳入鉴别诊断。用CD21和/或CD35等滤泡树突状细胞标志物进行确诊性免疫组化染色对诊断至关重要。鉴于该肿瘤有复发和转移的可能,正确鉴定该肿瘤至关重要。

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