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Follicular dendritic cell tumour/sarcoma: a commonly misdiagnosed tumour in the thorax

机译:滤泡性树突状细胞肿瘤/肉瘤:胸腔内常见的误诊肿瘤

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摘要

AIMS: Follicular dendritic cell sarcoma is a rare tumour reported to occur occasionally in association with the hyaline-vascular type of Castleman's disease (HVCD). Most cases arise in lymph nodes, although extranodal presentation is described. METHODS AND RESULTS: Clinical, radiological and histological characteristics, including diagnosis on pre-resection material, were assessed in seven intrathoracic cases from five males and two females with a median age of 38 years. Clinical symptoms were related to mass location, six cases presenting within central and/or posterior mediastinal compartments and one within the lungs. Positron emission tomography-computed tomography demonstrated marked fluoro-deoxy-glucose avidity and the prominent vessels traversing the lesions. Four of six cases (67%) were misdiagnosed initially. HVCD was present in three cases. Two cases with high mitotic rates recurred after resection. All were positive for at least one of the follicular dendritic cell markers (CD21, CD35 and CD23). Six of seven cases (86%) show cyclin D1 expression ranging from 5% to 90%. CONCLUSIONS: Follicular dendritic cell sarcoma is often misdiagnosed on biopsy and pathologists need to be aware of the tumour to request the relevant immunohistochemistry, especially in masses presenting in the central/posterior mediastinum with high vascularity and standardized uptake values. Background HVCD appears more common than previously thought.
机译:目的:滤泡性树突状细胞肉瘤是一种罕见的肿瘤,据报道与透明血管型Castleman氏病(HVCD)偶发。尽管描述了结外表现,但大多数病例都发生在淋巴结中。方法和结果:对7例胸腔内病例进行了临床,影像学和组织学检查,包括对切除前材料的诊断,其中5例男性和2例女性的中位年龄为38岁。临床症状与肿块位置有关,六例在纵隔中央和/或后纵隔内,一例在肺内。正电子发射断层扫描计算机断层扫描显示出明显的氟-脱氧-葡萄糖亲和力,并且突出的血管横穿病变。最初有6例病例中有4例(67%)被误诊。 HVCD出现在三个案例中。切除后复发2例有丝分裂率高。至少一种滤泡树突状细胞标志物(CD21,CD35和CD23)均为阳性。 7例中有6例(86%)显示cyclin D1表达范围为5%至90%。结论:滤泡性树突状细胞肉瘤在活检中经常被误诊,病理学家需要意识到肿瘤,要求进行相关的免疫组织化学检查,特别是在纵隔中央/后纵隔有高血管和标准化摄取值的肿块中。背景HVCD似乎比以前想像的更为普遍。

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