Recurrence of follicular dendritic cell sarcoma in tonsils after 7 years: a rare case report

Pratiksha Pawar, Shubhanshi Kangloo, Ameya Bihani, Kunal Gupta, Soma Yadav
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Abstract

Follicular dendritic cell sarcoma (FDCS) is a rare mesenchymal neoplasm. It arises from not only from lymph nodes but also from extra nodal tissues, either as acquired lymphoid tissue or as part of the organized constitutive lymphoid tissue. We here report this rare entity which developed again after 7 years post tonsillectomy in a 5-year old male patient. Patient underwent radical tonsillectomy and adjuvant treatment is awaited. Differential diagnosis includes large cell lymphoma, peripheral nerve sheath tumor, extracranial meningioma, malignant melanoma, metastatic carcinoma, ectopic thymoma, malignant fibrous histiocytoma, and interstitial reticulum cell sarcoma. Currently, the management of FDCS includes the therapeutic guidelines similar to that of high-grade soft tissue sarcomas that is complete surgical resection of the lesion with possibility of adjuvant radiotherapy and/or chemotherapy. The ideal combination of management of FDCS has yet to be defined.
扁桃体滤泡树突状细胞肉瘤7年后复发1例罕见报告
滤泡树突状细胞肉瘤是一种罕见的间充质肿瘤。它不仅起源于淋巴结,也起源于结外组织,作为获得性淋巴组织或作为有组织的本构性淋巴组织的一部分。我们在此报告一个5岁男性患者扁桃体切除术后7年再次发展的罕见实体。等待患者行根治性扁桃体切除术及辅助治疗。鉴别诊断包括大细胞淋巴瘤、周围神经鞘瘤、颅外脑膜瘤、恶性黑色素瘤、转移癌、异位胸腺瘤、恶性纤维组织细胞瘤和间质网细胞肉瘤。目前,FDCS的治疗指南类似于高级别软组织肉瘤的治疗指南,即完全手术切除病变,并可能辅以放疗和/或化疗。FDCS管理的理想组合尚未确定。
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