Aydin Erdinc, Ozluoglu Levent Naci, Demirhan Beyhan, Arikan Unser
Faculty of Medicine, Department of Otorhinolaryngology & Head and Neck Surgery, Baskent University, 6. Cadde No: 72/2, 06490 Bahcelievler-Ankara, Turkey.
Eur Arch Otorhinolaryngol. 2006 Dec;263(12):1155-7. doi: 10.1007/s00405-006-0124-9. Epub 2006 Aug 5.
Follicular dendritic cell sarcomas are unusual, and extranodal origin is extremely rare. The English literature contains only eight cases in which this sarcoma has been presented as a tonsillar mass. We report a new case of follicular dendritic cell sarcoma of the tonsil in a 76 year old woman. The patient underwent diagnostic tonsillectomy for a left tonsillar mass, and follicular dendritic cell sarcoma was diagnosed based on histopathological and immunoperoxidase findings. Postoperative radiotherapy was performed. The patient is alive and disease-free at 4 years of follow-up. Without a high index of suspicion, this entity can easily be missed. We believe that follicular dendritic cell sarcoma should be included in the differential diagnosis for any tonsillar mass.
滤泡树突状细胞肉瘤较为罕见,结外起源极为少见。英文文献中仅有8例该肉瘤表现为扁桃体肿物的报道。我们报告1例76岁女性扁桃体滤泡树突状细胞肉瘤的新病例。患者因左侧扁桃体肿物接受诊断性扁桃体切除术,根据组织病理学和免疫过氧化物酶检查结果确诊为滤泡树突状细胞肉瘤。术后进行了放射治疗。随访4年,患者存活且无疾病复发。若警惕性不高,该疾病很容易被漏诊。我们认为,对于任何扁桃体肿物,滤泡树突状细胞肉瘤都应列入鉴别诊断范围。