Cakir Ebru, Aydin N Engin, Samdanci Emine, Karadag Nese, Sayin Sadegul, Kizilay Ahmet
Department of Pathology, Inonu University, Faculty of Medicine, Malatya, Turkey.
J Pak Med Assoc. 2013 Mar;63(3):393-5.
Follicular dendritic cell sarcoma (FDCS) of the head and neck region, associated with Castleman's disease (CD), is an extremely rare entity. To the best of our knowledge, we report the first case demonstrating the transformation of the former into the latter as documented in the same lymph node disection material. A 45-year-old female presented to our hospital with right sided neck swelling. Radiologic imaging showed a well defined 3.5 x 3.5 cm mass of soft tissue at the right side of the neck with multiple bilateral cervical lymph nodes. Excision of the right neck mass with lymph node disection was performed. Microscopic examination and immunohistochemical findings showed features of follicular dendritic cell sarcoma. The associated lymph nodes exhibited changes consistent with hyaline-vascular type CD, follicular dendritic cell hyperplasia and foci of overgrowth in which FDCS possibly evolved. This report confirms the evolving of FDCS in the setting of follicular dendritic cell hyperplasia occurring in Castleman's disease.
头颈部与卡斯特曼病(Castleman病,CD)相关的滤泡性树突状细胞肉瘤(FDCS)是一种极为罕见的疾病。据我们所知,我们报告了首例在同一淋巴结切除标本中记录到的前者转化为后者的病例。一名45岁女性因右侧颈部肿胀就诊于我院。影像学检查显示右侧颈部有一个边界清晰的3.5×3.5 cm软组织肿块,双侧颈部有多个淋巴结。对右侧颈部肿块进行了切除及淋巴结清扫。显微镜检查和免疫组化结果显示为滤泡性树突状细胞肉瘤的特征。相关淋巴结呈现出与透明血管型CD一致的改变、滤泡性树突状细胞增生以及FDCS可能由此演变而来的过度生长灶。本报告证实了在Castleman病中滤泡性树突状细胞增生背景下FDCS的演变。