Singh Guddi Rani, Choudhary Vijayanand, Agrawal Rawi
Senior Resident, Department of Pathology, Indira Gandhi Institute of Medical Sciences , Patna, Bihar, India .
Additional Professor, Department of Pathology, Indira Gandhi Institute of Medical Sciences , Patna, Bihar, India .
J Clin Diagn Res. 2017 Feb;11(2):ED15-ED16. doi: 10.7860/JCDR/2017/23541.9275. Epub 2017 Feb 1.
Primary Ewing Sarcoma of the cranial bone is rare, contributing to only 1% of all Ewing Sarcomas. Primary cranial Ewing Sarcoma occurs most commonly in temporal bone followed by parietal and occipital bones. Sphenoid bone is less commonly involved. We report a case of Ewing Sarcoma of the sphenoid bone with intra-cranial extension in a 20-month-old boy. On CT scan a provisional diagnosis of rhabdomyosarcoma was made. Fine Needle Aspiration Cytology (FNAC) and histopathological examination of core needle biopsy showed small round cell tumour. On Immunohistochemistry (IHC), CD99 (MIC2) and FLI 1 were strongly positive and final diagnosis of Ewing Sarcoma was made. Considering the rarity of this unusual site, we report a case of primary Ewing Sarcoma arising in the sphenoid bone with erosion of adjacent bones and intra-cranial extension.
颅骨原发性尤因肉瘤罕见,仅占所有尤因肉瘤的1%。原发性颅骨尤因肉瘤最常发生于颞骨,其次为顶骨和枕骨。蝶骨较少受累。我们报告1例20个月大男孩的蝶骨尤因肉瘤伴颅内扩展。CT扫描初步诊断为横纹肌肉瘤。细针穿刺抽吸细胞学检查(FNAC)及粗针活检的组织病理学检查显示为小圆细胞肿瘤。免疫组织化学(IHC)检查显示,CD99(MIC2)和FLI 1呈强阳性,最终诊断为尤因肉瘤。鉴于此不常见部位的罕见性,我们报告1例起源于蝶骨并侵犯相邻骨质及颅内扩展的原发性尤因肉瘤病例。