Shukla Shailaja, Sharma Siddhartha, Langer Sabina, Sinha Madhu
Department of Pathology, Lady Hardinge Medical College & Smt. Sucheta Kriplani Hospital, New Delhi.
Indian J Pathol Microbiol. 2007 Oct;50(4):875-7.
Inflammatory myofibroblastic tumour formerly also known as inflammatory pseudotumour, was recognized initially in the lung and has been described in other visceral organs. It's occurrence in the subcutis is not well documented and its cytological appearance may be misinterpreted as malignant. This is the first case report of inflammatory myofibroblastic tumour of the subcutis in pediatric age group. A 12 year old female child presented with a subcutaneous swelling in the left anterior chest wall. FNA was performed and the cytological appearances were interpreted as malignant. Histopathology and immunohistochemistry revealed an inflammatory myofibroblastic tumour of the subcutis. FNA cytology is not very helpful in distinguishing inflammatory myofibroblastic tumour from malignant lesions especially soft tissue sarcomas. Awareness of it's occurrence in the subcutis is of importance for it's proper identification and treatment.
炎性肌纤维母细胞瘤以前也被称为炎性假瘤,最初在肺部被发现,也在其他内脏器官中有过描述。它在皮下组织中的发生情况记录并不充分,其细胞学表现可能被误诊为恶性。这是儿科年龄组皮下炎性肌纤维母细胞瘤的首例病例报告。一名12岁女童左侧前胸壁出现皮下肿物。进行了细针穿刺抽吸活检(FNA),细胞学表现被诊断为恶性。组织病理学和免疫组织化学检查显示为皮下炎性肌纤维母细胞瘤。FNA细胞学检查在区分炎性肌纤维母细胞瘤与恶性病变尤其是软组织肉瘤方面帮助不大。认识到它在皮下组织中的发生情况对于其正确识别和治疗很重要。