Department of Diagnostic Radiology and Organ Imaging, Faculty of Medicine, The Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, New Territories, Hong Kong.
Pediatr Blood Cancer. 2010 Jul 1;54(7):1029-31. doi: 10.1002/pbc.22391.
Inflammatory myofibroblastic tumour (IMFT) is a distinct entity with variable clinical presentation and therapeutic options. We present three paediatric cases of IMFT, originated from the lung, bladder and ovary respectively. All lesions were heterogeneous, with mixed solid/cystic components and infiltrative pattern, and were interpreted as aggressive malignant neoplasms initially due to their bizarre imaging appearance. The definitive diagnosis was derived from characteristic histopathological features.
炎性肌纤维母细胞瘤（IMFT）是一种具有不同临床表现和治疗选择的独特实体。我们报告了 3 例来自肺、膀胱和卵巢的儿童 IMFT 病例。所有病变均为异质性，具有混合实性/囊性成分和浸润性模式，由于其奇异的影像学表现，最初被误诊为侵袭性恶性肿瘤。明确的诊断来自特征性的组织病理学特征。
