Coulier B, Maldague P, Broze B, Gielen I
Department of Medical Imaging, Clinique St Luc, Bouge, Belgium.
JBR-BTR. 2008 Jul-Aug;91(4):149-52.
Inflammatory Fibroid Polyp (IFP) is an extremely rare tumour involving the gastrointestinal tract (GI) and especially the stomach and small bowel. It presents either as a solitary large or sessile lesion arising from the submucosa and despite a large size and sometimes infiltrating growth, the tumour is always benign and has a good prognosis. Histogenesis remains unknown and controversial. We report an ileal case presenting classically and typically with ileocolic intussusception. Diagnosis was made preoperatively with abdominal mdCT. The polyp itself does not have noteworthy radiological signs but must be included in the large essentially histological differential diagnosis of GI tumours.
炎性纤维性息肉(IFP)是一种极其罕见的肿瘤,累及胃肠道(GI),尤其是胃和小肠。它表现为起源于黏膜下层的单个大的或无蒂病变,尽管体积较大且有时呈浸润性生长,但该肿瘤始终为良性,预后良好。组织发生仍不清楚且存在争议。我们报告一例回肠病例,典型地表现为回结肠套叠。术前通过腹部多层螺旋CT(mdCT)做出诊断。息肉本身没有值得注意的放射学征象,但在胃肠道肿瘤的大体组织学鉴别诊断中必须考虑到。