Department of Surgery F, Durante General Surgery N, Sapienza University of Rome, Rome, Italy.
BMC Gastroenterol. 2010 Jan 26;10:10. doi: 10.1186/1471-230X-10-10.
Inflammatory myoglandular polyp (IMGP) is a rare non-neoplastic polyp of the large bowel, commonly with a distal localization (rectosigmoid), obscure in its pathogenesis. Up till now, 60 cases of IMGP have been described in the literature, but none located in the cecum.
We report a case of a 53-year-old man who was admitted to our hospital for further evaluation of positive fecal occult blood test associated to anemia. A colonoscopy identified a red, sessile, lobulated polyp of the cecum, 4.2 cm in diameter, partially ulcerated. The histological examination of the biopsy revealed the presence of inflammatory granulation tissue with lymphocytic and eosinophil infiltration associated to a fibrous stroma: it was diagnosed as inflammatory fibroid polyp. Considering the polyp's features (absence of a peduncle and size) that could increase the risk of a polypectomy, a surgical resection was performed. Histological examination of the specimen revealed inflammatory granulation tissue in the lamina propria, hyperplastic glands with cystic dilatations, proliferation of smooth muscle and multiple erosions on the polyp surface: this polyp was finally diagnosed as IMGP. There was also another little polyp next to the ileocecal valve, not revealed at the colonoscopy, 0.8 cm in diameter, diagnosed as tubulovillous adenoma with low grade dysplasia.
This is the first case of IMGP of the cecum. It is a benign lesion of unknown pathogenesis and must be considered different from other non-neoplastic polyps of the large bowel such as inflammatory cap polyps (ICP), inflammatory cloacogenic polyps, juvenile polyps (JP), inflammatory fibroid polyps (IFP), polyps secondary to mucosal prolapse syndrome (MPS), polypoid prolapsing mucosal folds of diverticular disease. When symptomatic, IMGP should be removed endoscopically, whereas surgical resection is reserved only in selected patients as in our case.
炎性肌纤维母细胞瘤性息肉(IMGP)是一种罕见的大肠非肿瘤性息肉,通常位于远端(直肠乙状结肠),其发病机制尚不清楚。迄今为止,文献中已描述了 60 例 IMGP,但均未发生在盲肠。
我们报告了 1 例 53 岁男性,因粪便潜血试验阳性伴贫血而收入我院。结肠镜检查发现盲肠有 1 个 4.2cm 大小、红色、无蒂、分叶状息肉,部分溃疡。活检的组织学检查显示存在伴有淋巴细胞和嗜酸性粒细胞浸润的炎症性肉芽组织和纤维基质:诊断为炎性纤维瘤。鉴于息肉的特征(无蒂和大小)可能增加息肉切除术的风险,故进行了手术切除。标本的组织学检查显示固有层有炎症性肉芽组织,增生的腺体伴有囊性扩张,平滑肌增生,息肉表面有多个糜烂:最终诊断为 IMGP。回盲瓣旁边还有另 1 个 0.8cm 大小的小息肉,结肠镜未发现,诊断为管状绒毛状腺瘤伴低级别异型增生。
这是首例盲肠 IMGP。它是一种病因不明的良性病变,必须与其他大肠非肿瘤性息肉区分,如炎性帽状息肉(ICP)、炎性泄殖腔息肉、幼年性息肉(JP)、炎性纤维瘤(IFP)、黏膜脱垂综合征(MPS)相关息肉、憩室病的息肉样脱垂黏膜褶皱。当有症状时,IMGP 应通过内镜切除,而手术切除仅适用于我们这种病例中的某些选择患者。