Bsirini Caroline, Tirumanisetty Pratyusha, Dytoc Joseph N, Agostini-Vulaj Diana, Steevens Christopher, Ullah Asad, Huber Aaron R
1 University of Rochester Medical Center, Rochester, NY, USA.
2 Unity Hospital, Rochester, NY, USA.
Int J Surg Pathol. 2019 Apr;27(2):221-224. doi: 10.1177/1066896918793944. Epub 2018 Aug 16.
Although pancreatic and gastric heterotopias are common findings in the gastrointestinal tract, heterotopic respiratory mucosa (HRM) in the rectum is extremely rare and has only been reported twice previously. We are presenting, to our knowledge, the third case of HRM in the rectum. A 56-year-old man with a history of chronic diarrhea presented for diagnostic colonoscopy, where he was found to have a rectal subepithelial nodule. He was subsequently referred to a tertiary medical center for further evaluation with rectal endoscopic ultrasound. Endoscopically, the nodule was hypoechoic, 2 to 3 mm in size, located in the submucosa, and did not appear to invade the muscularis propria. An uncomplicated endoscopic submucosal resection was subsequently performed. Microscopically, the nodule showed a multicystic complex lesion located in the submucosa, lined by ciliated pseudostratified columnar epithelium and surrounded by thin to moderately thick smooth muscle bundles and multiple lobules of seromucinous glands. There was associated acute and chronic inflammation. The rectum overlying the subepithelial lesion was lined by congested and edematous colonic mucosa and demonstrated no connection with the underlying cystic lesion. Immunohistochemical stains showed positive p63 basal cell staining in the respiratory epithelium of the lesion, while CDX2, TTF-1, and estrogen receptors were all negative. HRM is a benign nonneoplastic lesion with unclear etiology. Pathologists and gastroenterologists should be aware of this entity and consider it in their differential diagnosis for a subepithelial nodule in the rectum, keeping in mind that neoplastic processes can also develop in this location.
尽管胰腺和胃的异位在胃肠道中是常见的发现,但直肠中的异位呼吸道黏膜(HRM)极为罕见,此前仅报道过两例。据我们所知,我们正在呈现直肠HRM的第三例病例。一名有慢性腹泻病史的56岁男性因诊断性结肠镜检查就诊,在检查中发现他有一个直肠上皮下结节。随后他被转诊至一家三级医疗中心,接受直肠内镜超声进一步评估。在内镜下,该结节呈低回声,大小为2至3毫米,位于黏膜下层,似乎未侵犯固有肌层。随后进行了一次无并发症的内镜黏膜下切除术。显微镜下,该结节显示为位于黏膜下层的多囊性复合病变,内衬纤毛假复层柱状上皮,周围有薄至中等厚度的平滑肌束和多个浆液黏液性腺小叶。伴有急性和慢性炎症。上皮下病变上方的直肠内衬充血水肿的结肠黏膜,与下方的囊性病变无连接。免疫组织化学染色显示病变呼吸道上皮中p63基底细胞染色呈阳性,而CDX2、TTF - 1和雌激素受体均为阴性。HRM是一种病因不明的良性非肿瘤性病变。病理学家和胃肠病学家应了解这一实体,并在对直肠上皮下结节进行鉴别诊断时考虑到它,同时要记住该部位也可能发生肿瘤性病变。