Tanaka N, Seya T, Onda M, Kanazawa Y, Naitoh Z, Asano G, Hao K
First Department of Surgery, Nippon Medical School, Bunkyo-ku, Tokyo, Japan.
Surg Today. 1996;26(12):1010-3. doi: 10.1007/BF00309963.
Benign small bowel tumors seldom cause symptoms, due to the fluid content and distensibility of the small bowel. We herein present the case of a solitary ileal hamartoma causing melena and abdominal pain in a 24-year-old man. The diagnosis of a submucosal ileal tumor was made after performing small bowel barium studies. Surgical treatment was undertaken, and a histological examination of the excised lesion, which showed a partially ulcerated tumor surface and extended from the submucosa to the subserosa, revealed numerous cystic glands of various sizes together with bundles of proliferating smooth muscle cells. Histochemical and immunohistochemical investigations were performed for differential diagnosis, and the tumor features were consistent with a diagnosis of ileal myoepithelial hamartoma. In the literature, small intestinal myoepithelial hamartomas are quite rare and this is the first report of a myoepithelial hamartoma causing melena.
由于小肠的液体含量和扩张性,良性小肠肿瘤很少引起症状。我们在此报告一例24岁男性因孤立性回肠错构瘤导致黑便和腹痛的病例。在进行小肠钡剂造影检查后,诊断为回肠黏膜下肿瘤。进行了手术治疗,对切除病变进行组织学检查,结果显示肿瘤表面部分溃疡,从黏膜下层延伸至浆膜下层,可见大量大小不一的囊性腺体以及成束增生的平滑肌细胞。为进行鉴别诊断进行了组织化学和免疫组织化学研究,肿瘤特征符合回肠肌上皮错构瘤的诊断。在文献中,小肠肌上皮错构瘤相当罕见,这是首例导致黑便的肌上皮错构瘤报告。