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单发胃型 Peutz-Jeghers 息肉,酷似恶性胃肿瘤。

Solitary gastric Peutz-Jeghers type stomach polyp mimicking a malignant gastric tumor.

机构信息

Department of Pathology, Tungs' Taichung MetroHarbor Hospital, Wuqi Township, Taichung County 435, Taiwan, China.

出版信息

World J Gastroenterol. 2012 Apr 21;18(15):1845-8. doi: 10.3748/wjg.v18.i15.1845.

Abstract

Most cases of Peutz-Jeghers type polyps of the stomach are associated with mucocutaneous pigmentation and multiple intestinal polyposis. A solitary Peutz-Jeghers type polyp of the stomach is rare. We here report a case of a 71-year-old woman with a solitary Peutz-Jeghers type polyp of the stomach who presented with intolerable epigastric pain and weight loss of 5 kg over the prior two months. During the hospital treatment course for this patient, endoscopic examination revealed a bulging lesion with a central hole, mucosal ulceration, an asymmetrical wall thickness and a narrowing of the gastric lumen. A gastric biopsy further revealed ulceration with moderate dysplasia. The patient received endoscopic ultrasonography which showed a second subepithelial lesion that measured 4 cm × 3 cm. Computed tomography of the abdomen subsequently showed a thickened gastric wall with three visibly enlarged lymph nodes, all greater than 1 cm. The suspected diagnosis was malignant gastric cancer with lymph node metastases. The other lesion, which measured 2 cm × 2 cm × 1 cm was noted in the submucosa of the jejunum during surgery. The patient was treated using a subtotal gastrectomy and partial resection of the jejunal tumor. The final pathological report indicated a gastric Peutz-Jeghers type polyp with proliferation of smooth muscle bundles in the submucosal layer, and hyperplastic glands in the mucosal layer and ectopic pancreas of the jejunum. This is the first reported clinical case of a solitary Peutz-Jeghers type polyp of the stomach accompanying a lymph node enlargement and ectopic pancreas in the jejunum that simulates stomach cancer with lymph node metastases.

摘要

大多数胃型 Peutz-Jeghers 息肉与黏膜皮肤色素沉着和多发性肠息肉有关。胃孤立性 Peutz-Jeghers 型息肉很少见。我们在此报告一例 71 岁女性,患有胃孤立性 Peutz-Jeghers 型息肉,表现为无法忍受的上腹痛和两个月前体重减轻 5 公斤。在对该患者的住院治疗过程中,内镜检查显示有一个中央有孔的隆起性病变,伴有黏膜溃疡、不对称的壁厚度和胃腔狭窄。胃活检进一步显示溃疡伴中度异型增生。患者接受了内镜超声检查,显示第二个位于黏膜下层的病变,大小为 4cm×3cm。腹部计算机断层扫描随后显示胃壁增厚,有三个明显增大的淋巴结,均大于 1cm。疑似诊断为恶性胃癌伴淋巴结转移。在手术中,还在空肠黏膜下层发现了另一个 2cm×2cm×1cm 的病变。患者接受了胃大部切除术和空肠肿瘤部分切除术。最终的病理报告表明,胃 Peutz-Jeghers 型息肉伴有黏膜下层平滑肌束增生,黏膜层和空肠异位胰腺增生。这是首例报告的胃孤立性 Peutz-Jeghers 型息肉伴淋巴结肿大和空肠异位胰腺,模拟淋巴结转移的胃癌的临床病例。

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