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累及整个结肠和直肠的产生血管活性肠肽的神经节瘤病

Vasoactive intestinal polypeptide-producing ganglioneuromatosis involving the entire colon and rectum.

作者信息

Moon Suk-Bae, Park Kwi-Won, Jung Sung-Eun, Lee Seong-Cheol

机构信息

Department of Pediatric Surgery, Seoul National University Children's Hospital, Seoul 110-744, Korea.

出版信息

J Pediatr Surg. 2009 Mar;44(3):e19-21. doi: 10.1016/j.jpedsurg.2008.11.051.

Abstract

Vasoactive intestinal polypeptide (VIP) is known to cause the watery diarrhea, hypokalemia, and achlorhydria syndrome. A 14-year-old girl was admitted with a 4-year history of persistent uncontrollable diarrhea and hypokalemia. Computed tomographic evaluation of the neck, chest, and abdomen were normal. Numerous polyps covering the entire colon and rectum were noted on colonoscopy. The serum VIP level was 143 pg/mL. The patient underwent a total proctocolectomy with an ileal-J-pouch. The pathologic examination revealed ganglioneuromatosis. Postoperatively, the symptoms resolved, and the serum VIP level fell to lower than 5 pg/mL. This is an unusual case of the watery diarrhea, hypokalemia, and achlorhydria syndrome caused by ganglioneuromatosis of the entire colon and rectum.

摘要

已知血管活性肠肽(VIP)会引发水样腹泻、低钾血症和无胃酸综合征。一名14岁女孩因持续4年无法控制的腹泻和低钾血症入院。颈部、胸部和腹部的计算机断层扫描评估结果正常。结肠镜检查发现整个结肠和直肠布满了大量息肉。血清VIP水平为143 pg/mL。该患者接受了全直肠结肠切除术并进行回肠J袋重建。病理检查显示为神经节瘤病。术后症状消失,血清VIP水平降至5 pg/mL以下。这是一例由全结肠和直肠神经节瘤病引起的水样腹泻、低钾血症和无胃酸综合征的罕见病例。

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