继发于直肠腺癌的McKittrick Wheelock综合征。病例报告和诊断注意事项

Q4 Medicine
Claudia Alejandra Aceves Quintero, Santiago Taracena Pacheco, Itzel Vela Sarmiento
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引用次数: 0

摘要

McKittrick-Wheelock综合征是一种罕见的疾病,以慢性腹泻、急性肾损伤和水电解质失衡为特征,并伴有直肠大肿瘤,通常为绒毛腺瘤。病例报告一名69岁男性,慢性腹泻伴黏液。他接受了结肠镜活检,报告原位直肠腺癌,并接受了机器人辅助的结肠肛管吻合括约肌间切除术和保护性回肠造口术。该综合征于1954年被描述,表现为电解质失衡和急性肾损伤,继发于腹泻并伴有直肠绒毛腺瘤,通常症状持续时间较长。最常见的症状是带黏液的水样腹泻。最终的治疗方法是手术切除。结论虽然这是一种罕见的病理,但在慢性腹泻合并水电解质紊乱的病例中,它应被视为一种鉴别诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
McKittrick Wheelock Syndrome Secondary to Adenocarcinoma of the Rectum. Case Report and Diagnostic Considerations
Abstract Introduction McKittrick-Wheelock syndrome is a rare entity characterized by chronic diarrhea, acute kidney injury, and hydroelectrolytic imbalance associated with a large rectal tumor, frequently a villous adenoma. Case report A 69-year-old male with chronic diarrhea with mucus. He underwent a colonoscopy with biopsies, reporting adenocarcinoma of the rectum in situ, and underwent a robot assisted intersphincteric resection with colo-anal anastomosis and a protecitive ileostomy. Discussion Described in 1954, this syndrome is manifested by electrolyte imbalance and acute renal injury secondary to diarrhea associated with a rectal villous adenoma, often with long lasting symptoms. The most frequent symptom being watery diarrhea with mucus. The definitive treatment consists of surgical resection. Conclusion Although this is a rare pathology, it should be considered as a differential diagnosis in cases of chronic diarrhea associated with water and electrolyte disorders.
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来源期刊
Journal of Coloproctology
Journal of Coloproctology Medicine-Gastroenterology
CiteScore
0.60
自引率
0.00%
发文量
41
审稿时长
47 weeks
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