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发生于肛门直肠瘘的黏液腺癌。

Mucinous adenocarcinoma arising in an anorectal fistula.

作者信息

Venclauskas Linas, Saladzinskas Zilvinas, Tamelis Algimantas, Pranys Darius, Pavalkis Dainius

机构信息

Department of Surgery, Kaunas University of Medicine, Eiveniu 2, Kaunas, Lithuania.

出版信息

Medicina (Kaunas). 2009;45(4):286-90.

Abstract

UNLABELLED

Mucinous adenocarcinoma in association with chronic anal fistula is a rare case in clinical practice. The aim of this article was to report a rare case of anal gland mucinous adenocarcinoma in a patient who was treated in the Hospital of Kaunas University of Medicine.

CASE REPORT

A 70-year-old male was treated for anorectal fistula in the surgical department. Four operations were performed for perineal abscess during the period of 15 years. During the period of 15 years, the patient complained of purulent secretion from the perineal abscess. After the last operation, anorectal fistula developed. Multiple biopsies and scrapings of the fistulous track were taken for histological examination. Histological examination revealed mucinous adenocarcinoma, G2. Subsequently, the patient underwent endoanal ultrasound, computed tomography scan, and colonoscopy. The computed tomography scan did not show pathology in the abdomen, but showed soft tissue induration at the site of anorectal fistula. Colonoscopy investigation did not show any pathology in the rectum and bowels. Endoanal ultrasound findings showed soft tissue induration at the site of anorectal fistula, no tumor in the rectum wall. The patient underwent abdominoperineal resection. Histological examination after abdominoperineal resection revealed anal duct mucinous adenocarcinoma pT2 N0 L0 V0 R0, G2. Metastases to the mesenteric lymph nodes were not detected. On the eighth day after abdominoperineal resection, the patient was discharged from the hospital for follow-up.

SUMMARY

Mucinous adenocarcinoma in anorectal fistula is a rare condition. If surgical treatment for perineal abscess or anorectal fistula is not successful for a long time, mucinous adenocarcinoma should be suspected.

摘要

未标注

黏液性腺癌合并慢性肛瘘在临床实践中是罕见病例。本文旨在报告考纳斯医科大学医院收治的一例罕见的肛门腺黏液性腺癌病例。

病例报告

一名70岁男性因肛肠瘘在外科接受治疗。15年间因会阴脓肿进行了4次手术。在这15年期间,患者主诉会阴脓肿有脓性分泌物。最后一次手术后,发生了肛肠瘘。对瘘管进行了多次活检和刮片以进行组织学检查。组织学检查显示为黏液性腺癌,G2级。随后,患者接受了肛门内超声、计算机断层扫描和结肠镜检查。计算机断层扫描未显示腹部有病变,但显示肛肠瘘部位有软组织硬结。结肠镜检查未发现直肠和肠道有任何病变。肛门内超声检查结果显示肛肠瘘部位有软组织硬结,直肠壁无肿瘤。患者接受了腹会阴联合切除术。腹会阴联合切除术后的组织学检查显示肛管黏液性腺癌,pT2 N0 L0 V0 R0,G2级。未检测到肠系膜淋巴结转移。腹会阴联合切除术后第8天,患者出院进行随访。

总结

肛肠瘘中的黏液性腺癌是一种罕见情况。如果对会阴脓肿或肛肠瘘的手术治疗长期不成功,应怀疑黏液性腺癌。

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