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克-特综合征孤立性结直肠受累:一例广泛血管畸形病例

Isolated Colorectal Involvement in Klippel-Trenaunay Syndrome: A Case of Extensive Vascular Malformation.

作者信息

Ilyassov Nurbek, Shayakhmetov Yerzhan, Abdikarimov Anuar, Nurgaliev Erlan, Saberbekov Saken, Aralbayev Rakymzhan, Tokusheva Aiman, Kalina Vitaliy

机构信息

JSC National Scientific Medical Center, Astana, Kazakhstan.

International Oncological Tomotherapy Center "YMIT", Astana, Kazakhstan.

出版信息

Int Med Case Rep J. 2025 Aug 7;18:997-1002. doi: 10.2147/IMCRJ.S535985. eCollection 2025.

Abstract

BACKGROUND

Rectal vascular malformations associated with Klippel-Trenaunay syndrome are exceedingly rare. While their diagnosis may be straightforward when characteristic features are present, such cases remain of significant educational value due to their unusual presentation and potential for misdiagnosis.

CASE PRESENTATION

Our study aimed to describe a clinical case of a 45-year old female patient. There were complaints of pain in the perianal area and periodic bleeding during/after defecation, prolapse of hemorrhoids, general weakness. Colonoscopy revealed varicose veins of the rectum, hemangioma of the rectal mucosa, and chronic internal hemorrhoids. Multislice computed tomography of the pelvic organs with intravenous bolus contrast was performed. The preliminary clinical diagnosis was hemangioma of the rectal mucosa, and vascular malformation of the rectum was considered operable. In our clinic, the patient underwent several-stage surgery: (1) implantation of a temporary vena cava filter into the inferior vena cava, (2) two weeks later laparoscopic-assisted anterior resection of the rectum with preventive transverse colostomy and demucosation of the rectal mucosa, (3) after 7 months following discharge, the closure of transverse colostomy. Pathological examination of the gross specimen revealed that mucous membrane of the colon in a section extending 12.0 cm up to the distal edge of the resection is compacted, coarsely lumpy, grayish-bluish in color, with multiple blood-filled cavities. The postoperative period proceeded smoothly. Oral nutrition and patient's activity began on the 1st day. Primary healing of postoperative wounds was occurred. The patient was discharged in satisfactory condition on the 6th day post-surgery.

CONCLUSION

This clinical case is a case-of-interest due to its rare localization, asymptomatic course for a long time with a fairly large size of an excessively vascularized abnormal vascular formation. The appropriate approach to this pathology is laparoscopic surgery, which can be useful for both diagnostic and radical treatment of vascular malformations of the rectum.

摘要

背景

与克-特综合征相关的直肠血管畸形极为罕见。当出现特征性表现时,其诊断可能较为简单,但由于其不寻常的表现形式及误诊可能性,此类病例仍具有重要的教学价值。

病例介绍

我们的研究旨在描述一名45岁女性患者的临床病例。患者主诉肛周区域疼痛、排便时/排便后周期性出血、痔疮脱垂及全身乏力。结肠镜检查发现直肠静脉曲张、直肠黏膜血管瘤及慢性内痔。对盆腔器官进行了静脉团注造影的多层计算机断层扫描。初步临床诊断为直肠黏膜血管瘤,认为直肠血管畸形可进行手术治疗。在我们诊所,该患者接受了多阶段手术:(1)在下腔静脉植入临时腔静脉滤器;(2)两周后行腹腔镜辅助直肠前切除术并预防性横结肠造口及直肠黏膜脱黏膜术;(3)出院7个月后关闭横结肠造口。大体标本的病理检查显示,距切除远端边缘向上延伸12.0 cm的结肠段黏膜致密、粗糙呈块状、灰蓝色,有多个充满血液的腔隙。术后恢复顺利。术后第1天开始经口营养及患者活动。术后伤口一期愈合。患者术后第6天状况良好出院。

结论

该临床病例因其罕见的定位、长时间无症状病程且伴有相当大尺寸过度血管化的异常血管形成而备受关注。针对这种病理情况的合适方法是腹腔镜手术,其对直肠血管畸形的诊断和根治性治疗均可能有用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f20/12339189/36ba68d52d8c/IMCRJ-18-997-g0001.jpg

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