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肠系膜静脉特发性肌内膜增生——两例报告

Idiopathic myointimal hyperplasia of the mesenteric veins-a report of two cases.

作者信息

Uwah Martin, Bustamante-Lopez Leonardo, Devane Liam, Hoff John, Garcia-Henriquez Norbert, Kline Brian, Monson John R T, Albert Matthew

机构信息

AdventHealth Department of Colorectal Surgery, Surgical Health Outcomes Consortium (SHOC), Orlando, FL, USA.

出版信息

AME Case Rep. 2024 Aug 9;8:84. doi: 10.21037/acr-23-59. eCollection 2024.

Abstract

BACKGROUND

Idiopathic myointimal hyperplasia of the mesenteric veins (IMHMV) is a rare condition that poses a diagnostic challenge to surgeons and pathologists alike. Our aim is to describe two cases of IMHMV requiring operative intervention. The challenge going forward is accurately and systematically identifying factors from both a pathologic and clinical perspective that guide timely diagnosis and avoid unnecessary treatment.

CASE DESCRIPTION

A 37-year-old male with no significant past medical history was evaluated for a two-month history of abdominal pain, constipation, diarrhea and recent bleeding per rectum. Computed tomography (CT) scan revealed abnormal wall thickening with surrounding inflammatory changes and mesenteric edema involving the descending and sigmoid colon as well as the rectum. The patient was taken to the operating room where he underwent a laparoscopic-assisted extended left colectomy with end colostomy. The patient did well postoperatively and was ultimately meeting all goals for discharge by postoperative day 9. A 49-year-old male with a past medical history of hypertension, gastroesophageal reflux and recent coronavirus disease 2019 (COVID-19) infection was admitted to another hospital following several months of colitis of unknown etiology; unresponsive to antibiotics and steroids. CT scan revealed concentric, severe mural thickening and intramural edema of the distal descending colon extending to the rectum consistent with proctocolitis. The patient was taken to the operating room where he underwent a laparoscopic-assisted low anterior resection with end colostomy with findings of an extremely indurated, thickened left colon and rectum. The patient recovered from these additional interventions and was discharged home in stable condition on postoperative day 32.

CONCLUSIONS

A multidisciplinary team approach to this condition will be vital to administering the appropriate treatment modalities for future cases of IMHMV.

摘要

背景

肠系膜静脉特发性肌内膜增生(IMHMV)是一种罕见疾病,对外科医生和病理学家来说都具有诊断挑战性。我们的目的是描述两例需要手术干预的IMHMV病例。未来面临的挑战是从病理和临床角度准确、系统地识别指导及时诊断并避免不必要治疗的因素。

病例描述

一名37岁男性,既往无重大病史,因腹痛、便秘、腹泻及近期直肠出血两个月前来就诊。计算机断层扫描(CT)显示降结肠、乙状结肠及直肠壁异常增厚,周围有炎症改变及肠系膜水肿。患者被送往手术室,接受了腹腔镜辅助扩大左半结肠切除术及末端结肠造口术。患者术后恢复良好,术后第9天最终达到所有出院目标。一名49岁男性,有高血压、胃食管反流病史,近期感染新型冠状病毒肺炎(COVID-19),因病因不明的结肠炎数月后入住另一家医院;对抗生素和类固醇治疗无效。CT扫描显示降结肠远端至直肠同心性、严重壁增厚及壁内水肿,符合直肠结肠炎表现。患者被送往手术室,接受了腹腔镜辅助低位前切除术及末端结肠造口术,术中发现左半结肠和直肠极度硬结、增厚。患者从这些额外干预中恢复,术后第32天病情稳定出院。

结论

对于这种疾病,多学科团队方法对于为未来的IMHMV病例实施适当的治疗方式至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88f8/11459427/8ec08f9e71b8/acr-08-23-59-f1.jpg

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