Vargas Aignasse Ramiro A, Pantoja Pachajoa Diana A, Llahi Florencia, Parodi Matias, Doniquian Alejandro M, Viscido German R
General Surgery Department, Clínica Universitaria Reina Fabiola, Universidad Católica de Córdoba, Oncativo 1248, Córdoba Capital, Argentina.
General Surgery Department, Clínica Universitaria Reina Fabiola, Universidad Católica de Córdoba, Oncativo 1248, Córdoba Capital, Argentina.
Int J Surg Case Rep. 2023 Aug;109:108614. doi: 10.1016/j.ijscr.2023.108614. Epub 2023 Aug 4.
Meckel's diverticulum (MD) is a common congenital malformation of the digestive tract, often asymptomatic but occasionally leading to complications such as bowel obstruction and ischemia. Timely recognition and treatment of these complications are crucial.
We report the case of a 27-year-old male patient presenting with complete intestinal obstruction and ischemia of the ileum due to a fibrous band associated with MD. The patient presented with severe abdominal pain lasting for 10 h. Physical examination revealed a distended abdomen, antalgic position, and positive decompression. Laboratory tests showed leukocytosis and elevated lactic acid levels. Computed tomography revealed dilated small bowel loops with signs of intestinal ischemia. Emergency exploratory laparoscopy confirmed a complete ileum with ischemia and identified a fibrous band originating from the mesentery, strangulating the affected loop. The fibrous band was dissected and sectioned, confirming its association with the MD, which was resected with subsequent recovery of peristalsis and vascularization of the compromised segment. The patient had a favorable postoperative recovery without complications.
MD is a rare cause of bowel obstruction, requiring a high index of suspicion for diagnosis. Despite the challenges in preoperative identification, early surgical intervention is crucial to prevent adverse outcomes. This case emphasizes the importance of promptly recognizing and managing MD-related complications to optimize patient outcomes.
MD should be considered in cases of acute occlusive abdomen, despite its infrequent occurrence. Early diagnosis and timely surgical intervention are essential to minimize morbidity and mortality associated with MD-related complications.
梅克尔憩室(MD)是一种常见的消化道先天性畸形,通常无症状,但偶尔会导致肠梗阻和缺血等并发症。及时识别和治疗这些并发症至关重要。
我们报告一例27岁男性患者,因与MD相关的纤维带导致完全性肠梗阻和回肠缺血。患者出现严重腹痛持续10小时。体格检查发现腹部膨隆、强迫体位及减压阳性。实验室检查显示白细胞增多和乳酸水平升高。计算机断层扫描显示小肠袢扩张并有肠缺血迹象。急诊探查性腹腔镜检查证实回肠完全缺血,并发现一条源自肠系膜的纤维带,压迫受累肠袢。将纤维带分离并切断,证实其与MD相关,随后切除MD,受累肠段的蠕动和血运得以恢复。患者术后恢复良好,无并发症。
MD是肠梗阻的罕见原因,诊断时需要高度怀疑。尽管术前识别存在挑战,但早期手术干预对于预防不良后果至关重要。本病例强调了及时识别和处理与MD相关并发症以优化患者预后的重要性。
尽管MD在急性腹痛病例中发生率较低,但仍应予以考虑。早期诊断和及时手术干预对于将与MD相关并发症的发病率和死亡率降至最低至关重要。