Ali Muhammad, Farooq Omama, Fatima Mishal, Farooq Hajrah
Internal Medicine, Islamabad Medical Complex, Islamabad, PAK.
General Surgery, Islamabad Medical Complex, Islamabad, PAK.
Cureus. 2022 Jul 11;14(7):e26728. doi: 10.7759/cureus.26728. eCollection 2022 Jul.
Superior mesenteric artery (SMA) syndrome, also known as Wilkie's syndrome, is an uncommon disorder that involves a set of symptoms that primarily includes postprandial pain at times associated with intestinal obstruction. Although a rare disease in the general population, SMA syndrome has a high probability of occurrence in patients who are severely malnourished or have certain debilitating conditions leading to a loss of retroperitoneal fat. Here, we present the case of a 16-year-old male with a one-year history of postprandial abdominal pain associated with nausea, multiple episodes of vomiting, and abdominal distension. Amid a delayed diagnosis and multiple hospital visits, the patient's condition further deteriorated. Thereafter, computed tomography of the abdomen confirmed this rare diagnosis. Because the patient could not be further managed conservatively, laparoscopic duodenojejunostomy was planned and done. This case report highlights the various challenges in diagnosing this disease and highlights the importance of an early diagnosis so that patients can be managed effectively and timely.
肠系膜上动脉(SMA)综合征,也称为威尔基综合征,是一种罕见的疾病,其症状主要包括餐后疼痛,有时伴有肠梗阻。虽然在普通人群中是罕见疾病,但SMA综合征在严重营养不良或患有某些导致腹膜后脂肪减少的衰弱性疾病的患者中发生概率较高。在此,我们报告一例16岁男性患者,有一年餐后腹痛病史,伴有恶心、多次呕吐和腹胀。在诊断延迟和多次就诊期间,患者病情进一步恶化。此后,腹部计算机断层扫描证实了这一罕见诊断。由于患者无法进一步保守治疗,遂计划并实施了腹腔镜十二指肠空肠吻合术。本病例报告强调了诊断该疾病的各种挑战,并强调了早期诊断的重要性,以便能够有效及时地治疗患者。