Wrenn Sean M, Parsons Charles S, Yang Michelle, Malhotra Ajai K
University of Vermont Medical Center, Department of Surgery, 111 Colchester Avenue, Burlington, VT, 05401, United States.
University of Vermont Medical Center, Department of Surgery, 111 Colchester Avenue, Burlington, VT, 05401, United States; Beth Israel Deaconess Medical Center, Department of Surgery, 330 Brookline Avenue, Boston, MA, 02215, United States.
Int J Surg Case Rep. 2017;33:79-83. doi: 10.1016/j.ijscr.2017.02.040. Epub 2017 Feb 27.
Atrophic visceral myopathy is a pathological diagnosis characterized by atrophy of the smooth muscle layers of the viscera with intact ganglia. Rarely, it can present acutely as an intestinal pseudo-obstruction. We describe a rare case report and explore how this diagnosis can be distinguished from other forms of intestinal obstruction.
A 60-year-old male with a past medical history of hypothyroidism presented to the emergency department with a two-day history of worsening abdominal distention and pain associated with nausea and vomiting. Upon evaluation patient was found to have tachycardia, with abdominal distention and localized tenderness with peritonitis. Computed tomography demonstrated large bowel obstruction, likely caused by sigmoid volvulus. The patient underwent emergent laparotomy. Intra-operatively, the entire colon was found to be extremely dilated and redundant. With a working diagnosis of recurrent sigmoid volvulus causing intermittent large bowel obstruction, a sigmoid colectomy and primary anastomosis was performed. Pathology revealed atrophic visceral myopathy, with an extremely thin colonic wall and atrophic circumferential and longitudinal muscularis propria without inflammation or fibrosis. The ganglion cells and myenteric plexus were unaffected. Post-operatively, the patient developed prolonged ileus requiring nasogastric decompression and parenteral nutrition. The ileus resolved with pro-kinetic agents, and patient was discharged home on post-operative day fifteen.
Atrophic visceral neuropathy is a rare cause of intestinal pseudo-obstruction. While often presenting with chronic obstruction in younger populations, we present a rare late-onset acute presentation that may have been secondary to underlying hypothyroidism.
萎缩性内脏肌病是一种病理诊断,其特征为内脏平滑肌层萎缩而神经节完整。它很少会急性发作表现为假性肠梗阻。我们描述了一例罕见病例,并探讨如何将该诊断与其他形式的肠梗阻相鉴别。
一名60岁男性,有甲状腺功能减退病史,因腹胀、疼痛加重伴恶心、呕吐两天就诊于急诊科。经评估,患者有心动过速,伴有腹胀和局限性压痛及腹膜炎。计算机断层扫描显示大肠梗阻,可能由乙状结肠扭转引起。患者接受了急诊剖腹手术。术中发现整个结肠极度扩张且冗长。初步诊断为复发性乙状结肠扭转导致间歇性大肠梗阻,遂行乙状结肠切除术及一期吻合术。病理显示为萎缩性内脏肌病,结肠壁极薄,固有肌层环形和纵形肌萎缩,无炎症或纤维化。神经节细胞和肌间神经丛未受影响。术后,患者出现长时间肠梗阻,需要鼻胃管减压和肠外营养。使用促动力药物后肠梗阻缓解,患者于术后第15天出院。
萎缩性内脏神经病是假性肠梗阻的罕见病因。虽然该病在年轻人群中常表现为慢性梗阻,但我们报告了一例罕见的迟发性急性表现,可能继发于潜在的甲状腺功能减退。