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Segmental Absence of Intestinal Musculature in a 64-Year-Old Female: Case Report and Literature Review

机译:64岁女性肠道肌肉的节段性缺失:病例报告和文献复习

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Patient: Female, 64 Final Diagnosis: Segmental absence of intestinal musculature Symptoms: Abdominal discomfort Medication: — Clinical Procedure: Colectomy Specialty: Diagnostics, Laboratory Objective: Rare disease Background: Segmental absence of intestinal musculature is a well described entity in premature infants. It presents with peritonitis, bowel perforation, and obstruction. The diagnosis is based on pathologic observation of absence of intestinal musculature. Researchers hypothesized that this entity is a result of a vascular accident during embryogenesis. However, segmental absence of intestinal musculature is no longer limited to the pediatric population. Recently, a few cases have been described in adults with and without significant vascular diseases. This change in the age of the affected population with segmental absence of intestinal musculature makes the understanding of the pathogenesis of this entity even more challenging. Case Report: Here, we report a case of segmental absence of intestinal musculature in a 64-year-old female. The patient presented to the emergency room with sudden onset of abdominal pain and signs of peritonitis. Abdominal computed tomography showed free air in the abdomen. Laparotomy was performed, and a perforation involving the descending colon was identified. Left hemicolectomy was performed. Pathologic examination of the resected colon showed segmental absence of intestinal musculature. Conclusions: Although the pathologic diagnosis of segmental absence of intestinal musculature is straightforward, the assumption that this condition is limited to the pediatric population is a major player in overlooking this diagnosis in adults. Pathologists should be aware that this condition can present in adults and is segmental. Gross and microscopic examination of perforated intestine is required to reach the correct diagnosis. To our knowledge, twelve cases of this entity have been described in adults. Here we present the thirteenth case of segmental absence of intestinal musculature in an adult, and we discuss the clinical and pathologic findings of this entity as well as its pathogenesis.
机译:患者:女,64岁最终诊断:肠段肌无节段症状:腹部不适药物治疗:—临床程序:结肠切除术专长:诊断,实验室检查目的:罕见疾病背景:早产儿段段无肠肌结构是一个很好的描述。表现为腹膜炎,肠穿孔和阻塞。诊断是基于无肠肌肉组织的病理观察。研究人员假设该实体是胚胎发生期间血管意外的结果。但是,小肠肌肉的节段性缺失不再仅限于儿科人群。最近,已经描述了成年人中有或没有重大血管疾病的几例病例。在部分不存在肠道肌肉组织的情况下,受影响人群的年龄发生了变化,这使得对该实体发病机理的理解更具挑战性。病例报告:在这里,我们报告了一名64岁女性肠道肌肉分段缺失的病例。该患者突然出现腹痛和腹膜炎的迹象,出现在急诊室。腹部计算机断层扫描显示腹部自由空气。进行了剖腹手术,并发现了涉及降结肠的穿孔。进行左半结肠切除术。切除结肠的病理检查显示节段性肠肌组织缺失。结论:尽管对节段性肠肌肉组织缺乏进行病理学诊断很简单,但这种情况仅限于儿科人群的假设是忽略成人这种诊断的主要因素。病理学家应意识到这种情况可以在成人中出现并且是分段的。要进行正确的诊断,需要对穿孔的肠进行肉眼和显微镜检查。据我们所知,成人中已经描述了该实体的十二例。在这里,我们介绍了成年人中肠肌肉组织节段性缺失的第十三例,我们讨论了该实体的临床和病理学发现及其发病机理。

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