Idiopathic encapsulating peritoneal sclerosis: A case report.

IF 0.6 Q4 SURGERY International Journal of Surgery Case Reports Pub Date : 2025-01-01 Epub Date: 2024-11-30 DOI:10.1016/j.ijscr.2024.110694
Kammoun Neirouz, Ben Romdhane Haifa, Trabelsi Mohamed Mehdi, Ben Salah Faicel, Ben Hassine Mohamed, Jerraya Hichem
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Abstract

Introduction: Encapsulating peritoneal sclerosis is a rare disease, characterized by subocclusive symptoms. Idiopathic forms could be challenging, as they are often mistaken for other conditions. We present a case mistaken for an internal hernia.

Case report: A 52-year-old male patient, who was complaining of abdominal pain and bloating for 6 months. He presented due to worsening of his symptoms. A CT scan was then performed evoking an internal hernia. Emergency surgery via laparoscopy revealed encapsulating peritoneal sclerosis with a cocoon-like fibrous tissue encasing the bowel. A conversion by a midline incision was performed for enterolysis and fibrous tissue resection.

Discussion: Encapsulating peritoneal sclerosis (EPS), is a rare disease. Because of the rigid capsule surrounding the loops, symptomatology includes recurrent occlusive symptoms. The incidence of this pathology is unknown. EPS is often associated with peritoneal dialysis(PD), infections, and systemic inflammatory disorders. Idiopathic cases, like in our patient, are often misdiagnosed pre-operatively. The treatment focuses on the management of the underlying cause if identified. Corticoids are proposed in inflammatory diseases while switching to hemodialysis or the use of tamoxifen and immunosuppressive therapies are proposed in case of PD. In case of failure of the conservative approaches or in case of emergency, a peritonectomy and enterolysis could be performed despite being at high risk of recurrence and mortality.

Conclusion: We aimed to describe a case misdiagnosed as an internal hernia to raise awareness among practitioners about this condition.

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特发性包膜性腹膜硬化1例。
简介:包膜性腹膜硬化症是一种罕见的疾病,以亚封闭症状为特征。特发性形式可能具有挑战性,因为它们经常被误认为是其他疾病。我们报告一个被误认为是腹内疝的病例。病例报告:男性,52岁,主诉腹痛、腹胀6个月。他是由于症状恶化而来的。然后进行了CT扫描,引起了内部疝气。通过腹腔镜急诊手术发现包裹性腹膜硬化症,茧状纤维组织包裹肠。通过中线切口进行肠溶和纤维组织切除。讨论:包裹性腹膜硬化(EPS)是一种罕见的疾病。由于环周围的硬囊,症状包括复发性闭塞症状。这种病理的发生率尚不清楚。EPS通常与腹膜透析(PD)、感染和全身炎症性疾病有关。特发性病例,如本例患者,术前常被误诊。治疗的重点是管理的根本原因,如果确定。在炎症性疾病中,当转向血液透析或使用他莫昔芬时,建议使用皮质激素;在PD的情况下,建议使用免疫抑制疗法。如果保守入路失败或在紧急情况下,尽管有很高的复发和死亡风险,仍可以进行腹膜切除术和肠溶术。结论:我们的目的是描述一个病例误诊为内部疝,以提高认识的从业者对这种情况。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.10
自引率
0.00%
发文量
1116
审稿时长
46 days
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