2015
DOI: 10.5152/ucd.2015.2786
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Idiopathic encapsulating sclerosing peritonitis

Abstract: Sclerosing encapsulating peritonitis (SEP)/abdominal cocoon syndrome is a rare condition that is generally identified in young females. The exact cause is still unknown. Timely and accurate imaging and diagnosis play a critical role for morbidity and mortality. It is usually diagnosed during surgery. The initial treatment should be conservative, and aggressive surgical approach should be avoided as much as possible. Herein, we aimed to review the clinical features of SEP based on a patient who underwent surger… Show more

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Cited by 11 publications
(12 citation statements)
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References 7 publications
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“…Furthermore, an aggressive surgical approach may lead to an increased risk of intraoperative enterotomy and subsequent enterocutaneous fistula formation. Medical treatments such as tamoxifen, corticosteroids and other immunosuppressive agents have been reported in the management of SEP [ 9 ]. We report a significant improvement in the patient’s condition with conservative management, consisting of bowel rest and nutritional support.…”
Section: Discussionmentioning
confidence: 99%
“…Furthermore, an aggressive surgical approach may lead to an increased risk of intraoperative enterotomy and subsequent enterocutaneous fistula formation. Medical treatments such as tamoxifen, corticosteroids and other immunosuppressive agents have been reported in the management of SEP [ 9 ]. We report a significant improvement in the patient’s condition with conservative management, consisting of bowel rest and nutritional support.…”
Section: Discussionmentioning
confidence: 99%
“…Inflammatory cells are always present, but leukocyte infiltration is not a must for diagnosis [14]. In the pathogenesis of cocoon formation, It is thought that fibrogenic cytokines are released from fibroblasts trigger neoangiogenesis and peritoneal fibrosis [15,16].…”
Section: Discussionmentioning
confidence: 99%
“…Histologically, the sac of PE is the crystalloid peritoneum, which is normal, has no fibrosis and no adhesion with the intestine. However, AC often presents with omental dysplasia or absence, and the sac is formed of thickened collagen and fibrous tissue, which may be accompanied by nonspecific chronic inflammation (26,32,33). In addition, AC also needs to be identified with tuberculosis, peritoneal mesothelioma and peritoneal pseudomyxoma (27,32,33).…”
Section: Discussionmentioning
confidence: 99%