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复杂性阑尾炎继发腹壁坏死性筋膜炎:一例报告

Necrotizing Fasciitis of the Abdominal Wall Secondary to Complicated Appendicitis: A Case Report.

作者信息

Falconi Sirin, Wilhelm Christopher, Loewen Jocelin, Soliman Basem

机构信息

Surgery, Texas Tech University Health Sciences Center School of Medicine, Lubbock, USA.

General Surgery, Texas Tech University Health Sciences Center School of Medicine, Amarillo, USA.

出版信息

Cureus. 2023 May 29;15(5):e39635. doi: 10.7759/cureus.39635. eCollection 2023 May.

Abstract

Acute appendicitis is one of the most common surgical emergencies worldwide. Many complications can occur secondary to complicated appendicitis including abscess formation, gangrene, sepsis, and perforation, rarely, leading to abdominal wall necrotizing fasciitis. The incidence of necrotizing fasciitis as a complication of ruptured appendicitis is extremely uncommon. The formation of an enterocutaneous fistula leading to this complication further emphasizes the rarity of such occurrence with few cases reported in the literature. Herein, we present a case of abdominal wall necrotizing fasciitis in a 72-year-old female presenting to the local emergency room with complaints of severe suprapubic abdominal pain associated with abdominal distension and acute onset foul-smelling drainage. Physical exam was significant for suprapubic and right lower quadrant abdominal tenderness with associated large indurated tender lesion and purulent weeping with large ecchymosis. Abdominal computed tomography (CT) revealed extensive subcutaneous emphysema, a large cavity with layering fluid extending into the peritoneal space, and a possible fistula formation between the intra-abdominal cavity and subcutaneous tissue. Following the diagnosis of probable necrotizing fasciitis secondary to fistula formation, the patient underwent emergent exploratory laparotomy and extensive debridement of necrotic tissue. In this report, we take the opportunity to highlight the importance of promptly recognizing and treating this uncommon complication and maintaining a high level of suspicion to prevent life-threatening consequences.

摘要

急性阑尾炎是全球最常见的外科急症之一。复杂阑尾炎可继发许多并发症,包括脓肿形成、坏疽、脓毒症和穿孔,极少情况下会导致腹壁坏死性筋膜炎。坏死性筋膜炎作为阑尾炎破裂的并发症,其发生率极为罕见。导致这种并发症的肠皮肤瘘的形成进一步凸显了这种情况的罕见性,文献中报道的病例很少。在此,我们报告一例72岁女性腹壁坏死性筋膜炎病例,该患者因严重耻骨上腹痛伴腹胀及急性发作的恶臭引流物就诊于当地急诊室。体格检查发现耻骨上和右下腹压痛明显,伴有大的硬结性压痛病变及脓性渗液和大片瘀斑。腹部计算机断层扫描(CT)显示广泛的皮下气肿、一个有分层液体的大腔隙延伸至腹膜腔,以及腹腔与皮下组织之间可能存在瘘管形成。在诊断为可能继发于瘘管形成的坏死性筋膜炎后,患者接受了急诊剖腹探查术及广泛的坏死组织清创术。在本报告中,我们借此机会强调及时识别和治疗这种罕见并发症以及保持高度怀疑以防止危及生命后果的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/565c/10305508/1628a3641144/cureus-0015-00000039635-i01.jpg

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