低级别阑尾粘液瘤的诊断不确定性和处理方法--病例报告和文献综述。

IF 0.4 Q4 SURGERY Journal of Surgical Case Reports Pub Date : 2024-11-18 eCollection Date: 2024-11-01 DOI:10.1093/jscr/rjae717
Charles Lu, Veysel K Embel, Mackenzie E Fox, Robin Donne, Glenn S Parker
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引用次数: 0

摘要

低级别阑尾粘液瘤(LAMN)是一种罕见的肿瘤,在接受阑尾切除术的患者中约占 1%。其表现往往各不相同,因此诊断具有挑战性。及时发现和治疗对防止破裂至关重要,破裂可能导致假性腹膜肌瘤。我们描述了一个 41 岁男性的病例,他因急性右下腹痛前来就诊。临床印象与阑尾炎一致,临床怀疑潜在的恶性肿瘤。患者被送入手术室,接受了探查性开腹手术和右半结肠切除术,发现了低级别阑尾粘液瘤。低级别阑尾粘液瘤的表现和影像学检查结果各不相同,因此其诊断极具挑战性。早期识别和治疗是防止发展为假性腹膜肌瘤的当务之急。我们的病例报告旨在为现有文献做出贡献,并对现有知识进行回顾。
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Diagnostic uncertainty and management of low-grade appendiceal mucinous neoplasm-a case report and review of the literature.

Low-grade appendiceal mucinous neoplasm (LAMN) is a rare entity identified in ~1% of patients undergoing appendectomy. The presentation often varies, making diagnosis challenging. Timely identification and treatment are critical to prevent rupture, which may lead to pseudomyxoma peritonei. We describe the case of a 41-year-old male who presented for evaluation of acute right lower quadrant abdominal pain. The clinical impression was consistent with appendicitis with a clinical suspicion for underlying malignancy. The patient was brought to the operating room for an exploratory laparotomy and right hemicolectomy, revealing low-grade appendiceal mucinous neoplasm. The diagnosis of low-grade appendiceal mucinous neoplasm can be challenging given the variable presentation and imaging findings. Early recognition and treatment are imperative to prevent progression to pseudomyxoma peritonei. Our case report seeks to contribute to the ongoing literature and provide a review of the current knowledge.

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来源期刊
CiteScore
0.70
自引率
0.00%
发文量
559
审稿时长
11 weeks
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