Pereira Soares Inês, Sampaio Mesquita António, Ramos Luís, Ussene Esperança, Cunha Florbela
Paediatrics, Unidade Local de Saúde Estuário do Tejo - Hospital de Vila Franca de Xira, Lisbon, PRT.
General Surgery, Unidade Local de Saúde Estuário do Tejo - Hospital de Vila Franca de Xira, Lisbon, PRT.
Cureus. 2025 Mar 10;17(3):e80323. doi: 10.7759/cureus.80323. eCollection 2025 Mar.
Appendiceal mucinous neoplasms are neoplastic appendicular lesions resulting from the abnormal accumulation of mucin in the appendix. These neoplasms can be asymptomatic or present with vague, nonspecific symptoms. Although generally considered benign, they carry the risk of severe complications such as pseudomyxoma peritonei. We present a 17-year-old boy with fever and suprapubic pain radiating to the right lower quadrant, with no definitive clinical, imaging, or intraoperative macroscopic diagnosis, who was found to have an appendiceal mucinous neoplasm. He underwent complete resection of the appendix with negative margins, without the need for further treatment. As a rare entity in pediatric patients, these neoplasms pose both diagnostic and therapeutic challenges with ongoing debate regarding the best surgical approach, appropriate adjuvant therapy, duration of follow-up, and imaging techniques for their management. This case highlights an unusual way of diagnosing an uncommon neoplasm.
阑尾黏液性肿瘤是阑尾的肿瘤性病变,由阑尾中黏蛋白的异常蓄积引起。这些肿瘤可能无症状,或表现为模糊、非特异性的症状。虽然通常被认为是良性的,但它们有发生严重并发症如腹膜假黏液瘤的风险。我们报告一名17岁男孩,有发热及耻骨上区疼痛并向右下腹放射,临床、影像学及术中宏观检查均无明确诊断,最终发现患有阑尾黏液性肿瘤。他接受了阑尾完整切除,切缘阴性,无需进一步治疗。作为儿科患者中的罕见疾病,这些肿瘤在诊断和治疗方面都具有挑战性,关于最佳手术方式、合适的辅助治疗、随访时间以及用于其管理的影像学技术仍存在争议。本病例突出了一种诊断罕见肿瘤的不寻常方法。