A Pediatric Case of Mixed Acinar-Neuroendocrine Carcinoma

J. Youn, H. Son, Sung-Eun Jung, Hyun Young Kim
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引用次数: 1

Abstract

Mixed acinar-neuroendocrine carcinoma (MANEC) is a malignant pancreatic tumor that rarely occurs in children. It is diagnosed pathologically according to the proportion of neuroendocrine cells present, highlighting the need for surgical biopsy. A 13-year-old boy presented with a 10-cm palpable mass on CT. Surgical resection was performed, and the pathological diagnosis was MANEC. There were no postoperative complications, and the patient was discharged from the hospital 10 days after surgery. He is presently undergoing adjuvant chemotherapy. We reviewed historical MANEC cases published in the English literature. We concluded that pathological analysis of a surgically resected specimen is necessary for an accurate diagnosis of MANEC, and that publication of more cases is needed to determine the optimal management strategy for MANEC.
小儿腺泡-神经内分泌混合性癌1例
混合性腺泡-神经内分泌癌(MANEC)是一种少见的儿童胰腺恶性肿瘤。根据神经内分泌细胞的比例进行病理诊断,强调手术活检的必要性。一个13岁的男孩在CT上表现为一个10厘米可触及的肿块。手术切除,病理诊断为MANEC。术后无并发症,术后10天出院。他目前正在接受辅助化疗。我们回顾了在英语文献中发表的历史MANEC病例。我们的结论是,手术切除标本的病理分析对于准确诊断MANEC是必要的,需要发表更多的病例来确定MANEC的最佳治疗策略。
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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