SPONTANEOUS RUPTURE OF WILMS’ TUMOR PRESENTING AS ACUTE APPENDICITIS: A RARE CASE PRESENTATION

Q4 Medicine
H. Lip, T. J. Huei, P. Vellusamy
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引用次数: 0

Abstract

In Malaysia, incidence of Wilms’ Tumor (WT) is rare, with only 8 cases reported over four years according to the Malaysia Cancer Registry Report (2012-2016). Reports of spontaneous rupture of WT are scarce and the commonest presentation of this entity is a palpable mass in the abdomen. Herein, we report on the unusual presentation of an 11-year-old boy with typical symptoms of acute appendicitis. The child was subjected to an initial open appendicectomy and diagnosed intra-operatively with a right sided ruptured renal mass. Subsequent investigation leading to the diagnosis of a ruptured Wilms’ tumor and its treatment is discussed in this case presentation.
肿瘤自发破裂表现为急性阑尾炎:罕见病例
在马来西亚,威尔姆斯肿瘤(WT)的发病率很低,根据马来西亚癌症登记报告(2012-2016),四年内仅报告了8例。WT自发性破裂的报告很少,这种实体最常见的表现是腹部可触及的肿块。在此,我们报告一名11岁男孩的不寻常表现,他有典型的急性阑尾炎症状。该儿童接受了首次开放性阑尾切除术,术中诊断为右侧肾肿块破裂。随后的研究导致威尔姆斯肿瘤破裂的诊断及其治疗在本病例中进行了讨论。
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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CiteScore
0.30
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