Giant Renal Angiomyolipoma: A Case Report

S. Nawrocki, A. Lachowski
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Abstract

Renal Angiomyolipoma (AML), moreover known as a renal hamartoma, is a solid tumor with no malignant characteristics. The inheritance pattern of renal AML is autosomal dominant. If the lesion grows to a large size, a series of clinical manifestations and important complications might also occur. This research paper presents a case of huge renal AML in a 47-year-old lady, who visited the Emergency Department of Bahrain Defence Forces Hospital with right-sided abdominal pain of sudden onset. The patient underwent a total right nephrectomy. The resected mass was sized 10.5 x 13 x 14 cm. Postoperative histopathological examination confirmed the lesion as a huge renal AML. Due to the huge size of the tumor, it is crucial to record similar cases, along with their diagnosis and treatment. Keywords: Abdominal pain, Angiomyolipoma, Hamartoma, Kidney Neoplasms, Nephrectomy
巨大肾血管平滑肌脂肪瘤1例
肾血管平滑肌脂肪瘤(AML),又称肾错构瘤,是一种无恶性特征的实体瘤。肾性AML的遗传模式为常染色体显性。如果病变发展到较大,还可能出现一系列临床表现和重要的并发症。本文报告一位47岁的女士,因右侧突然腹痛到巴林国防军医院急诊科就诊,患严重肾性急性髓性白血病。病人接受了全右肾切除术。切除肿块大小为10.5 x 13 x 14 cm。术后组织病理学检查证实病变为巨大的肾性急性髓性白血病。由于肿瘤体积巨大,记录类似病例及其诊断和治疗是至关重要的。关键词:腹痛,血管平滑肌脂肪瘤,错构瘤,肾肿瘤,肾切除术
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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