Adrenal Cortex Carcinoma: One of the Rarest Retroperitoneal Tumors in children

D. Hanine, B. Rouijel, A. E. Baoudi, M. Kisra
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Abstract

Adrenocortical Carcinoma (ACC) are rare tumors that have a bimodal distribution, the first peak is in children less than five years and the second around the fifth decade [1]. Although most adult ACC are non-functional, in the pediatric age group, nearly 95% are functional [2]. Virilization is the most common abnormality and Cushing’s syndrome and hyperaldosteronism are less frequent [3]. We begin the review with a clinical case of a 16-month-old infant, and then we will discuss this very rare pathology as well as its management.
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肾上腺皮质癌:儿童腹膜后最罕见的肿瘤之一
肾上腺皮质癌(Adrenocortical Carcinoma, ACC)是一种罕见的肿瘤,呈双峰分布,第一个高峰发生在5岁以下的儿童,第二个高峰发生在50岁左右[1]。虽然大多数成人ACC是非功能性的,但在儿童年龄组中,近95%是功能性的[2]。男性化是最常见的异常,库欣综合征和高醛固酮增多症较少见[3]。我们首先回顾一个16个月大的婴儿的临床病例,然后我们将讨论这种非常罕见的病理及其管理。
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