儿童肾上腺偶发瘤

Q4 Medicine Revista Romana de Pediatrie Pub Date : 2021-12-31 DOI:10.37897/rjp.2021.4.4
M. Dumitrașcu, Alice Elena Ghenea, Mihaela Popescu, A. Dumitrașcu, M. Carsote, C. Mehedințu, F. Șandru
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引用次数: 1

摘要

“偶发瘤”一词涉及医学的多个学科,特别是在现代医学时代,随着调查工具的巨大进步,增加了这一实体的流行病学含义。“内分泌偶发瘤”一词主要用于肾上腺和垂体(较少用于甲状腺,用“甲状腺结节”一词代替)。成人肾上腺偶发瘤(AAI)预计可在5-20%的人群中发现,这取决于年龄组、合共病、放射学/影像学方法(发病率随年龄增长而增加),而在儿童中没有。我们的目标是概述儿科AI (PAI)的频谱作为各种组织学和内分泌条件的总称。这是一篇简短的文学述评。纳入标准为:PubMed已发表的论文,扩展文章(英语),出版年份在2016年至2021年之间;选择是基于临床相关性。其中包括70个参考文献。PAI可能与多种皮质、髓质肿瘤有关,而AAI多为肾上腺皮质腺瘤,预后良好。AAI诊断(不仅基于放射学,也基于内分泌评估)特别强调肾上腺皮质癌或发展为恶性肿瘤,而在儿童人群中偶发肾上腺皮质癌的可能性并不罕见(非功能性模式在儿童中比在成人中更常见)。神经嵴源性肿瘤可能位于肾上腺水平;神经节神经瘤是一种良性肿瘤,通常是偶然发现的,而神经母细胞瘤大多是侵袭性的,临床表现暗示恶性肿瘤更常见,而不是完全无症状。10-14%的嗜铬细胞瘤是偶然发现的;然而,肾上腺切除术是必要的,无论表型。PAI是一个大的多学科领域,在某些领域仍有争议。关键信息是,在一个表面健康的孩子身上意外发现肾上腺肿块需要仔细检查;由于肾上腺切除术提供了足够的组织学报告,以维持内分泌和影像学检查,因此系列随访不太可能是选择性的方法(与成人人群相反)。
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Pediatric adrenal incidentaloma
The term of “incidentaloma” involves multiple disciplines of the medicine, especially on the era of modern medicine with massive progress of investigations tools that increased the epidemiological implications of this entity. “Endocrine incidentaloma” represents a term mostly used for adrenals and pituitary glands (and less used for thyroid where it is replaced by the term of “thyroid nodule”). Adult adrenal incidentaloma (AAI) is expected to be found up to 5-20% of population depending on age group, co-morbidities, radiological/imaging method (the incidence increases with age), and not in children. We aim to overview the spectrum of pediatric AI (PAI) as an umbrella term for various histological and endocrine conditions. This is a brief narrative review of literature. Inclusion criteria are: PubMed published papers, in extenso articles (English language), the year of publication between 2016 and 2021; the selection is based on clinical relevance. A number of 70 references is included. PAI may be related to various tumors of the cortex and medulla, while AAI mostly means an adrenocortical adenoma with a very good prognostic. AAI diagnostic (based not only on radiological, but also an endocrine assessment) exceptionally underlines an adrenocortical carcinoma or evolves to a malignancy while in pediatric population the eventuality of an incidental adrenocortical carcinoma is not so rare (the non-functional pattern is more frequent in children than in adults). Neural crest-derived tumors may be located at adrenal levels; while ganglioneuroma is a benign tumor which typically respects the incidental detection, neuroblastoma is mostly aggressive and the clinical presentation suggestive for a malignancy is more frequent rather than a completely asymptomatic picture. 10-14% of pheochromocytomas are incidentally detected; however, the adrenalectomy is imperative, regardless the phenotype. PAI represents a large multidisciplinary field which is still a matter of debate in certain areas. The key message is the fact that accidental detection of an adrenal mass on an apparently healthy child needs careful examination; serial follow-up is less likely the elective approach (opposite to adult population) since adrenalectomy provides adequate histological report in order to sustain the endocrine and imaging workup.
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4 weeks
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