Le masse surrenaliche nella sindrome di Beckwith-Wiedemann: un algoritmo diagnostico

Author:

Borraccetti Natalia1,Bruno Ivana2,Lambertini Anna Giulia1,Casadio Luca2,Radice Caterina2,Donati Ilaria3,Piccinini Giancarlo2,Minguzzi Maria Teresa4,Marchetti Federico2

Affiliation:

1. Scuola di Specializzazione in Pediatria, Università di Ferrara

2. UOC di Pediatria e Neonatologia, Ospedale di Ravenna, AUSL della Romagna

3. UO di Genetica Medica, AUSL della Romagna

4. UOC di Radiodiagnostica, Ospedale di Ravenna, AUSL della Romagna

Abstract

Children with Beckwith-Wiedemann syndrome (BWs) have an increased risk of developing embryonic tumours during the first few years of life. Predisposition to the development of tumours is closely related to molecular subtype and therefore the cancer screening programme should be individualized on the basis of the genotype. Among the most common tumours, those with adrenal origin even if they show benign characteristics should be evaluated to rule out the hypothesis of severe tumours such as neuroblastoma. The paper reports the case of a newborn with BWs who showed an adrenal mass shortly after birth. To evaluate the lesion, though there is little available literature on the subject, one of the few existing algorithm for the diagnosis and follow-up was used. In case of ultrasound detection of an adrenal mass the algorithm first considers age, size and type of consistency (cystic or solid).

Publisher

Medico e Bambino

Subject

General Medicine

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. La sindrome Beckwith-Wiedemann;Medico e Bambino;2023-09-07

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