Case Report: Plummer's adenoma in Prader-Willi syndrome.

GH therapy Plummer’s adenoma children subclinical hyperthyroidism thyroid nodule

Journal

Frontiers in pediatrics
ISSN: 2296-2360
Titre abrégé: Front Pediatr
Pays: Switzerland
ID NLM: 101615492

Informations de publication

Date de publication:
2024
Historique:
received: 28 02 2024
accepted: 22 07 2024
medline: 23 8 2024
pubmed: 23 8 2024
entrez: 23 8 2024
Statut: epublish

Résumé

Thyroid nodules in children are less common than in adults but they are approximately two- to three-fold more likely to be malignant in children. Among thyroid nodular diseases, Plummer's adenoma occurs very rarely in pediatrics, and currently, there is no literature providing evidence of this diagnosis in patients with Prader-Willi syndrome (PWS). We report the case of a 9-year-old Caucasian boy affected by PWS presenting with a rapidly growing palpable mass in the thyroid lodge associated with subclinical hyperthyroidism. Laboratory and other examinations (thyroid ultrasound, fine-needle aspiration of the nodule, and scintigraphy) were strongly suggestive for Plummer's adenoma; therefore, the patient underwent left hemithyroidectomy surgery, and anatomo-pathological examination confirmed the diagnosis. Our case describes the first evidence of an isolated follicular adenoma in children with PWS. Surgery is the only therapeutic option in younger children. Further evidence is needed to assess the possible correlation between these two conditions and the existence of potential risk factors.

Identifiants

pubmed: 39175805
doi: 10.3389/fped.2024.1388437
pmc: PMC11338776
doi:

Types de publication

Case Reports Journal Article

Langues

eng

Pagination

1388437

Informations de copyright

© 2024 Corica, Toscano, Moleti, Pepe, Campenni, Fadda, Dionigi, Romeo, Aversa and Wasniewska.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The authors declared that they were an editorial board member of Frontiers at the time of submission. This had no impact on the peer review process and final decision.

Auteurs

Domenico Corica (D)

Pediatric Unit, Department of Human Pathology of Adulthood and Childhood "G. Barresi", University of Messina, Messina, Italy.

Fabio Toscano (F)

Pediatric Unit, Department of Human Pathology of Adulthood and Childhood "G. Barresi", University of Messina, Messina, Italy.

Mariacarla Moleti (M)

Endocrinology Unit, Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.

Giorgia Pepe (G)

Pediatric Unit, Department of Human Pathology of Adulthood and Childhood "G. Barresi", University of Messina, Messina, Italy.

Alfredo Campenni (A)

Nuclear Medicine Unit, Department of Biomedical and Dental Sciences and Morpho-Functional Imaging, University of Messina, Messina, Italy.

Guido Fadda (G)

Section of Pathological Anatomy, Department of Human Pathology of Adulthood and Childhood "Gaetano Barresi", University of Messina, Messina, Italy.

Gianlorenzo Dionigi (G)

Division of Surgery, Istituto Auxologico Italiano, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Milano, Italy.

Carmelo Romeo (C)

Pediatric Surgery Unit, Department of Human Pathology of Adulthood and Childhood "Gaetano Barresi", University of Messina, Messina, Italy.

Tommaso Aversa (T)

Pediatric Unit, Department of Human Pathology of Adulthood and Childhood "G. Barresi", University of Messina, Messina, Italy.

Malgorzata Wasniewska (M)

Pediatric Unit, Department of Human Pathology of Adulthood and Childhood "G. Barresi", University of Messina, Messina, Italy.

Classifications MeSH