Pediatric primary hyperparathyroidism: Surgical pathology and long-term outcomes in sporadic and familial cases.
Am J Surg
; 225(4): 699-702, 2023 04.
Article
em En
| MEDLINE
| ID: mdl-36270819
ABSTRACT
BACKGROUND:
Primary Hyperparathyroidism (PHPT) is rare in pediatric patients. Data regarding surgical outcomes are scarce.METHODS:
Single-center retrospective review (1994-2020) of patients ≤21 years undergoing surgery for PHPT.RESULTS:
66 patients were identified (61% female, 17 ± 3 years). 71% of patients were symptomatic at diagnosis. 32% of patients had known familial syndromes, most commonly MEN-1. 23% of patients without a known mutation had genetic testing, 22% positive. 56% of the total and 19% of the familial cohort underwent focused exploration. Single gland disease was found in 19% of familial vs 85% of sporadic cases, p < 0.00001. Persistence was 9%, all in the sporadic group, p = 0.11. Recurrence was 15% 38% in the familial vs 2% in the sporadic groups, p=0.0004. Time to recurrence was 59 months (Q1-38, Q3-95), familial 61 vs 124 months sporadic, p=0.001.CONCLUSION:
Pediatric PHPT is frequently sporadic, although 5% of apparent sporadic cases are secondary to syndromes. Familial cases have higher rates of recurrence, requiring closer follow-up.Palavras-chave
Texto completo:
1
Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Patologia Cirúrgica
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Neoplasia Endócrina Múltipla Tipo 1
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Hiperparatireoidismo Primário
Limite:
Child
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Female
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Humans
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Male
Idioma:
En
Revista:
Am J Surg
Ano de publicação:
2023
Tipo de documento:
Article