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Ovarian tumors in children: how common are lesion recurrence and metachronous disease? A UK CCLG Surgeons Cancer Group nationwide study.
Braungart, S; Craigie, R J; Farrelly, P; Losty, P D.
Afiliación
  • Braungart S; Department of Paediatric Surgery, Royal Manchester Children's Hospital, Manchester, UK; Department of Paediatric Surgery, Alder Hey Children's Hospital, Liverpool, UK. Electronic address: sarah.braungart@doctors.org.uk.
  • Craigie RJ; Department of Paediatric Surgery, Royal Manchester Children's Hospital, Manchester, UK. Electronic address: Ross.craigie@mft.nhs.uk.
  • Farrelly P; Department of Paediatric Surgery, Royal Manchester Children's Hospital, Manchester, UK. Electronic address: Paul.farrelly@mft.nhs.uk.
  • Losty PD; Department of Paediatric Surgery, Alder Hey Children's Hospital, Liverpool, UK; University of Liverpool, Liverpool, L69 3BX, UK. Electronic address: Paul.losty@liverpool.ac.uk.
J Pediatr Surg ; 55(10): 2026-2029, 2020 Oct.
Article en En | MEDLINE | ID: mdl-31837839
ABSTRACT

BACKGROUND:

Ovarian tumors in children are rare, mature teratoma being the most common histological entity. Robust guidelines to aid patient follow-up after resection are distinctly lacking. Although mature teratoma has a very good prognosis following complete resection, small studies have reported the occurrence of metachronous disease and recurrence to a variable degree (2.5-23% of patients). Nevertheless, there are surgeons who recommend no follow-up is required for these children after primary tumor resection. We investigated the incidence of (i) recurrence and (ii) metachronous disease in pediatric patients following ovarian tumor resection.

METHODS:

Retrospective multicenter study amongst UK pediatric surgical oncology centers. Females <16 years with diagnosis of ovarian tumor from 2006 to 2016 were included. Functional/neonatal ovarian cysts were excluded.

RESULTS:

Three hundred ten patients with ovarian tumors treated at 12 surgical oncology centers were identified. Mean age at surgery was 11 years [IQR 8-14]. Most common diagnosis were mature teratoma (57%, 177 cases), immature teratoma (10.9%, 34 cases) and serous cystadenoma (7.7%, 24 cases). 8.1% (25 cases) of all females were identified with tumor recurrence/ metachronous disease. 5.1% (9 cases) of patients with mature teratoma had recurrent/ metachronous disease. Most of these patients were diagnosed at routine clinic follow-up.

CONCLUSION:

Our study clearly shows that ovarian tumor recurrence(s) and metachronous disease occur, even in "benign" ovarian tumors. We recommend female pediatric patients should have robust follow-up care plans after primary diagnosis and resection of ovarian tumor(s). LEVEL OF EVIDENCE STATEMENT This is a level II evidence study. It is a retrospective multicentre collaborative study which summarizes data from a national cohort of children.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Ováricas / Teratoma / Recurrencia Local de Neoplasia Tipo de estudio: Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Child / Female / Humans País/Región como asunto: Europa Idioma: En Revista: J Pediatr Surg Año: 2020 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Ováricas / Teratoma / Recurrencia Local de Neoplasia Tipo de estudio: Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Child / Female / Humans País/Región como asunto: Europa Idioma: En Revista: J Pediatr Surg Año: 2020 Tipo del documento: Article