Gastric tumors in children: single-center study with emphasis on treatment of repeated recurrence.
Adolescent
Child
Child, Preschool
Female
Gastrectomy
/ methods
Gastrointestinal Neoplasms
/ pathology
Hamartoma
/ pathology
Humans
Infant
Infant, Newborn
Male
Neoplasm Recurrence, Local
/ surgery
Neoplasms, Muscle Tissue
/ pathology
Neurilemmoma
/ pathology
Retrospective Studies
Survival Analysis
Teratoma
/ pathology
Treatment Outcome
Gastric tumors
Pediatric
Recurrence
Stomach
Surgery
Journal
Pediatric surgery international
ISSN: 1437-9813
Titre abrégé: Pediatr Surg Int
Pays: Germany
ID NLM: 8609169
Informations de publication
Date de publication:
Aug 2020
Aug 2020
Historique:
accepted:
11
06
2020
pubmed:
21
6
2020
medline:
15
12
2020
entrez:
21
6
2020
Statut:
ppublish
Résumé
Analysis of surgical management and survival of pediatric patients with gastric tumors treated at our institution. A retrospective study of patients with primary gastric tumors treated between 1993 and 2018 was conducted. Eight patients, five girls and three boys, were diagnosed with gastric tumors at an average age of 10.4 years (1 day-15.4 years). Surgical management included Billroth type I procedure in five and tumor excision in three patients. Histology revealed gastrointestinal stromal tumor (GIST) in four patients and one of each of schwannoma, myofibroblastic tumor, hamartoma and teratoma. Microscopically clear margins were reported in six patients. Repeated local recurrence occurred in three patients (2 × GIST, 1 × myofibroblastic tumors) who consequently underwent three, four and six reoperations. One of these patients had liver metastases, which were managed with ligation of the hepatic arteries. This patient was also diagnosed with a lung hamartoma, which was treated with a lobectomy. Survival rate was 100% with a median follow-up of 8.6 years (7 months-25.5 years). Gastric tumors are rare in children and represent a management challenge. Repeated recurrence of GISTs and myofibroblastic tumors remains frequent even after complete resection and may necessitate multiple surgeries, therefore patients require a lifelong follow-up.
Identifiants
pubmed: 32561985
doi: 10.1007/s00383-020-04698-w
pii: 10.1007/s00383-020-04698-w
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM