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[Retroperitoneal lipoblastoma in an infant. A case report]. / Lipoblastoma retroperitoneal en un lactante. Caso clínico.
Valderrama S, Javier; Schnettler R, David; Zamorano H, Marcelo; Lahsen H, Juan Pablo.
Afiliação
  • Valderrama S J; Licenciado en Medicina, Universidad Católica del Maule, Talca, Chile.
  • Schnettler R D; Cirujano Pediátrico, Magíster en Bioética, Facultad de Medicina Universidad Católica del Maule, Servicio de Cirugía Infantil, Hospital Regional de Talca, Talca, Chile. Electronic address: dschnettlerrod@yahoo.com.
  • Zamorano H M; Cirujano Pediátrico, Urólogo Pediátrico, Facultad de Medicina Universidad Católica del Maule, Servicio de Cirugía Infantil, Hospital Regional de Talca, Talca, Chile.
  • Lahsen H JP; Anátomo Patólogo, Facultad de Medicina Universidad Católica del Maule, Unidad de Anatomía Patológica, Hospital Regional de Talca, Talca, Chile.
Rev Chil Pediatr ; 87(3): 199-203, 2016.
Article em Es | MEDLINE | ID: mdl-26613629
INTRODUCTION: Lipoblastoma is a benign neoplasia of the adipose tissue. It is a rare conditionand almost exclusively presents in children under 3 years old. It usually occurs in extremities as a painless volume increase of progressive growth, with the definitive diagnosis being established by pathological and cytogenetic analysis. The treatment of choice is complete resection, and follow-up period of up to five years is recommended due to a recurrence of up to 25%. OBJECTIVE: To present an unusual location of this uncommon condition in an infant, and review the related literature. CASE REPORT: A sixteen-month child with an increase in abdominal growth of six-months progression, associated with a decreased food intake, and with no other symptoms. The imaging study revealed a lipoid-like image compromising almost the entire abdominal cavity, very suggestive of lipoblastoma. A resection was performed on an 18cm diameter retroperitoneal tumour that rejected the adjacent organs. Histological analysis was enough to confirm diagnosis without the need for cytogenetic analysis. The follow-up showed no recurrence of the disease. CONCLUSION: Given the rarity of this disease and its unusual presentation, we communicate this clinical case, in order to be considered in the differential diagnosis of abdominal mass in chilhood.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Retroperitoneais / Lipoblastoma Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Infant Idioma: Es Revista: Rev Chil Pediatr Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Chile País de publicação: Chile

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Retroperitoneais / Lipoblastoma Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Infant Idioma: Es Revista: Rev Chil Pediatr Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Chile País de publicação: Chile