Síndrome lumbocostovertebral. Reporte de un caso

Mónica Galarza-Armijos, Luis Marcano-Sanz, Miurkis Endis-Miranda, Mauricio Siavichai-Romero

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

Resumen

Introduction. Lumbocostovertebral syndrome is a rare anomaly that affects the vertebral bodies, ribs and muscles of the abdominal wall, and can be associated with multiple congenital abnormalities. It requires multidisciplinary management and early surgical treatment to avoid complications. Clinical case. The case of a 10-day-old male neonate is reported, who presented from birth 2 right lumbar tumors, one that increased in size with crying, corresponded to a lumbar hernia, and the other, to myelomeningocele. In complementary studies, rib fusion, fusion of lumbar and sacral vertebral bodies (hemivertebrae), and abdominal wall defect with protrusion of intestinal contents were evidenced. The lumbar hernia was closed with prosthetic reinforcement with a bovine pericardium, without complications. Conclusion. In extensive defects, such as the one reported in this patient, it may be advisable to use prosthetic material. The bovine pericardium appears as a safe, well tolerated and effective option for these patients in par-ticular. This syndrome is a rare entity, which requires a multidisciplinary team for early surgical resolution and thus avoid complications.

Título traducido de la contribuciónLumbocostovertebral syndrome. A case report
Idioma originalEspañol
Páginas (desde-hasta)151-155
Número de páginas5
PublicaciónRevista Colombiana de Cirugia
Volumen37
N.º1
DOI
EstadoPublicada - 17 dic. 2022
Publicado de forma externa

Palabras clave

  • Abdominal hernia
  • Congenital abnormalities
  • Hernia
  • Lumbar vertebrae
  • Meningomyelocele
  • Syndrome

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