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Tumor dissemination through surgical tracts in diffuse intrinsic pontine glioma.
Lobon-Iglesias, Maria-Jesus; Santa-Maria Lopez, Vicente; Puerta Roldan, Patricia; Candela-Cantó, Santiago; Ramos-Albiac, Monica; Gomez-Chiari, Marta; Puget, Stephanie; Bolle, Stephanie; Goumnerova, Liliana; Kieran, Mark W; Cruz, Ofelia; Grill, Jacques; Morales La Madrid, Andres.
Afiliación
  • Lobon-Iglesias MJ; 1Department of Pediatric and Adolescent Oncology and.
  • Santa-Maria Lopez V; 2Team "Target Identification and Innovative Anticancer Therapies in Pediatric Cancers," Centre National de la Recherche Scientifique Unité Mixte de Recherche 8203, Villejuif.
  • Puerta Roldan P; 3Department of Pediatric Hematology and Oncology.
  • Candela-Cantó S; 4Pediatric Neuro-Oncology, Department of Pediatric Hematology and Oncology.
  • Ramos-Albiac M; 5Department of Pediatric Neurosurgery, and.
  • Gomez-Chiari M; 5Department of Pediatric Neurosurgery, and.
  • Puget S; 6Department of Radiation Oncology, Hospital Vall d'Hebron, Barcelona, Spain.
  • Bolle S; 7Department of Radiology, Hospital Sant Joan de Déu.
  • Goumnerova L; 8Department of Pediatric Neurosurgery, Necker Sick Children's Hospital and University Paris-Descartes, Paris, France.
  • Kieran MW; 9Department of Radiation Therapy, Gustave Roussy and University Paris-Saclay, Villejuif.
  • Cruz O; 10Department of Neurosurgery, Boston Children's Hospital; and.
  • Grill J; 11The Pediatric Brain Tumor Program, Department of Pediatric Oncology, Dana-Farber Boston Children's Cancer and Blood Disorders Center, Boston, Massachusetts.
  • Morales La Madrid A; 3Department of Pediatric Hematology and Oncology.
J Neurosurg Pediatr ; 22(6): 678-683, 2018 Dec 01.
Article en En | MEDLINE | ID: mdl-30192215
ABSTRACT
OBJECTIVEDiffuse intrinsic pontine glioma (DIPG) is a highly aggressive and lethal brainstem tumor in children. In the 1980s, routine biopsy at presentation was abandoned since it was claimed "unnecessary" for diagnosis. In the last decade, however, several groups have reincorporated this procedure as standard of care or in the context of clinical trials. Expert neurosurgical teams report no mortality and acceptable morbidity, and no relevant complications have been previously described. The aim of this study was to review needle tract dissemination as a potential complication in DIPG.METHODSThe authors retrospectively analyzed the incidence of dissemination through surgical tracts in DIPG patients who underwent biopsy procedures at diagnosis in 3 dedicated centers. Clinical records and images as well as radiation dosimetry from diagnosis to relapse were reviewed.RESULTSFour patients (2 boys and 2 girls, age range 6-12 years) had surgical tract dissemination in 3 cases in the needle tract and in 1 case in the Ommaya catheter tract. The median time from biopsy to identification of dissemination was 5 months (range 4-6 months). The median overall survival was 11 months (range 7-12 months). Disseminated lesions were in the marginal radiotherapy field (n = 2), out of the field (n = 1), and in the radiotherapy field (n = 1).CONCLUSIONSAlthough surgical tract dissemination in DIPG is a rare complication (associated with 2.4% of procedures in this study), it should be mentioned to patients and family when procedures involving a surgical tract are proposed. The inclusion of the needle tract in the radiotherapy field may have only limited benefit. Future studies are warranted to explore the benefit of larger radiotherapy fields in patients with DIPG.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Biopsia / Puente / Neoplasias del Tronco Encefálico / Glioma / Invasividad Neoplásica Límite: Child / Female / Humans / Male Idioma: En Revista: J Neurosurg Pediatr Asunto de la revista: NEUROCIRURGIA / PEDIATRIA Año: 2018 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Biopsia / Puente / Neoplasias del Tronco Encefálico / Glioma / Invasividad Neoplásica Límite: Child / Female / Humans / Male Idioma: En Revista: J Neurosurg Pediatr Asunto de la revista: NEUROCIRURGIA / PEDIATRIA Año: 2018 Tipo del documento: Article
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