Tumor dissemination through surgical tracts in diffuse intrinsic pontine glioma
OBJECTIVE Diffuse 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...
| Autores: | , , , , , , , , , , , , |
|---|---|
| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2018 |
| País: | España |
| Institución: | Fundació Sant Joan de Déu |
| Repositorio: | r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu |
| OAI Identifier: | oai:fsjd.fundanetsuite.com:p14880 |
| Acceso en línea: | https://fsjd.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=14880 |
| Access Level: | acceso abierto |
| Palabra clave: | DIPG dissemination biopsy oncology |
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Tumor dissemination through surgical tracts in diffuse intrinsic pontine gliomaLobon-Iglesias MJSanta-Maria Lopez VPuerta Roldan PCandela-Cantó SRamos-Albiac MGomez-Chiari MPuget SBolle SGoumnerova LKieran MWCruz OGrill JMorales La Madrid ADIPGdisseminationbiopsyoncologyOBJECTIVE Diffuse 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. METHODS The 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. RESULTS Four 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). CONCLUSIONS Although 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.AMER ASSOC NEUROLOGICAL SURGEONS2018info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttps://fsjd.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=14880Journal of Neurosurgery-PediatricsISSN: 19330707ISSNe: 19330715reponame:r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déuinstname:Fundació Sant Joan de DéuInglésinfo:eu-repo/semantics/openAccessoai:fsjd.fundanetsuite.com:p148802026-05-27T12:37:41Z |
| dc.title.none.fl_str_mv |
Tumor dissemination through surgical tracts in diffuse intrinsic pontine glioma |
| title |
Tumor dissemination through surgical tracts in diffuse intrinsic pontine glioma |
| spellingShingle |
Tumor dissemination through surgical tracts in diffuse intrinsic pontine glioma Lobon-Iglesias MJ DIPG dissemination biopsy oncology |
| title_short |
Tumor dissemination through surgical tracts in diffuse intrinsic pontine glioma |
| title_full |
Tumor dissemination through surgical tracts in diffuse intrinsic pontine glioma |
| title_fullStr |
Tumor dissemination through surgical tracts in diffuse intrinsic pontine glioma |
| title_full_unstemmed |
Tumor dissemination through surgical tracts in diffuse intrinsic pontine glioma |
| title_sort |
Tumor dissemination through surgical tracts in diffuse intrinsic pontine glioma |
| dc.creator.none.fl_str_mv |
Lobon-Iglesias MJ Santa-Maria Lopez V Puerta Roldan P Candela-Cantó S Ramos-Albiac M Gomez-Chiari M Puget S Bolle S Goumnerova L Kieran MW Cruz O Grill J Morales La Madrid A |
| author |
Lobon-Iglesias MJ |
| author_facet |
Lobon-Iglesias MJ Santa-Maria Lopez V Puerta Roldan P Candela-Cantó S Ramos-Albiac M Gomez-Chiari M Puget S Bolle S Goumnerova L Kieran MW Cruz O Grill J Morales La Madrid A |
| author_role |
author |
| author2 |
Santa-Maria Lopez V Puerta Roldan P Candela-Cantó S Ramos-Albiac M Gomez-Chiari M Puget S Bolle S Goumnerova L Kieran MW Cruz O Grill J Morales La Madrid A |
| author2_role |
author author author author author author author author author author author author |
| dc.subject.none.fl_str_mv |
DIPG dissemination biopsy oncology |
| topic |
DIPG dissemination biopsy oncology |
| description |
OBJECTIVE Diffuse 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. METHODS The 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. RESULTS Four 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). CONCLUSIONS Although 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. |
| publishDate |
2018 |
| dc.date.none.fl_str_mv |
2018 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
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article |
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publishedVersion |
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https://fsjd.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=14880 |
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https://fsjd.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=14880 |
| dc.language.none.fl_str_mv |
Inglés |
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Inglés |
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info:eu-repo/semantics/openAccess |
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openAccess |
| dc.publisher.none.fl_str_mv |
AMER ASSOC NEUROLOGICAL SURGEONS |
| publisher.none.fl_str_mv |
AMER ASSOC NEUROLOGICAL SURGEONS |
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Journal of Neurosurgery-Pediatrics ISSN: 19330707 ISSNe: 19330715 reponame:r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu instname:Fundació Sant Joan de Déu |
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Fundació Sant Joan de Déu |
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r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu |
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r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu |
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