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Decoding pediatric spinal tumors: a single-center retrospective case series on etiology, presentation, therapeutic strategies, and outcomes.
Lenga, Pavlina; Kühlwein, Daniel; Grutza, Martin; Issa, Mohammed; Hinz, Felix; Sahm, Felix; Selt, Florian; Milde, Till; Günther, Patrick; Unterberg, Andreas W; Krieg, Sandro M; Damaty, Ahmed El.
Afiliação
  • Lenga P; Department of Neurosurgery, Heidelberg University Hospital, Heidelberg, Germany. pavlina.lenga@med.uni-heidelberg.de.
  • Kühlwein D; Department of Neurosurgery, University of Heidelberg, Im Neuenheimer Feld 400, 69120, Heidelberg, Germany. pavlina.lenga@med.uni-heidelberg.de.
  • Grutza M; Department of Neurosurgery, Heidelberg University Hospital, Heidelberg, Germany.
  • Issa M; Department of Neurosurgery, Heidelberg University Hospital, Heidelberg, Germany.
  • Hinz F; Department of Neurosurgery, Heidelberg University Hospital, Heidelberg, Germany.
  • Sahm F; Department of Neuropathology, Institute of Pathology, Heidelberg University Hospital, Heidelberg, Germany.
  • Selt F; Department of Neuropathology, Institute of Pathology, Heidelberg University Hospital, Heidelberg, Germany.
  • Milde T; Hopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany.
  • Günther P; Clinical Cooperation Unit Pediatric Oncology, German Cancer Research Center (DKFZ) and German Consortium for Translational Cancer Research (DKTK), Heidelberg, Germany.
  • Unterberg AW; National Center for Tumor Diseases (NCT), Heidelberg, Germany.
  • Krieg SM; Department of Pediatric Hematology and Oncology, Heidelberg University Hospital, Heidelberg, Germany.
  • Damaty AE; Hopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany.
Neurosurg Rev ; 47(1): 557, 2024 Sep 06.
Article em En | MEDLINE | ID: mdl-39240372
ABSTRACT

INTRODUCTION:

Spinal tumors (ST) often result in dire prognosis, carrying risks such as permanent paralysis, sensory loss, and sphincter dysfunction. Data on their incidence and etiology in pediatric populations are markedly scant. Our study investigates the etiology, clinical manifestation, treatment, and outcomes of pediatric ST.

METHODS:

We conducted a retrospective review of our institutional pediatric oncology and neurosurgery database, examining 14 patients under 18 years admitted with ST due to oncological diseases since 2005. We analyzed the clinical presentations, evaluations, molecular diagnostics and treatments for these patients.

RESULTS:

The study spanned 15 years and included 14 pediatric patients, each diagnosed with distinct spinal tumor entity. The mean patient age was approximately 19.6 ± 10.1 months. Severe axial pain along the vertebral column was observed in 13 patients, while acute neurological deterioration manifested in 7 patients. As a first-line intervention, 13 patients underwent decompressive surgery through laminectomy and tumor resection, and only one patient received chemotherapy solely. Before surgery, seven patients were unable to walk; post-surgery, six of them regained their ability to ambulate. The diagnosis encompassed a range of neoplasms two instances of Ewing sarcoma, 3 instances of teratoma, one case presenting an atypical teratoid Rhabdoid tumor, two instances each of low-grade astrocytoma and neuroblastoma, and single instances of ependymoma, meningioma, rhabdomyosarcoma, and embryonal tumors with multilayered rosettes (ETMRs). Three patients succumbed two years after initiating therapy.

CONCLUSION:

Despite their rarity, intraspinal tumors in pediatric patients pose substantial therapeutic challenges. The intertwined complexities of the disease entity and the patient's neurological status demand swift initiation of an individualized therapeutic strategy. This crucial step helps optimize outcomes for this patient cohort, who frequently grapple with debilitating health conditions. Inclusion of these patients within a registry is mandatory to optimize treatment outcomes due to their rarity in pediatric population.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Coluna Vertebral Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Coluna Vertebral Idioma: En Ano de publicação: 2024 Tipo de documento: Article