Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1975 3
1976 3
1977 1
1978 2
1979 3
1980 2
1981 2
1983 2
1984 3
1986 4
1987 6
1988 2
1989 2
1990 7
1991 1
1992 1
1993 3
1994 3
1995 3
1996 2
1997 4
1998 3
1999 6
2000 4
2001 6
2002 2
2003 4
2004 5
2005 2
2006 2
2007 8
2008 4
2009 9
2010 7
2011 2
2012 4
2013 5
2014 4
2015 2
2016 4
2017 5
2018 3
2019 4
2020 2
2021 8
2022 5
2023 1
2024 1

Text availability

Article attribute

Article type

Publication date

Search Results

157 results

Results by year

Filters applied: . Clear all
Quoted phrase not found in phrase index: "Childhood spinal cord tumor"
Page 1
Updates in the classification of ependymal neoplasms: The 2021 WHO Classification and beyond.
Kresbach C, Neyazi S, Schüller U. Kresbach C, et al. Brain Pathol. 2022 Jul;32(4):e13068. doi: 10.1111/bpa.13068. Epub 2022 Mar 21. Brain Pathol. 2022. PMID: 35307892 Free PMC article. Review.
Ependymal neoplasms occur at all ages and encompass multiple tumor types and subtypes that develop in the supratentorial compartment, the posterior fossa, or the spinal cord. ...This review summarizes how recent findings regarding biology, molecular …
Ependymal neoplasms occur at all ages and encompass multiple tumor types and subtypes that develop in the supratentorial compa …
Pediatric spinal tumors.
Hsu W, Jallo GI. Hsu W, et al. Handb Clin Neurol. 2013;112:959-65. doi: 10.1016/B978-0-444-52910-7.00016-7. Handb Clin Neurol. 2013. PMID: 23622304 Review.
Although tumors of the central nervous system in children constitute the second most prevalent tumor type of childhood, spinal cord tumors account for less than 10% of pediatric central nervous system tumors. ...Treatment is based on tumor type, …
Although tumors of the central nervous system in children constitute the second most prevalent tumor type of childhood, spi
Oncologic emergencies.
Kelly KM, Lange B. Kelly KM, et al. Pediatr Clin North Am. 1997 Aug;44(4):809-30. doi: 10.1016/s0031-3955(05)70531-9. Pediatr Clin North Am. 1997. PMID: 9286286 Free article. Review.
The prognosis for the child with cancer has improved dramatically over the past decades. ...Respiratory or circulatory failure may arise from compression of the SVC or airway. Epidural spinal cord compression by tumor may lead to irreversible paraplegi …
The prognosis for the child with cancer has improved dramatically over the past decades. ...Respiratory or circulatory failure may ar …
Advances in Treatment of Diffuse Midline Gliomas.
Cacciotti C, Wright KD. Cacciotti C, et al. Curr Neurol Neurosci Rep. 2023 Dec;23(12):849-856. doi: 10.1007/s11910-023-01317-8. Epub 2023 Nov 3. Curr Neurol Neurosci Rep. 2023. PMID: 37921944 Review.
PURPOSE OF REVIEW: Diffuse midline gliomas (DMGs) generally carry a poor prognosis, occur during childhood, and involve midline structures of the central nervous system, including the thalamus, pons, and spinal cord. ...
PURPOSE OF REVIEW: Diffuse midline gliomas (DMGs) generally carry a poor prognosis, occur during childhood, and involve midlin …
Neonatal Central Nervous System Tumors.
Shahab S, Fangusaro J. Shahab S, et al. Clin Perinatol. 2021 Mar;48(1):35-51. doi: 10.1016/j.clp.2020.11.003. Epub 2021 Jan 11. Clin Perinatol. 2021. PMID: 33583506 Review.
Central nervous system (CNS) tumors, including brain and spinal cord tumors, are the most common solid tumors of childhood. ...This article reviews neonatal CNS tumors, specifically their clinical presentation, imaging findings, treatment, prognosis, a …
Central nervous system (CNS) tumors, including brain and spinal cord tumors, are the most common solid tumors of childhood
Spine and spinal cord tumours in children: a diagnostic and therapeutic challenge to healthcare systems.
Wilne S, Walker D. Wilne S, et al. Arch Dis Child Educ Pract Ed. 2010 Apr;95(2):47-54. doi: 10.1136/adc.2008.143214. Arch Dis Child Educ Pract Ed. 2010. PMID: 20351151 Review.
Only 2% of childhood tumours occur in the spine and spinal cord; yet these tumours account for a disproportionate degree of morbidity in children with cancer. ...This article reviews the pathology and presentation of spine and spinal cord tumour …
Only 2% of childhood tumours occur in the spine and spinal cord; yet these tumours account for a disproportionate degre …
Diagnosis and management of brain and spinal cord tumors in the neonate.
Hwang SW, Su JM, Jea A. Hwang SW, et al. Semin Fetal Neonatal Med. 2012 Aug;17(4):202-206. doi: 10.1016/j.siny.2012.03.001. Epub 2012 Mar 30. Semin Fetal Neonatal Med. 2012. PMID: 22465555 Review.
Congenital central nervous system (CNS) tumors are rare, accounting for <5% of childhood CNS tumors. Although the definition remains arbitrary, 'congenital' is often defined as CNS tumors diagnosed at birth or within a few months after birth. ...Choroid plexus tumors (p …
Congenital central nervous system (CNS) tumors are rare, accounting for <5% of childhood CNS tumors. Although the definition remai …
Spinal cord ependymomas in children and adolescents.
Benesch M, Frappaz D, Massimino M. Benesch M, et al. Childs Nerv Syst. 2012 Dec;28(12):2017-28. doi: 10.1007/s00381-012-1908-4. Epub 2012 Sep 8. Childs Nerv Syst. 2012. PMID: 22961356 Review.
BACKGROUND: Spinal cord ependymomas are very rare among children and adolescents. ...METHODS: The present review summarizes the currently available literature on childhood spinal cord ependymomas. RESULTS: Although overall survival rates are fav …
BACKGROUND: Spinal cord ependymomas are very rare among children and adolescents. ...METHODS: The present review summarizes th …
Primary Paraspinal and Spinal Epidural Non-Hodgkin Lymphoma in Childhood.
Kurucu N, Akyüz C, Varan A, Akçören Z, Aydin B, Yalçin B, Kutluk T. Kurucu N, et al. J Pediatr Hematol Oncol. 2021 Apr 1;43(3):e395-e400. doi: 10.1097/MPH.0000000000001858. J Pediatr Hematol Oncol. 2021. PMID: 32520843
Primary paraspinal/spinal epidural lymphoma (PPSEL) is rare in childhood. Here, we retrospectively evaluated patients with PPSEL treated in our department. ...Most common symptoms were pain and limb weakness. Physical examination revealed spinal cord c …
Primary paraspinal/spinal epidural lymphoma (PPSEL) is rare in childhood. Here, we retrospectively evaluated patients with PPS …
Paediatric spinal cord low-grade gliomas-evaluation and management of post-surgical residual disease.
Silva AHD, Constantinides M, Valetopoulou A, Sgardelis P, Mankad K, D'Arco F, Jankovic I, Thompson D. Silva AHD, et al. Childs Nerv Syst. 2022 Mar;38(3):577-586. doi: 10.1007/s00381-021-05412-4. Epub 2021 Dec 2. Childs Nerv Syst. 2022. PMID: 34855000
PURPOSE: To assess the evaluation and management of post-surgical residual disease for low-grade intramedullary spinal cord tumours (IMSCT) in childhood. METHODS: A single-centre retrospective review of low-grade IMSCTs treated between 2000 and 2019. ...
PURPOSE: To assess the evaluation and management of post-surgical residual disease for low-grade intramedullary spinal cord tu …
157 results