Congenital Midline Spinal Hamartoma in a 5-Month-Old Infant.

There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

Abstract

Congenital midline spinal hamartoma is a very rare tumor-like proliferation that mostly occurs during childhood. It consists of mature, well-differentiated ectodermal and mesodermal elements that present in an abnormal location and are mostly associated with neurofibromatosis type 1 and spinal dysraphism.

Related collections

Author and article information

Journal

Journal ID (iso-abbrev): World Neurosurg

Title: World neurosurgery

Publisher: Elsevier BV

ISSN (Electronic): 1878-8769

ISSN (Print): 1878-8750

Publication date (Electronic): January 2021

Volume: 145

Affiliations

[1 ] Department of Neurosurgery, Prof. Dr. W. Z. Johannes Kupang Regional General Hospital, Kupang, East Nusa Tenggara, Indonesia.

[2 ] Department of Neurosurgery, Prof. Dr. W. Z. Johannes Kupang Regional General Hospital, Kupang, East Nusa Tenggara, Indonesia. Electronic address: chrislauren11@gmail.com.

[3 ] Department of Pathology Anatomy, Prof. Dr. W. Z. Johannes Kupang Regional General Hospital, Kupang, East Nusa Tenggara, Indonesia.

Article

Publisher Item ID: S1878-8750(20)32073-8

DOI: 10.1016/j.wneu.2020.09.065

PubMed ID: 32949805

SO-VID: a9c30638-b7fe-4d31-8c5b-8be41d583725

History

Keywords: Congenital,Spinal dysraphism,Spinal cord tumor,Oncology,Hamartoma

Data availability:

Keywords: Congenital, Spinal dysraphism, Spinal cord tumor, Oncology, Hamartoma

Comments

Comment on this article

scite_

Cited by 3

See all cited by