Spontaneous resolution of a Cervicothoracic syrinx in a child. Case report and review of the literature

Anthony M. Avellino; Gavin W. Britz; James R. McDowell; Dennis W. Shaw; Richard G. Ellenbogen; Theodore S. Roberts

doi:10.1159/000028760

Spontaneous resolution of a Cervicothoracic syrinx in a child. Case report and review of the literature

Anthony M. Avellino, Gavin W. Britz, James R. McDowell, Dennis W. Shaw, Richard G. Ellenbogen, Theodore S. Roberts

Research output: Contribution to journal › Article › peer-review

49 Scopus citations

Abstract

A child with near complete spontaneous resolution of a cervicothoracic syrinx and improvement in a Chiari type I malformation without surgical intervention is presented. The child was followed clinically with serial magnetic resonance (MR) imaging and has remained neurologically stable over an 11-year period. To our knowledge, only 3 pediatric cases of spontaneous resolution of a spinal cord syrinx as documented by MR imaging without surgical intervention have been reported. This case contributes to the literature on the natural history of syringes.

Original language	English (US)
Pages (from-to)	43-46
Number of pages	4
Journal	Pediatric Neurosurgery
Volume	30
Issue number	1
DOIs	https://doi.org/10.1159/000028760
State	Published - Jan 1 1999

Keywords

Chiari type I malformation Magnetic resonance imaging
Spinal cord
Syringomyelia

ASJC Scopus subject areas

Pediatrics, Perinatology, and Child Health
Clinical Neurology

Access to Document

10.1159/000028760

Cite this

@article{67309c4fbe104b6a915930c2030b1dee,

title = "Spontaneous resolution of a Cervicothoracic syrinx in a child. Case report and review of the literature",

abstract = "A child with near complete spontaneous resolution of a cervicothoracic syrinx and improvement in a Chiari type I malformation without surgical intervention is presented. The child was followed clinically with serial magnetic resonance (MR) imaging and has remained neurologically stable over an 11-year period. To our knowledge, only 3 pediatric cases of spontaneous resolution of a spinal cord syrinx as documented by MR imaging without surgical intervention have been reported. This case contributes to the literature on the natural history of syringes.",

keywords = "Chiari type I malformation Magnetic resonance imaging, Spinal cord, Syringomyelia",

author = "Avellino, \{Anthony M.\} and Britz, \{Gavin W.\} and McDowell, \{James R.\} and Shaw, \{Dennis W.\} and Ellenbogen, \{Richard G.\} and Roberts, \{Theodore S.\}",

year = "1999",

month = jan,

day = "1",

doi = "10.1159/000028760",

language = "English (US)",

volume = "30",

pages = "43--46",

journal = "Pediatric Neurosurgery",

issn = "1016-2291",

publisher = "S. Karger AG",

number = "1",

}

TY - JOUR

T1 - Spontaneous resolution of a Cervicothoracic syrinx in a child. Case report and review of the literature

AU - Avellino, Anthony M.

AU - Britz, Gavin W.

AU - McDowell, James R.

AU - Shaw, Dennis W.

AU - Ellenbogen, Richard G.

AU - Roberts, Theodore S.

PY - 1999/1/1

Y1 - 1999/1/1

N2 - A child with near complete spontaneous resolution of a cervicothoracic syrinx and improvement in a Chiari type I malformation without surgical intervention is presented. The child was followed clinically with serial magnetic resonance (MR) imaging and has remained neurologically stable over an 11-year period. To our knowledge, only 3 pediatric cases of spontaneous resolution of a spinal cord syrinx as documented by MR imaging without surgical intervention have been reported. This case contributes to the literature on the natural history of syringes.

AB - A child with near complete spontaneous resolution of a cervicothoracic syrinx and improvement in a Chiari type I malformation without surgical intervention is presented. The child was followed clinically with serial magnetic resonance (MR) imaging and has remained neurologically stable over an 11-year period. To our knowledge, only 3 pediatric cases of spontaneous resolution of a spinal cord syrinx as documented by MR imaging without surgical intervention have been reported. This case contributes to the literature on the natural history of syringes.

KW - Chiari type I malformation Magnetic resonance imaging

KW - Spinal cord

KW - Syringomyelia

UR - https://www.scopus.com/pages/publications/0032930988

UR - https://www.scopus.com/inward/citedby.url?scp=0032930988&partnerID=8YFLogxK

U2 - 10.1159/000028760

DO - 10.1159/000028760

M3 - Article

C2 - 10202308

AN - SCOPUS:0032930988

SN - 1016-2291

VL - 30

SP - 43

EP - 46

JO - Pediatric Neurosurgery

JF - Pediatric Neurosurgery

IS - 1

ER -

Spontaneous resolution of a Cervicothoracic syrinx in a child. Case report and review of the literature

Abstract

Keywords

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this