Literature DB >> 17877266

Tethering tracts in spina bifida occulta: revisiting an established nomenclature.

Sharad Rajpal1, M Shahriar Salamat, R Shane Tubbs, David R Kelly, W Jerry Oakes, Bermans J Iskandar.   

Abstract

OBJECT: The goal of the present study goal was to systematically confirm the previously recognized nomenclature for tethering tracts that are part of the spectrum of occult spinal dysraphic lesions.
METHODS: The tethering tract in 20 patients with spina bifida occulta underwent histological examination with H & E staining and epithelial membrane antigen (EMA) immunolabeling, and additional selected specimens were stained with Masson trichrome.
RESULTS: All tethering tracts contained fibrous connective tissue. Four tracts were lined with epithelial cells and either originated within a dermoid cyst, terminated at a skin dimple/sinus opening, or had both of these characteristics. No tethering tracts exhibited EMA positivity or meningeal elements. Although all tethering tracts originated in juxtaposition to the spinal cord, their termination sites were variable.
CONCLUSIONS: Based on histological findings and presumed embryological origin, the authors broadly classified tethering tracts terminating within the dura mater, epidural space, or lamina as "short tethering tracts" (STTs). The STTs occurred mostly in conjunction with split cord malformations and had a purely fibrous composition. Tethering tracts terminating superficial to the overlying lamina were classified as "long tethering tracts" (LTTs), and the authors propose that these are embryologically distinct from STTs. The LTTs were of two varieties: epithelial and nonepithelial, the former being typically associated with a skin dimple or spinal cord (epi)dermoid cyst. In fact, analysis of the data suggested that not every tethering tract terminating in or on the skin should be classified as a dermal sinus tract without histological confirmation, and because no evidence of meningeal tissue-lined tracts was detected, the use of the term "meningocele manqué" may not be appropriate.

Entities:  

Mesh:

Year:  2007        PMID: 17877266     DOI: 10.3171/SPI-07/09/315

Source DB:  PubMed          Journal:  J Neurosurg Spine        ISSN: 1547-5646


  6 in total

1.  Spinal dermal sinus and pseudo-dermal sinus tracts: two different entities.

Authors:  Juan F Martínez-Lage; María José Almagro; Belén Ferri-Ñiguez; Virginia Izura Azanza; Cristina Serrano; Ernesto Domenech
Journal:  Childs Nerv Syst       Date:  2010-10-27       Impact factor: 1.475

2.  Spinal inclusion cysts.

Authors:  Dominic N P Thompson
Journal:  Childs Nerv Syst       Date:  2013-09-07       Impact factor: 1.475

Review 3.  Meningocele manqué: a comprehensive review of this enigmatic finding in occult spinal dysraphism.

Authors:  Cameron Schmidt; Ellie Bryant; Joe Iwanaga; Rod J Oskouian; W Jerry Oakes; R Shane Tubbs
Journal:  Childs Nerv Syst       Date:  2017-06-15       Impact factor: 1.475

4.  Split cord malformation concomitant with spinal teratoma without open spinal dysraphism.

Authors:  Jülide Hazneci; Feryal Bastacı; Ali Börekci; Özden Çağlar Öztürk; Merih İş; Adnan Somay; Murat Şakir Ekşi; Erhan Çelikoğlu
Journal:  Childs Nerv Syst       Date:  2022-06-10       Impact factor: 1.532

5.  Coexistence of a human tail and congenital dermal sinus associated with lumbosacral lipoma.

Authors:  Kazuhiro Samura; Takato Morioka; Kimiaki Hashiguchi; Fumiaki Yoshida; Yasushi Miyagi; Takashi Yoshiura; Satoshi O Suzuki; Tomio Sasaki
Journal:  Childs Nerv Syst       Date:  2008-08-09       Impact factor: 1.475

6.  An Unusual Case of Torticollis: Split Cord Malformation with Vertebral Fusion Anomaly: A Case Report and a Review of the Literature.

Authors:  Dong Hyun Ye; Da Yeong Kim; Eun Jae Ko
Journal:  Children (Basel)       Date:  2022-07-20
  6 in total

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