Literature DB >> 29260294

Fatty filum terminale (FFT) as a secondary tethering element in children with closed spinal dysraphism.

Ankush Gupta1, Vedantam Rajshekhar2.   

Abstract

PURPOSE: The purpose of this study was to assess the prevalence of FFT as an additional tethering element in children operated for closed spinal dysraphism, where FFT was not the primary tethering pathology.
METHODS: This is a retrospective study of 195 children (< 18 years of age) who underwent surgery for closed spinal dysraphism and did not have FFT as the primary diagnosis. All patients were operated during the period 2005-2017 by a single surgeon. The commonest diagnosis was a lipomyelomeningocele (LMMC, n = 81, 41.5%), followed by split cord malformations (SCM, types I and II, n = 61, 31.3%), dermal sinus (n = 28, 14.4%), and dermoid cyst (n = 10, 5.1%). Factors such as age and sex, presenting symptoms, intraoperative findings, and radiological presence of a FFT on a magnetic resonance imaging (MRI) were documented, and the relationship between the primary diagnoses and presence of FFT was analyzed.
RESULTS: FFT as a secondary finding was seen in 63 patients (32.3%). The mean age of the cohort was 54 months (4.5 years) and the sex distribution was relatively even (51.8% girls). The commonest symptom at presentation was a swelling in the back, followed by lower limb weakness. The mean duration of symptoms was nearly 30 months. FFT was seen on the MRI and confirmed intraoperatively in 55 patients (28.2%). There were 8 patients (4.1%) where a FFT was seen intraoperatively, but was not diagnosed on the preoperative MRI. In 16 patients, FFT was seen > 2 segments away from the primary tethering pathology, 8 of which mandated a second skin incision for sectioning of the FFT. Secondary FFT was most commonly associated with a SCM (types I and II combined) and was seen in 42.6% of those patients. It was least commonly associated with intradural dermoid cysts.
CONCLUSION: The presence of a secondary FFT should be considered and actively sought on preoperative thin-slice T1W axial MR images in the sacral region in all patients with spinal dysraphism. Even if a FFT is not seen on preoperative MR images, the filum should be explored and sectioned if it is in the vicinity of the primary surgical field, especially in patients with SCM.

Entities:  

Keywords:  Fatty filum; Filum terminale; Spinal dysraphism; Split cord; Tethered cord

Mesh:

Year:  2017        PMID: 29260294     DOI: 10.1007/s00381-017-3700-y

Source DB:  PubMed          Journal:  Childs Nerv Syst        ISSN: 0256-7040            Impact factor:   1.475


  33 in total

1.  Gross and microscopic study of the filum terminale: does the filum contain functional neural elements?

Authors:  Samson Sujit Kumar Gaddam; Vissa Santhi; Srinivasa Babu; Geeta Chacko; Ramakrishna Appala Baddukonda; Vedantam Rajshekhar
Journal:  J Neurosurg Pediatr       Date:  2012-01       Impact factor: 2.375

Review 2.  Spinal cord traction, vascular compromise, hypoxia, and metabolic derangements in the pathophysiology of tethered cord syndrome.

Authors:  Aristotelis S Filippidis; M Yashar Kalani; Nicholas Theodore; Harold L Rekate
Journal:  Neurosurg Focus       Date:  2010-07       Impact factor: 4.047

3.  Normal diameter of filum terminale in children: in vivo measurement.

Authors:  K D Yundt; T S Park; B A Kaufman
Journal:  Pediatr Neurosurg       Date:  1997-11       Impact factor: 1.162

4.  The association of the epidermoid cyst of the filum terminale, intradural spinal lipoma, tethered cord, dermal sinus tract, and type I diastematomyelia in a child.

Authors:  Hakan Ak; Tugay Atalay; Ismail Gülşen
Journal:  World Neurosurg       Date:  2014-08-19       Impact factor: 2.104

5.  Intraoperative mapping of sacral nervous system (S2-4).

Authors:  G Samson Sujit Kumar; Vedantam Rajshekhar; K Srinivasa Babu
Journal:  Br J Neurosurg       Date:  2006-12       Impact factor: 1.596

6.  Acquired chiari malformation type I associated with a fatty terminal filum. Case report.

Authors:  Taylor J Abel; Abhineet Chowdhary; Patrik Gabikian; Richard G Ellenbogen; Anthony M Avellino
Journal:  J Neurosurg       Date:  2006-10       Impact factor: 5.115

7.  Cutting filum terminale is very important in split cord malformation cases to achieve total release.

Authors:  Mustafa Barutcuoglu; Mehmet Selcuki; Deniz Selcuki; Sukru Umur; Mesut Mete; Seren Gulsen Gurgen
Journal:  Childs Nerv Syst       Date:  2014-12-03       Impact factor: 1.475

Review 8.  Split cord malformation: Part II: Clinical syndrome.

Authors:  D Pang
Journal:  Neurosurgery       Date:  1992-09       Impact factor: 4.654

9.  Tight filum terminale syndrome in children: analysis based on positioning of the conus and absence or presence of lumbosacral lipoma.

Authors:  Nan Bao; Zhi-Hua Chen; Shuo Gu; Qi-Min Chen; Hui-Ming Jin; Cheng-Ren Shi
Journal:  Childs Nerv Syst       Date:  2007-06-06       Impact factor: 1.475

10.  Spinal dysraphism: A challenge continued to be faced by neurosurgeons in developing countries.

Authors:  Amit Agrawal; Sunil Sampley
Journal:  Asian J Neurosurg       Date:  2014-04
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  3 in total

1.  Early- and long-term surgical outcomes in 109 children with lipomyelomeningocele.

Authors:  Tarang K Vora; Shabari Girishan; Ranjith K Moorthy; Vedantam Rajshekhar
Journal:  Childs Nerv Syst       Date:  2021-01-06       Impact factor: 1.475

2.  Real spinal cord injury without radiologic abnormality in pediatric patient with tight filum terminale following minor trauma: a case report.

Authors:  Qin Chuan Liang; Bo Yang; Yun Hai Song; Pin Pin Gao; Ze Yang Xia; Nan Bao
Journal:  BMC Pediatr       Date:  2019-12-23       Impact factor: 2.125

3.  Surgical histopathology of a filar anomaly as an additional tethering element associated with closed spinal dysraphism of primary neurulation failure.

Authors:  Takato Morioka; Nobuya Murakami; Satoshi O Suzuki; Nobutaka Mukae; Takafumi Shimogawa; Ai Kurogi; Tadahisa Shono; Masahiro Mizoguchi
Journal:  Surg Neurol Int       Date:  2021-07-27
  3 in total

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