<%server.execute "isdev.asp"%> Split notochord syndrome: A rare variant Dhawan V, Kapoor K, Singh B, Kochhar S, Sehgal A, Dada R - J Pediatr Neurosci
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CASE REPORT
Year : 2017  |  Volume : 12  |  Issue : 2  |  Page : 177-179
 

Split notochord syndrome: A rare variant


1 Department of Anatomy, All India Institute of Medical Sciences, New Delhi, India
2 Department of Anatomy, Government Medical College and Hospital, Chandigarh, India
3 Department of Anatomy, Chhattisgarh Institute of Medical Sciences, Bilaspur, Chhattisgarh, India
4 Department of Radiology, Government Medical College and Hospital, Chandigarh, India
5 Department of Obstetrics and Gynaecology, Government Medical College and Hospital, Chandigarh, India

Date of Web Publication10-Aug-2017

Correspondence Address:
Vidhu Dhawan
Room No. 1027-A, Laboratory of Molecular Reproduction and Genetics, Department of Anatomy, All India Institute of Medical Sciences, Ansari Nagar, New Delhi - 110 029
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/jpn.JPN_120_16

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   Abstract 

Split notochord syndrome represents an extremely rare and pleomorphic form of spinal dysraphism characterized by a persistent communication between the endoderm and the ectoderm, resulting in splitting or deviation of the notochord. It manifests as a cleft in the dorsal midline of the body through which intestinal loops are exteriorized and even myelomeningoceles or teratomas may occur at the site. A rare variant was diagnosed on autopsy of a 23+4-week-old fetus showing a similar dorsal enteric fistula and midline protruding intestinal loops in thoracolumbar region. The anteroposterior radiograph showed a complete midline cleft in the vertebral bodies from T11to L5region, and a split in the spinal cord was further confirmed by ultrasonography. Myelomeningocele was erroneously reported on antenatal ultrasound. Thus, awareness of this rare anomaly is necessary to thoroughly evaluate the cases of such spinal defects or suspected myelomeningoceles.


Keywords: Dorsal enteric fistula, spinal dysraphism, split notochord syndrome


How to cite this article:
Dhawan V, Kapoor K, Singh B, Kochhar S, Sehgal A, Dada R. Split notochord syndrome: A rare variant. J Pediatr Neurosci 2017;12:177-9

How to cite this URL:
Dhawan V, Kapoor K, Singh B, Kochhar S, Sehgal A, Dada R. Split notochord syndrome: A rare variant. J Pediatr Neurosci [serial online] 2017 [cited 2019 Aug 24];12:177-9. Available from: http://www.pediatricneurosciences.com/text.asp?2017/12/2/177/212790



   Introduction Top


Split notochord syndrome (SNS) represents an extremely rare and pleomorphic form of spinal dysraphism characterized by a wide spinal defect and a persistent communication between endoderm and ectoderm.[1],[2] In its basic form, it consists of a neural tube defect with an endo-ectodermal fistula opening in the dorsal aspect, varying in location from distal ileum/cecum or in the large intestine.[3] Several variants have been reported with gastrointestinal tracts such as dorsal enteric fistula or diverticulum, imperforate anus, duplicated colon, and central nervous system (CNS) including meningocele, neurenteric cysts, duplicated spine, or sacral agenesis. Less frequent presentations include bladder exstrophy, bladder or urethral duplication, and teratomas.[4],[5]


   Case Report Top


Less than 35 cases have been reported in the literature till now, and one such case was examined on routine fetal autopsy done in the Anatomy Department of Government Medical College, Chandigarh, India. The mother, a primigravida, was admitted for termination of pregnancy considering the antenatal ultrasound which reported a myelomeningocele in the lower thoracolumbar region. The gestational age of the fetus was 23+4 weeks (crown-rump length 17.85 cm). There was no history of fever or exposure to any teratogenic agents. The family history was unremarkable, with no consanguinity reported.


   Observations Top


Gross observations

The fetus presented with following anomalies:

  1. A big gap in the vertebral column in the thoracolumbar region. Protuberant bony mass (sacrum) in the lumbosacral region [Figure 1]a
  2. Midline herniating loop - In thoracolumbar region, 5.7 cm from the root of neck, measuring 2.9 cm from its attachment to the dorsum [Figure 1]a and [Figure 1]b
  3. Enteric fistulous opening - 0.2 cm and 0.6 cm to the right of the first [Figure 1]a.
Figure 1: Gross observations of fetus showing midline herniating loop measuring 2.9 cms (right arrow), enteric fistulous opening (left arrow), protuberant bony mass (star) (Figure 1a and 1b). Superficial dissection of back showing posterior midline thoracolumbar diastasis with herniating bowel loops (star) and dorsal enteric fistula (left arrow) (Figure 1c and 1d)

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On dissection of back

  1. Superficial [Figure 1]c
    1. Skin - Normal
    2. Posterior midline thoracolumbar diastasis of vertebral column (2.6 cm × 2.0 cm) with herniating distal ileal loops
    3. Dorsal enteric fistula
  2. Deep [Figure 1]d
    1. Complete splitting of spinal cord
    2. Protuberant bony mass - Sacrum with slight posterior convexity.


Radiographic findings

  1. Anteroposterior [Figure 2]a
    Figure 2: Midline vertical cleft (T11–L5) (a), flattening of vertebral concavity (b)

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    1. Complete midline vertical cleft in T11–L5 vertebral bodies
    2. Butterfly appearance due to lateral fanning of the hemivertebrae
  2. Lateral [Figure 2]b - Flattening of the concavity of vertebral column.


Ultrasound findings

  1. Split cord in the lower thoracic and lumbar region with the presence of overlapping bowel loops
  2. Normal spinal cord contour in the cervical and upper thoracic level [Figure 3]a and [Figure 3]b.
    Figure 3: Ultrasonography findings: Lower thoracic - split cord (a), lower thoracic, upper lumbar: Bowel loops (b)

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   Discussion Top


Spinal dysraphisms consist of a wide variety of congenital malformations resulting from defective embryogenesis of the spinal cord and vertebrae. Spinal dysraphisms show a relatively uniform incidence in all ethnic groups, with no geographic and socioeconomic variations. SNS is usually discovered in the 1st year of life affects both sexes and mostly involve cervical or thoracic regions.[2] Owing to its pleomorphism, this condition has rarely been identified prenatally, with only two cases reported in the last 20 years.[1],[2] The malformations featuring spinal dysraphisms can occur as isolated lesions or in combination with a wide range of anomalies of both CNS and other systems. The SNS belongs to a group of complex occult spinal dysraphisms out of the open (spina bifida cystica) and closed (spina bifida occulta) varieties of spinal dysraphisms. The most common occult forms of spinal dysraphism are lipomas, split cord malformations (diastematomyelia and diplomyelia), dermal sinuses and dermoid tumors, myelocystoceles, tight filum terminale, neuroenteric cysts, and caudal agenesis.[6]

The pathogenesis of the condition is not completely known. One hypothesis for the SNS refers to the persistence or partial obliteration of an accessory neurenteric canal that connects the yolk sac and the amniotic cavity in the 3rd week of gestation. The most widely accepted theory suggests a primary midline notochordal integration defect and paraxial mesoderm changes resulting in split notochord, which is not completely separated from primitive intestine. This leads to herniation of endoderm and underlying primitive intestine which adhere to the dorsal ectoderm and eventually rupture.[3] No clear etiology has been documented, but approximately 50% of the cases are related to maternal nutritional deficiency, especially folic acid. The use of supplementary folic acid may reduce neural tube defects by up to 72.68%. Other causes are zinc and Vitamin A deficiency, high nitrates or Vitamin A excess, altered carbohydrate metabolism (e.g., diabetes mellitus, hyperinsulinemia).[7]

The importance of genetic factors is evidenced by a 3-fold higher incidence in consanguineous marriages as well as monozygotic twins. The role of the Sonic Hedgehog gene (shh) on chromosome 7q36 acting as a morphogen for dorsoventral patterning of somites, anteroposterior polarity of limb, and left-right asymmetry has been documented.[8]

The present case represents a case of SNS located in the lower thoracic (T11) to lumbar region. Myelomeningocele was erroneously reported on the prenatal ultrasound done at 23+4 weeks of gestation. However, the lesions are so different from each other with such a wide range of associated anomalies that each one might be considered a unique variant.[5],[9],[10]

Although the anomaly is grossly evident at birth, the prenatal recognition of the condition can help in prompt management of such cases. The present case was not diagnosed prenatally. Appropriate and detailed preoperative imaging studies, combining nuclear magnetic resonance and contrast fistulography, are of utmost importance for proper surgical planning and management may vary from case to case.[9],[11] A poor prognosis for survival has been described in the literature, with only 12 survivors being reported.


   Conclusion Top


SNS is an extremely rare disorder with <35 cases described in literature before the present case. This report demonstrates that awareness of this rare anomaly is necessary as it can be suspected prenatally whenever a spinal defect is detected together with gastrointestinal variants. This calls for thorough evaluation of cases of hemivertebrae and suspected myelomeningoceles.

The study was supported by Government Medical College and Hospital, Chandigarh, India.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

 
   References Top

1.
Almog B, Leibovitch L, Achiron R. Split notochord syndrome - Prenatal ultrasonographic diagnosis. Prenat Diagn 2001;21:1159-62.  Back to cited text no. 1
[PUBMED]    
2.
Agangi A, Paladini D, Bagolan P, Maruotti GM, Martinelli P. Split notochord syndrome variant: Prenatal findings and neonatal management. Prenat Diagn 2005;25:23-7.  Back to cited text no. 2
[PUBMED]    
3.
Jesus LE, França CG. A rare variant of neuroenteric cyst: Split notochord syndrome. J Pediatr (Rio J) 2004;80:77-80.  Back to cited text no. 3
    
4.
Kanmaz T, Demirbilek S, Oztürk A, Baykara S, Yücesan S. The split notochord syndrome with dorsal enteric fistula. Indian J Pediatr 2002;69:729-30.  Back to cited text no. 4
    
5.
van Ramshorst GH, Lequin MH, Mancini GM, van de Ven CP. A case of split notochord syndrome: A child with a neuroenteric fistula presenting with meningitis. J Pediatr Surg 2006;41:e19-23.  Back to cited text no. 5
[PUBMED]    
6.
Tortori-Donati P, Rossi A, Cama A. Spinal dysraphism: A review of neuroradiological features with embryological correlations and proposal for a new classification. Neuroradiology 2000;42:471-91.  Back to cited text no. 6
[PUBMED]    
7.
Netto JM, Bastos AN, Figueiredo AA, Pérez LM. Spinal dysraphism: A neurosurgical review for the urologist. Rev Urol 2009;11:71-81.  Back to cited text no. 7
    
8.
Chiang C, Litingtung Y, Lee E, Young KE, Corden JL, Westphal H, et al. Cyclopia and defective axial patterning in mice lacking Sonic hedgehog gene function. Nature 1996;383:407-13.  Back to cited text no. 8
[PUBMED]    
9.
Srivastava P, Gangopadhyay AN, Gupta DK, Sharma SP. Split notochord syndrome associated with dorsal neuroenteric fistula: A rare entity. J Pediatr Neurosci 2010;5:135-7.  Back to cited text no. 9
[PUBMED]  [Full text]  
10.
Yazici MU, Ekinci S, Turkmen OK, Yalcin EG, Ciftci AO, Gucer S, et al. Recurrent hemoptysis and a mass in the thorax in an infant: The split notochord syndrome. European J Pediatr Surg Rep 2014;2:38-42.  Back to cited text no. 10
[PUBMED]    
11.
Asagiri K, Yagi M, Tanaka Y, Akaiwa M, Asakawa T, Kaida A, et al. Acase of split notochord syndrome with congenital ileal atresia, the total absence of a colon, and a dorsal enteric cyst communicating to the retroperitoneal isolated ceca with a vesical fistula. Pediatr Surg Int 2008;24:1073-7.  Back to cited text no. 11
[PUBMED]    


    Figures

  [Figure 1], [Figure 2], [Figure 3]



 

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    Abstract
   Introduction
   Case Report
   Observations
   Discussion
   Conclusion
    References
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