Revision 40 for 'Diastematomyelia'
Diastematomyelia (also known as a split cord malformation) refers to a type of spinal dysraphism when there is a longitudinal split in the spinal cord. Although traditionally it has been distinguished from diplomyelia (in which the cord is duplicated rather than split) the term split cord malformation (SCM) is advocated to encompass both conditions 6. For the purposes of this articles the terms diastematomyelia and split cord malformation are used interchangeably.
Split cord malformations are a congenital abnormality and account for approximately 4% of all congenital spinal defects 6.
The majority of patients with diastematomyelia are symptomatic, presenting with signs and symptoms of tethered cord, although patients wil mild type II (see below) may be minimally affected or entirely asymptomatic 6. Presenting symptoms include:
- leg weakness
- low back pain
Patients with diastematomyelia also frequently have other associated annomalies including:
Split cord malformations are divided into two types according to presence of a dividing septum and single vs dual dural sac.
- type I : duplicated dural sac, with common midline spur and usually symptomatic
- type II : single dural sac containing both hemicords; impairment less marked
Type I is the classic diastematomyelia, characterised by 1-6:
- duplicated dural sac
- hydromyelia common
- midline spur often present (osseous or osteocartilaginous)
- vertebral abnormalities: hemivertebrae / butterfly vertebrae / spina bifida / fusion of laminae of adjacent levels
- skin pigmentation / haemangioma / hypertrichosis (hair patch) are common
- patients are usually symptomatic presenting with scoliosis and tethered cord syndrome
Type II is milder than type I, and lack many of the features of latter.
- single dural sac and no spur / septum
- cord divided, sometimes incompletely so
- hydromyelia may be present
- spina bifida may be present, but other vertebral anomalies are far less common
- patients a less symptomatic or may even be asymptomatic
Split cord malformations are more common in the lower cord but can sometimes occur at multiple levels.
- 50 % occur between L1 and L3
- 25 % occur between T7 and T12
An associated bony, cartilagenous or fibrous spur projecting through the dura mater forwards from the neural arch is visible in 33% of cases 1.
Vertebral anomalies (spina bifida, butterfly or hemivertebrae) are common. Laminar fusion associated with a neural arch defect is a good predictor of diastematomyelia and occurs the level of the defect, or at an adjacent level.
There presence of an extra echogenic focus in the midline between the foetal spinal posterior elements has been described as a reliable sign 2.
- multi level spina bifida
- widening of interpedicular distance : but this may be remote from the site of the spur
- as associated scoliosis
- anteroposterior narrowing of vertebral bodies
CT is able to better image many of the features seen on plain films and in addition may demonstrate the bony septum. Modern scanners are also able to visualise the cord.
MRI is the modality of choice for assessing children with split cord malformations. As well as being able to elegantly demonstrate the cord and presence of hydromyelia (if present), it can also assess for the presence of the numerous associated anomalies (see above).
Usually there is little in the way of a differential diagnosis when the cord has been adequately imaged and features are typical (especially now that diplomyelia is considered part of the same spectrum by many authors 6).