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| Patient: 2 year old male |
| History: 2 year old male with history of macrocrania and developmental delay. |
| Images: |
| Findings: MR of the brain demonstrate multiple enlarged Virchow Robin spaces mostly in the periventricular location. |
| Diagnosis: Probable mucopolysacchridosis. |
| Discussion: Mucopolysacchridosis Lysosomal storage disorder resulting from deficient enzyme GAGs deposits in lysosomes and interfere with degradation GAGs accumulate in cells and excreted in urine Clinical features - varies with type most patients have macrocephaly developmental retardation - prominent in type I, II, III, and VII skeletal involvement prominent in types IV and VI Imaging features general - delayed myelination, atrophy, varying degrees of hydrocephalus white matter changes CT - diffuse low attenuation w/i cerebral white matter MR - diffuse areas of T1 & T2 prolongation sharply defined foci in corpus callosum, basal ganglia, and cerebral white matter iso to CSF on all sequence enlarged perivascular (Virchow-Robin) spaces progress to become larger and more diffuse like leukodystrophy atrophy & white matter changes earliest in type I, II, III, and VII later in life in type IV and VI spinal abnormality - may lead to cord compression frequently occurs in type IV and VI C1-2 atlantoaxial subluxation from laxity of transverse ligament or hypoplasia/absence of odontoid chronic subluxation may lead to ligamentous hypertrophy MR - shortened odontoid w/ soft tissue mass C1 and C2 dural thickening thoracic vertebral body gibbus deformity (Morquio most common) |
| References: Barkovich et al. Pediatric Neuroimaging. pg 134-137; 4th ed. Lippincott Williams & Wilkins 2005. |
| Comments: No comments posted. |
| Additional Details:
Case Number: 11543327 The reader is fully responsible for confirming the accuracy of this content. |