Classical imaging findings of Dyke-Davidoff-Masson syndrome.

To cite: Anandpara KM, Aswani Y, Hira P. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/bcr-2014206682 DESCRIPTION A 14-year-old girl, known case of seizure disorder since 10 years and mild mental retardation, presented with progressive left-sided hemiparesis and a recent increase in the frequency of seizures. Significant history included a developmental lag. A CT of the brain revealed marked cortical hemiatrophy on the right side with prominence of ipsilateral ventricular system (figure 1). Neuroparenchymal changes were accompanied with ipsilateral calvarial thickening and hyperpneumatisation of the paranasal sinuses on the right (figure 2). A diagnosis of Dyke-DavidoffMasson syndrome (DDMS) was thus established. The pathophysiology of DDMS includes cortical hemiatrophy secondary to one-sided cerebral vascular insult, and may be congenital or acquired. 2 The absence of sulcation in the former differentiates between the two. Compensatory widening of the diploic space and paranasal sinuses occurs as a consequence. Mimics of DDMS include Sturge-Weber syndrome (which shows the characteristic port wine stain, extensive pial enhancement and dystrophic calcification), Rasmusens encephalitis (in which calvarial changes are typically absent) and unilateral complete occlusion of the middle cerebral artery (in which the hemiatrophy is in the territory of the middle cerebral artery vascular supply). However, a combined clinical and radiological approach makes the diagnosis of DDMS straightforward. Neuroimaging in the form of CT or MRI is the gold standard and early detection is possible due to the classical findings.