Dyke-Davidoff-Masson Syndrome: A Case Report and Review of Literature

被引:11
|
作者
Younas, Amna, Jr. [1 ]
Saim, Muhammad [2 ]
Maqsood, Hamza [3 ]
Younus, Shifa [4 ]
Raza, Muhammad Hassan [5 ]
机构
[1] Russells Hall Hosp, Med, Dudley, England
[2] Nishtar Med Univ, Dept Cardiol, Multan, Pakistan
[3] Nishtar Med Univ, Dept Cardiovasc Med, Multan, Pakistan
[4] Nishtar Med Univ, Dept Radiol, Multan, Pakistan
[5] Nishtar Med Univ, Dept Internal Med, Multan, Pakistan
关键词
cerebral atrophy; hemiplegia; seizures; ddms; CEREBRAL HEMIATROPHY; CHILDHOOD;
D O I
10.7759/cureus.11919
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Dyke-Davidoff-Masson syndrome (DDMS) is a rare neurological disorder that results from brain injury in intrauterine or early years of life. Prominent cortical sulci, dilated lateral ventricles, cerebral hemiatrophy, hyperpneumatization of the frontal sinus, and compensatory hypertrophy of the skull are the characteristic findings. We describe a male patient who presented with generalized tonic-clonic seizure and left-sided body weakness and neuroimaging findings of cerebral hemiatrophy, dilatation of right lateral ventricle, right frontal sinus hyperpneumatization, and asymmetric calvarial thickening. Knowledge of its features on imaging enables timely and accurate diagnosis, allowing appropriate management.
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页数:5
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