Cortical dysgenesis: Hemimegalencephaly is determined as a cortical dysgenesis in this new classification[3]. Hemimegalencephaly is a hamartomatous malformation characterized by overgrowth of all or part of one cerebral hemisphere. Three different types are described. First type is isolated hemimegalencephaly, which is no hemicorporal hypertrophy and not associated with cutaneous or systemic involvement (Figure 1). Second type is hemimegalencephaly associated with various neurocutaneous syndromes such as neurofibromatosis type 1, epidermal nevus syndrome, proteus syndrome, and tuberous sclerosis and also typically including hemicorporal hypertrophy of the ipsilateral part of the body. The last and the rarest one is total hemimegalencephaly associated with hypertrophy of the ipsilateral cerebellar hemisphere and brainstem. The cerebral cortical structures may be normal or dysplastic[14,15].

Open in New Tab   Full Size Figure   Download Figure

Figure 1 A 10-year-old boy with hemimegalencephaly. Coronal T1-weighted magnetic resonance image shows hypertrophy of the left cerebral hemisphere, mild enlargement of the left lateral ventricle, hamartoma (white arrow) in postero-medial area of the right thalamus.

Unlike other types of FCDs, FCD type II (FCD-II) is accepted in-group of cortical dysgenesis in the new classification of Barkovich et al[3] FCD-II has divided into two subgroups as type a and b[16]. FCD-II is characterized by focal area of cortical thickening, marked blurring of gray and white matter junction, and in some cases signal change in adjacent white matter on T2-weighted and FLAIR images[17]. On the other hand, it is harder to identify FCD-IIa than FCD-IIb, and FCD-IIa cannot be always detected on MRI[16].

FCDs can mimic gliomas. FCD-II often occurs in extra-temporal location especially frontal region, whereas a temporal location suggests gliomas[18]. Since the cortical dysplasia primarily affect the gray matter and generally not associated with edema and gliosis, the increased signal on T2-weighted images is less distinct in FCDs when compared with the tumors (Figure 2). Gliomas may cause mass effect and frequently show intravenous contrast enhancement[1].

Open in New Tab   Full Size Figure   Download Figure

Figure 2 Focal cortical dysplasia type IIb of the left frontal cortex in a 3-year-old girl. Axial T2-weighted (A) and coronal T1-weighted (B) magnetic resonance images reveal a slight increase of white matter signal on T2-weighted image, significant blurring on T1-weighted image in gray matter-white matter junction (arrow).

Microcephaly: Congenital microcephaly refers to a head circumference of patient < 3 standard deviation below normal for that age without history of intrauterine damage[1]. There is also another microcephaly entity, which is classified in abnormal postmigrational development group. This type patients born with normal or small head size, and severe microcephaly progresses within 1-2 years after the birth[3].

Microcephaly with a simplified gyral pattern is a mild form of microlissencephaly, and characterized with profound microcephaly, significantly decreased number of sulci, sulcation abnormality, but normal cortical thickness (Figure 3). This malformation is generally not associated with other congenital structural anomalies[1].

Open in New Tab   Full Size Figure   Download Figure

Figure 3 An 8-year-old girl with microlissencephaly. Axial T2-weighted images (A, B) show reduction in the number and depth of the sulcus, thickened cortex (white arrows) with choroidal fissure cyst (black arrow). Thinning of posterior parts of the corpus callosum is also seen on sagittal three-dimensional (3D) T1-weighted image (C).

Periventricular heterotopia (subependymal nodular): Heterotopia is an abnormal location of neurons anyplace between the subependymal region of the lateral ventricles and cerebral cortex secondary to arrest of radial migration[1].

Periventricular (subependymal nodular) heterotopias are often bilateral and placed adjacent to the walls of the lateral ventricles, frequently in the peritrigonal regions, the temporal and occipital horns[1]. The characteristic appearances of nodular heterotopia are small, round or oval shaped nodules isointense with gray matter on all MR sequences, located in subependymal layer, and do not show contrast enhancement (Figure 4). Periventricular heterotopia may project into the ventricular lumen (Figure 5)[1].

Open in New Tab   Full Size Figure   Download Figure

Figure 4 An 18-year-old boy with subependymal heterotopia. Axial inversion recovery T1-weighted image shows gray matter nodules located adjacent to bilateral periventricular temporal horn region (arrows).

Open in New Tab   Full Size Figure   Download Figure

Figure 5 A 7-mo girl with subependymal heterotopia. Sagittal T1-weighted image shows gray matter nodule located in the periventricular region that protrudes into the ventricular wall (arrow).

Subcortical heterotopia (Band heterotopia): Subcortical band heterotopias (SCH) are located within the subcortical or deep white matter between the ventricular epandimal surface and the cerebral cortex. SCH may be in various forms including nodular, curvilinear or mixed. Thin overlying cortex and shallow sulci are characteristic findings for SCH (Figure 6)[1,19].

Open in New Tab   Full Size Figure   Download Figure

Figure 6 A 12-year-old boy with subcortical heterotopia. Sagittal 3D T1-weighted image shows large nodular form subcortical heterotopia (arrows) extends from the ventricle into the white matter in frontotemporal region.

SCH is a rare developmental malformation seen primarily in female and may be familial with X-linked dominant inheritance. On MRI, it shows a characteristic two parallel layers of gray matter separated by a thin white matter layer (3-layer cake: A thin outer ribbon, a very thin layer of white matter and a thick inner band (Figure 7)[1,19].

Open in New Tab   Full Size Figure   Download Figure

Figure 7 An 8-year-old girl with subcortical heterotopia. Sagittal 3D T1-weighted image shows band heterotopia (double cortex) located between the ventricular wall and the cerebral cortex (arrows).

Lissencephaly: Lissencephaly is defined as smooth brain and characterized with the absent normal gyral and sulcal pattern of the brain. The neocortex of lissencephalic patients lacks the normal cortical lamination and contains four layers instead of the six[19]. Classic or type 1 lissencephaly appears as a complete or incomplete agyria. The complete form is characterized with smooth surface of entire brain. In the incomplete form, which is more commonly seen type, temporal lobes and inferior regions of frontal lobes have some gyral formation (Figure 8). The important MRI findings of classical lissencephaly are hourglass configuration, thick cortex and thin subcortical white matter, pachygyria-agyria areas, lack of gray-white matter interdigitation, and shallow Sylvian fissure[1,19].

Open in New Tab   Full Size Figure   Download Figure

Figure 8 A 5-year-old girl with incomplete lissencephaly. Axial T1-weighted (A) and sagittal 3D T1-weighted (B) magnetic resonance images show pachygyria in frontotemporal region.

Cobblestone malformation: Cobblestone lissencephaly or formerly called type 2 lissencephaly is characterized by a nodular cortical surface accompanied by ocular anomalies and congenital muscular disorders[1]. Cobblestone lissencephaly has been divided into three different groups based on severity: (1) Cobblestone lissencephaly occurs in various genetic conditions, with Walker-Warburg syndrome being the most severe form; (2) Fukuyama congenital muscular dystrophy, the mildest form; and (3) muscle-eye brain disease, the moderate form. Congenital muscular dystrophy is a key feature (Figure 9)[19].

Open in New Tab   Full Size Figure   Download Figure

Figure 9 An 18-year-old boy with cobblestone lissencephaly. Axial T2-weighted image (A) shows incomplete lissencephaly in right occipital region (white arrows). Sagittal 3D T1-weighted image (B) reveals multiple areas of shallow microgyri (black arrows) in the parietal and temporal lobes.

Polymicrogyria: Polymicrogyria (PMG) is caused by an interruption in normal cerebral cortical development in the late neuronal migration or early postmigrational development periods[20]. The cortical surface appears thick and irregular or can have multiple small gyri separated by shallow sulci.

In the cases of PMG, the cerebral cortex may be affected various degrees: Unilateral or bilateral; asymmetrical or symmetrical; single focal focus, multifocal, or diffuse. Around the Sylvian fissure, mostly posterior perisylvian area is the most common location (Figure 10)[21].

Open in New Tab   Full Size Figure   Download Figure

Figure 10 A 7-year-old boy with polymicrogyria. Axial 3D T1-weighted image shows bilateral perisylvian polymicrogyria (arrows).

For identifying PMG the combination of three characteristics on MR images has been used: (1) abnormal gyral pattern; (2) increased cortical thickness; and (3) irregularity of the cortical–white matter junction due to packing of microgyri[22]. These can be readily detected when thin sliced volumetric images are obtained[21].

Schizencephaly: Schizencephaly is characterized by unilateral or bilateral full thickness cleft that is extending from the subarachnoid spaces to the ventricular system, and lined with gray matter[23]. The cleft is often found in perisylvian areas, and may be small (closed lip type) or large (open lip type)[24]. It may be associated with other malformations such as agenesis or dysgenesis of optic nerves, septum pellucidum (Figure 11), corpus callosum or hypocampus[25].

Open in New Tab   Full Size Figure   Download Figure

Figure 11 A 12-year-old boy with schizencephaly. T2-weighted coronal (A) and T1-weighted axial (B) images show oblique gray matter lined holohemispheric cleft (arrows) extending into the lateral ventricle that suggest open lip type schizencephaly with agenesis of septum pellucidum.

FCD: FCD type I (FCD-I) and type III (FCD-III) are in this group according to Barkovich et al[3] new MCD classification.

FCD-I is a malformation presenting with abnormal cortical layering, either settle with radial cortical lamination and maturation of neurons (FCD-Ia) or the six-layered tangential cortical lamination of the neocortex (FCD-Ib). The combination of these two subgroups is categorized as FCD-Ic[16].

MRI examination of FCD-I cases is usually normal[15]. Hippocampal atrophy is frequently coexistent with FCD-I[17]. In some cases, prominent segmental or lobar hypoplastic/atrophic changes and decrease the volume of subcortical white matter (Figure 12), sulcal and gyral pattern abnormalities may be seen. The most common location of FCD-I is the temporal lobe[1,17].

Open in New Tab   Full Size Figure   Download Figure

Figure 12 An 18-year-old girl with focal cortical dysplasia type I. Axial fluid attenuated inversion recovery image shows blurring at gray-white matter junction with normal gray matter signal in the posterior of the left frontal lobe (arrows).

FCD-III is divided into four subgroups; FCD-IIIa is in combination with hippocampal sclerosis. FCD-IIIb is associated with adjacent glial or glioneuronal tumors (i.e., DNET, ganglioglioma). FCD-IIIc is characterized with cortical lamination abnormalities adjacent to vascular malformations, whereas FCD-IIId is associated with any other acquired lesions in early life period (i.e., post-traumatic lesions, ischemic injury, encephalitis)[3,16,17].