Anatomic variants in Dandy-Walker complex
Maria Claudia Jurcă1, Kinga Kozma, CodruŢa Diana Petcheşi
1Department of Morphological Sciences, Department of Surgical Disciplines, Faculty of Medicine and Pharmacy, University of Oradea, Romania; opticlar@gmail.com.
Insights
Dandy-Walker complex (DWC) is a group of central nervous system malformations. Diagnosis relies on clinical and imaging data, with varied presentations requiring tailored management.
Area of Science:
- Neurology
- Developmental Biology
- Medical Imaging
Background:
- Dandy-Walker complex (DWC) encompasses diverse central nervous system malformations.
- Includes Dandy-Walker malformation, Dandy-Walker variant, mega cisterna magna, and posterior fossa arachnoid cyst.
- Characterized by posterior fossa abnormalities and variable vermian and fourth ventricle involvement.
Observation:
- Presents four cases illustrating the morphological and clinical spectrum of DWC.
- Diagnosis integrated clinical signs (macrocephaly, seizures) with imaging (X-ray, CT, MRI).
- Observed diverse presentations including rare associations like neurofibromatosis and congenital anomalies.
Findings:
- Two cases diagnosed with Dandy-Walker complex.
- One case of Dandy-Walker variant associated with neurofibromatosis.
- One case of posterior fossa arachnoid cyst with Horner's syndrome and cardiac defects.
Implications:
- Highlights the variability in clinical, radiological, and functional manifestations of DWC.
- Emphasizes the need for comprehensive diagnostic approaches.
- Underscores the requirement for individualized therapeutic strategies for DWC patients.
Abstract:
Dandy-Walker complex (DWC) is a malformative association of the central nervous system. DWC includes four different types: Dandy-Walker malformation (vermis agenesis or hypoplasia, cystic dilatation of the fourth ventricle and a large posterior fossa); Dandy-Walker variant (vermis hypoplasia, cystic dilatation of the fourth ventricle, normal posterior fossa); mega cysterna magna (large posterior fossa, normal vermis and fourth ventricle) and posterior fossa arachnoid cyst. We present and discuss four cases with different morphological and clinical forms of the Dandy-Walker complex. In all four cases, diagnosis was reached by incorporation of clinical (macrocephaly, seizures) and imaging [X-ray, computed tomography (CT), magnetic resonance imaging (MRI)] data. Two patients were diagnosed with Dandy-Walker complex, one patient was diagnosed with Dandy-Walker variant in a rare association with neurofibromatosis and one patient was diagnosed with a posterior fossa arachnoid cyst associated with left-sided Claude Bernard-Horner syndrome, congenital heart disease (coarctation of the aorta, mitral stenosis) and gastroesophageal reflux. In all forms of DWC, the clinical, radiological and functional manifestations are variable and require adequate diagnostic and therapeutic measures.
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