Book contents
- Frontmatter
- Contents
- List of contributors
- List of abbreviations
- Preface
- Section 1 Bilateral Predominantly Symmetric Abnormalities
- Section 2 Sellar, Perisellar and Midline Lesions
- Section 3 Parenchymal Defects or Abnormal Volume
- 77 Hippocampal Sclerosis
- 78 Wallerian Degeneration
- 79 Rasmussen Encephalitis
- 80 Chronic Infarct
- 81 Post-Traumatic Atrophy
- 82 Postoperative Defects
- 83 Porencephalic Cyst
- 84 Schizencephaly
- 85 Hemimegalencephaly
- 86 Sturge–Weber Syndrome
- 87 Benign External Hydrocephalus
- 88 Normal Pressure Hydrocephalus
- 89 Alzheimer Disease
- 90 Frontotemporal Lobar Degeneration
- 91 Huntington Disease
- 92 Congenital Muscular Dystrophies
- 93 Dandy-Walker Malformation
- 94 Microcephaly
- 95 Hydranencephaly
- 96 Acquired Intracranial Herniations
- Section 4 Abnormalities Without Significant Mass Effect
- Section 5 Primarily Extra-Axial Focal Space-Occupying Lesions
- Section 6 Primarily Intra-Axial Masses
- Section 7 Intracranial Calcifications
- Index
- References
87 - Benign External Hydrocephalus
from Section 3 - Parenchymal Defects or Abnormal Volume
Published online by Cambridge University Press: 05 August 2013
- Frontmatter
- Contents
- List of contributors
- List of abbreviations
- Preface
- Section 1 Bilateral Predominantly Symmetric Abnormalities
- Section 2 Sellar, Perisellar and Midline Lesions
- Section 3 Parenchymal Defects or Abnormal Volume
- 77 Hippocampal Sclerosis
- 78 Wallerian Degeneration
- 79 Rasmussen Encephalitis
- 80 Chronic Infarct
- 81 Post-Traumatic Atrophy
- 82 Postoperative Defects
- 83 Porencephalic Cyst
- 84 Schizencephaly
- 85 Hemimegalencephaly
- 86 Sturge–Weber Syndrome
- 87 Benign External Hydrocephalus
- 88 Normal Pressure Hydrocephalus
- 89 Alzheimer Disease
- 90 Frontotemporal Lobar Degeneration
- 91 Huntington Disease
- 92 Congenital Muscular Dystrophies
- 93 Dandy-Walker Malformation
- 94 Microcephaly
- 95 Hydranencephaly
- 96 Acquired Intracranial Herniations
- Section 4 Abnormalities Without Significant Mass Effect
- Section 5 Primarily Extra-Axial Focal Space-Occupying Lesions
- Section 6 Primarily Intra-Axial Masses
- Section 7 Intracranial Calcifications
- Index
- References
Summary
Specific Imaging Findings
Benign external hydrocephalus (BEH) is characterized by an increased amount of fluid in the subarachnoid spaces (SAS), with density and signal intensity following CSF, typically in the bilateral frontal regions and along the interhemispheric fissure. Enlarged SAS follow the contour of gyri and appear symmetric between the two hemispheres. Additional imaging features include widening of the suprasellar cistern and normal to slightly increased ventricular size. The distance between the frontal gyri and the skull and between the mesial frontal gyri and the anterior interhemispheric fissure measures more than 5 mm. MRI or Doppler ultrasound can confirm the presence of transversing leptomeningeal vessels within the extra-axial collections. MRI can rule out associated chronic subdural hematomas or hygromas.
Pertinent Clinical Information
Increased head circumference above the 95th percentile, full fontanelles, and frontal bossing are the most common clinical findings. Patients are usually referred for imaging when the head size has rapidly increased over the course of months. A family history of macrocephaly is often present. BEH is usually diagnosed between 3 and 8 months of age and is more common in male infants. Transient gross motor delay can be observed and is usually attributed to the added head weight in the macrocephalic infant. Otherwise BEH is usually not associated with developmental delay or neurological deficit. Once the diagnosis of BEH is established, clinical follow-up is required to confirm normal development and no treatment is necessary. In selected cases, follow-up imaging at 18–24 months of age can be considered and should show resolution of the abnormality.
- Type
- Chapter
- Information
- Brain Imaging with MRI and CTAn Image Pattern Approach, pp. 179 - 180Publisher: Cambridge University PressPrint publication year: 2012