Tag: cerebrospinal fluid

The brain's intricate structure is revealed in this frontal section, showcasing key components of the basal nuclei and surrounding features. This image highlights the striatum with its subdivisions, the globus pallidus, lateral ventricle, and corpus callosum, providing a clear view of their spatial relationships within the cerebral cortex. Understanding these elements is essential for grasping motor control, cognitive functions, and overall neurological health.

The cranial fossae form the foundation of the cranial cavity, providing structural support and protection to the brain while housing critical neurovascular structures. This anatomical illustration highlights the anterior, middle, and posterior cranial fossae, showcasing their distinct roles in supporting different brain regions. The superior and lateral views of the skull reveal how these fossae are organized to accommodate the brain's complex architecture.

The illustration depicts a classic presentation of lumbar myelomeningocele, showing the external sac containing cerebrospinal fluid (CSF) protruding posteriorly from the lumbar region of the spine.

Step back in time with this rare medical photograph of a 16-year-old female patient diagnosed with hydrocephalus and occipital encephalocele from 1917. This black-and-white image provides a historical perspective on the treatment and presentation of these neurological conditions, offering valuable lessons for medical students and professionals today. Explore the clinical significance, historical context, and modern advancements related to these conditions in this detailed analysis.

The image depicts a neonate with a significant occipital encephalocele, visible as a large sac-like protrusion from the back of the infant's head. Encephalocele is a severe congenital neural tube defect characterized by herniation of brain tissue and meninges through a defect in the skull. This particular case shows a substantial occipital encephalocele with intact skin coverage and visible vascularity. The condition requires prompt multidisciplinary evaluation and neurosurgical intervention to minimize complications and optimize developmental outcomes. Early diagnosis, careful surgical planning, and comprehensive follow-up care are essential components in the management of this challenging congenital anomaly.