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A condition marked by an excessive accumulation of cerebrospinal fluid resulting in dilation of the cerebral ventricles and raised intracranial pressure; may also result in enlargement of the cranium and atrophy of the brain. SYN: hydrocephaly. [hydro- + G. kephale, head]
- communicating h. type of h. in which there is an abnormality in cerebrospinal fluid absorption; there is no obstruction to cerebrospinal fluid flow in the ventricular system or where the cerebrospinal fluid passes into the spinal canal.
- double compartment h. independent supra- and infratentorial h. usually due to a veil occlusion of the aqueduct of Sylvius.
- external h. 1. accumulation of fluid in the subarachnoid spaces of the brain; 2. accumulation of fluid in the subdural space owing to a persistent communication between the subarachnoid and subdural spaces.
- h. ex vacuo h. due to loss or atrophy of brain tissue; less commonly associated with raised intracranial pressure.
- noncommunicating h. SYN: obstructive h..
- normal pressure h. a type of h. developing usually in older people, due to failure of cerebrospinal fluid to be absorbed by the pacchionian granulations, and characterized clinically by progressive dementia, unsteady gait, urinary incontinence, and usually, a normal spinal fluid pressure. SYN: occult h..
- obstructive h. h. secondary to a block in cerebrospinal fluid flow in the ventricular system or between the ventricular system and spinal canal. SYN: noncommunicating h..
- otitic h. a form of h. associated with otitis media and thrombosis of one or both sigmoid sinuses of the dura, characterized by marked increase in cerebrospinal fluid pressure.
- postmeningitic h. ventricular dilation following meningitis and secondary to obstruction of cerebrospinal fluid pathways.
- posttraumatic h. ventricular dilation following injury, due either to impaired circulation and/or absorption of cerebrospinal fluid or due to loss of brain substance (h. ex vacuo).
- primary h. SYN: congenital h..
- secondary h. an accumulation of fluid in the cranial cavity, due to meningitis or obstruction to the venous flow.
- thrombotic h. increase in cerebrospinal fluid and of intracranial pressure following thrombosis of the cerebral veins or sinuses; caused by septic infection, dehydration, tuberculosis, typhoid, leukemia, and other conditions.
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hy·dro·ceph·a·lus -'sef-ə-ləs, Brit also -'kef- n, pl -li -.lī an abnormal increase in the amount of cerebrospinal fluid within the cranial cavity that is accompanied by expansion of the cerebral ventricles, enlargement of the skull and esp. the forehead, and atrophy of the brain
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n.
an abnormal increase in the amount of cerebrospinal fluid within the ventricles of the brain. In childhood, before the sutures of the skull have fused, hydrocephalus makes the head enlarge. In adults, because of the unyielding nature of the skull, hydrocephalus raises the intracranial pressure with consequent drowsiness and vomiting. Hydrocephalus may be caused by obstruction to the outflow of cerebrospinal fluid from the ventricles or a failure of its reabsorption into the cerebral sinuses. spina bifida may be associated with hydrocephalus in childhood. Treatment involves treating the underlying cause and, if necessary, diverting the excess cerebrospinal fluid into the abdominal cavity, where it is absorbed. This is achieved by tunnelling a thin tube from the ventricles to the abdomen (ventriculo-peritoneal shunt) or atrium (ventriculo-atrial shunt).
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hy·dro·ceph·a·lus (hi″dro-sefґə-ləs) [hydro- + -cephalus] a condition marked by dilatation of the cerebral ventricles, most often occurring secondary to obstruction of the cerebrospinal fluid pathways (see ventricular block, under block), and accompanied by an accumulation of cerebrospinal fluid within the skull; the fluid is usually under increased pressure, but occasionally may be normal or nearly so. In children it may occur prior to closure of the skull sutures and is typically characterized by enlargement of the head, prominence of the forehead, brain atrophy, mental deterioration, and convulsions. In adults the syndrome includes incontinence, imbalance, and dementia. It may be congenital or acquired and may be of sudden onset (acute h.) or be slowly progressive (chronic or primary h.). Called also hydrocephaly, hydrencephaly, and hydrencephalus. hydrocephalic adjMedical dictionary. 2011.