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The superior cerebellar veins pass partly forward and medialward, across the superior cerebellar vermis.They end in the straight sinus, [1] and the internal cerebral veins, partly lateralward to the transverse and superior petrosal sinuses.
The venous drainage of the cerebrum can be separated into two subdivisions: superficial and deep. The superficial system. The superficial system is composed of dural venous sinuses, sinuses (channels) within the dura mater. The dural sinuses are therefore located on the surface of the cerebrum.
CSF returns to the vascular system by entering the dural venous sinuses via arachnoid granulations. [2] These are outpouchings of the arachnoid mater into the venous sinuses around the brain, with valves to ensure one-way drainage. [2] This occurs because of a pressure difference between the arachnoid mater and venous sinuses. [3]
Glymphatic flow was initially believed to be the complete answer to the long-standing question of how the sensitive neural tissue of the CNS functions in the perceived absence of a lymphatic drainage pathway for extracellular proteins, excess fluid, and metabolic waste products.
These sinuses play a crucial role in cerebral venous drainage. A dural venous sinus, in human anatomy, is any of the channels of a branching complex sinus network that lies between layers of the dura mater, the outermost covering of the brain, and functions to collect oxygen-depleted blood. Unlike veins, these sinuses possess no muscular coat.
Cranial venous outflow obstruction, also referred to as impaired cranial venous outflow, impaired cerebral venous outflow, cerebral venous impairment is a vascular disorder that involves the impairment of venous drainage from the cerebral veins of the human brain. [1] [2] The cause of cranial venous outflow obstruction is not fully understood.
The granulations exhibit a thinner stalk that penetrates through the wall of a venous sinus, and a distended head formed within the lumen of the sinus. The head consists of a trabecular collagenous core that is largely covered by a dural cupula, except for an apical cap — some 0.3 mm in diameter — of arachnoid cells attached directly to the ...
Beginning in 1937 Batson began a series of injection experiments investigating the anatomy and physiology of the cerebrospinal venous system. [2] His carefully documented results demonstrated the continuity of the venous systems of the brain and the spine, as injections of contrast dyes into venous systems feeding into the spinal venous plexus led to the appearance of contrast material in the ...