Epidemiology Not rare, an important cause of new daily persistent headaches among young & middle age individuals Prevalence: ~1 per 50,000, previously.

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Presentation transcript:

Epidemiology Not rare, an important cause of new daily persistent headaches among young & middle age individuals Prevalence: ~1 per 50,000, previously probably underdiagnosed F:M ~ 2:1, onset in 4 th or 5 th decade Associated with connective tissue disorders (Marfan, Ehler Danlos) JAMA 2006.;295(19):

Etiology & Pathogenesis Generally caused by spinal CSF leak Precise cause remains largely unknown, underlying structural weakness of spinal meninges is suspected Hx of trivial traumatic events elicited in 1/3 Wide variety of dural defects; simple dural hole, fragile meningeal diverticula, absence of dura cover spinal nerve root JAMA 2006.;295(19):

Etiology & Pathogenesis Decreased CSF volume may be final common pathway in pathophysiology Altered distribution of craniospinal elasticity due to spinal CSF leak may be final common pathway So, “spontaneous spinal CSF leak” are preferred terms JAMA 2006.;295(19):

Diffuse pachymeningeal (dural) enhancement Bilateral subdural effusion/hematomas Downward displacement of brain Enlargement of pituitary gland Engorgement of dural venous sinuses Prominence of spinal epidural venous plexus Venous sinus thrombosis & isolated cortical vein thrombosis AJNR 2008.; 29:

Monroe-Kellie Rule Sum of volumes of intracranial blood, CSF & cerebral tissue must remain constant in an intact cranium Loss of CSF can be compensated by increased vascular component or by increased intracranial CSF component JAMA 2006.;295(19):

Monroe-Kellie Rule Accounting for pachymeningeal enhancement, engorged venous structures, pituitary hyperemia and subdural effusions Subdural hematoma may caused by tearing of bridging veins or rupture of thin wall vessels in subdural zone Sagging of brain is caused by loss of CSF buoyancy JAMA 2006.;295(19):

AJNR 2008.; 29: Diffuse, uniform thickness Located at convexity, along falx cerebri, tentorium & posterior fossa dura Disappears after successful treatment Diffuse Pachymeningeal, (Dural) Enhancement

Bilateral Subdural Effusion/Hematomas Incidence: 10-50% Tend to be thin (2-7 mm), typically occur over supratentorial convexity Have variable MR signal, depending on protein conc. & presence of blood Disappear after successful treatment

Downward Displacement of The Brain Low lying cerebellar tonsils Effacement of prepontine cistern, flattening of pons against clivus Effacement of perichiasmatic cistern with bowing of optic chiasm over pituitary fossa

Engorgement of Dural Venous Sinuses On T1W the middle 1/3 of dominant transverse sinus, shows convex borders All venous sinuses become engorged The falx & tentorium show marked enhancement AJNR 2007 ; 28:

Prominent of Epidural Venous Plexus AJNR 2009.; 30: Occasionally patients may even present with a compressive myelopathy due to a prominent venous epidural plexus.

Spinal Extradural Fluid Collections From: AJNR 2009.; 30:147-51

Treatment Many cases resolved spontaneously There is no randomized control trial evaluation of the treatment option Conservative approach: bed rest, oral hydration, caffeine intake, use of abdominal binder JAMA 2006.;295(19):

Treatment Mainstay of treatment is epidural blood patch (EBP) - epidural injection of autologous blood into epidural space Effective in relieving symptoms in ~1/3, presumable by dural temponade and sealing the leak If unsuccessful, it can be repeated JAMA 2006.;295(19):

Treatment If EBP fail, direct EBP or percutaneous placement of fibrin sealant is recommended Requires knowledge of exact site of CSF leak Surgical Rx is reserved for Pt who failed nonsurgical Rx Often successful when focal CSF leak is identified Ligation or placement of muscle pledget JAMA 2006.;295(19):

Pre- post Tx appearance Left: MRI shows ‘saggin’ brain & large pituitary gland. Right: after Tx & symptom resolution the brain & gland have a normal appearance.

Pituitary gland changes in Intracranial Hypotension Pre- & post treatment changes. The pituitary gland was initially enlarged & after Tx it becomes normal in size.

CT myelography Radioisotope cisternography MR myelography MR imaging Intrathecal Gd-enhanced MR ► Most common site of CSF leak reported as the cervicothoracic junction & thoracic area, could be single or multiple sites

Complications Patient with known intracranial hypotension who rapidly deteriorated shows cerebellar, brainstem & cord infarctions. AJNR 2009, doi: /ajnr.A1749

Intracranial hypotension due to Post op spinal CSF leak Patient had a tumor resection from the thoracic vertebrae & developed intracranial hypotension found to be due to paraspinal thoracic pseudomeningocele.

Intracranial hypotension complicated by cortical vein thrmbosis Iatrogenic- post LP- intracranial hypotension with cortical vein thrombosis (arrow).

References Spontaneous spinal cerebrospinal fluid leaks and intracranial hypotension. JAMA 2006; 295(19): Diffuse pachymeningeal hyperintensity and subdural effusion/hematoma by FLAIR MRI in patients with spontaneous intracranial hypotension. AJNR 2008; 29: The venous distention sign: a diagnostic sign of intracranial hypotension. AJNR 2008; 28: Intradural spinal vein enlargement in intracranial hypotension. AJNR 2005; 26: Diagnostic criteria for spontaneous spinal CSF leaks and intracranial hypotension. AJNR 2008; 29: Detection of CSF leak in spinal CSF leak syndrome using MR myelography: correlation with radioisotope cisternography. AJNR 2008; 29: Gadolinium-enhanced MR cisternography to evaluate dural leaks in intracranial hypotension syndrome. AJNR 2008; 29: Diagnostic value of spinal MRI in spontaneous intracranial hypotension syndrome. AJNR 2009; 30: False localizing sign of C1-2 CSF leak in spontaneous intracranial hypotension. J Neurosurg 2004; 100:639-44