Bilateral Cavernous Sinus Lesions
Anne G. Osborn, MD, FACR
DIFFERENTIAL DIAGNOSIS
Common
Pituitary Macroadenoma
Meningioma
Metastasis, Skull Base
Lymphoma, Metastatic, Intracranial
Less Common
Neurofibromatosis Type 2
Carotid-Cavernous Fistula
Thrombosis, Cavernous Sinus
Chordoma, Clivus
Plasmacytoma
Neurosarcoid
Langerhans Histiocytosis, Skull Base
Rare but Important
Pseudotumor, Intracranial
Leukemia
Extramedullary Hematopoiesis
Germ Cell Neoplasms
Erdheim-Chester Disease
Benign Nonmeningothelial Tumors
ESSENTIAL INFORMATION
Key Differential Diagnosis Issues
Is lesion intrinsic to cavernous sinus (CS)?
Does it arise from skull base or extracranial tissues?
Is it destructive?
Helpful Clues for Common Diagnoses
Pituitary Macroadenoma
Pituitary gland indistinguishable from mass (gland IS the mass)
Enlarged, “figure-of-eight” mass
Extends laterally through thin medial dural wall into CS
May surround, encase ICAs but rarely occludes
Mass typically isointense with brain, enhances strongly/uniformly
Dynamic MR shows mass enhances more slowly than CS
If symptoms of pituitary apoplexy, hemorrhage common
Sphenoid sinusitis often present
Meningioma
Uni- > bilateral
Thick, uniformly enhancing dura along lateral walls
Variable extension into CS proper
Look for “dural tail” (thickening along tentorium, middle fossa)
Look for obliteration of CSF in Meckel caves
May extend inferiorly along clivus
Metastasis, Skull Base
Permeative, destructive mass
Hematogenous spread from extracranial primary common (e.g., breast)
Most commonly centered in central skull base (BOS), secondary extension into CS
May also be direct geographic extension from nasopharyngeal carcinoma
CS involvement can be uni-, bilateral; symmetric or asymmetric
Sagittal T1, coronal T1 C+ FS scans useful
Lymphoma, Metastatic, Intracranial
Primary central BOS lymphoma rare
Uni- > bilateral
Isointense, avidly enhancing
Associated cranial nerve, meningeal (dural) lesions common
Tumor often surrounds, encases but does not occlude cavernous ICAs
Helpful Clues for Less Common Diagnoses
Neurofibromatosis Type 2
Multiple schwannomas, meningiomas
Most common CS schwannoma = trigeminal (Meckel cave)
Look for meningiomas of CS, optic nerve sheath, tentorium
Look for bilateral vestibular schwannomas (VS, diagnostic of NF2), evidence for prior CPA/temporal bone surgery
One VS + other schwannoma, meningioma highly suggestive
Carotid-Cavernous Fistula
Uni- > bilateral carotid-cavernous fistulas
Look for CS “flow voids” in addition to ICAs
Look for ↑ superior ophthalmic vein(s) (SOV)
CTA helpful screening study
DSA to delineate fistula site(s)
Thrombosis, Cavernous Sinus
Can be spontaneous, sterile, or septic (thrombophlebitis)
Look for infection in paranasal sinuses, orbits
Nonenhancing areas within intensely enhancing CS
Lateral dural wall, CS septations enhance, thrombus does not
Look for ↑ SOVs
Chordoma, Clivus
Destructive T2 hyperintense mass centered in clivus
Large lesions may invade CS
Displace but rarely occlude ICAs
Chondrosarcoma may mimic
Usually unilateral, arises from petro-occipital fissure
Plasmacytoma
Solitary destructive mass of central BOS
Centered in sphenoid sinus, clivus
Isointense, strongly enhancing mass
Bi- > unilateral
Neurosarcoid
CS rare site
Look for other lesions
Pituitary, infundibular stalk lesion
Cranial nerve involvement
Dural-based masses
Infiltrating CS mass(es)
Lesions enhance strongly, uniformly
Bone destruction rare
Langerhans Histiocytosis, Skull Base
Osteolysis with sharply defined scalloped margins ± soft tissue mass
Varies from small punched out lesion to widespread diffuse bony involvement
May destroy almost entire BOS
Homogeneous enhancement
Helpful Clues for Rare Diagnoses
Pseudotumor, Intracranial
90% of intracranial pseudotumors occur without orbital disease
Tolosa-Hunt syndrome (painful ophthalmoplegia) when CS involved
Uni- > bilateral
Look for associated meningeal thickening (can be extensive)
Bone invasion, destruction may occur
Leukemia
Paranasal sinus/orbit involvement typical
Bilateral CS involvement rare
Extramedullary Hematopoiesis
CS involvement rare
Look for associated dural-based masses (calvarium, spine)
Germ Cell Neoplasms
Rare; typically involve pituitary gland/stalk
Erdheim-Chester Disease
Rare non-Langerhans cell histiocytosis
Disseminated xanthogranulomatous infiltrative disease of unknown originStay updated, free articles. Join our Telegram channel
Full access? Get Clinical Tree