Prayson Infection Flashcards
Epidural abcess
Most common organsims: Streptococcus and Staphylococcus. Usually 2/2 extension from bones (trauma, osteomyelitis) > soft tissue
Spinal- Staph aureus, Lumbar and thoracic, more common than intracranial
Intracranial - extension from sinus infection
Subdural abcess
1 Strep, #2 Staph. Bone/sinus infection via thrombophlebitis. Dorsolateral cerbrum, frontal pole, and interhemispheric fissure. Spinal rare
Leptomeninges
Fever, HA, nausea, vomiting, confusion, nuchal rigidity, Kernig’s and Brudzinski’s signs.
Neonatal- Strep agalactiae (Group B, exudate over vertex) and E. coli (hemorrhage, necrotizing, arteritis, necrosis) are most common, Proteus, Listeria (microabcesses)
Children- Nisseria meningitidis (basal aspect of brain, Waterhous Friederichesen)
Adults- S. pneumonia, Listeria monocytogenes
Abcess
#1 Streptococcus #2 gram-negative bacilli #3 Staphylococcus frequently multiple organisms
Mycobacterium tuberculosis
Necrotizing granulomas; Ziehl-Neelsen & Fite have low yeild (<50%)
CSF: lymphocyte predom
Epidural- extension from vertebral infxn (Pott’s), subdural- milliary or en-plaque, abcsess-tuberucloma, meningitis- base of brain, neutrophils, endarteritis.
Mycobacterium avium
Perivascular macrophages with orgasisms
Sarcoid
Non-casseating granulomas, base of brain post. fossa, Optic nerve and chiasm common, near vessels in meninges,
Whipple’s dx
Tropheryma whippelii, gram + actinomyocete. Males, dementia, gaze palsies, and myoclonus. PAS+ organsims in perivascular macs
Early Syphilis
Treponema pallidum; Steiner, Warthin-Starry, Dieterle stains. Subacute secondary lymphocytic meningitis, meningovascular lymhs, plasma cells, and gummata (central necrosis surrounded by epithelioid histiocytes, no organisms), arteritis, Heubner’s endarteritis obliterans, pachymeningitis cervicalis.
General paresis Syphilis
Progressive dementia, Argyll Robertson pupils, late frotnal atrophy, subacute encephalitis, loss of neurons, astrocytosis, perivascular inflammation, microglial with iron. Spirochetes hard to identify. 3 year course
Lissauer’s dementia
Cuased by syphilis (7-8 year course), variant of general paresis. Epileptic or aapoplectic attacks, temporal atrophy w/ pseudolaminar degenration.
Tabes Dorasalis
Degeneration of spinal dorsal roots and columns, lumbosacral and lower thoracic cord, dorsal root ganglia unaffected.
Caused by syphillis. Pain, loss of reflexes, loss of pain sensation and joint position, ataxia, Charcot joints. Optic nerve atrophy
Congenital syphilis
Meningovascular inflammation with obstructive hydrocephalus. Keratitis, chroiretinits, and deafness. cerebellar general paresis
Lyme disease
Borrelia burgdorferi, spirochete transmitted by ioxodid tick. Lymphoplasmacytic leptomeningitis, crainial neuropathy. Erythema chroncia migrans, cardiac involvement, and arthritis.
Actinomycosis
BT w/ fungal like morphology, thin filaments. Gram +, acid fast -. Sulfur granules, cervicofacial entry. Granulomas and basilar meningitis