Neuropathology Review Questions 113012 Match the tumor with

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Neuropathology Review Questions 11/30/12

Neuropathology Review Questions 11/30/12

Match the tumor with the description 1. Antoni A areas Schwannoma 2. Antoni B

Match the tumor with the description 1. Antoni A areas Schwannoma 2. Antoni B areas Schwannoma 3. Verocay bodies Schwannoma 4. Axons present between tumor cells Neurofibroma 5. Plexiform type strongly associated with NF 1 Neurofibroma • • Neurofibroma Schwannoma Both Neither

Schwannoma • Neoplastic schwann cells in two basic patterns – Antoni A • Compact

Schwannoma • Neoplastic schwann cells in two basic patterns – Antoni A • Compact • Spindle cells • Collagen abundant – Antoni B • Loose • Stellate round cells • Microcysts

Schwannoma • Verocay bodies – In Antoni A areas – Anuclear areas with palisading

Schwannoma • Verocay bodies – In Antoni A areas – Anuclear areas with palisading cells

Schwannoma • • Benign No sex predominance Mean age 40 -50 years Occasionally multiple

Schwannoma • • Benign No sex predominance Mean age 40 -50 years Occasionally multiple – With NF 2 or schwannomatosis • • Neural crest origin Frequently affect sensory nerves May be cystic, hemorrhagic S 100 positive

Schwannoma • Intracranial – Superior vestibular nerve • Internal acoustic meatus at root entry

Schwannoma • Intracranial – Superior vestibular nerve • Internal acoustic meatus at root entry zone – Trigeminal nerve • Middle fossa, posterior fossa or both • Spinal – Intraspinal or dumbell shaped • • Head & Neck Posterior mediastinum Retroperitoneum Flexor surfaces of extremities

Neurofibroma • Peripheral nerve sheath tumor – Mix of Schwann cells, perineural cells, fibroblasts

Neurofibroma • Peripheral nerve sheath tumor – Mix of Schwann cells, perineural cells, fibroblasts • Hypocellular with mucoid matrix • Collagen bundles follow nerve fibers • Entrapped axons, ganglion cells • Tactilelike structures – Resemble Meissnerian corpuscles

Neurofibroma • • Any age No sex predominance Not intracranial Solitary cutaneous nodules –

Neurofibroma • • Any age No sex predominance Not intracranial Solitary cutaneous nodules – From small terminal nerves • Potential for malignant transformation

Neurofibroma Types • Cutaneous – Painless, unencapsulated – Solitary, low malignant potential • Multiple

Neurofibroma Types • Cutaneous – Painless, unencapsulated – Solitary, low malignant potential • Multiple = NF 1 • Intraneural – Large nerve trunks – NF 1 (plexiform = pathognomonic for NF 1) – “bag of worms” – Malignant potential

Schwannoma Neurofibroma Extremities Trunk Eccentric to nerve Incorporates nerve Globular, fusiform or diffuse Encapsulated

Schwannoma Neurofibroma Extremities Trunk Eccentric to nerve Incorporates nerve Globular, fusiform or diffuse Encapsulated No capsule Tan-yellow, opaque Gray-tan, opalescent Occasionally cystic Non-cystic Highly cellular Low-moderate cellularity Antoni A/B Uniphasic pattern Axons absent Axons present Schwann cells Multiple cells No mast cells Mast cells present Rare malignancy Malignant potential NF 2 association NF 1 assosciation

Match the time period after an infarct with the histologic appearance 1. Lipid laden

Match the time period after an infarct with the histologic appearance 1. Lipid laden macrophages first appear 5 -7 d 2. Fibrillary astrocytes at periphery >3 mo 3. Gemistocytic astrocytes at periphery 10 -20 d 4. Polymorphonuclear infiltrate 1 -2 d 5. Neuronal necrosis first apparent 12 -24 h • • • 12 -24 h 1 -2 d 5 -7 d 10 -20 d >3 mo

Infarction • 12 -24 hours – Ischemic neuronal necrosis • Possibly as little as

Infarction • 12 -24 hours – Ischemic neuronal necrosis • Possibly as little as one hour – Softening & discoloration – Circumscribed pallor

Infarction • 1 -2 days: PMN infiltration • 2 -5 days: Astrocyte retraction balls,

Infarction • 1 -2 days: PMN infiltration • 2 -5 days: Astrocyte retraction balls, BBB breakdown, edema • 5 days: Macrophages (gitter cells), neovascularization • 2 weeks: Gemistocytic astrocytes • 3 months: Fibrillary astrocytes, preservation of outer cortical layer

Infarct

Infarct