ABPath Neuropathology flashcards
ABPath Neuropathology · Build recall with a focused review session.
32 cards. Read the term and the definition here. The deck at the top of this page is optional.
- Brodmann area 4
- Primary motor cortex located in the precentral gyrus; contains Betz giant pyramidal cells whose axons form the corticospinal tract.
- Internal capsule posterior limb
- White matter tract between thalamus and lentiform nucleus; carries corticospinal, corticobulbar, and sensory fibers and is a common site of lacunar infarction.
- CA1 sector
- Pyramidal cell region of the hippocampus most vulnerable to hypoxia and ischemia; also an early site of neurofibrillary tangle formation in Alzheimer disease.
- Circle of Willis
- Anastomotic ring at the brain base formed by anterior cerebral, internal carotid, posterior communicating, and posterior cerebral arteries with anterior communicating artery.
- Glioblastoma definition
- IDH-wildtype diffuse astrocytic glioma with necrosis or microvascular proliferation, or with TERT promoter mutation, EGFR amplification, or +7/-10.
- Oligodendroglioma criteria
- Diffuse glioma with IDH mutation and whole-arm 1p/19q codeletion; histology often shows uniform round cells with perinuclear halos and chicken-wire vasculature.
- Lewy body
- Eosinophilic neuronal cytoplasmic inclusion composed of alpha-synuclein and ubiquitin; found in substantia nigra and cortex in Lewy body disease.
- Creutzfeldt-Jakob disease histology
- Spongiform change with neuronal loss and gliosis; definite diagnosis requires demonstration of protease-resistant prion protein by immunoblot or immunohistochemistry.
- Meningioma grade 2 criteria
- Brain invasion, at least four mitoses per 10 high-power fields, or three of five atypical features including necrosis, sheet-like growth, and macronucleoli.
- Alzheimer ABC score
- Combined Braak tangle stage, Thal amyloid phase, and CERAD neuritic plaque score that assigns low, intermediate, or high Alzheimer disease neuropathologic change.
- MGMT promoter methylation
- Epigenetic silencing of the DNA repair gene MGMT that predicts improved response to temozolomide in glioblastoma and is assessed by methylation-specific PCR.
- WHO CNS5 grading
- Tumor grade integrates histologic features with molecular markers such as IDH status, 1p/19q codeletion, CDKN2A/B deletion, and H3 K27M mutation.
- Intraoperative consultation timing
- Frozen section diagnosis typically rendered within 20 to 30 minutes to guide surgical extent; final report usually issued within 24 to 48 hours.
- CLIA proficiency testing
- Regulatory requirement that laboratories demonstrate ongoing accuracy for immunohistochemistry and molecular assays through external proficiency surveys and documented validation.
- Brain-only autopsy
- Limited postmortem examination restricted to the central nervous system, performed with next-of-kin consent and often used for neurodegenerative disease research.
- Peer review QA
- Quality assurance process in which a sample of cases is re-reviewed by a second pathologist to identify diagnostic discrepancies and drive corrective action.
- Muscle biopsy freezing
- Skeletal muscle is snap-frozen in isopentane cooled by liquid nitrogen to preserve enzyme histochemistry; formalin fixation destroys ATPase and oxidative enzyme staining.
- Sural nerve biopsy
- Standard site for peripheral nerve sampling; tissue is divided for glutaraldehyde electron microscopy, paraffin histology, and teased fiber preparations.
- Fiber typing ATPase
- Myosin ATPase incubation at pH 9.4 stains type II fibers dark and type I light; preincubation at pH 4.3 reverses the pattern.
- Retinoblastoma specimen handling
- Enucleated eye is oriented at the optic nerve margin; fresh tumor is submitted for genetic testing and the globe sectioned to assess invasion.
- CSF cytology sensitivity
- Detection of leptomeningeal malignancy improves with repeat lumbar punctures and cytospin or cell block preparation rather than single samples.
- Corneal button orientation
- Excised corneal tissue must be oriented with marking sutures and assessed for endothelial cell density and stromal pathology before transplantation.
- Gomori trichrome
- Muscle stain that highlights mitochondria and ragged red fibers in red; useful in mitochondrial myopathy and nemaline rod evaluation.
- Coagulative necrosis
- Pattern of ischemic cell death in most solid organs preserving tissue architecture; brain instead undergoes liquefactive necrosis after infarction.
- Congo red amyloid
- Histochemical stain binding amyloid beta-pleated sheets, producing apple-green birefringence under polarized light; thioflavin T shows fluorescence.
- Virchow triad
- Three contributors to thrombosis: endothelial injury, abnormal blood flow or stasis, and hypercoagulability of the blood.
- Granulomatous inflammation
- Chronic inflammation with epithelioid histiocytes and multinucleated giant cells, seen in tuberculosis, sarcoidosis, and fungal infection.
- Antigen retrieval
- Heat or enzymatic pretreatment that unmasks epitopes cross-linked by formalin fixation, improving immunohistochemical staining sensitivity.
- Grade versus stage
- Grade describes tumor differentiation and biologic aggressiveness; stage describes anatomic extent of disease including nodal and distant spread.
- Endogenous peroxidase
- Intrinsic tissue peroxidase activity that can cause false-positive immunohistochemistry unless blocked with hydrogen peroxide before detection.
- Fibroblast growth factor signaling
- Receptor tyrosine kinase pathway regulating proliferation and angiogenesis; FGFR alterations occur in gliomas and other tumors and are therapeutic targets.
- Middle cerebral artery embolism
- Most common site of cerebral embolic occlusion, causing contralateral hemiparesis and aphasia when the dominant hemisphere is involved.