Page 13 of 16

PA34.1-3,PA35.1 | Nervous System & Eye — Practice Quiz

Practice 12 questions · Untimed · Unlimited attempts

Click any question card to reveal the correct answer.

Q1 PA34.3 1 pt

A 6-year-old child presents with fever, neck stiffness, and petechial rash for 18 hours. Lumbar puncture is performed. Which CSF profile is MOST consistent with bacterial meningitis?

A Glucose 55 mg/dL (serum 90 mg/dL), protein 35 mg/dL, cells 8/mm³ (90% lymphocytes)
B Glucose 18 mg/dL (serum 92 mg/dL), protein 210 mg/dL, cells 1,800/mm³ (95% neutrophils)
C Glucose 48 mg/dL (serum 90 mg/dL), protein 80 mg/dL, cells 120/mm³ (80% lymphocytes), cobweb clot on standing
D Glucose 60 mg/dL (serum 90 mg/dL), protein 28 mg/dL, cells 4/mm³, India ink preparation positive

Click to reveal answer

Q2 PA34.3 1 pt

A 28-year-old immunocompetent medical student develops headache and low-grade fever over 3 days. CSF analysis: opening pressure 160 mmH₂O, appearance clear, cells 110/mm³ (92% lymphocytes), protein 55 mg/dL, glucose 58 mg/dL (simultaneous serum glucose 95 mg/dL). Gram stain and culture are negative. Which diagnosis fits BEST?

A Bacterial meningitis
B Viral (aseptic) meningitis
C Tuberculous meningitis
D Cryptococcal meningitis

Click to reveal answer

Q3 PA34.3 1 pt

A 45-year-old HIV-negative patient with prolonged fever, night sweats, and weight loss presents with meningism. CSF: cells 180/mm³ (85% lymphocytes), protein 320 mg/dL, glucose 28 mg/dL (serum 88 mg/dL). After standing overnight the tube shows a fine 'cobweb' clot. AFB smear is pending. Which meningitis type does this profile MOST likely represent?

A Viral meningitis
B Bacterial meningitis
C Tuberculous meningitis
D Eosinophilic meningitis

Click to reveal answer

Q4 PA34.2 1 pt

On histology of a brain tumour biopsy, you observe areas of necrosis with a rim of densely packed, hyperchromatic tumour cells arranged in a radial pattern around the necrotic core. Microvascular proliferation with glomeruloid tufts is also present. Which tumour and molecular marker best characterises this finding?

A Oligodendroglioma — 1p/19q co-deletion
B Glioblastoma (Grade IV) — IDH-wildtype
C Medulloblastoma — WNT pathway activation
D Meningioma — NF2 mutation

Click to reveal answer

Q5 PA34.2 1 pt

A 55-year-old woman undergoes craniotomy for a parasagittal mass compressing the brain from outside. Histology shows meningothelial cells arranged in concentric whorls with laminated, concentrically calcified spherical structures. The tumour is well-delineated and does not infiltrate brain parenchyma. What is the diagnosis?

A Schwannoma
B Meningioma
C Glioblastoma
D Oligodendroglioma

Click to reveal answer

Q6 PA34.2 1 pt

Brain biopsy of a frontal lobe tumour in a 35-year-old man shows uniform round nuclei surrounded by clear cytoplasmic halos ('fried-egg' artefact) and a delicate branching vasculature resembling 'chicken wire'. Molecular analysis reveals co-deletion of chromosomes 1p and 19q. What is the diagnosis?

A Astrocytoma, IDH-mutant
B Oligodendroglioma
C Glioblastoma, IDH-wildtype
C Ependymoma

Click to reveal answer

Q7 PA34.2 1 pt

A 7-year-old boy presents with morning headache, vomiting, and ataxia. MRI shows a midline posterior fossa mass filling the 4th ventricle. Histology reveals densely packed small blue cells with hyperchromatic nuclei and scant cytoplasm forming circular arrangements around a central fibrillary core. Which feature and tumour does this BEST describe?

A Flexner-Wintersteiner rosettes — retinoblastoma
B Homer-Wright rosettes — medulloblastoma
C Perivascular pseudorosettes — ependymoma
D True ependymal rosettes — ependymoma

Click to reveal answer

Q8 PA34.2 1 pt

A 30-year-old woman with neurofibromatosis type 2 (NF2) develops hearing loss and tinnitus. MRI reveals a well-circumscribed, enhancing mass at the cerebellopontine angle attached to the vestibulocochlear nerve (CN VIII). Histology shows two alternating patterns: cellular areas with nuclear palisading ('Verocay bodies') and loose myxoid areas. Which tumour is this?

A Meningioma
B Schwannoma (acoustic neuroma)
C Neurofibroma
D Glioblastoma

Click to reveal answer

Q9 PA34.2 1 pt

A 60-year-old woman with known breast carcinoma develops multiple ring-enhancing lesions at the grey-white junction of both cerebral hemispheres. Biopsy of one lesion shows nests of epithelial cells with ductal features surrounded by reactive gliosis. What is the MOST likely diagnosis and key pathological clue?

A Glioblastoma — pseudopalisading necrosis
B Cerebral metastasis — epithelial nests at grey-white junction
C Primary CNS lymphoma — perivascular cuffing of lymphoid cells
D Oligodendroglioma — 1p/19q co-deletion

Click to reveal answer

Q10 PA35.1 1 pt

A 2-year-old girl is brought to the ophthalmologist because her mother noticed a white reflex from the right eye in photographs (leukocoria). Examination under anaesthesia shows a white intraocular mass. Enucleation is performed. Histology reveals small blue cells forming rosettes with a central lumen lined by columnar cells resembling primitive photoreceptors. Which genetic mechanism BEST explains the hereditary form of this tumour?

A Gain-of-function mutation in KRAS oncogene (chromosome 12p)
B Two-hit inactivation of the RB1 tumour suppressor gene (chromosome 13q14)
C TP53 mutation with loss of heterozygosity at chromosome 17p
D NF2 deletion on chromosome 22q

Click to reveal answer

Q11 PA35.1 1 pt

A retinoblastoma patient successfully treated in childhood later develops a painful swelling of the distal femur at age 18. Biopsy of the femoral lesion shows malignant spindle and osteoid-producing cells. Which statement BEST explains this second malignancy?

A Radiation-induced meningioma from prior orbital radiotherapy
B Germline RB1 mutation predisposes to osteosarcoma as a second primary tumour
C Chemotherapy-induced leukaemia due to alkylating agents
D Metastatic spread of the original retinoblastoma via the optic nerve

Click to reveal answer

Q12 PA35.1 1 pt

On histology of an enucleated eye from a 3-year-old, you identify two types of rosettes. Type 1 shows tumour cells arranged around a central LUMEN with no cytoplasmic processes filling it; Type 2 shows cells around a central mass of FIBRILLAR cytoplasmic processes with NO lumen. Which pairing correctly identifies both rosette types and their associated tumours?

A Type 1 = Homer-Wright (medulloblastoma); Type 2 = Flexner-Wintersteiner (retinoblastoma)
B Type 1 = Flexner-Wintersteiner (retinoblastoma); Type 2 = Homer-Wright (medulloblastoma/neuroblastoma)
C Type 1 = Perivascular pseudorosette (ependymoma); Type 2 = Flexner-Wintersteiner (retinoblastoma)
D Type 1 = True ependymal rosette; Type 2 = Homer-Wright (medulloblastoma)

Click to reveal answer