Case studies · Psychiatry · 26 October 2026

Schizophrenia case study

The case

Patient: A 22‑year‑old male, college student, unmarried, living in a shared hostel.

Presenting complaint: “I hear voices telling me to do things” – duration 6 months.

History of presenting illness:

Past psychiatric history: None documented. No prior psychiatric treatment.

Medical history: Unremarkable. No known chronic illnesses.

Family history: Mother has a history of major depressive disorder; paternal uncle diagnosed with schizophrenia.

Substance use: Occasional cannabis use (≈1 joint/week) for the past 2 years; denies alcohol, tobacco, or other illicit drugs.

Social history: Lives in a hostel, attends engineering college, average academic performance before symptom onset.

Review of systems: No headache, fever, weight loss, or seizures. No recent infections or trauma.

Examination

Parameter Finding
General Thin, appears apathetic, poor eye contact
Vital signs BP 118/76 mm Hg, HR 78 bpm, RR 14 /min, Temp 36.8 °C, SpO₂ 98 % on room air
Mental status exam • Appearance: Disheveled, unkempt<br>• Behavior: Cooperative but mildly psychomotor retardation<br>• Speech: Low volume, occasional poverty of speech<br>• Mood: “I feel empty” (subjective), affect blunted<br>• Thought process: Disorganized, loose associations<br>• Thought content: Auditory hallucinations, delusions of persecution and reference<br>• Perception: Visual hallucinations present<br>• Cognition: MMSE 24/30 (orientation intact, 2‑point recall deficit, impaired attention)<br>• Insight: Poor (denies illness)
Neurological No focal deficits, normal gait, reflexes 2+ bilaterally
Other systems Unremarkable

Initial investigations

Test Result Units / Reference
CBC Hb 13.2 g/dL; WBC 7.8 ×10⁹/L; Platelets 240 ×10⁹/L Normal
Serum electrolytes Na 138 mmol/L; K 4.2 mmol/L; Cl 102 mmol/L; HCO₃⁻ 24 mmol/L Normal
Fasting glucose 92 mg/dL Normal
Liver function AST 22 U/L; ALT 18 U/L; Bilirubin 0.8 mg/dL Normal
Renal function Creatinine 0.9 mg/dL; BUN 12 mg/dL Normal
Thyroid profile TSH 2.1 µIU/mL; Free T4 1.1 ng/dL Normal
Serum calcium, magnesium Within normal limits
Urine drug screen Positive for THC (cannabis) only
HIV, VDRL Non‑reactive
MRI brain (non‑contrast) No focal lesions, normal ventricles, no demyelination
EEG Normal background activity, no epileptiform discharges
Serum vitamin B12 420 pg/mL (normal)
Urine routine Normal

The patient is admitted to the psychiatry ward for further evaluation and management.


Questions

  1. What is the most likely diagnosis?
  2. Which clinical findings in the history and examination point toward this diagnosis, and why are alternative diagnoses less likely?
  3. List the essential investigations that should be performed to confirm the diagnosis and rule out mimics, and explain the relevance of each.
  4. Outline a comprehensive management plan (pharmacological and non‑pharmacological) for this patient, including acute, stabilization, and maintenance phases.
  5. Discuss the potential short‑ and long‑term complications of the illness and its treatment, and strategies to monitor and prevent them.

Answers

1. Diagnosis

Schizophrenia, chronic type (DSM‑5‑TR 2022 criteria).

The diagnosis aligns with the International Classification of Diseases, 11th Revision (ICD‑11, 2022) “Schizophrenia spectrum disorder”.

2. Clinical findings supporting the diagnosis

Finding Reason it supports schizophrenia Why alternatives are less likely
Auditory & visual hallucinations lasting > 6 months Core positive symptom; persistent > 1 month is required for schizophrenia. Hallucinations due to substance‑induced psychosis usually resolve within weeks of abstinence; the patient’s cannabis use is low‑frequency and does not explain chronicity.
Delusions of reference & persecution Typical first‑rank symptoms (Jaspers) strongly associated with schizophrenia. Delusional disorder would have non‑bizarre delusions without hallucinations and without marked functional decline.
Negative symptoms (blunted affect, avolition) Negative domain is characteristic of schizophrenia and predicts poorer functional outcome. Major depressive disorder can cause anhedonia, but would also have pervasive low mood, guilt, and suicidal ideation, which are absent.
Cognitive impairment (MMSE 24/30) Cognitive deficits are a core feature of schizophrenia, especially in attention and working memory. Dementia is unlikely at age 22; neurocognitive disorders present with progressive decline and often memory‑dominant deficits.
Family history of schizophrenia Increases genetic liability (≈10 % concordance in first‑degree relatives). Family history of mood disorders would raise suspicion for bipolar disorder with psychotic features, but the mood symptoms are not prominent.
Absence of mood elevation or depressive episodes Rules out bipolar or major depressive disorder with psychotic features. Mood‑congruent psychosis would show clear mood episodes, which are not reported.
Normal neuroimaging & labs Excludes organic causes (e.g., temporal lobe epilepsy, brain tumour). Substance‑induced psychosis would often have a temporal relationship with intoxication/withdrawal; the patient’s cannabis use is low‑dose and chronic, not acute.

3. Essential investigations

Investigation Purpose Expected/normal result in schizophrenia
Complete blood count, electrolytes, renal & liver panels Baseline before antipsychotic initiation; detect metabolic derangements that may be worsened by medication. Typically normal; any abnormality would prompt treatment modification.
Thyroid function tests Thyroid dysfunction can mimic psychosis (e.g., hyperthyroidism). Normal in this case, ruling out thyroid‑related psychosis.
Urine drug screen Exclude substance‑induced psychosis (e.g., amphetamines, cocaine). Positive for THC only; low‑dose cannabis rarely causes chronic psychosis, but it is documented as a risk factor.
Serology for HIV, syphilis (VDRL) Infections can present with neuropsychiatric symptoms. Negative, excluding these mimics.
MRI brain (or CT if MRI unavailable) Detect structural lesions (tumour, demyelination, vascular insult). Normal; supports primary psychiatric etiology.
EEG Rule out seizure‑related psychosis (e.g., temporal lobe epilepsy). Normal background; no epileptiform activity.
Vitamin B12, folate Deficiencies can cause neuropsychiatric manifestations. Normal; deficiency unlikely.
Pregnancy test (if female) – not applicable here.
Baseline metabolic panel for antipsychotic monitoring (fasting glucose, lipid profile) Many atypical antipsychotics cause metabolic syndrome; baseline needed for future comparison. Not yet performed; should be ordered before starting medication.

These investigations satisfy the NICE Clinical Guideline NG221 (2023) for psychosis and schizophrenia which recommends a minimum “basic screen” plus targeted tests based on clinical suspicion.

4. Comprehensive management plan

A. Acute phase (first 2–4 weeks)

  1. Pharmacotherapy

    • First‑generation antipsychotic (FGA): Haloperidol 2–5 mg PO BID, titrate to 10 mg/day as needed, monitoring extrapyramidal symptoms (EPS).
    • Or second‑generation antipsychotic (SGA) – preferred per NICE 2023: Risperidone 2 mg PO daily, titrate to 4–6 mg/day.
    • Rationale: SGAs have lower EPS risk and treat both positive and negative symptoms. Risperidone has robust evidence in young adults.
    • Baseline metabolic monitoring: Fasting glucose, lipid profile, weight, waist circumference.
  2. Adjunctive medication

    • Benztropine 1 mg PO BID if EPS develop (e.g., parkinsonism).
    • Low‑dose lorazepam 0.5 mg PO q6h PRN for severe agitation, not exceeding 2 mg/day.
  3. Non‑pharmacological

    • Safe environment: Remove potential self‑harm objects, ensure 1‑to‑1 observation if risk of acting on command hallucinations.
    • Psychoeducation: Brief session with patient and family about illness, medication, and expected course.
    • Sleep hygiene & regular meals to stabilize circadian rhythm.

B. Stabilization phase (weeks 4–12)

  1. Medication optimization

    • Aim for the lowest effective dose; switch to an SGA with favorable metabolic profile (e.g., aripiprazole 10–15 mg daily) if weight gain or hyperglycemia emerges.
    • Therapeutic drug monitoring (plasma levels) is optional for clozapine but not for risperidone/haloperidol.
  2. Psychosocial interventions

    • Cognitive‑behavioral therapy for psychosis (CBTp): 12‑weekly sessions focusing on reality testing of hallucinations and coping strategies.
    • Supported employment / educational assistance: Liaise with college disability services to arrange a reduced workload and tutoring.
  3. Family interventions

    • Family psychoeducation (6–8 sessions) to improve expressed emotion, reduce relapse risk (per McFarlane model, 2022).
  4. Physical health monitoring (every 4 weeks)

    • Weight, BMI, fasting glucose, lipid panel, blood pressure.

C. Maintenance/long‑term phase (≥12 weeks)

  1. Continuation of antipsychotic at the maintenance dose (usually 50–75 % of the acute dose).

  2. Relapse‑prevention strategies

    • Adherence support: Pill boxes, SMS reminders, depot formulation (e.g., Risperidone long‑acting injection 25 mg IM every 2 weeks) if oral adherence is poor.
    • Regular follow‑up: Every 3 months for the first year, then 6 monthly if stable.
  3. Rehabilitation

    • Social skills training, vocational rehabilitation, and peer‑support groups.
  4. Monitoring for treatment‑emergent side effects

    • EPS: Use the Simpson‑Angus Scale; treat with anticholinergics or switch to a lower‑risk SGA.
    • Metabolic syndrome: Follow American Diabetes Association (ADA) 2023 criteria – weight gain ≥5 % of baseline, fasting glucose ≥100 mg/dL, triglycerides ≥150 mg/dL, HDL‑C <40 mg/dL (men).
  5. Consideration of clozapine

    • Indicated if treatment‑resistant schizophrenia (failure of ≥2 antipsychotics at adequate doses for ≥6 weeks).
    • Baseline ANC ≥1500 cells/µL, then weekly for first 6 months, bi‑weekly for next 6 months, then monthly.

5. Complications and prevention

Complication Short‑term risk Long‑term risk Monitoring / Prevention
Suicide Elevated during acute psychosis, especially with command hallucinations. Persistent risk, especially with depressive features. Columbia‑Suicide Severity Rating Scale (C‑SSRS) at each visit; safety plan; crisis hotline.
Medication‑induced EPS Acute dystonia (hours‑days), akathisia (days‑weeks). Tardive dyskinesia (months‑years). Use Simpson‑Angus and Abnormal Involuntary Movement Scale (AIMS); prefer SGAs; consider dose reduction or switch.
Metabolic syndrome Weight gain, hyperglycemia within weeks of SGA initiation. Diabetes mellitus, cardiovascular disease. Baseline & periodic labs; lifestyle counseling; consider metformin if BMI ≥ 30 kg/m² and glucose ↑.
Substance‑use relapse Cannabis may exacerbate psychosis. Dual diagnosis worsens prognosis. Motivational interviewing; referral to addiction services.
Social/occupational decline Poor school attendance, isolation. Chronic disability, homelessness. Early vocational rehab, supported housing programs.
Clozapine‑induced agranulocytosis (if used) Neutropenia within first 6 months. Life‑threatening infection. Strict ANC monitoring per Clozapine REMS (2022).
Legal/forensic issues Acting on command hallucinations may lead to aggression. Criminal charges, incarceration. Risk assessment, involuntary hospitalization if dangerous, liaison with legal services.

Key learning points


Practice MCQs

1. A 22‑year‑old man presents with auditory hallucinations for 7 months, delusions of persecution, and marked social withdrawal. Which of the following is the most appropriate next step in management?

A. Start high‑dose haloperidol (20 mg/day) immediately.
B. Order a full metabolic panel, thyroid function, and urine

Practise cases like this one

Get a new patient case, answer the examiner's questions by voice or text, and get marked — free.

Try a case on MEDOST

More in Psychiatry

Bipolar disorder – diagnosis and managementSchizophrenia – Diagnostic Criteria & Management

The patient is invented for teaching. AI-assisted study material for exam revision. Always confirm with standard textbooks and current guidelines; not medical advice.