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Created August 13, 2025 15:17
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Fictional Patient History – Oncology Case Study
(All names, dates, and details are fabricated for educational and platform‑testing purposes. This is not real patient data and does not constitute medical advice.)


1. Identifying Information

Item Details
Patient ID ONC‑2025‑0187
Name Ms. Elena M. Alvarez
Age 58 years
Sex Female
Race/Ethnicity Hispanic/Latina
Preferred Language English (primary) / Spanish (secondary)
Occupation School‑age child care provider (full‑time)
Marital Status Married, spouse works as a mechanic
Residence Urban apartment, 2‑bedroom, in a multi‑family building (moderate socioeconomic status)

2. Chief Complaint (CC)

“I’ve been coughing up blood-tinged sputum for the past three weeks and I’ve lost a lot of weight without trying.”


3. History of Present Illness (HPI)

Timeline Symptoms / Findings Pertinent Details
6 months ago Persistent, non‑productive cough; occasional wheeze; mild dyspnea on exertion (climbing two flights of stairs). Attributed to “seasonal allergies”; treated with over‑the‑counter antihistamines; no imaging performed.
3 months ago Increase in cough frequency; occasional nocturnal cough; “raw” sensation in throat; occasional hoarseness. Self‑prescribed cough syrup (dextromethorphan); no relief.
2 months ago First episode of hemoptysis (≈ 5 mL bright red blood mixed with sputum). Prompted ED visit; chest X‑ray reported “possible right upper lobe infiltrate”; discharged with antibiotics for presumed pneumonia.
1 month ago Persistent hemoptysis (now streaks of blood daily, occasional larger episodes up to 10 mL). Weight loss: 12 lb (≈ 5.5 kg) despite unchanged diet; fatigue; decreased appetite; occasional night sweats.
2 weeks ago Progressive dyspnea at rest; mild chest tightness; occasional palpitations. Denies fever, chills, recent travel, or known TB exposure.
Present Ongoing cough with blood-tinged sputum, 3–4 episodes daily; 15‑lb weight loss (total since symptom onset); fatigue; reduced exercise tolerance; occasional dysphagia to solids. No new medications; no recent trauma; no known sick contacts.

4. Past Medical History (PMH)

Condition Details
Hypertension Diagnosed 8 years ago; controlled on lisinopril 10 mg daily.
Hyperlipidemia On atorvastatin 20 mg nightly; LDL last measured 112 mg/dL (2 years prior).
Type 2 Diabetes Mellitus Diagnosed 3 years ago; metformin 500 mg BID; latest HbA1c 6.9 % (6 months ago).
Obstructive Sleep Apnea CPAP use nightly (compliant).
Seasonal Allergic Rhinitis Fluticasone nasal spray PRN.
No prior surgeries No gallbladder, appendectomy, or thoracic surgeries.
Vaccinations Up‑to‑date: influenza (2024), COVID‑19 (boosted 2023), pneumococcal (PCV13 + PPSV23).

5. Family History (FH)

Relation Age / Status Conditions
Mother Deceased at 71 (cardiac arrest) Hypertension, coronary artery disease
Father Alive, 84 Former smoker (30 pack‑years), COPD, died of lung cancer at 78
Sister (younger) 55, alive Breast cancer (diagnosed 2022, lumpectomy + radiation)
Brother 60, alive “Benign” colon polyps (removed 2021)
Paternal grandmother Deceased at 68 Ovarian cancer

Notable: Two first‑degree relatives with malignancies (father – lung cancer, sister – breast cancer) and a paternal grandmother with ovarian cancer suggest possible hereditary predisposition.


6. Social History (SH)

Item Details
Tobacco Never smoker (0 pack‑years).
Alcohol Social drinker: 1–2 glasses of wine on weekends.
Illicit drug use Denies.
Occupational exposures Working in daycare; occasional exposure to cleaning chemicals (bleach, ammonia). No known asbestos, radon, or silica exposure.
Living conditions Lives with husband; nonsmoking household; moderate indoor air quality.
Physical activity Walks 15 minutes daily; limited recently due to dyspnea.
Diet Mixed diet; reports decreased appetite over the past month.
Travel No recent international travel; last trip to Mexico 2 years ago (no known illness).
Support system Strong family support; husband and adult children involved in care.

7. Review of Systems (ROS) – Positive Findings

System Positive Findings
Constitutional Weight loss (15 lb), fatigue, night sweats.
Respiratory Chronic cough with hemoptysis, dyspnea on exertion, occasional wheeze.
Cardiovascular Palpitations (occasional), mild chest tightness.
Gastrointestinal Dysphagia to solids, decreased appetite.
Neurologic No headaches, seizures, or focal deficits.
Skin No new lesions or rashes.
Psychiatric Anxious about diagnosis; occasional low mood related to weight loss.
Other No hematuria, no joint pain.

8. Physical Examination (PE) – Findings (Date: 2025‑08‑08)

Area Findings
General Thin, mildly distressed, alert, oriented ×3.
Vital Signs BP 138/84 mmHg, HR 96 bpm (regular), RR 20/min, Temp 37.2 °C (99 °F), SpO₂ 94 % on room air (improved to 96 % after brief ambulation).
HEENT No cervical lymphadenopathy; oral mucosa pink, no lesions; flexible nasolaryngoscopy (performed in clinic) shows mild edema of the right posterior pharyngeal wall, no mass.
Neck Supple; no jugular venous distention; no palpable thyroid nodules.
Chest/Lungs Decreased breath sounds over right upper zone; scattered crackles over right middle field; occasional wheezes on expiration; no egophony.
Heart Regular rate/rhythm; normal S1, S2; no murmurs or rubs.
Abdomen Soft, non‑tender, no organomegaly; bowel sounds normal.
Extremities No clubbing (Nail beds normal), no edema; peripheral pulses palpable.
Neurologic Cranial nerves II‑XII intact; strength 5/5 in all extremities; sensation intact.
Skin No lesions, bruising, or rashes.

9. Initial Diagnostic Work‑up (ordered in ED & Outpatient)

Test Result / Interpretation
Chest X‑ray (PA & Lateral) Right upper lobe mass (~4 cm), possible cavitation; right hilar prominence.
CT Chest with contrast 4.2 × 3.8 cm spiculated mass in the right upper lobe; mediastinal lymphadenopathy (stations 2R, 4R); no pleural effusion; small right‑sided pulmonary emboli ruled out.
PET‑CT Hypermetabolic right upper lobe lesion (SUVmax 12.5); hypermetabolic mediastinal nodes (SUV 7.8); no distant metastases identified (no adrenal, bone, or brain uptake).
Bronchoscopy with broncho‑alveolar lavage (BAL) & endobronchial biopsies Endobronchial mass visualized; biopsy obtained. BAL negative for acid‑fast bacilli, fungal cultures, and cytology.
Pathology (Core biopsy) Moderately differentiated non‑small cell lung carcinoma (NSCLC), adenocarcinoma subtype; EGFR wild‑type; ALK negative; ROS1 negative; PD‑L1 expression 55 % (22C3 assay).
Molecular profiling No targetable mutations (KRAS G12C negative, BRAF V600E negative, MET exon 14 skipping negative).
Complete blood count (CBC) WBC 7.8 ×10⁹/L, Hb 11.2 g/dL (normocytic), Platelets 210 ×10⁹/L.
Comprehensive metabolic panel (CMP) Normal renal and hepatic function; glucose 118 mg/dL (fasting).
LDH 190 U/L (slightly elevated).
Baseline pulmonary function tests (PFTs) FEV1 78 % predicted; FVC 85 % predicted; DLCO 72 % predicted — acceptable for systemic therapy.
Echocardiogram LVEF 60 %; no wall motion abnormalities.
Brain MRI No intracranial lesions.
Baseline performance status ECOG 2 (ambulatory, capable of self‑care but unable to carry out any work activities).

10. Staging (AJCC 8th Edition)

Parameter Value
Primary tumor (T) T2a – tumor >3 cm but ≤5 cm in greatest dimension, without invasion of the visceral pleura.
Regional nodes (N) N2 – metastasis in ipsilateral mediastinal and/or subcarinal lymph nodes.
Distant metastasis (M) M0 – no distant spread identified.
Overall Stage Stage IIIA (T2a N2 M0).

11. Initial Management Plan (as of 2025‑08‑12)

Component Details
Multidisciplinary Tumor Board Review Thoracic surgery, medical oncology, radiation oncology, pulmonology, radiology, pathology, palliative care, and genetics.
Systemic Therapy Chemo‑immunotherapy per current guideline (e.g., carboplatin + paclitaxel plus pembrolizumab) given PD‑L1 ≥50 % and lack of targetable driver mutation.
Radiation Oncology Consider definitive concurrent chemoradiation (60 Gy in 30 fractions) if surgical resection deemed non‑feasible; evaluate for consolidative radiation after systemic therapy response.
Surgical Evaluation Mediastinoscopy/EBUS‑TBNA to confirm N2 disease; assess surgical candidacy for lobectomy (right upper lobectomy) after neoadjuvant therapy.
Supportive Care • Smoking cessation reinforcement (patient already a never smoker). • Nutritional counseling (high‑calorie, protein‑rich diet). • Pain management (acetaminophen PRN, low‑dose opioids if needed). • Pulmonary rehabilitation referral.
Genetic Counseling Due to family history of multiple cancers, offer germline testing (e.g., BRCA1/2, TP53, ATM) and discuss eligibility for clinical trials.
Follow‑up Repeat PET‑CT after 4–6 cycles of systemic therapy to reassess response and restage.
Clinical Trials Screening for enrollment in trials evaluating novel immunotherapy combinations or adjuvant targeted agents (e.g., KRAS G12C inhibitors, even though mutation negative, trial may explore other pathways).
Patient Education Discuss disease nature, treatment options, potential side effects (immune‑related adverse events, neuropathy, myelosuppression), and goals of care. Provide written material in English and Spanish.
Advance Care Planning Initiate conversation about preferences, document POLST if appropriate, involve palliative care early for symptom management.

12. Teaching Points & Learning Objectives

  1. Differential Diagnosis of Chronic Hemoptysis – Importance of early imaging in persistent cough, especially with blood‑tinged sputum.
  2. Staging of NSCLC – How T, N, M components directly influence therapeutic pathways (surgery vs. concurrent chemoradiation).
  3. Molecular Testing – Routine pan‑cancer NGS panels guide targeted therapy selection; PD‑L1 expression informs immunotherapy eligibility.
  4. Multidisciplinary Care – Coordinating thoracic surgery, oncology, radiation, and supportive services improves outcomes and reduces delays.
  5. Family History & Hereditary Cancer Syndromes – Recognizing potential hereditary predisposition (e.g., BRCA, TP53) and the role of germline testing.
  6. Management of Treatment‑Related Toxicities – Monitoring for immune‑related adverse events (colitis, pneumonitis) and providing prompt intervention.
  7. Psychosocial Support – Addressing anxiety, nutritional deficits, and providing culturally sensitive education (bilingual resources).

13. Disclaimer

The above case is a fully fictional construct intended solely for educational, training, or platform‑testing purposes. It does not represent a real patient. Clinical decisions should always be individualized and made in consultation with qualified health‑care professionals.

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