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Step 2 CK · Internal Medicine · Hematology/Oncology

Oncologic Emergencies

When the clock is the diagnosis: act before the scan, before the culture

Hematology/Oncology·General Oncology·4 min read·9 high-yield points·Reviewed by Veli Bakalov, MD @HemeOncBuddy
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The principle: treat first, confirm second

The clock is the diagnosis. In oncologic emergencies the correct first move often comes before definitive imaging or culture results: antibiotics before culture results (febrile neutropenia), dexamethasone before the MRI (cord compression), saline before the bisphosphonate (hypercalcemia), and apheresis before treating the clone (hyperviscosity, leukostasis). Time-to-treatment drives outcome.

First moves in oncologic emergencies
EmergencyRecognizeFirst actionAvoid
Febrile neutropeniaANC <500 plus fever ≥38.3 °CAntipseudomonal β-lactam within 1 hourWaiting for cultures
HypercalcemiaConfusion, dehydration, suppressed PTHAggressive IV isotonic salineLoop diuretics unless overloaded
Cord compressionBack pain plus weakness or a sensory levelIV dexamethasone, then whole-spine MRIDelaying steroids for imaging
Tumor lysisHigh K, phosphate, uric acid; low calciumIV fluids plus rasburicase or allopurinolCalcium for asymptomatic hypocalcemia
Hyperviscosity, leukostasisBleeding, visual change, confusion, hypoxiaPlasmapheresis or leukapheresisRed cell transfusion
Pericardial tamponadeBeck triad, pulsus paradoxusUrgent pericardiocentesisDelaying drainage

Febrile neutropenia

ANC <500or expected to fall below 500 within 48 hours
38.3 °Csingle temperature (or 38.0 °C sustained for 1 hour)
≤60 minto the first antibiotic dose

Occult infection. Neutropenia blunts the usual signs of inflammation (little pus, minimal infiltrate, scant pyuria), so fever may be the only clue. Draw blood cultures, including from any central line, but do not delay treatment. Avoid rectal examinations and rectal temperatures.

Empiric antipseudomonal monotherapy. Give cefepime, piperacillin-tazobactam, or a carbapenem (meropenem) within 60 minutes. Pseudomonas coverage is the non-negotiable core, which is why ceftriaxone is inadequate. Add vancomycin only for suspected line, skin, or soft-tissue infection, hemodynamic instability, pneumonia, or known MRSA. Fever persisting beyond 4–7 days of antibiotics prompts empiric antifungal therapy; carefully selected low-risk patients may be treated as outpatients with oral ciprofloxacin plus amoxicillin-clavulanate.

Metabolic emergencies: hypercalcemia and tumor lysis

Hypercalcemia of malignancy is most often humoral, via PTHrP, and native PTH is low or suppressed, the key contrast with primary hyperparathyroidism. Symptoms are stones, bones, groans, and psychiatric overtones, with a short QT interval and a polyuria-driven dehydration that worsens the hypercalcemia.

Three mechanisms of hypercalcemia of malignancy
MechanismTypical tumorsLabs
Humoral (PTHrP), most commonSquamous cell lung and head and neck, renal, bladderHigh PTHrP, low PTH
OsteolyticMyeloma, breastLow PTH; lytic lesions
1,25-vitamin D productionLymphomaHigh calcitriol, low PTH
  1. IV isotonic salineNow: rehydrates and drives calciuresis.
  2. CalcitoninFast bridge; tachyphylaxis by ~48 hours.
  3. IV bisphosphonateZoledronic acid; durable effect in 2–4 days.
  4. DenosumabIf bisphosphonate-refractory or in renal failure.
Hypercalcemia sequence: saline (now) → calcitonin (bridge) → zoledronate (durable)

Adjuncts. Avoid loop diuretics unless the patient is volume-overloaded. Glucocorticoids help vitamin D–mediated (lymphoma) hypercalcemia, and dialysis is reserved for severe, refractory cases with renal failure.

Tumor lysis syndrome follows treatment of bulky, high-turnover tumors: hyperkalemia, hyperphosphatemia, hyperuricemia, and hypocalcemia (three highs, one low), driving arrhythmia and acute kidney injury. Hydrate hard and give rasburicase (high risk) or allopurinol; check G6PD before rasburicase, which causes hemolysis and methemoglobinemia in G6PD deficiency. Urine alkalinization is no longer recommended. Treat hyperkalemia urgently; give calcium only for symptomatic hypocalcemia or cardiac effects, because calcium given into a high phosphate precipitates. Refractory cases need dialysis.

Compressive emergencies: cord, SVC, and effusions

Malignant epidural spinal cord compression starts with progressive back pain (worse when recumbent or at night), then weakness, a sensory level, and late bowel and bladder dysfunction such as urinary retention. The thoracic spine is most often involved; common primaries are prostate, breast, lung, and myeloma. Ambulatory status at diagnosis predicts the outcome.

  1. Back pain plus weaknessSensory level, urinary retention.
  2. IV dexamethasone nowOn clinical suspicion; do not wait for imaging.
  3. Urgent whole-spine MRIThe gold standard.
  4. Radiation or surgeryRadiation oncology and neurosurgery decompress.
Cord compression order of operations

Do not delay steroids for imaging: neurologic recovery is time-dependent.

Superior vena cava syndrome. Obstruction causes facial, neck, and upper-extremity swelling, plethora, distended neck and chest-wall veins, and dyspnea worse when bending forward. Causes include small cell and squamous lung cancer, non-Hodgkin lymphoma, thymoma, and indwelling-catheter thrombosis. Diagnose with contrast CT and, when the patient is stable, obtain tissue before treating; then treat the cause (radiation or chemotherapy for a tumor; anticoagulation and catheter removal for catheter thrombosis) and stent if severe. Stridor or cerebral edema warrants emergent stenting.

Malignant effusions. Pleural effusions (lung, breast) cause dyspnea and are drained by thoracentesis; recurrence is managed with pleurodesis or an indwelling pleural catheter. Pericardial effusions can produce cardiac tamponade, with Beck triad (hypotension, distended neck veins, muffled heart sounds), pulsus paradoxus, and electrical alternans, requiring urgent pericardiocentesis. Malignant effusions are typically exudative with malignant cytology.

Viscosity emergencies: hyperviscosity and leukostasis

Hyperviscosity syndrome vs leukostasis
FeatureHyperviscosity syndromeLeukostasis
CauseParaprotein, usually IgM from Waldenström (also myeloma)Hyperleukocytosis: blasts >100,000/μL, usually AML
FindingsMucosal bleeding, visual changes (dilated "sausage-link" retinal veins), headache, confusion, vertigoLungs: dyspnea, hypoxia; brain: headache, confusion, visual changes
Urgent treatmentPlasmapheresis to remove the paraprotein, then treat the cloneCytoreduction: leukapheresis, hydroxyurea, induction chemotherapy

Why IgM? Waldenström macroglobulinemia is a lymphoplasmacytic lymphoma secreting pentameric IgM (MYD88 mutation); the large molecule stays in the vessels and thickens the blood.

In both syndromes, transfusing red cells first raises whole-blood viscosity and worsens sludging; remove the protein or cytoreduce instead.