Oncologic Emergencies Flashcards

1
Q

Hypercalcemia

Path:

S/Sx:

Dx:

Tx:

A

Hypercalcemia

Path:

  • Humoral vs. local osteolysis
  • Majority: squamous cell ca -> increased PTHrP -> Humoral hypercalcemia of malignancy

S/Sx:

  • Acute pancreatitis, acute renal insufficiency, nephrolithiasis
  • Less common: short QT, ST elevation, MI-like, AMS

Dx:

  • PTH and PTHrP
  • Chem panel + Mg, Phos
  • ECG

Tx:

  • Mild-Mod: No urgent tx, avoid increased Ca by increasing hydration, minimizing thiazides, lithium, and bedrest
  • Severe:
    • Hydrate NS 200-300cc/h and maintain UO at 100-150cc/h
    • Block Ca reabsorption: calcitonin 4 IU/kg, recheck Ca
      • If persistently high continue calcitonin every 6-12h
      • Add bisphosphonate/Zoledronic acid/pamidronate
    • Dialysis if Ca > 18-20 with (+) Neuro symptoms
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2
Q

Tumor Lysis Syndrome

Path:

S/Sx:

Dx:

Tx:

A

Tumor Lysis Syndrome

Path:

  • Tumor cells die -> renal tubular damage -> electrolyte abnormalities
  • More common in heme malignancy or large solid tumor burden
  • High LDH and bone marrow involvement lead to higher risk

S/Sx:

  • HYPERphosphatemia and HYPOcalcemia
  • AKI, hyperkalemia, hyperuricemia
  • Arrythmia, seizure, death

Dx:

  • Chem panel: phos, ca, K, uric acid
  • ECG
  • Cairo-Bishop score = 0-5

Tx:

  • All: Prevent AKI with hydration pre-, intra-, and post-chemotherapy
  • Mod risk: Ppx allopurinol to decrease xanthines
  • High risk: Rasburicase IV
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3
Q

SIADH

Path:

S/Sx:

Dx:

Tx:

A

SIADH

Path: Tumor (sclc primarily) -> ectopic ADH over-production

S/Sx:

  • H2O retention with decreased UO
  • HYPOnatremia and HYPOosmolality
  • AMS, somnolence, weakness

Dx:

  • Low serum osmolality: Hyponatremia + Hypo-osmolality
  • High urine osmolality: Urine Osm > 100 + Urine Na > 40
    • Concentrated; Low UO
  • Normal K, normal pH
  • Low serum uric acid

Tx:

  • Severe / symptomatic:
    • Hypertonic Saline
    • Do NOT correct more than 8-12 mEq in 24h
  • Fluid restriction, salt tablets
  • Loop diuretic vs vasopressin –> reabsorb sodium
  • Tx underlying cancer
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4
Q

Lambert Eaton Myasthenic Syndrome

Path:

S/Sx:

Dx:

Tx:

A

Lambert Eaton Myasthenic Syndrome

Path:

  • Autoimmune Ab block calcium channel -> decreased acetylcholine available at synapse
  • SCLC and some Hodgkin lymphoma are most common underlying cancers

S/Sx:

  • Limb weakness (slow, proximal, progressive)
  • Dry mouth, oropharyngeal weakness, ptosis
  • Hyporeflexia +/- severe weakness +/- neuromsk respiratory failure

Dx:

  • Autoantibodies against Ca channels
  • CT chest to look for SCLC

Tx:

  • Amifampridine 15-30mg divided into 3-4 doses daily
  • Pyridostigmine​
  • IVIG 2g/kg over 2-5d
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5
Q

Adverse effects of Radiation Therapy

Oropharyngeal:

GI:

Neurologic:

Dermatologic:

Chronic:

A

Adverse effects of Radiation Therapy

Oropharyngeal:

  • Dental caries, decreased saliva
  • Mucositis in 1st week: caked yeast overgrowth -> pain
  • Loss of taste 2nd week: dry mouth contributes; anorexia/weight loss ensues

GI:

  • Enteritis / proctitis: common in intestinal and pelvic cancers
  • Acute: fever, abd cramp, anorexia, N/V, tenesmus, urgency, diarrhea, incontinence, hematochezia
    • Tx: analgesics, antispasmodics, antidiarrheals, supportive IV hydration
  • Chronic: Endarteritis obliterans (ischemia), progressive worsening, fistula development
    • Tx: diet, supportive, CPN, surgical resection/repair if fistula develops

Neurologic:

  • Acute encephalopathy (responsive to steroids)

Dermatologic:

  • Erythema, increased melanin
  • Decreased sweat gland function
  • Increased sensitivity
  • Hair loss

Chronic:

  • Delayed wound healing
  • Dry eyes
  • Radiation necrosis
  • Tissue fibrosis, lymphedema
  • Diffuse cerebral atrophy (decades s/p treatment)
  • Personality/cognitive/gait changes
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6
Q

Colorectal Cancer

Epi:

Risks:

Screening:

S/Sx:

Dx:

Tx:

A

Colorectal Cancer

Epi: 2nd leading cause ca death, 95% are adenocarcinomas

Risks: Age > 60; IBD; AA; Male; Hx cancer; Diet; Family Hx

Screening:

  • High Risk: <50 years old, colo q5y
    • PMHx adenoma, serrated polyps, colon ca, IBD, genetic syndrome
    • FHx 1st degree relative with adenoma or colorectal cancer
    • FHx 2nd degree relative with hx colorectal cancer
  • Medium Risk: 50 years old
    • Fecal occult blood yearly; FIT yearly; FIT-DNA 1-3y
    • Flex-sig q5y, or q10y with yearly FIT
    • Colo q10 years
  • >76 years old: Individualized; >85 years old: Do not screen

S/Sx:

  • Fatigue, weight loss, nausea, anorexia
  • Change in bowels, discharge, bloating, pain, straining
  • Melanic/bloody stool, iron deficiency anemia
  • Palpable abd or rectal mass
  • Jaundice with liver mets

Dx:

  • Gold Standard: Colonoscopy with biopsy
  • CBC (anemia), Chem (post renal AKI), LFTs (liver mets)
  • CT AP with IV and PO contrast
  • Carcinoembryonic antigen (CEA) aids in prognosis
  • CT guided needle biopsy
  • Metastatic
    • PET, MRI, bone scan
    • Oncogenes: RAS, BRAF (poor prognosis, no benefit from tx)
  • Tumor molecular testing: epidural growth factor receptor (tyrosine kinase receptor target for tx)

Tx:

  • Stage 0, I, IIa
    • Surgery: resection and surveillance with or without adjuvant therapy
    • Colectomy +/- removal of nearby lymph nodes may be needed in Stg II
  • Stage III
    • Partial colectomy + lymph removal AND…
    • Chemo: determined by EGFR, KRAS, BRAF
      • First line: Flouroucacil + Oxiplatin, irinotecan, leucovorin
      • Second line: Capecitabine, trifluridine, tipiracil
    • XRT: used as adjunct in stage IIb or III along with chemo and used in rectal cancer to limit metastasis
  • Stage IV
    • Targeted monoclonal Ab therapy if mets or non-resectable tumor
      • Bevacizumab, cetuximab, panitumumab, regorfenib
    • Immune Tx for advanced dz, mets
      • Checkpoint inhibitors (Nivolumab, pemrolizumab)
  • Follow Up
    • Physical exam q3 months for 3 years, then q6 months for year 4-5
    • CEA q3mo for 3y
    • Chest CT yearly for 3y
    • CT abd yearly for 3y
    • Colo at 1 year then q5 years
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7
Q

Breast Cancer

Epi:

S/Sx:

Dx:

Tx:

A

Breast Cancer

Epi:

  • Most common Ca in females (other than skin); 12% of US women; nonmet>met
  • Risks: Age >50, Hx cancer, nulliparity, late 1st pregnancy, early menarche, late menopause, dense breast, hx radiation, FHx
  • Type 1: HER2 (-) and Hormone Receptor (+)
  • Type 2: HER2 (+) and Hormone Receptor (+) or (-)
  • Familial: 10% d/t mutation in p53, BRCA1, or BRCA2 tumor suppressor genes

S/Sx:

  • Palpable, hard, painful breast or axilla lump; focal inflammation
  • 60% are in Upper Outer quadrant
  • Nipple discharge (unilateral and bloody)
  • Change in breast size/shape; skin dimpling, new nipple inversion, ulceration

Dx:

  • Screen: >40 or >50 q2y, controversial
  • Clinical exam sitting and supine
    • Lump is hard, irregular, assymmetrical, fixed to skin/muscle
  • Imaging: Bilateral mammogram -> Biopsy (core)
    • Vs. MRI for high risk Vs. ultrasound +/- biopsy for < 30y/o
    • Pulm Sx: Chest CT w/ contrast
    • Abd Sx: A/P CT w/ contrast
    • Bone pain or elevated alk phos: Bone scan
  • Molecular testing: HER2/neu gene mutation over expression a/w aggressive tumors
  • Labs: CBC, CMP, LFTs, Alk Phos

Tx:

  • Local/Non-Metastatic:
    • Lumpectomy + XRT + axillary LN dissection (if +sentinel LN bx) works as well as mastectomy
    • +/- Neoadjuvant (preop) treatment (anthracycline plus taxane +/- XRT)
      • Also for systemic tx
    • Targeted:
      • HER2+ add HER/neu protein with trastuzumab and lapatinib
      • HR+ add target progesterone/estrogen (better prognosis than HR -)
  • Advanced/Mets:
    • Palliative surgery and XRT
    • Systemic tx with endocrine tx, chemo, and/or targeted tx based on HR, HER2, PDL1, BRCA, comorbidites, severity
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8
Q

Lung Cancer

Epi:

Screening:

S/Sx:

Dx:

Tx:

A

Lung Cancer

Epi:

  • Central: Small Cell Carcinoma (10%), Squamous Cell Carcinoma
  • Peripheral: NSC Carcinoma (90%) (adenocarcinoma, large cell, bronchoalveolar)
  • Males: 1st cancer deaths; Female: 2nd cancer death

Screening:

  • CXR NOT sensitive screening tool
  • Age 55-80, 30pk year hx, quit <15y: Low Dose CT Chest q3 years
  • High risk (age, educ, COPD, CXR, smoking): PLCO2 plus Annual CT Chest

S/Sx:

  • 25% Asymptomatic with peripheral tumor; dx s/p metastastic lesion
  • Nonspecific: dyspnea; pain in chest, ribs, back, pelvis; anorexia, weight loss
  • Specific: Cough, hoarse, recurrent laryngeal nerve, hemoptysis
    • Central location: atelectasis and SVC syndrome
    • Evasion: pleural effusion
    • Paraneoplastic syndrome: SIADH, hypercalcemia, hypercoagulable state
    • Apiceal: Horner’s syndrome (T1 nerve damage) causing unilateral miosis, ptosis, facial anhidrosis
    • Pancoast: Apical tumor with brachial plexus and sympathetic ganglion involvement -> pain, paresthesias, arm weakness

Dx:

  • CXR: compare to priors
  • Definitive: BIOPSY
  • Sputum cytology: high Sp, low Se (better for central tumor)
  • Bronchoscopy, percutaneous needle bx, pleural fluid analysis
  • VATS
  • PET: High Se, moderate Se
  • Molecular testing: mutatious analysis guides therapy
    • EGFR, ALK, ROS, PDL1

Tx:

  • Guided by cell type, comorbidity, lung function
  • Refer to onc, IR, pal care, surg
  • SCC: 1 lung + ipsilateral LN
    • Definitive surgery (wedge resection vs lobectomy)
    • Chemo (cisplatin vs carboplatin)
    • Survival: 8-12wks untreated; Ch/XRT: 5yr 10-15%
  • SCC: BL lung +/- BL LN vs distant mets
    • Chemo: cisplatin or carboplatin AND etoposide
    • +/- radiation
    • Survival: 5y 1-2%
  • NSCC:
    • Surgery: definitive if early / slow spread
    • Resection + chemo: advanced
  • Staging
    • 1: tracheal/bronchial lining: surgery and XRT
    • 2: invading parenchyma: surgery and XRT
    • 3a: LN involvement: surg, chemo, XRT, brachytx
    • 3b: Widespread lung dz nonresectable: brachytx, chemo, xrt, palliative
    • 4: Lung ca and mets: pal chemo
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9
Q

Chemo Induced Complications

Cardiomyopathy

Pulmonary

Neurological

Secondary Cancers

A

Chemo Induced Complications

Cardiomyopathy:

  • Patho: Damages myocytes -> CHF, LV dysf
  • CTX: Anthracycline agents (Doxorubicin)
  • Dx: Monitor LV ejection fraction serially
  • Tx: ACEIs, carvedilol, antioxidants (Vit E)

Pulmonary

  • Patho: Pulmonary fibrosis, esp in older smoker with renal failure
  • CTX: Amrubicin, bleomycin, carmustine
  • Dx: Monitor serial PFTs
  • Tx: D/c agent, admin oral/IV corticosteroids (short term benefit)

Neurological

  • Patho: Peripheral Neuropathy (glove and stocking) d/t mitrochondrial toxicity or nerve inflammation
    • Common, up to 60% of chemo patients
    • Decreased proprioception leads to falls
  • CTX: Plantinum (cisplatin, oxaliplatin), taxanes, vinca alkaloids
  • Dx: Clinical
  • Tx: Duloxetine, Venlafaxine; Ø Gabapentinoids (ineffective)

Secondary Cancers

  • Patho: Chemo increases risk for secondary cancer 5-10 years later
  • CTX: Non-Hodgkins Lymphoma treatment increases risk for AML and Myeloma
  • Dx: Monitor labs periodically
  • Tx: Guideline based
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10
Q

Neutropenic Fever

Path:

Time course:

S/Sx:

Dx:

Tx:

A

Neutropenic Fever

Path:

  • Chemo -> bone marrow suppression -> decreases ALL hemopoetic lineages -> ANC under 500 (or expected to drop in next 24h) -> Fever
  • Or, malignancy renders neutrophils ineffective (functional neutropenia)

Time course: 7-14d post chemotherapy

S/Sx:

  • Lesions, rash, bruising of skin, perineum, anus
  • Hot, red, swollen joint with msk pain

Dx:

  • Fever >38.3oC plus ANC <500
  • CBC w/ diff; chem panel; LFTs; UA; lactic acid; CRP; blood cultures

Tx:

  • Low Risk: Neutropenia <7d, no comorbidities, normal CXR, adequate social support, easy access to hospital
    • Outpt abx and f/u in 72h
  • High Risk: Neutropenia >7d, ANC < 100 following chemo, acute comorbidities (HoTN, AMS, PNA, Abd pain)
    • Hospitalize
    • Begin empiric broad spectrum abx
  • Antibiotics
    • High risk + clinically well: B-Lactam with PsA coverage
    • High risk + clinically sick: Add aminoglycoside vs. FQ for double gram neg coverage
    • Suspicion for Gram Pos: Add Vanco
    • Persistent fever s/p broad spectrum: Add Antifungal (ampho B, caspo, itra, vori)
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11
Q

DIC of Malignancy

Path:

S/Sx:

Dx:

Tx:

A

DIC of Malignancy

Path:

  • Leukemia (APL > AML > ALL) > Adenocarcinomas
  • Gradual coagulation activation with chronic consumption of factors and platelets

S/Sx:

  • VTE common
  • Less fulminant than DIC of sepsis/trauma

Dx:

  • Normal coags initially, then progressive decrease in platelets and fibrinogen, with increased INR

Tx:

  • Treat underlying malignancy
  • APL: initiate chemo within 24h
  • Admin blood, cryo, FFP, platelets
  • Consider Vena Cava filter
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12
Q

Hyperleukocytosis / Leukostasis

Path:

S/Sx:

Dx:

Tx:

A

Hyperleukocytosis / Leukostasis

Path:

  • Acute leukoemias (especially AML) -> severe leukocytosis -> hyperviscosity
  • Can lead to microvascular obstruction, vessel wall rupture, bleeding, hypoxia

S/Sx:

  • CNS: HA, dizziness, decreased LOC, focal deficit, ICH
  • Opth: Blurry vision, blindness, papilledema, retinal hemorrhage and thrombosis
  • Pulm: Dyspnea, tachypnea, hypoxia, crackles, pulmonary infiltration, respiratory failure
  • CV: MI, ischemia
  • Other: Fever, renal failure, priapism, VTE, DIC, tumor lysis syndrome

Dx:

  • WBC as high as 100 x 109

Tx:

  • Leukapheresis
  • Hydroxyurea: prevents rapid reaccumulation of blasts during treatment
  • Caution with RBC transfusion -> worsen viscosity
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13
Q

Hypercoagulability of Malignancy

Path:

S/Sx:

Dx:

Tx:

A

Hypercoagulability of Malignancy

Path:

  • All cancer (esp GI, pancreatic, ovarian, and lung) -> prothrombotic / fibrinolytic tumor cell proteins and cytokines -> host cell inflammatory response -> prothrombotic state

S/Sx:

  • Unilateral leg swelling
  • Chest pain, dyspnea, tachycardia, hemoptysis

Dx:

  • Coags, Ultrasound, clinical suspicion

Tx:

  • LMWH then transition to PO warfarin vs. DOAC
  • Emotional support
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14
Q

Typhlitis

Path:

S/Sx:

Dx:

Tx:

A

Typhlitis

Path:

  • Heme malignancy vs. chemo -> neutropenic and necrotizing enterocolitis
  • Leads to acute, life threatening infection of intestine, cecum, ileocecum

S/Sx:

  • Fever with abdominal pain in a neutropenic / immunosuppressed patient
    • Especially 3wks s/p chemo
  • N/V, liquid bloody stools, distended abd
  • Acute abdomen (firm, guarding, rebound tenderness) = bowel perforation

Dx:

  • Suspect bowel perf -> CT: Mesenteric stranding with wall thickening, dilated bowel, and free air in abdomen

Tx:

  • Free air, GIB -> surgery (high mortality d/t low platelets)
  • No peritoneal signs -> abx and bowel rest with NGT
    • Will be treating polymicrobial infection
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15
Q

Engraftment

Path:

S/Sx:

Dx:

Tx:

A

Engraftment

Path:

  • Autologous stem cell transplant (moreso than allogenic) -> release of cytokines -> sepsis-like reaction 1-2wks s/p txp

S/Sx:

  • Fever of unknown origin
  • May be indistinguishable from sepsis until s/p (-) cultures (or autopsy)
  • Mimics GVHD: palmar rash, non-cardiogenic pulmonary edema with hypoxia, weight gain, diarrhea

Dx:

  • (-) cultures with classic symptom cluster
    • Fever, total body erythema, respiratory distress, AKI, transaminitis, GIB, hematuria

Tx:

  • Supportive care, IV fluids
  • Presume sepsis initially
  • APAP and benadryl
  • IV corticosteroids
  • MV and CRRT prn
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16
Q

ALL: Acute Lymphocytic Leukemia

Path:

Epi:

S/Sx:

Dx:

Tx:

A

ALL: Acute Lymphocytic Leukemia

Path: ABnormal overproduction from the lymphocyte lineage

Epi: 80% young children; poor prognosis in adults; increases risk for brain tumor

S/Sx:

  • Constitutional cancer symptoms
  • Bone pain
  • Chest pain, SOB
  • Bleeding, hepatosplenomegaly, generalized lymphadenopathy

Dx:

  • 1st get Smear: pancytopenia with blasts
  • Marrow: 30% Blast Cells, (+) cALLa, (+) TdT, (+) periodic Acid-Schiff
  • Anemia and thrombocytopenia
  • Hyperuricemia, azotemia
  • Consider cytogenetic studies, chromosome analysis, LP screen for brain mets

Tx:

  • Heme/onc consult
  • Chemo: Combo plus TK1
  • Ppx CNS ARA-C
  • Supportive: hydration, transfusion, abx
  • Allopurinol 100-200mg TID prior to chemo
  • Acetazolamide 500mg to alkalinize urine
  • Dialysis prior to chemo if persistently uremic
17
Q

AML: Acute Myelocytic Leukemia

Path:

Epi:

S/Sx:

Dx:

Tx:

A

AML: Acute Myelocytic Leukemia

Path: Abnormal overproduction from myelocyte (neutrophil) lineage OR chemo related

Epi: >60yo with increased risk as age increases; Benzene/Radiation exposure

S/Sx:

  • Constitutional cancer symptoms
  • Bleeding: bruising, petechiae, gingival, epistaxis, increased risk for DIC

Dx:

  • CBC smear: Pancytopenia with blast cells
  • Marrow: Sudan Black (+), myeloperoxicase (+)
  • CMP: HYPERkalemia, HYPERphosphatemia
  • Hyper uricemia d/t cell destruction
  • Coags: thin
  • HLA typing for stem cell transplant

Tx:

  • Heme/onc consult
  • M3 variant: vit A; all others, Chemo
  • Chemo, XRT, stem cell txp, and maintenance therapy
  • Supportive: Hydration, transfusion, abx
  • Allopurinol, acetazolamide, +/- dialysis prior to chemo
18
Q

CLL: Chronic Lymphocytic Leukemia

Path:

Epi:

S/Sx:

Dx:

Tx:

A

CLL: Chronic Lymphocytic Leukemia

Path: Insidious proliferative disorder of lymphoid lineage -> abnormal B lymphocytes

Epi: Geriatric, increased risk with age; Genetic predisposition; M>F

S/Sx:

  • Painless lymphadenopathy (80%)
  • Hepatosplenomegaly (50%)
  • Asymptomatic +/- constitutional cancer symptoms
  • Skin nodules and infiltrates

Dx:

  • CBC: Lymphocytosis 40k-150k with >75% circulating cells
  • Smear: Smudge Cells
  • Decreased Gamma Globulin (advanced dz)
  • Bone Marrow Biopsy > 30% Blasts
  • Staging:
    • 0 lymphocytosis - 15y
    • 1 lymphadenopathy - 15y
    • 2 - Organomegaly
    • 3 - Anemia - 2y
    • 4 - Thrombocytopenia - 2y

Tx:

  • Heme/onc consult
  • If old and asx - Do Nothing
  • Early: watch and wait, chemo when symptomatic
  • Maintenance: annual flu vax, q5y pneumococcal vax, NO live vax’s
  • If young and donor = give stem cell txp
19
Q

CML: Chronic Myelogenous Leukemia

Path:

Epi:

S/Sx:

Dx:

A

CML: Chronic Myelogenous Leukemia

Path: Insidious excessive granulocytosis with Philadelphia chromosome

Epi: 25-60 yo; 80% remission at 4y; 70% have blast crisis

S/Sx:

  • Anemia: fatigue, SOB, chest pain
  • Thrombocytopenia: Bleeding, bruising
  • Granulocytopenia: Infections
  • Hepatosplenomegaly
  • Bone pain with pathologic fractures

Dx:

  • CBC: WBC 15k to 500K
  • Diff: Blasts < 5%, (+) Philadelphia Chromosome
  • CMP: HYPERkalemia, HYPERphosphatemia
  • Hyperuricemia
  • PCR: BCR/ABL gene (+)
  • Coags: thin
  • Bone Marrow Biopsy: Sudan Black (+); myeloperoxidase (+)
  • HLA typing for stem cell txp

Tx: Imatinib

  • Will turn into blast crisis -> AML
20
Q

Hodgkin’s Lymphoma

Path:

Epi:

S/Sx:

Dx:

Tx:

A

Hodgkin’s Lymphoma

Path: Contiguous spread of Reed Sternberg cells -> spread along predictable path from cervical node

Epi: 50% d/t Epstein Barr; increased risk in HIV; Genetic vs Toxic; M>F; bimodal age distribution

S/Sx:

  • Painless lymph enlargement in neck
  • Fever, weight loss, night sweats, pruritis, splenomegaly, abd mass, mediastinal mass

Dx:

  • CBC: Eosinophilia, thrombocytosis, leukocytosis
  • Lymph biopsy = definitive, (+) Reed Sternberg Cells
  • Elevated ESR and Alk Phos
  • Monitor LFTs, LDH
  • Monitor for TLS: Calcium and uric acid
  • Staging: CT C/A/P; CXR: mass +/- hilar adenopathy
    • Is it above only, or both above and below, the diaphragm?

Tx:

  • XRT + Chemo (ABVD vs. CHOP)
  • Thoracic XRT portal (Mantel: t-shape covers supraclavicular and mediastinal nodes)
  • Lymphoma radiosensitive? Tumor will reduce immediately
  • 5 Year Px: St 4 65%
21
Q

Non-Hodgkin’s Lymphoma

Path:

Epi:

S/Sx:

Dx:

Tx:

A

Non-Hodgkin’s Lymphoma

Path: Diverse, generalized group of lymphocytic and hystocytic malignancies with NO Reed Sternberg cells and NO predictable contiguous spread

Epi: Viral infxn, immunosuppression, hx ionizing radiation or toxic chemical exposure all increase risk

S/Sx: Similar to Hodkin’s painless lymphadenopathy, but widespread

Dx:

  • CBC: early anemia -> bone marrow infiltration
  • Lymph node biopsy = definitive (NO Reed Sternberg)
  • LFTs and LDH: monitor
  • Ca, Uric acid, ESR: monitor
  • CT C/A/P for staging
  • Lumbar puncture if c/f CNS lymphoma

Tx:

  • Heme/onc consult
  • Chemo, XRT, biologic/MAB + maintenance
22
Q

Multiple Myeloma

Path:

Epi:

S/Sx:

Dx:

Tx:

A

Multiple Myeloma

Path: Beta-Lymphocutes secrete antibodies -> infiltrate marrow, lymph, liver, spleen, kidneys

Epi: Insidious onset over 40 yeaars old; AAM, hx XRT, genetic, exposure, obesity, other plasma cell dz

S/Sx:

  • CRAB: hyperCalcemia, Renal failure, Anemia, Bone pain
  • Present with infxn/pneumonia, bone pain, pathologic fx
  • Hypercalcemia, leukopenia, AKI, anemia, thrombocytopenia

Dx:

  • Bence Jones proteinuria
  • Serum protein electrophoresis: Total serum protein ELEVATED
  • Bone marrow biopsy >10% plasma

Tx:

  • Younger donor: stem cell txp
  • Older non donor: Chemo, XRT, immune tx/Mabs, exchange transfusion