Rosen & Barkin's 5-Minute Emergency Medicine Consult (420 page)

Read Rosen & Barkin's 5-Minute Emergency Medicine Consult Online

Authors: Jeffrey J. Schaider,Adam Z. Barkin,Roger M. Barkin,Philip Shayne,Richard E. Wolfe,Stephen R. Hayden,Peter Rosen

Tags: #Medical, #Emergency Medicine

BOOK: Rosen & Barkin's 5-Minute Emergency Medicine Consult
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CODES
ICD9

732.1 Juvenile osteochondrosis of hip and pelvis

ICD10
  • M91.10 Juvenile osteochondrosis of head of femur, unspecified leg
  • M91.11 Juvenile osteochondrosis of head of femur, right leg
  • M91.12 Juvenile osteochondrosis of head of femur, left leg
LEUKEMIA
Linda Mueller
BASICS
DESCRIPTION
  • Neoplasms of WBCs that have undergone a malignant transformation
  • Hyperleukocytosis:
    • Occurs with WBC >100,000/mm
      3
    • Leads to occlusions of small vessels primarily in brain or lungs
    • Present with confusion, stupor, or shortness of breath
Chronic Myelogenous Leukemia
  • Overproduction of granulocytic WBCs (neutrophils)
  • Neutrophil function preserved
  • Thrombocytosis
  • Basophilia
  • Philadelphia chromosome present in bone marrow of >95%
Chronic Lymphocytic Leukemia
  • Most common leukemia in adults
  • Overproduction of monoclonal lymphocytes
  • Cells accumulate in lymph nodes, bone marrow, liver, spleen
  • Particularly prone to herpes virus infections
Acute Leukemias
  • Proliferation of undifferentiated immature cells:
    • Acute myelogenous leukemia (AML)—immature myeloid cells
    • Acute lymphocytic leukemia (ALL)—immature lymphoid cells (blasts)
  • Rapidly fatal
ETIOLOGY
  • Cause unknown
  • Familial clustering in chronic lymphocytic leukemia (CLL)
  • Increased incidence of AML, ALL, and chronic myelogenous leukemia (CML) with ionizing radiation
Pediatric Considerations
  • Usually have ALL:
    • Most common pediatric cancer
  • 60–80% remission in those who are standard risk
  • Better overall prognosis, except if <1 yr of age
  • May develop leukostasis at lower levels
  • Allopurinol dose is 3 mg/kg.
  • Ceftazidime dose is 50 mg/kg.
Pregnancy Considerations
  • 90% of leukemias are AML or ALL.
  • Myeloid leukemias are more common.
  • CLL is very rare in pregnancy.
  • Chemotherapeutics may cause birth defects and/or preterm labor.
  • Same prognosis as nonpregnant; do not delay therapy.
  • Transfuse earlier than nonpregnant; keep hemoglobin >9.8 mg/dL.
Geriatric Considerations

More likely to present with CLL and CML

DIAGNOSIS
SIGNS AND SYMPTOMS
Chronic Myelogenous Leukemia
  • Asymptomatic
  • Fatigue
  • Weight loss
  • Left upper quadrant pain, tenderness
  • Abdominal fullness
  • Splenomegaly (most common)
  • Later stage:
    • Headaches
    • Bone pain
    • Arthralgias
    • Fever
    • Leukotactic symptoms:
      • Dyspnea
      • Drowsiness
      • Confusion
Chronic Lymphocytic Leukemia
  • Asymptomatic
  • Fatigue
  • Lethargy
  • Weight loss
  • Lymphadenopathy
  • Splenomegaly
  • Hepatomegaly
Acute Myelogenous Leukemia
  • Fever
  • Fatigue
  • Pallor
  • Headache
  • Angina
  • Congestive heart failure, dyspnea on exertion
  • Bone pain
  • Granulocytic sarcoma (isolated mass of leukemic blasts)
  • Easy bleeding (thrombocytopenia):
    • Petechiae
    • Ecchymosis
    • Epistaxis
    • Hemorrhage
  • Infections (granulocytopenic)
  • Organ involvement with advanced ALL:
    • Lymphadenopathy
    • Hepatomegaly
    • Splenomegaly
    • Leukemic meningitis:
      • Headache
      • Nausea
      • Seizures
History
  • Radiation exposure
  • Exposure to alkylating agents
  • Recent viral infection, particularly Epstein–Barr
Physical-Exam
  • Signs of bleeding (petechiae, purpura)
  • Hepatomegaly and splenomegaly
  • Presence of chloromas (AML blast tumors)
  • Sausage-like hemorrhagic retinal veins are pathognomic for hyperviscosity.
ESSENTIAL WORKUP
  • CBC/platelets:
    • CML:
    • WBC range, 10,000–1 million/mm
      3
    • Neutrophils predominate.
    • Thrombocytosis in 50%
  • CLL:
    • Absolute lymphocytosis >5,000
    • WBC range, 40,000–150,000/mm
      3
  • Acute leukemia (AML/ALL):
    • Anemia
    • Thrombocytopenia
    • Elevation/depression of WBCs
DIAGNOSIS TESTS & NTERPRETATION
Lab
  • Electrolytes, BUN, creatinine, glucose, calcium
  • Uric acid level:
    • Frequently elevated, especially in ALL
  • Lactate dehydrogenase:
    • Increased in acute leukemias
  • Coagulation profile:
    • PT/PTT, fibrinogen, fibrin-split products
    • If disseminated, suspect intravascular coagulation.
  • Blood/urine cultures if fever
  • Arterial blood gases/pulse oximetry for shortness of breath
Imaging

CXR for infectious workup

Diagnostic Procedures/Surgery
  • Bone marrow biopsy:
    • Required to make diagnosis
    • CML—hypercellular with myeloid hyperplasia
    • CLL—lymphocytosis (30–100%)
    • Acute leukemia—hypercellular with blast cells, which replace normal marrow
  • Leukocyte alkaline phosphatase test:
    • Decreased in neutrophils in CML
  • Ph1 chromosome present in CML
DIFFERENTIAL DIAGNOSIS
  • CML:
    • Lymphoma
    • Myeloproliferative syndromes
    • Systemic lupus erythematosus
    • Infection—bacterial, fungal, mycobacterial
  • CLL:
    • Pertussis
    • Infectious lymphocytosis
    • Cytomegalovirus
    • Epstein–Barr virus/mononucleosis
    • Hepatitis
    • Rubella
  • Acute leukemia:
    • Aplastic anemia
    • Leukemoid reactions to infections
TREATMENT
INITIAL STABILIZATION/THERAPY
  • 100% oxygen for hypoxia/shortness of breath
  • IV access with 0.9% NS
  • Initiate platelet transfusion for severe bleeding from thrombocytopenia.
  • Begin broad-spectrum antibiotics for fever and granulocytopenia.
  • Treat disseminated intravascular coagulation (see “Disseminated Intravascular Coagulation”).
ED TREATMENT/PROCEDURES
  • Treat leukostasis:
    • Rehydrate with 500-mL bolus (20 mL/kg) IV 0.9% NS
    • Administer acetazolamide to alkalinize urine.
    • Initiate allopurinol.
    • Arrange for leukapheresis.
    • Whole-brain radiation or dexamethasone for CNS effects
    • Administer hydroxyurea for CML: 20–30 mg/kg single dose daily
  • Transfuse packed RBCs for symptomatic anemia:
    • May require irradiated, filtered, and HLA-type–specific blood
  • Post-ED treatment:
    • CLL:
      • Chemotherapy
      • Prednisone for immune-mediated thrombocytopenia
      • Radiation to localized nodular masses/enlarged spleen
    • CML:
      • Interferon therapy
      • Chemotherapy
      • Bone marrow transplantation
    • ALL:
      • Chemotherapy
      • CNS prophylaxis with intrathecal–methotrexate/cranial radiation
      • Bone marrow transplantation
    • AML:
      • Chemotherapy
      • Bone marrow transplantation
MEDICATION
First Line
  • Aggressive IVF, start with normal saline, then alkalinize
  • Packed RBC and platelets as needed
Second Line
  • Ceftazidime if febrile
  • Allopurinol or rasburicase and diuretics if at risk for tumor lysis

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