Hematology and Oncology Flashcards

1
Q

Anemia

A

Hemoglobin concentration too low to deliver adequate oxygen to meet demands. Hgb concentration < 2 standard deviations below the mean for age, gender, and race.

Causes: Many!
- Acute: Viral illness, oncologic diagnosis, inflammation.

S/S: Common in young children. Pallor, tachycardia, fatigue, lethargy, shortness of breath.

Dx: CBC, Reticulocyte count, Ferritin, Fe, TIBC, FEP, Hemoglobin electrophoresis, Peripheral smear, Additional screens for hemolytic anemia.

Tx: Treatment is based on underlying cause. Extremely low hgb with significant side effects requires transfusion.

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2
Q

Thalassemia - Alpha

A

Sx

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3
Q

Immune Thrombocytopenia Purpura

A

Idiopathic low platelet count.

  • Cause is unknown, but may be immune. May occur as a result of disease such as oncologic or infection.
  • Platelet count < 50, 000 or < 10, 000
  • Acute or chronic.

Dx: CBC, may need bone marrow smear.

Tx: Based on acute or chronic presentation. If no bleeding, usually no treatment. If moderate bleeding, IVIG or anti-D or platelet infusion, especially associated with another acute illness.

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4
Q

Neutropenia

A

Decreased neutrophils with normal hemoglobin and platelet count, May be associated with viral or oncologic illness.

Dx: ANC

Tx: G-CSF, or if chronic, no treatment.

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5
Q

Pancytopenia

A

Low hgb, platelets, and WBC.

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6
Q

Leukocytosis

A

WBC higher than normal, often associated with leukemia, infection, or significant inflammation.

Dx: WBC

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7
Q

Sickle Cell Anemia

A

Deoxygenated hemoglobin S polymerizes and distorts the shape of the red blood cells. Sickled blood cells are more prone to hemolysis. Vaso-occlusive pain crisis and intrapulmonary thrombosis are two clinical manifestations. Acute crises and infection occur with pain.

Dx: Hemoglobin electrophoresis.

  • Can identify hemoglobin S and hemoglobin A SSD on newborn screen.
  • Splenomegaly is a common feature early in life.

Complications: Jaundice, cholestasis, pallor, fatigue, chronic pain, decreased exercise tolerance, cardiomegaly, stroke, aplastic, hypoplastic, hyperhemolytic crisis. Acute splenic sequestration, Chest Syndrome, Stroke, Acute Vascular Compromise.

Serious S/S: Fever, unusual fatigue, lethargy, pallor, acute splenic enlargement, shortness of breath, hypoxia, protracted vomiting, sudden loss of speech, weakness in an arm or leg.

Tx: Prophylaxis is usually with PCN.

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8
Q

Stroke

A

Ischemic or hemorrhagic. Dysfunction of brain activity due to interruption of blood flow in brain.

  • Ischemic strokes occur with cardiac disease, hematologic disorders (SSD), primary vasculitis, lipid abnormalities, metabolic abnormalities, dehydration, shock.
  • Hemorrhagic strokes occur with vascular malformation, cavernous malformation, aneurysm, brain tumor, thrombocytopenia or other hematologic problems, coagulopathies, spontaneous dissection.

PE: Neurologic evaluation, skin assessment, abdominal exam, cardiac evaluation, rash or petechiae.

S/S: Acute neurologic symptoms, headache, confusion and lethargy.

Dx: History, neurologic exam, head CT or MRI/MRA, labs (CBC, coags, LFTs, CMP, ESR).
- Acute and chronic monitoring.

Tx: Focused on underlying cause, anticoagulation therapy may or may not be warranted.
- Evaluation of CBC, maintain low hgb/hct, exchange transfusion, urea

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9
Q

Disseminated Intravascular Coagulation

A

Acquired, life-threatening complication resulting from a variety of disease processes including sepsis, trauma, malignancy, vascular irregularities, liver failure and pregnancy. Results when excessive fibrinogen and platelets are deposited in the microvascular system.

S/S: Diffuse bleeding and thrombosis with coagulation abnormalities by laboratory analysis.

Tx: Treat underlying condition, blood products, vit K.

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10
Q

Hemolytic Uremic Syndrome

A

Bacterial verotoxins cause damage to microvessels in circulation, resulting in inflammation and thrombosis leading to decrease in glomerular filtration rate, hematuria, proteinuria, and oliguria.

  • HUS is MOST common cause of renal failure.
  • Typical causative factor is E. coli 0157

S/S: Incubation period 3-5 days, abdominal pain, nonbloody diarrhea, fever, then progresses to bloody diarrhea. Other symptoms are pallor, fever, weakness, petechiae, hematuria, and hematemesis.

Dx: Based on clinical findings and labs - electrolytes with increased BUN and creatinine. Stool culture positive for E. coli 0157.

Tx: Preventing renal failure with diuretics, fluid management and assessment.
- May need dialysis!

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11
Q

Most Common Types of Pediatric Cancers

A
  1. Leukemia
  2. Brain and other nervous system tumors
  3. Neuroblastoma
  4. Wilm’s Tumor
  5. Lymphoma
  6. Rhabdomyosarcoma
  7. Retinoblastoma
  8. Bone Cancer (osteosarcoma, Ewings)

Dx: CBC, electrolytes, ESR, CT, MRI, plain xray

Tx: Per specific cancer presentation

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12
Q

Acute Lymphoblastic Leukemia (ALL)

A

Blood cell cancer.

  • Most common malignancy.
  • Usually affects ages 2-5 years, but can occur in older children.

S/S: Clinical presentation includes fever, bone pain, anorexia, weight loss, pallor and mucosal bleeding, lymphadenopathy, splenomegaly, hepatosplenomegaly.

Dx: CBC, peripheral blood smear, bone marrow smear, electrolytes, uric acid, LDH.

Tx: Based on oncology group.
- Includes induction and maintenance chemotherapy

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13
Q

Acute Myelocytic Leukemia (AML)

A

Blood cell cancer.

  • 20% of all leukemias.
  • Presents with coagulopathies and chloromas.

S/S: Clinical presentation includes fever, bone pain, anorexia, weight loss, pallor and mucosal bleeding, lymphadenopathy, splenomegaly, hepatosplenomegaly.

Dx: CBC, peripheral blood smear, bone marrow smear, electrolytes, uric acid, LDH.

Tx: Based on oncology group.

  • Includes induction and maintenance chemotherapy
  • Bone marrow transplant.
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14
Q

Neuroblastoma

A

Extracranial solid tumor.
- MOST common in children < 1 year of age.

S/S: Palpable mass, 60% in abdomen. Bruising, pallor, fatigue, bone pain, fever, hepatosplenomegaly, lymphadenopathy, periorbital bruising.

Dx: CBC, liver and renal function, coags, VMA/HVA (urine), CXR, abdominal film, CT and MRI.

Tx: Tumor staging, surgical resection and chemotherapy, BMT for high risk tumors.

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15
Q

Wilm’s Tumor

A

Unilateral or bilateral solid tumor of the kidney.

  • MOST common renal neoplasm in children.
  • Median age is 2-3 years old.

S/S: Often idenitifed by parent or family member. Some have pain, microscopic or gross hematuria, malaise, fever, HTN.

Tx: Nephrectomy or partial resection, chemotherapy.

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16
Q

Retinoblastoma

A

Retinal tumor, unilateral or bilateral, noted with leukocoria and strabismus, often genetic.

S/S: Noted physical exam, ophthalmological evaluation.

Tx: Individualized therapy with surgery, chemotherapy, cryotherapy, and radiation.

17
Q

Brain Tumors

A

Most common solid tumor.

  • 2nd to leukemia in childhood cancers.
  • Many different types and placements.

S/S: Typical presentation is headache with morning vomiting, increased ICP, personality changes, poor performance in school, lethargy, irritability.

Dx: CT or MRI

Tx: Depends on severity of symptoms and location of tumor.
- Usually involves surgical resection, radiation, and chemotherapy.

18
Q

Bone Tumors

A

Solid tumors.

  • Average age is 13-17 years old.
  • Ewings, Osteogenic Sarcoma
  • Most common area of involvement is distal femur or proximal tibia.

S/S: Presents with pain over affected area, fever, weight loss, increased ESR.

Dx: Imaging with plain films first, followed by MRI

Tx: Resection and chemotherapy

19
Q

Fever and Neutropenia

A

Fever with low WBC and ANC.

S/S: Fever, lethargy, shock.

Dx: BCx, CBC, electrolytes.

Tx: High dose broad spectrum antibiotics, fluids, symptom management.
- ICU, if indicated.

20
Q

Typhlitis/Intra-abdominal Emergency

A

Necrotizing enterocolitis occurs from infectious source in neutropenic patients.

S/S: Right lower quadrant abdominal pain, +/- fever, mucocitis.

Tx: Surgical consult for emergency bowel perforation, serial xrays or CT.

21
Q

Tumor Lysis Syndrome

A

Massive tumor cell lysis with the release of large amounts of potassium, phosphate, and nucleic acid. Can affect neurological, pulmonary, and renal function.

S/S: Can be asymptomatic, but with hyperkalemia, hyperphosphatemia, and hyperuricemia. Nausea, vomiting, diarrhea, anorexia, lethargy, hematuria, heart failure, cardiac dysrhythmias, seizures, muscle cramps, tetany, syncope, and possible sudden death.

Tx: Prevention is key to management! Rasburicase and allopurinol are medical therapy. Aggressive IV fluid hydration.

22
Q

Superior Vena Cava Syndrome (SVC)

A

Compression of the superior mediastinal structures, ultimately compromising flow to heart.

S/S: Distended neck veins, tachypnea, hypoxia, SOB, signs of decreased cardiac output.

Dx: CXR, CT

Tx: Airway management, decrease pressure.

23
Q

Mass Syndromes

A

Abdominal, spinal compression via tumor mass.

S/S: Altered neurologic condition/status, pain, compartment syndrome.

Tx: Decrease mass effect via radiation or chemotherapy.