NUR 232 Cancer Week 10 Student view
Week 10: Cellular Regulation
Focus on childhood cancers:
Ewing's Sarcoma
Osteosarcoma
Hodgkin's Lymphoma
Leukemia
Wilm's Tumor
Cure for Childhood Cancer initiatives
Cellular Regulation
Scope:
Proliferation: Production of new cells through growth and division.
Differentiation: Process where less specialized cells become more specialized.
Physiologic Consequences
Normal Cellular Growth and Reproduction:
Replication and Differentiation.
Abnormal Growth and Reproduction:
Benign Neoplasm: Non-cancerous growth.
Malignant Neoplasm: Cancerous growth that invades surrounding tissues.
Cellular Regulation Risk Factors
Age: Risk increases with older age.
Smoking: Tobacco exposure raises cancer risk.
Infectious agents: Exposure can lead to certain cancers.
Radiation: UV and ionizing radiation can cause mutations.
Nutrition and Activity: Poor diet and lack of exercise affect health.
Carcinogens: Chemicals that promote the formation of cancer.
Racial/Socioeconomic Disparities: Access to healthcare and resources vary.
Genetics: Family history increases risk.
Assessment
Methods:
History: Personal and family medical history.
Physical Exam: Check for signs and symptoms.
Diagnostic Tests: Essential for cancer identification.
Radiographic Tests: Imaging to visualize abnormalities.
Direct Visualization and Lab Tests: For cellular analysis.
Pathology: Examining tissue for cancer cells.
Classification: Grading and staging per Giddens (pg. 107-108).
Clinical Management
Prevention:
Primary: Avoiding disease onset.
Secondary: Early detection and intervention.
Collaborative Interventions:
Surgery: Removal of tumors.
Radiation: Targeting cancer cells with radiation.
Chemotherapy: Drug treatment to kill cancer cells.
Hormonal therapy: Blocks hormone production.
Targeted therapy: Attacks specific cancer cells.
Biologic therapy: Uses the immune system to fight cancer.
Bone Marrow and Stem Cell Transplantation: Replacement of damaged bone marrow.
Interrelated Concepts
Key Areas:
Infection
Elimination
Immunity
Fluid & Electrolytes
Nutrition
Pain
Anxiety
Fatigue
Coping
Sexuality
Bone Marrow and Leukemia
Pathophysiology:
Competition for nutrients and infiltration leads to ( RBC ) and ( WBC ) abnormalities.
Types of Leukemia:
Acute: Rapidly progressing population of immature white blood cells.
Generalized CNS hyper-metabolism can occur with leukemia.
Manifestations:
Anemia, increased infection risk, bleeding, pain.
Classification of Leukemia
Types:
Classified by affected ( WBC ).
Common Types in Children:
ALL (Acute Lymphoblastic Leukemia)
AML (Acute Myelogenous Leukemia).
Generally, boys are more affected than girls; Caucasians > African Americans.
Clinical Manifestations of Leukemia
Symptoms Include:
Pale, febrile, irritable, anorexia, easy bruising, joint pain, organ involvement, hepatosplenomegaly, lymphadenopathy.
Diagnosis of Leukemia
Tests:
History and Physical Exam: Initial assessments.
Peripheral Blood Smear: Identify immature leukocytes.
Bone Marrow Aspiration/Biopsy: Definitive diagnosis through cell examination.
Treatment of Leukemia
Management:
Includes history, physical exam, and various tests (CBC, bone marrow biopsy).
Treatment plans often involve chemotherapy and potential bone marrow transplants.
Hodgkin Lymphoma
Malignancy of the Lymph System:
Primarily affects lymph nodes; can metastasize to other organs (spleen, liver).
Associated with the Epstein-Barr virus (EBV).
Diagnosis of Hodgkin Lymphoma
Biopsy:
Identifies Reed-Sternberg cells unique to Hodgkin Lymphoma.
Commonly diagnosed in adolescents, especially males.
Clinical Manifestations of Hodgkin Lymphoma
Symptoms:
Enlarged lymph nodes (supraclavicular, cervical), low-grade fever, weight loss, night sweats, rash, itching.
Treatment of Hodgkin Lymphoma
Approach:
Combined radiation and chemotherapy typically yield excellent long-term prognosis.
Non-Hodgkin Lymphoma
Incidence Rates:
10 children per 1 million under 20 years old.
Risk Factors:
Infection (EBV), immunodeficiency, DNA repair syndromes, previous cancer treatments.
Characteristics of Non-Hodgkin Lymphoma
Heterogeneous: Multiple causes and variations in morphology.
Clinical Manifestations: Vary based on site and extent; usually widespread at diagnosis.
Survival Rates: Approximately 85% to 95% of children with limited disease involvement can be cured.
Bone Tumors
Common Types:
Osteosarcoma: Most frequent bone tumor in adolescents.
Manifestations: Localized pain and palpable mass; confirmed via imaging and biopsy.
Therapeutic Management: Involves surgery and chemotherapy.
Ewing's Sarcoma
Characteristics:
Second most common bone cancer in children, affecting pelvis, long bones, and chest wall.
Treatment includes radiation and chemotherapy.
Wilm's Tumor
Nephroblastoma:
Most common malignant renal tumor in childhood, presents as abdominal mass/swelling.
Generally has a high survival rate.