Blood Disorders 2 Flashcards
thalassemia
a hemoglobin disorder that has some effect on the bones and patients present with a range of anemic symptoms
thalassemia pathogenesis
a-chain: high affinity for oxygen and will not release O2 to cells
b-chain: interferes with normal maturation of RBCs and contributes to early destruction
extraoral characteristics thalassemia
a-thalassemia: mild to moderate signs of anemia
b-thalassemia: minor, intermedia, major (bone malformations and stunted growth)
radiographic bone changes thalassemia
jaw: honeycomb trabecular pattern
skull: hair-on-end trabecular pattern
megaloblastic anemia is caused by
Vitamin B12 deficiency
folic acid deficiency
megaloblastic anemia pathogenesis
normal RBCs have a nucleus while maturing, but once the maturation process is complete the nucleus is ejected
perioral characteristics megaloblastic anemia
glossitis “beefy red,” smooth, sore appearance
pale ulcerated mucosa
possible cleft lip and/or palate
megaloblastic anemia dental implications
abnormal vital signs
refer for medical evaluation
female patients of childbearing age
what are the two anemias with bone changes
sickle cell disease and thalassemia
sickle cell crisis
episodic exacerbations brought on by cold, stress, physical exertion, dehydration, acidosis, infectious agents, hypoxia or a low level of oxygen
sickling of many RBC, occluding the microvasculature in many areas, such as the chest, abdomen and bones, causing extreme pain
sickle cell disease perioral/intraoral characteristics
bone trabecular changes: skull “hair-on-end” trabecular pattern caused by bone marrow expansion similar to the thalassemias
periapical “step-ladder” trabecular pattern between posterior teeth
sickle cell disease dental implications
use local anesthetics with little or no vasoconstrictors (avoid epi)
anemia associated with chronic disease or disorders
treatment of these conditions usually eliminates the anemia
cancer, chronic inflammatory disease, renal disease, hypertension, prosthetic heart valves, turbulent blood flow
aplastic anemia
bone marrow fails to produce any of the blood cells usually due to destruction of pluripotential stem cells
extraoral characteristics of aplastic anemia
classic symptoms of anemia
bleeding tendencies
infections
severe perio infections
spontaneous gingival bleeding
polycythemia
excess RBCs, can impair flow
three forms of polycythemia
relative polycythemia
secondary polycythemia
primary: caused by proliferative neoplastic disease, clinical manifestations
lymphoid stem cell
lymphocytes
myeloid stem cell
monocytes
granulocytes
platelets
erythrocytes
disease of WBCs can be broken into two categories
diseases of the leukocytes (Neutropenia, agranulocytosis, cyclic neutropenia)
lymphomas: Hodgkin Lymphoma, Non-Hodgkin Lymphoma, Leukemia, Multiple Myeloma
neutropenia etiology
adverse reaction to a drug
many types
neutropenia pathogenesis
genetic of caused as reaction to infection
results in increased susceptibility to infections
neutropenia extraoral characteristics
fatigue, fever, malaise, extreme weakness
vital signs
skin infections (will not have exudate or erythema present)
upper respiratory infections
genitourinary tract infection
neutropenia perioral/intraoral characteristics
oral infections
oral ulcers
perio infections
rapid, progressive loss of periodontal attachment
can lead to premature loss of dentition