7. Clinical Considerations (Hematology) Pt. II Flashcards

1
Q

Disorders of Red Blood Cells

Vitamin B12 and Folate deficiency
• Vitamin B12 (cobalamin) and folic acid are needed for RBC formation.
• Risk factors for folate deficiency include poor ____, alcoholism, history of ____ disorders, and pregnancy (especially during the third trimester).
• Pernicious anemia is caused by a deficiency of ____, a substance secreted by the gastric parietal cells that is necessary for absorption of vitamin B12.
• Most patients with pernicious anemia have ____ with decreased intrinsic factor and hydrochloric acid secretion.

A

diet
malabsorption
intrinsic factor
chronic atrophic gastritis

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2
Q

Disorders of Red Blood Cells

Vitamin B12 and Folate deficiency

  • ____ patients are at an increased risk of developing vitamin B12 deficiency because their digestive tracts have been altered.
  • In healthy adults, ____ (released by the parietal cells in the stomach) binds with vitamin B12 in the duodenum. The binded vitamin B12 is then absorbed in the ____.
  • In patients who have had gastric bypass surgery, most of the stomach and duodenum are bypassed, ____ the breakdown of vitamin B12 and its binding with intrinsic factor.
A

bariatric
intrinsic factor
ileum

limiting

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3
Q

Disorders of Red Blood Cells
G6PD deficiency
• Glucose-6-phosphate dehydrogenase (G6PD) is a ____ enzyme that prevents oxidative damage to cells by promoting detoxification of ____.
• G6PD is expressed in all tissues; however, when the enzyme is abnormally low, this biochemical process is markedly reduced in ____, rendering these cells strongly vulnerable to oxidative stress.
• In G6PD deficiency, hemolysis can be precipitated by diverse factors, such as ____ drugs, infectious diseases, and ingesting ____.

A

cytoplasmic X chromosome-linked
free radicals

RBC

oxidative
fava beans

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4
Q

Disorders of Red Blood Cells

G6PD deficiency
• Patients with G6PD deficiency exhibit an increased incidence of drug sensitivity with ____ (sulfamethoxazole), aspirin, and ____ being the prime offenders.
• Dental ____ may accelerate the rate of hemolysis in patients with this type of anemia.

A

sulfonamides
chloramphenicol
infection

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5
Q

Disorders of Red Blood Cells

Sickle cell anemia
• In patients with sickle cell anemia, distortion of the RBC into a sickled shape results from ____ or ____ blood pH.
• Cellular rigidity and membrane damage occur, and ____ sickling is the result. The net effects of these changes are ____, increased blood viscosity, reduced ____, hypoxia, increased adhesion of RBCs, vascular ____, and further sickling.

A
deoxygenation
decreased
irreversible
erythrostasis
blood flow
occlusion
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6
Q

Disorders of Red Blood Cells

Sickle cell anemia
• Complications of sickle cell anemia can occur at any age, but patients in the following age groups are more likely to manifest certain complications:

Birth to 20 years of age: Painful events, ____, acute ____ syndrome (fever, chest pain, wheezing, cough, and hypoxia), acute anemia, and infection.

From 20 to 40 years of age: ____ of hip and shoulder joints, leg ulcers, priapism, liver disease, and gallstones

Older than 40 years of age: Pulmonary ____, nephropathy, proliferative retinopathy, and cardiac enlargement, heart murmurs, and sudden death from arrhythmias.

A

stroke
chest

osteonecrosis
hypertension

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7
Q

Disorders of Red Blood Cells
Sickle cell anemia
• Patients with sickle cell anemia can receive ____ dental care during non-crisis periods; however, ____ and complicated procedures should be avoided.
• The goal during routine care is to ____ a crisis

A

routine
long
prevent

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8
Q

Disorders of Red Blood Cells

Sickle cell anemia
• Appropriate restorative and preventive dental care are important because oral infection can precipitate a ____. If infection occurs, it must be treated quickly.
• For routine dental care, appointments should be ____ to minimize stress.
• The use of ____ in the local anesthetic is controversial because some believe it may impair circulation and cause vascular occlusion. However, the ____ of a vasoconstrictor outweigh the risk of local impairment of circulation.
• ____ and dehydration should be prevented.

A
crisis
short
epinephrine
benefits
hypoxia
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9
Q

Disorders of Red Blood Cells
Sickle cell anemia
• ____ can be used, with at least ____% oxygen concentration provided.
• ____ must be used with extreme caution.
• ____ should be avoided because suppression of the respiratory center by these agents leads to hypoxia and acidosis, which may precipitate an acute crisis.

A

nitrous oxide
50
intravenous
opiates

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10
Q

• What kind of anemia does he have?
• His MCV is low so it is a ____ anemia
• What are the types of microcytic anemias? ____ deficiency, Thalassemia, Anemia of
____ disease, ____
• When I was rotating in hematology we would get really excited about serum ferritin levels
• What I want you guys to know is “that they can run lab tests to determine which one of
these it is”. Not important for you guys to know
• This patient came back with iron deficiency anemia

A

microcytic

iron
chronic
sideroblastic

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11
Q

• So why did he lose conciseness? Why did he fall?
• Whats syncope? Fainting
• Whats happening with the brain? Not getting enough oxygen so global cerebral
____. Thats why he loss conciseness. He has anemia so his oxygen carrying capacity is very ____ and also is hypotensive and tachycardia which indicates ____ depletion so that puts you at risk for orthostatic hypotension (standing up too quickly and fainting)

A

hypoperfusion
low
volume

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12
Q

• Hemorrhagic shock is probably class ____ stage. His blood pressure was decreased and his heart rate increased. He probably loss 1.5L of blood which was due to an upper GI bleed

A

III

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13
Q

Disorders of White Blood Cells
• Disorders of white blood cells (WBCs) in dental patients can substantially influence clinical decision making as well as the delivery of care because WBCs constitute the primary ____ against microbial infections and are critical for mounting an immune response.
• Defects in WBCs can manifest as delayed ____, infection, or mucosal ____ and, in some cases, may be fatal.

A

defense
healing
ulceration

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14
Q

Disorders of White Blood Cells
• Leukocytes (WBCs) respond to an inflammatory process or injury.
• Normal levels of WBCs for are ____/uL
• ____ is an increase in the number of circulating WBCs and ____ as a reduction in the number of circulating WBCs.
• In a complete blood count (CBC), the differential measures the ____ of the various types of white cells present.
• The differential usually includes ____, bands, eosinophils, ____ and lymphocytes.

A
4300-10800
leukocytosis
leukopenia
percentage
neutrophils
monocytes
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15
Q

Disorders of White Blood Cells
• A thorough ____ for evidence of WBC disorders is essential in all patients who present for dental treatment.
• Patients with leukemia or lymphoma may be at risk for catastrophic outcomes if the disease is not detected before dental treatment is started.
• Patients with leukemia whose disease has not been diagnosed may experience serious ____ complications after surgical procedures, may have altered ____ of surgical wounds, and are prone to postsurgical ____.

A

assessment
bleeding
healing
infection

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16
Q

Disorders of White Blood Cells

  • Specific questions regarding blood disorders and cancer in family members, weight loss, fever, swollen or enlarged lymph nodes, and bleeding tendencies should be asked.
  • Examination of the head, neck, and mouth should include a thorough inspection of the oropharynx, head, and cervical and ____ lymph nodes.
  • ____ examination is important for identifying abnormalities suggestive of invasive neoplasms.
  • ____ films also provide insight into potential osteolytic lesions associated with WBC disorders.
A

supraclavicular
cranial nerve
panoramic

17
Q

Disorders of White Blood Cells
• A patient who displays the classic signs or symptoms of leukemia, lymphoma, or multiple myeloma should be promptly referred directly to a ____.
• Screening laboratory tests should include a ____ with differential (total and differential WBC counts, hemoglobin, hematocrit, platelet count) and a ____ for cell morphologic study.
• If screening tests are ordered by the dentist and one or more results are abnormal, the patient should be promptly referred for ____ evaluation and treatment.

A

physician
CBC
smear
medical

18
Q

Leukemia
Disorders of White Blood Cells
• Leukemia is cancer of the WBCs that affects the ____ and ____ blood. It involves exponential proliferation of a clonal ____ or ____ cell and occurs in both ____ and chronic forms.
• Acute leukemia is a rapidly progressive disease that results from accumulation of ____, nonfunctional WBCs in the marrow and blood. Chronic leukemias have a ____ onset, which allows production of ____ numbers of more mature, ____ cells.

A
bone marrow
circulating
myeloid
lymphoid
acute

immature
slower
larger
functional

19
Q
Leukemia
• Four types of leukemia:
Disorders of White Blood Cells
  • \_\_\_\_ (AML)
• \_\_\_\_ (ALL)
• \_\_\_\_ (CML)
• \_\_\_\_(CLL
A

acute myelogenous leukemia
acute lymphocytic leukemia
chronic myelogenous leukemia
chronic lymphocytic leukemia

20
Q

Leukemia – Clinical considerations
• Patients with leukemia are prone to develop gingival ____, ulceration, and oral infection.
• It is caused by infiltration of atypical and ____ WBCs . It occurs in up to ____% of those with acute leukemia and 10% of those with chronic leukemia.
• A localized mass of leukemic cells is known as a ____. These extramedullary tumors have been observed in the ____ tissues (maxilla, palate) and ____ tissues (gingiva, tongue, oral mucosa) of the maxillofacial complex.

A
enlargement
immature
granulocytic sarcoma
chloroma
hard
soft
21
Q

Leukemia – Clinical considerations
• The gingiva is boggy and ____ easily and is exacerbated by thrombocytopenia.
• Due to granulocytopenia, at least one third of patients have recurrent ____, nonhealing wounds, oral ulcerations, and fever.
• Enlargement of the ____, lymph nodes, spleen, and gingiva occurs as a result of leukemic infiltration of these tissues.
• Oral ____ is extremely important and invasive procedures (extractions, biopsies) should be ____ if possible.

A
bleeds
infections
tonsils
hygiene
avoided
22
Q

Lymphoma
Disorders of White Blood Cells
• Lymphoma is cancer of the ____ organs and tissues that presents as discrete tissue masses.
• Lymphomas are classified by ____ type (B cell, T cell, MALT, plasma cell), ____ (small or large cell, cleaved or noncleaved nucleus), and ____ behavior (of low, intermediate, and high grade);
• There are over 20 types, but the 2 main categories are ____, and ____.
• The initial signs of these diseases often occur in the mouth (____) and in the ____ region.

A
lymphoid
cell
appearance
clinical
hodgkin lymphoma
non-hodgkin lymphoma

waldeyer ring
H+N

23
Q

Lymphoma
Disorders of White Blood Cells
• Hodgkin lymphoma presents most commonly as a painless mass or a group of firm, nontender, enlarged lymph nodes, often affecting the ____ nodes or the ____ nodes (in >50% of cases).
• Non-Hodgkin lymphoma is marked by enlarged lymph nodes, fever, and weight loss.

In contrast with Hodgkin lymphoma, which often begins with a ____ focus of tumor, NHL usually is ____ when first detected.
• About 20% to 40% of lymphomas develop ____ of lymph nodes and are termed ____ lymphomas

A

mediastinal
neck

single
multifocal
outside

extranodal

24
Q

Lymphoma
Disorders of White Blood Cells
• Lymphomas are the ____ most common malignant lesions in the maxillofacial region (behind ____ + ____ neoplasms),
• In the maxillofacial region these are frequently found in the ____ glands or intraoral ____

A
third
SCCa
salivary
salivary
mucosa
25
Q

Disorders of White Blood Cells

  • Multiple myeloma is a lymphoproliferative disorder that results from overproduction of cloned malignant ____ cells that results in multiple tumorous masses scattered throughout the skeletal system.
  • Malignant plasma cells secrete monoclonal ____ and various cytokines.
  • Monoclonal gammopathy of undetermined significance (MGUS), consisting of increased numbers of ____ cells with no other ____ manifestations, may precede MM.
A

plasma
immunoglobulins
plasma
clinical

26
Q

Disorders of White Blood Cells

Multiple myeloma
• The disease consists of ____ and myeloma cell proliferation, ____ production, bone resorption, and bone marrow ____.
• Resorption of bone leads to release of calcium and serum ____.
• Bone marrow replacement leads to ____, leukopenia, thrombocytopenia, and eventually a decrease in plasma ____.
• Increased plasma ____ contributes to altered ____ function, excessive bleeding, renal impairment, and neuropathy.

A

plasma
immunoglobulin
replacement

hypercalcemia
anemia
immunoglobulins

viscosity
function

27
Q

Disorders of White Blood Cells

Multiple myeloma
• Patients with MM may have ____ lesions, soft tissue lesions, and soft tissue deposits of amyloid.
• Dental radiographs may show “____” lesions or mottled areas that represent areas of tumor.
• An ____-like protein is found sometimes in oral soft tissues.

A

jaw
punched-out
amyloid

28
Q

Disorders of White Blood Cells

Multiple myeloma
• Patients are often treated with ____ to prevent hypercalcemia and bone resorption -> These patients are at risk for ____ with dental procedures.

A

IV bisphosphonates

MRONJ

29
Q

Disorders of White Blood Cells
• When a patient presents with a diagnosis of a WBC disorder it is important to understand the diagnosis as well as the stage of treatment.
• Pretreatment care should include oral ____ instructions that emphasize the importance of meticulous plaque removal. Caries and infection should be eliminated before ____ is begun.

A

hygiene

chemotherapy

30
Q

Disorders of White Blood Cells
• Patients who are undergoing chemotherapy or radiotherapy are susceptible to many oral complications, including ____, neutropenia, infection, excessive ____, graft-versus-host disease (GVHD), and alterations in ____ and development.

A

mucositis
bleeding
growth

31
Q

Dental management - Mucositis
• Patients who are undergoing chemotherapy or radiotherapy are susceptible to many oral complications, including ____, neutropenia, infection, excessive bleeding, ____, and alterations in growth and development.
• Mucositis usually begins ____ days after initiation of chemotherapy and resolves after ____ of chemotherapy.
• Affected mucosa becomes ____, raw, and tender.
Breakdown of the epithelial barrier produces oral
____ that may become secondarily infected.

A
mucositis
graft-versus-host disease
7 to 10
cessation
red
ulcerations
32
Q

Dental management - Mucositis
• The treatment of mucositis is ____.
• Oral ____ should be maintained to minimize
infection complications.
• A ____ (____ free) can be used to clean the surface of the ulcers.
• A topical ____ mouth rinse and systemic analgesics makes the mouth more comfortable so the patient can maintain their nutrition.

A
palliative
hygiene
mouth rinse
alcohol
anesthetic
33
Q

Dental management - Neutropenia
• Oral infection is less of a problem in patients with ____ leukemia than in those with ____ leukemia because the cells are more mature and functional in chronic leukemia. However, in the ____ stages of both CML and CLL, infection can become a serious complication.

• Because of ____, signs of infection are often masked in patients with leukemia. The swelling and erythema usually associated with oral infection are often less ____.

A
acute
chronic
later
neutropenia
distinctive
34
Q

Dental management - Neutropenia
• ____ infections (bacterial, fungal, and viral) are common with ____ being the most common. This should be treated with topical and sometimes parenteral ____.
• ____ virus infection is also common. To prevent recurrence ____ antiviral agents are given to HSV antibody– positive patients who are undergoing chemotherapy.

A
opportunistic
candidiasis
antifungals
recurrent herpes simplex
prophylactic
35
Q

Disorders of White Blood Cells
• ‘____ clot’ or ‘____ clot’: Disorganized clot with incomplete fibrin formation, rich in erythrocytes.
• Generally the result of ____ hemorrhage characterized by slow, oozing ____ red blood.
• Remember, upon vessel injury, platelets adhere into vWF in subendothelial tissue → aggregate → primary hemostatic plug. Platelets stimulate the plasma coagulation factors, which leads to the generation of a fibrin clot.
• If this process is disturbed (platelet deficiency, etc.) you can see a disorganized clot form.

A

liver
currant jelly
venous
dark