Chapter 30: Lewis - Hematologic System

Pallor of skin or nail beds can be indicative of what?

Low hemoglobin levels which means low oxygen. Low hemoglobin is a type of anemia.

Flushing

Too much hemoglobin due to polycythemia, and congestion of capillaries. Flushing of the palms of the hands or soles of the feet are a possible indication of anemia.

Jaundice

This is an accumulation of bile pigment caused by rapid or excessive hemolysis or liver damage.

Cyanosis

Reduce hemoglobin, excessive concentration of deoxyhemoglobin in the blood

Excoriation

scratching from intense pruritus

Pruritus

Hodgkins lymphoma, cutaneous lymphomas, inflitrative leukemias, increased bilirubin

Leg ulcers

Sickle cell disease

Angioma

Benign tumor consisting of blood or lymph vessels. Most are congenital, some may disappear spontaneously.

Telangiectasia

Small angioma with tendency to bleed. Focal red lesions, course or fine red lines. This can be due to dilation of small vessels.

Spider nevus

Type of telangiectasia. It has a round red central portion and branching radiations resembling a spider. Usually on face, neck, or chest. Elevated estrogen levels as in pregnancy or liver disease.

Purpura

Conditions like petechiae, ecchymosis (bruise) or other small hemorrhages in the skin and mucous membrane. This can be due to low platelets or clotting factors resulting in hemorrhage into the skin. Vascular abnormalities, break in blood vessel walls resulting in trauma

Chloroma

A tumor arising from myeloid tissue and containing a pale green pigment. Can be caused by acute myelogenous leukemia that has infiltrated the skin.

Plasmacytoma

Tumor arising from abnormal plasma cells. Can be caused by multiple myeloma that has infiltrated the tissue.

Jaundiced sclera

Due to accumulation of bile pigment resulting from rapid or excessive hemolysis or liver disease or infiltration.

Conjuctival pallor

Due to low hemoglobin levels

Blurred vision, diplopia, visual field cuts

Can be caused by anemia, extreme leukocytosis, polycythemia may cause visual abnormalities. Thrombocytopenia may cause intraoccular hemorrhage with visual abnromalities. Excessive clotting may cause thromboses in the circulation to the brain that cause visual field cuts

Smooth tongue

Tongue surface is smooth and shiny, mucosa is thin and red from decreased papillae. This can be due to pernicious anemia or iron-deficiency anemia.

Bone pain in pelvis, ribs, spine, or sternum

Can be due to multiple myeloma related to enlarged tumors that stretch periosteum, bone invasion by leukemia cells. Bone demineralization resulting from various malignancies. Sickle cell disease.

Joint swelling

this can occur due to hemophilia and sickle cell anemia as bleeding occurs into the joint causing inflammation.

Lymphadenopathy

Enlarged lymph nodes that may be tender to the touch. This can be due to infection, foreign infiltration. systemic disease such as leukemia, lymphoma, Hodgkin's lymphoma, and metastatic cancer.

Tachycardia

compensatory mechanism in anemia to increase cardiac output.

palpitations

feeling the heartbeat, flutter, or pound in the chest. This can be due to anemia, fluid volume overload, hypotension with impending syncope, hypertension, or dysrhythmias.

orthostasis

This is when heart rate goes up about 20 beat per minute or when blood pressure goes down 20 from baseline when moving from a lying position to either sitting or standing. This is a common manifestation in anemia, especially if also accompanied by low blood volume.

Hypotension

Hypotension is a systolic blood pressure below 90 or a drop of 40 from baseline. This may indicate an infectious process, blood loss, or compromised cardiovascular compensatory mechanism.

Hypertension

Hypertension is a blood pressure greater than 140/90. This usually occurs as a compensatory mechanism for anemia.

Sternal tenderness

Leukemia resulting from increased bone marrow cellularity can cause an increase in pressure and bone erosion.

Low oxygen saturation

This can be decreased due to severe cases of anemia

Hepatomegaly

Leukemia, cirrhosis, or fibrosis secondary to iron overload from sickle cell disease or thalassmeia can cause this.

Splenomegaly

Can be caused due to anemia, thrombocytopenia, leukemia, lymphomas, leukopenia, mononucleoisis, malaria, cirrohosis, trauma, portal hypertension.

Distended abdomen

Lymphoma may manifest as abdominal adenopathy, masses or bowel obstruction.

Parasthesias of feet and hands; ataxia

This can be due to a colbamin deficiency or folate deficiency

Weakness

Low hemoglobin levels, anemia

headache, nuchal rigidity

this is a pain in the cranium, potentially invovling one area or extending form the frontal area to the back of the neck. Headaches can be due to mild to moderate anemia. Severe headaches with or without visual disturbances may signal intracranial hemorrhage due to thrombocytopenia.

Normal hemoglobin levels

This is to help us measure the gas-carrying capacity of RBC. In females, 12-16, in males, 14-18.

Normal hematocrit levels

This is to measure the packed cell volume of RBCs expressed as a percentage of the total blood volume. In females, 36-46, in males, 42-52.

Normal WBC

This is the measurement of total leukocytes. 5,000-10,000

Normal platelets

This is the number of total platelets available, and it tells us what the person's clotting ability looks like. 150,000-400,000

Normal RBC

This is total circulating RBCs. In females, 4.2 to 5.4. In males, 4.7 - 6.1.

Normal aPTT

This is activated partial thromboplastin time. This is an assessment of intrinsic coagulation by measuring clotting factors specific to intrinsic pathway. It is longer in patients using heparin. 25-35 seconds by book standard.

Normal PT

Prothrombin time. This is an assessment of extrinsic coagulation by measurement of clotting factors specific to extrinsic pathway. 11-12.5 seconds on chart, but 11-16 per book.

thromboplastin

Enzyme released by damaged cells that convert prothrombin to thrombin.

Prothrombin

Enzyme that coverts fibrinogen to fibrin after it is converted to thrombin.

D-dimer

Measures breakdown of fibrin products. This is used as an adjunctive measure in diagnosis of hypercoagulable conditions like DIC or pulmonary embolism. Usually used to rule out DVT, but not used to diagnose. < 250/L is normal

INR Internationalized ratio

This is a standardized system of reporting PT based on a reference calibration model and calculated by comparing the patient's PT with a control value. reference level is 2-3
= desired effects with warfarin.

Bilirubin

measures the degree of RBC hemolysis or liver's inability to excrete normal quantities of bilirubin. three forms to look at. Total: 0.2-1.2, Direct: 0.1-0.3. Indirect: 0.1-1.0

Coombs test

This helps to differentiate among the types of hemolytic anemias. Detection of immune antibodies and RH factor. Normal value would be negative.

ESR is erythrocyte sedimentation rate

This is a measurement of sedimentaion or settling of RBCs in 1 hour. This helps us know if a patient is experiencing inflammation. During inflammation, alteration of plasma proteins can resulti in aggregation of RBCs and making them heavier. The faster the sedimentation rate, the higher the ESR. Less than 30 mm/hr.

Colbamin

Colbamin needed to produce RBCs, normal amount is 200-835

Ferritin

Amount of stored circulating iron. normal is 10-250

Folic acid

Folic acid is needed for RBC production. Normal is 3-16

Serum iron

Amount of total iron used and stored. 50-175

Total iron-binding capacity (TIBC)

This is a measurement of all proteins available for binding iron. Transferring represents the largest quantity of these proteins. 250-425

Reticulocyte count

Measurement of immature RBCs which is a reflection of bone marrow activity. 0.5%-1.5% of RBC count.

Transferrin

This is the largest of proteins that bind to iron. It is increased in most people with iron deficiency anemia. 190-380 mL

Transferrin saturation

Decreased in iron-deficiency anemia and increased in hemolytic and megaloblastic anemia. 15%-50%.

Normal WBC

...