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93 Cards in this Set
- Front
- Back
hypersegmented neutrophils, gastritis, parasthesias/numbness, low Hct, palor, icteric... is most likely what deficiency?
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Vitamin B12-peripheral nerves are usually affected first, posterior columns become impaired and p complain of balance problems.
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what is the hallmark symptom of B12 deficiency?
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megaloblastic anemia
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a type of autoimmune anemia. Antibodies are directed against intrinsic factor or parietal cells which produce intrinsic factor
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pernicious anemia
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what is the MC dietary deficiency that leads to anemia?
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occult blood loss
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what are some examples of bleeding disorders?
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occult blood loss
inadequate PLT's ITP |
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what are some manifestations of ITP?
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isolated thrombocytopenia, purpura, epistaxis
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an autoimmune disorder in which an IgG autoantibody is formed that binds to platelets. Destruction of pLT takes place in spleen. Common in childhood, precipitated by viurs.
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Idiopathic (autoimmune) Thrombocytopenic Purpura
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what are some examples of some infectious processes that lead to ITP?
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viral: varicella,
sequele: GI, URI |
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what is the primary tx for ITP?
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corticosteroids; IVIG= intravenous Immunoglobulins
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Factor VIII deficiency: aka?
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Hemophilia A
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VonWillebrand's deficiency: aka?
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Co-Factor VIII deficiency
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Hemophilia B: aka?
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Factor IX deficiency
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if p is dx c ITP, and is unresponsive to corticosteroid treatment, what is the most aggressive tx and last resort?
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spleenectomy
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which blood test is timing the extrinsic cascade?
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PT
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which blood test times the intrinsic cascade?
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PTT
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what is the hallmark of the ITP disease?
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thrombocytopenia: <10,000
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what is the name of the co-existant autoimmune hemolytic anemia usually seen in ITP?
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Evan's Syndrome: + anemia, reticulocytosis, spherocytes on peripheral smear
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what is the MC type of drug-induced thrombocytopenia?
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HIT
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IgG autoantibody that reacts with platelet factor 4 (PF4) that is usually in a complex with heparin causes what reaction?
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HIT
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after you confirm your dx of HIT, what is the first thing you do?
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stop heparin
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virchow's triad?
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damage to vessel wall
stasis of blood hypercoaguable state |
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thrombocytopenia, elevated serum LDH, microangiopathic hemolytic anemia, neurologic and renal abnormalities... are usually indicitive of what disorder?
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thrombotic thrombocytopnic purpura
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what is the hallmark of TTP: thrombotic thrombocytopenic purpura
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microangiopathic blood picture with shistocytes, etc.
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definitive tx for TTP?
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large-volume plasmapheresis: fresh-frozen plasma!
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what are some examples of microangiopathic hemolytic anemias?
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TTP, ITP, DIC, HELLP, HIT, HUS
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MAHA, thrombocytopenia, renal failure, elevated LDH, is indicitive of what disorder?
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Hemolytic Uremia Syndrome
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a form of severe preeclampsia, (very elevated BP, thrombocytopenia) may progress to DIC is called?
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HELLP syndrome: hemolysis, elevated liver enzymes, low plt
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a direct antibody test that is given to a patient with hemolysis to identify which antiobdy IgG or IgM is involved?
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COOMBS test
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most often measured to evaluate the presence of tissue damage. This enzyme is in many body tissues, especially the heart, liver, kidney, skeletal muscle, brain, blood cells, and lungs
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LDH: Lactate dehydrogenase; Lactic acid dehydrogenase
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what does the BUN reflect?
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proteins in liver that get converted to urea
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a medical condition characterized by abnormal levels of urea, creatinine, various body waste compounds, and other nitrogen-rich compounds in the blood as a result of insufficient filtering of the blood by the kidneys.
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azotemia
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a toxic condition resulting from renal failure, when kidney function is compromised and urea, a waste product normally excreted in the urine, is retained in the blood. it can lead to disturbances in the platelets and hypersomnia, among other effects.
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uremia
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this condition is MC in children, presents like renal failure; hemolysis of RBC's and decreased plt's. Petechiae, purpura, SOB, fatigue, epistaxis?
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HUS: hemolytic uremic syndrome
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more common in adults, presents with HA, seizures, altered mental status, bleeding, thrombosis, is most likely what disorder?
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TTP
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It is the most common type of pituitary tumor. S/S are caused by too much prolactin in the blood (hyperprolactinemia) or by pressure of the tumor on surrounding tissues.
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prolactinoma
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how do you treat prolactinomas?
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with drugs that inhibit the production of prolactin= dopamine antagonists aka Bromocriptine or cabergoline
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cold nodule=?
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a hypoactive nodule. it does not absorb contrast on CT scan. usually malignant.
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some systemic symptoms, such as low-grade fever, night sweats, weight loss, pruritus, or fatigue. painless lymphadenopathy
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Hodgkin's lymphoma
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membrane defects, spherocytosis , hereditary elliptocytosis, hemoglobinopathies are examples of what types of anemias?
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intrinsic hemolytic anemias
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immune, microangiopathic, lymphoproliferative diseases, TTP, HUS, DIC are examples of what type of anemia?
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extrinsic hemolytic anemias
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a tumor of the adrenal gland causes severe HTN, palpitations, flushing, irriatibilty is known as what rare disease?
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pheochromocytoma
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what is the best way to differentiate between Hyperthyroid and pheochromocytoma?
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pheo has more severe and paroxsymsmal HTN
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what is the most definitive way to confirm Pheo?
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MIBG scintiscan
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syndromes of these tumors are inherited as autosomal dominant traits and cause a predisposition to the development of tumors in different tissues, particularly involving endocrine glands
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MEN 1: multiple endocrine neoplasia
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what is the main risk factor for multiple endocrine neoplasia?
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familial history
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what is the first clinical manifestation of MEN-1?
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hyperparathyroidism: hypercalcemia
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what is the normal range for calcium?
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8.5-10.5
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an enlargement of one parathyroid gland is called?? and it accounts for 96% of all patients with primary hyperparathyroidism?
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parathyroid adenoma
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what is the term for an enlargement of all 4 parathyroid glands
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hyperplasia
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what is the definitive treatment of hyperparathyroidism?
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surgery
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an uncommon disorder caused by destruction or dysfunction of the adrenal cortices. characterized by chronic deficiency of cortisol, aldosterone and adrenal androgens and causes skin pigmentations
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addison's disease= chronic adrenocortical insufficiency
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what is the most common cause of addison's disease in the U.S?
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autoimmune destruction of the adrenal cortex
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what two hormones are lacking in addison's disease?
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glucocorticoid (cortisol)
mineralcorticoid (aldosterone) |
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what is the sole purpose of the parathyroid glands?
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to regulate calcium
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what are some of the side effects of hypercalcemia?
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feeling of being "run down" poor sleep habits, irritability, memory decrese
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what is the MC cause of excess hormone production?
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the development of a benign tumor in one of the parathyroid glands
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what test is used to identify adenomas or hyperplastic parathyroids?
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MIBI: methoxyisobutyl isonitrile
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what is the name of the disease that affects multiple endocrine glands; is classified into two types?
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Polyendocrine Deficiency syndrome
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schmidt's syndrome?
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type II Polyendocrine Def.
adults underactive thyroid slow sexual develop. diabetes vitiligo |
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what infection accounts for 20 % of cases of primary adrenal insuff in developed countries?
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TB
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what are the main clinical features of addison's disease?
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fatigue
weight loss GI disturbances hypoglycemia depression pigmentation (if elevated ACTH production) |
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what is the most specific test for diagnosing Addison's ?
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ACTH stimulation test
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what is the acute tx for addison's (crisis)
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IV hydrocortisone and 0.9% saline
(add dextrose if hypoglycemia present) |
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what is lifelong tx for patient dx with addison's
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hydrocortisone and fludrocortisone
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the excess secretion of aldosterone into the blood is from an abnormal adrenal gland/s, usually seen with HTN.
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Conn's aka primary hyperaldosteronism
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what is the most rigorous method of diagnosis to test for Conn's
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test aldosterone and renin
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what are the 3 hallmark findings in conn's syndrome?
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HTN
elevated aldosterone decreased RENIN |
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what is the definitive tx for CONN's?
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adrenalectomy.
in the meantime; treat with spironolactone (blocks aldosterone) |
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if a patient has hypotension or hyperkalemia what disease should be a part of your diff?
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addison's
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a steroid hormone (mineralocorticoid family) produced by the outer-section (zona glomerulosa) of the adrenal cortex in the adrenal gland to regulate sodium and potassium balance in the blood.
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aldosterone
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excess production of cortisol by the adrenal glands causes what syndrome?
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cushings
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what is the most common cause of excess steroids in the blood and its side effects?
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long term use of steroid medication for other disorders
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how do you determine excess cortisol from a pituitary tumor or an adrenal tumor?
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pituitary tumor secretes too much ACTH, increase cortisol and increase ACTH serum levels.
Adrenal tumor: composed of adrenal producing cells, and normal pituitary will sense excess cortisol and stop making ACTH! |
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what is the major cause of ACTH dependent cushings syndrome?
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pituitary tumors 60%
lung cancers 5% |
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what is the cause of ACTH independent cushings syndrome?
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benign adrenal tumors (adenoma) 25%
malignant 10% |
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what is the most sensitive test for cushings?
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24 hour cortisol serum
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this disease of the adrenal medula causes "attacks" of HA, perspiration, palpitations, HTN, Nausea, abdominal pain
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pheochromocytoma
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elevated urine metanephrine (VMA) and elevated urine catecholamines is indicitive of what disorder?
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pheochromocytoma
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what are the 3 main categories of anemias?
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Impaired production
Bleeding Hemolytic |
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acquired anemia caused by IgG autoantibody, spherocytes and reticulocytes on peripheral, + Coombs is indicitive of ?
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autoimmune hemolytic anemia
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a liver-derived protein that participates in response or with IgG/IgM, it binds to RBC and participates in immune-mediated hemolysis
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complement
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what is CREST ?
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the limited form of scleroderma:
Calcinosis Raynaud's syndrome Esophageal Dysmotility Sclerodactyl Telangiectasia |
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what are some examples of microcytic processes?
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MCV <80: "sits"
Sideroblastic anemia Iron Def Thalassemia Minor Sideroblastic |
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what are some representative examples of the macrocytic anemias?
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MCV > 100:
megaloblastic: folate def B12 def. drug induced Nonmegaloblastic: liver disease, hypothyroid |
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differential with normocytic anemia?
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MCV 80-100:
aplastic anemia myelophthsic diorders anemia of chronic disease uremia |
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what are some of the enteric organisms that reside in GI normally?
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e.coli, proteus, klebsiella
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macrophages in tissues aka?
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histocytes
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macrophages in brain
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microglial
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macrophages in liver aka?
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kupfer cells
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patients labs return with an elevated RENIN and elevated Aldosterone...where does this indicate the problem?
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within the kidneys:
caused by pressure loss, kidnes will raise renin |
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labs return with decreased RENIN and INCREASED ALD? what can you suspect?
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hyperaldosteronism
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you perform a 24 hour urine on patient you suspect has PHEO. what will you see?
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increased VMA which are the byproducts of catecholamines
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what test allows us to see pheo BEST?
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MIBI scan
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