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79 Cards in this Set
- Front
- Back
pt presents with palpitations, fatigue, HA, glossitis, flat thin nails.
1.What is the most likely dx? |
iron deficiency anemia
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in FE def what will the TIBC ans % st and ferritin levels be?
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TIBC is high
% sat is low Ferritin is low |
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what is the most specific test of iron deficiency?
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a low MCV.
only seen with Fe def and thalassemia |
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what is the best test to distinguish between Fe def and anemia of chronic disease?
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ferritin
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what is the bone marrow storage form of iron?
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ferritin
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what does transferrin do?
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made in liver and transports iron to bone marrow to be used so it is high in Fe def.
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what is the mcc of massive lower GI bleeding in adults?
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diverticulosis
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what does elevated CEA tell you
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coon cancer with mets to liver?
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what are the 3 risks for polyps becoming cancer?
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villous component
2 cm or greater sessile |
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pt has a megaloblastic anemia with hypersegmented neutraphils. what is the cause?
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B12/folate def
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what anemia is associated with LDH, high indirect bili, and pancytopenia
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B12/folate
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pt presents with neuropathy, ataxia, +rhomberg, dementia and anemia. what is the cause?
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B12 deficiency
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what are causes of b12 def?
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1. pernicious anemia with anti-pareital factor and intrinsic factor antibodies
2. partial gastrectomy with removal of ileum. 3. metformin |
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treatment of pernicious anemia? what are the side effects of treatment?
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Im or SubQ B12
side effects are thrombocytosis so have to give ASA also and hypokalemia because the new RBCs are using it up. |
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what are causes of folate deficiency ?
how to dx it? |
causes: alcohol, pregnancy, jejunal probs like crohns and celiac, drugs (sulfasalzine, mtx, 5-FU), hemolysis
dx with RBC folate levels not serum folate |
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Sickle cell complications and causes:
1. What causes aplastic crisis? 2. what causes chest syndrome? 3. what causes sickle cell crisis? 4. what causes osteomyelitis typically? |
1. parvovirus B19 with retic count of zero
2. plugging of vasculature and requiring transfusion 3. infection/dehydration/hypoxia 4. salmonella |
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Sickle cell
1. how it is passed? 2. what are typical WBC, Hgb, platelets? 3. what is treatment? 4. when do you see howell jolly bodies? |
1. autosomal recessive, have Hgb S
2. elevated WBC, low Hgb, elevated platelets 3. hydroxyurea to increase fetal hgb 4. spleen autoinfarction |
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pt has low MCV with no anemia an target cells. Dx?
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thalassemia
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Who has alpha thal?
Who has beta thal minor? |
Alpha is asians (will hav normal hgb electrophoresis)
beta is greeks, Mediterranean |
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Hemolytic anemia. What is the dx?
1. high MCHC, abnormal osmotic fragility test 2/2 loss of spectrin on RBC membrane? 2. +Ham's test, and budd chiari is associated with it. only hemolytic anemia without iron overload seen 3. heinz bodies? |
1. spherocytosis
2. paroxysmal noctural hemoglobinuria 3. G6PD def |
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in hemolytic anemia...
1. what is haptoglobin level? 2. bilirubin level? 3. LDH? 4. retic count? |
1. low
2. high indirect 3. high 4. high |
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what causes ITP?
what is treatment in adults? |
caused by IgG antibody against platelets
tx with steroids, IVIG, splenectomy, rituximab, thromboplastin receptor agonists |
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what vaccines should be given before splenectomy?
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pneumovax
H flu meningococcal |
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What is the typical presentation of TTP?
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FAT RN
fever, anemia, thrombocytopenia, renal failure, neurologic changes see LOW ADAMTS13 levels |
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what is tx of TTP?
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plasmaphereis or rituximab
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in a mixing study if pt labs normalize what is the cause?
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factor def
if not its an inhibitor |
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what is the most common bleeding disorder?
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von willebrands
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1. how is VWF def passed?
2. what is bleeding time, PTT, and PT/INR? 3. how to treat it? |
1. autosomal dominant
2. prolonged bleeding time and PTT but NORMAL PT/INR 3. treat with DDVAP if mild but cryoprecipitate or factor 8 concentrate if more severe. |
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what meds can cause platelet problems?
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ASA, NSAIDS, H-2 blockers and heparin
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what is the treatment for HIT?
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argotroban or hirudin before test results of HIT antibodies come back. Can also used fondaparinux now
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in DIC-- what will fibrinogen, platelets, d-dimer and Pt/PTT be?
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low fibrinogen
low platelets prolonged PtPTT and high d dimer. tx with FFP and underlying condition |
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if pt has abnormal ristocetin assay what should you think of on test?
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von willebrands
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how long after stopping heparin after an acute thrombotic event should Antithrombin level be checked and why?
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2 week drug free can check AT because heparin lowers AT, and lowers protein C and S
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which clotting disorder has the highest thrombotic risk?
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antithrombin deficiency -very rare
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if pt has true protein C or S deficiency what are they are risk for when starting coumadin?
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coumadin skin necrosis
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What two disorders will cause BOTH arterial and venous clots?
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anticardiolipin antibody syndrome and hyperhomocysteinemia
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pt presets after multiple second trimester spontaneous abortions. what labs should be checked?
What is the treatment? |
check anti-cardiolipin antibodies and lupus anticoagulant for anticardiolipin antibody syndrome
treat with coumadin lifelong with INR 2-2.5 for first and 3-3.5 for recurrent or arterial clot |
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what is mechanism for factor V leiden and how to dx?
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activated prot C resistance and dx by PCR which picks up the mutation
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how to dx prothrombin gene mutation G20210A?
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DNA test
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what is treatment of hyperhomocysteinemia?
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folate 1mg/day
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how do OCPs increase risk of VTW 4 fold?
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lowers prot c/s and icnreases fibrinogen and prothrombin
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pt presents complaining of puritis and hives after a warm shower.
dx? labs? tx? complications? |
1. polycythemia vera
2. high LAP score, low EPO levels, high RBC mass, pancytosis 3. phlebotomy weekly until hct below 45 and ASA, and myelosupressives later. 4. splenic infarct and AML risk |
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what diseases have the JAK 2 mutation?
how can you treat it? |
polycythemia vera, myelofibrosis, essential thrombocytopenia
tx with ruxolitinib |
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what is alloimmunuztion?
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development of antibodies to foreign RBC antigens- ocurs in 10% of transfusions
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how much should one unit of blood increase hgb?
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one hgb
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pt presents in respiratory failure 6 hours after a blood transfusion. what is the dx and cause?
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TRALI due to donor WBC antibodies binding iwth host WBC and sequestering in the lung
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pt presents with leukocytosis, night sweats, splenomegaly, philedelphia crhomosome and LOW LAP score (key!)
what is dx and tx? |
CML and treat with imatinib (first line) or hydroxyurea+interferon
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how does imatinib work?
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protein tyrosine kinase inhibitor of Bcr-Abl tyrosine kinase gene
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elderly person presents with elevated lymphocytes and smudge cells.
what is dx and when should treatment be started and what is tx? |
CLL usually b cell.
treat at stage 3 or 4 when anemia or thrombocytopenia with fludarabine. |
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auer rods and 30% blasts in BM think what kind of cancer
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AML
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what is treatment for M3 (promyelocytic) AML?
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all-trans retinoic acid (ATRA)
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what will uric acid level, K, phos, and ca levels be in tumor lysis syndrome and what is treatment?
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high uric acid, K, phos,
low ca give allopurinol plus hydration |
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what cancer to think of in kids with bone pain?
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ALL- 85% cure rate
CALLA CD 10+ has best prognosis |
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pt presents with pancytopenia, massive splenomegaly and TARTRATE- RESISTANT ACID PHOSPHATASE. what is dx? and tx?
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hairy cell leukemia (an indolent b cell non-hodgkins lymphoma
treat with interferon |
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what are side effects of interferon?
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depression and thyroid problems?
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what is a leukemoid rxn and what can cause it?
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persisten WBC of 30-50,000 that are mature and not clonally derived due to C. diff colitis, alcoholic hepatitis, and TB
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pt presents with fevers, night sweats, weight loss, painful nodes with etoh ingestion and reed sternberg cells
Dx? tx? |
nodular sclerosing hodgkins lymphoma
tx stage 3 adn 4 with chemo ABVD (adriamycin, bleomycin, vinblastine, dacarbazine) and XRT to involved nodes |
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is hodgkins or non hodgkins better survival?
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hodgkins
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older pt presents with bone pain and high LDH and hx of crohns (or other autoimmune disease). what is dx and tx?
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non-hodgkins most liley burkitts (t 8:14)
tx with XRT and rituximab |
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black pt presents with renal failure, bone pain, high calcium, thrombocytopenia.
1. what is dx? 2. what are the classic findings in urine 3. what type of cells are involved? 4. what type of antibodies are involved? 5. what test should be ordered? 6. what is treatment |
1. Multiple myeloma
2. bence-jones protiens in urine 3. b cell malignancy 4. IgG usually invovled (if IgM it is Waldenstroms) 5. order a skeletal survey not a bone scan 6. melphalan and prednisone |
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what does POEMS syndrome stand for?
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polyneuropathy that is usually distal and symmetric and papilledema
organomegaly endocrinopathy or edema m-protien (myeloma variant) skin hyperpigmentation it is a plasma cell disorder |
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50 year old african american male presents with low back pain and no hx of trauma. what should be ruled out?
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prostate cancer
mets are blastic with high alk phos |
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what drug can decrease prostate cancer risk by 40% and how does it work?
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finasteride- a 5a reductase inhibitor that inhibits conversion of testosterone to dihydrotestosterone and shrinks prostate tissue
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what is the number 1 cause of Ca death in men and women
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lung cancer
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what are lung cancer risk factors?
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smoking, passive smoke, asbestos, arsenic, radon, genetics
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where is squamous cell and small cell (oats) and adenocarcinoma seen in the lung?
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squamous and small cell are central and adeno is peripheral
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what is seen on CXR in adenocarcinoma?
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cannonball mass
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ectopic hormones : name the cancer is comes from
1. ADH 2. ACTH 3. erythropoietin 4. hcG 5 calcitonin 6. AFP 7. CEA 8. pth related peptide 9. serotonin |
1. small cell
2. small cell 3. squamous cell lung cancer, renal cell CA, hepatomas 4. choriocarcinoma 5. medullary cancer of thyroid 6. hepatoma 7. colon cancer with liver mets 8. squamous of lung, breast and renal 9. carcinoid |
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pt presents with myasthenia like illness and is diagnose by EMG with eaton-lambert syndrome. what should you look for next?
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small cell lung cancer or lymphoma
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if pt has DVT associated with a malignancy what should anticoagulation be?
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LMWH - not warfarin!
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if pt presents with acanthosis nigricans and is not found to have DM what else should you look for?
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gastric cancer
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who is most at risk for breast cancer?
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nulliparous women, late first pregnancy, and family history
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if pt has breast cancer with HER2 protein expression what should be the treatment?
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herceptin
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what is most common finding on bx of breast cancer?
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infiltrating ductal cell cancer
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staging breast cancer.
stage 1? stage 2? stage 3? stage 4? |
1. <2cm
2. 2-5cm 3. >5cm 4. chest wall, skin, mets |
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breast cancer treatment
1. if positive lymph nodes what should be treatment? 2. if ER/PR what should be treatment? 3. what are risks of the treatment for question 2? |
1. chemo
2. tamoxifen 3. risks are endometrial cancer, cataracts, and DVTs |
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pt has colon polyps and osteomas and soft tissue tumors. what is syndrome?
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gardners syndrome
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what cancer is strep bovis endocarditis associated with?
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colon cancer
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for pain in cancer pt on exam what should you give?
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acetaminophen first then long acting narcs sooner than later
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