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92 Cards in this Set

  • Front
  • Back
cornerstone of treatment for SCLC (limited-stage and extensive-stage)
Combination chemotherapy
define limited-stage disease SCLC
disease limited to one hemithorax, with hilar and mediastinal LAD that can be encompassed within one radiotherapy portal
thalassemia that presents with normal hemoglobin electrophoresis results
α-thalassemia trait
pentad of findings in TTP
fever, neurologic deficits, thrombocytopenia, microangiopathic hemolytic anemia, kidney impairment
how is mantle cell lymphoma diagnosis confirmed?
presence of overexpression of cyclin D1 and a t(11;14) translocation in the malignant lymphoid cells
CD4-positive T-cell leukemia characterized by major skin involvement
mycosis fungoides
what is Sézary syndrome?
cutaneous lymphoma with prominent leukemic phase; sometimes considered a late stage of mycosis fungoides with lymphadenopathy
provides independent prognostic information in CLL
β2-microglobuin level, heavy gene mutational status, and cytogenetics
test to establish diagnosis of CML
fluorescence in situ hybridization (FISH) assay for t(9;22)
conditions where JAK 2 is positive
polycythemia vera (95%) and essential thrombocythemia and primary myelofibrosis (50-60%)
heterophile antibody test
infectous mononucleosis
useful in the management of the hormonal symptoms of neuroendocrine tumors when they are present and may slow progression of metastatic carcinoid tumors
octreotide, a somatostatin analogue
when is R hemicolectomy indicated in carcinoid tumors of ileocecal area
large carcinoid tumors (≥2 cm) of appendix or tumors of appendix of any size with aggressive histology (high-grade neuroendocrine tumors or adenocarcinomas)
treatment of locally advanced anal cancer
RT + 5FU and mitomycin
is surgery indicated in anal cancer?
stages I, II, and III potentially cured with RT + chemo, without disfiguring operation
how to confurm adherence to hydroxyurea therapy in sickle patients
check MCV (should show macrocytosis)
treatment of acute chest syndrome
(ABx, O2, pain meds, don't overhydrate, transfusion) empiric broad-spectrum antibiotics, supplemental oxygen, pain meds (diminish chest splinting), and avoid overhydration; transfusion if hypoxic despite o2
appropriate breast cancer follow-up
H&P + mammography
causes of PRCA (4)
parvovirus B19 infection, myelodysplasia, large granular lymphocytosis, thymoma
??diagnostic of large granular lymphocytosis
Flow cytometry revealing CD57+ T cells and clonality on T-cell receptor gene rearrangement studies
lab findings in PRCA caused by parvovirus infection
giant pronormoblasts in bone marrow biopsy, and no large granular lymphocytes on PBS
poor prognostic features of melanoma (3)
thickness greater than 0.75 mm, a positive deep margin, or lymphovascular invasion
most common complication of sickle cell trait
hematuria due to papillary necrosis
purpose of γ-irradiation of erythrocytes
eradicates lymphocytes (minimizes GVHD)
advantages of leukoreduction of blood product
less febrile nonhemolytic transfusion reactions, CMV transmission, and alloimmunization (but not anaphylaxis)
Young men with a predominant tumor location in the mediastinum and retroperitoneum
extragonadal germ cell cancer syndrome, (check HCG and AFP)
monoclonal antibody against vascular endothelial growth factor
Bevacizumab
a monoclonal antibody that interferes with the HER2/neu receptor
trastuzumab or Herceptin
side effects of traztuzumab
Heart failure (esp when used with anthracycline)
side effects of tamoxifen
increased risk for thromboembolic disease and endometrial cancer
agent used for ER-positive breast cancer
tamoxifen
mutation in severe congenital neutropenia
neutrophil elastase gene
work up for autoimmune neutropenia
antineutrophil antibody assay
Diagnosis of APS
venous or arterial thromboembolism or pregnancy morbidity (3 or + first-trimester miscarriages or one fetal death) and positive laboratory results ([dRVVT], ACL Ab, β2 GPI) on two occasions 12 weeks apart
mutations associated with mild to moderate hyperhomocysteinemia
Methylene tetrahydrofolate reductase mutations
how to minimize risk of alloimmnization in patients with SCD
phenotypically matched for the C, E, and K antigens
who should undergo yearly mammography and breast MRI
patients who received mantle radiation, carriers of the BRCA1 or BRCA2 mutation
side effect of bevacizumab
disrupt normal vasculature, resulting in POOR WOUND HEALING and vascular catastrophes, including bleeding or thromboses
diagnostic of hairy cell leukemia
dry aspirate on bone marrow sampling and finding of lymphoid cells with hair-like projections
treatment of hairy cell leukemia
cladribine, highly curable
describe headache of brain mets
maximum intensity on waking up, severe and persistent despite analgesia
How to manage pregnant with SCD in a painful crisis
Fluids, O2, morphine (not teratogenic)
low risk prostate cancer
T1 or T2 cancer with Gleason score <8 and PSA <20
when is antiandrogen therapy considered in prostate cancer?
newly diagnosed + high-risk + received radiation therapy OR hormone-sensitive metastatic cancercancer
when is radical prostatectomy indicated in prostate cancer?
younger patients with organ-confined disease and a life expectancy greater than 10 years
treatment of diffuse large B cell lymphoma
R-CHOP (rituximab plus cyclophosphamide, doxorubicin, vincristine, prednisone) x six cycles, high-dose chemotherapy and autologous HSCT for recurrent
Treatment of newly diagnosed acute lymphoblastic leukemia.
induction chemo with daunorubicin, vincristine, L-asparaginase, prednisone
BCR-ABL inhibitor used for the treatment of chronic myeloid leukemia
imatinib
Anticoagulants approved for the treatment of HIT
argatroban + lepirudin (direct thrombin inhibitors) and danaparoid (heparinoid)
Pulmo nodule vs lung mass
pulmo NODULE = nodule up to 3 cm diameter surrounded by normal lung and no LAD vs. MASS = >3 cm
when should lung nodules be followed?
low risk </=4mm, follow-up not required; highi risk <4mm, follow up in 1 year. low-risk (never smokers, no first-degree relative with lung cancer, or significant radon or asbestos exposure); high-risk (smoking history, environmental exposure)
treatment of CUPS in woman with axillary LAD
axillary LAD without other findings = treat as stage II breast cancer
the only malignancy in which removing the primary tumor in the setting of metastatic disease can improve overall outcome rather than just reduce local symptoms.
Kidney cancer
diagnosis of multiple myeloma
bone marrow biopsy showing 10% or more clonal plasma cells
diagnosis of symptomatic myeloma
requires evidence of end-organ damage (hypercalcemia, kidney dysfunction, anemia, and/or bone disease) related to myeloma
greatest reduction in cancer risk for patients who are (+) for BRCA
bilateral salphingo-oophorectomy and bilateral mastectomy
chronic myeloproliferative disorder characterized by overproduction of megakaryocytes and bone marrow stromal cell-mediated collagen deposition
primary myelofibrosis
high risk features of primary myelofibrosis
age >65; fever, night sweats, and weight loss >/=10%; Hb <10 g/dL (100 g/L);WBC > 25,000/µL (25 × 109/L); and circulating blasts of >/=1%
what is SEVERE aplastic anemia?
>/=2 of: ANC 200 to 500/µL, Plt <20,000/µL, and retic <0.2%
VERY SEVERE aplastic anemia
ANC <200/µL
aplastic anemia in young man occurs after viral infection. which viral infections can cause this?
EBV, CMV
define limited stage SCLC
disease limited to one hemithorax, with hilar and mediastinal LAD that can be encompassed within one radiotherapy portal.
treatment of SCLC
limited stage - RT and chemo; extensive - chemo only
patient on tamoxifen develops menopausal symptoms - what is your treatment?
venlafaxine
What is retinoic acid syndrome?
In APL patients who receive ATRA, 25% develope syndrome of fever, hypotension, dyspnea, peripheral edema, weight gain, AKI due to ATRA-induced differentiation; MECHANISM is due to release of cytokines from promyelocytes leading to capillary leak
manifestations of tumor lysis syndrome
hyperkalemia, hyperuricemia, hyperphosphatemia, hypocalcemia, AKI, DIC
how to treat a pregnant patient with DVT?
LMWH throughout pregnancy + 6 weeks after delivery
4 side effects of Tamoxifen
VTE, endometrial cancer, hot flushes, cataracts.
warfarin reversal for life-threatening bleeding (2)
vitamin K, 10 mg IV over 1 hour, plus prothrombin complex concentrate (PCC)
what is prothrombin complex concentrate (PCC)?
lyophilized plasma products that contain each of the vitamin K-dependent coagulation factors
associated with increased RDW
iron, folate, or vitamin B12 deficienty
treatment of head and neck cancer in general
locoregionally advanced (stages III and IVA and IVB without mets) combination of radiation, chemo and surgery. early-stage (stages I and II) head and neck cancer receive surgery or radiation with curative intent
when is iron chelation indicated in beta thalassemia?
high ferritin and transferrin saturation, even without SSx of iron overload
what are bite cells?
cells with eccentrically located hemoglobin confined to one side of the cell seen in g6pd
differentiate WAIHA from cold agglutinin disease
direct Coombs (antiglobulin) test is frequently strongly positive for IgG and negative or weakly positive for complement in WAIHA,
diagnostic test to establish PNH
cytometric analysis for CD55 and CD59
how to prevent DVT in pregnant?
LMWH
how to prevent DVT in pregnant with APAS?
LMWH or UFH + ASA
rare NMJ transmission disorder caused by antibodies directed against presynaptic voltage-gated P/Q-type calcium channels
Lambert-Eaton myasthenic syndrome
how to diagnose Lambert-Eaton myasthenic syndrome
EMG and assays for P/Q-type calcium channel antibodies
differentiate cobalamin from folate deficiency
cobalamin deficiency presents with neuro symptoms + elevated MMA and homocysteine; folate does not have neuro symptoms
findings in smear of MDS
leukoerythroblastic picture, nucleated RBCs and a left shift in WBC; megathrombocytes, teardrop cells
treatment for acquired hemophilia with severe bleeding
rFVIIa
treatment for DIC with severe bleeding
FFP and CP
what is the pathophysiology of TRALI?
caused by antileukocyte antibodies in the donor blood product directed against recipient leukocytes, which then sequester in the lungs, usually during or within 6 hours of a transfusion
etiology of acute hemolytic transfusion reaction
most commonly caused by a clerical error leading to ABO incompatibility. hypotension and DIC develop very early in the transfusion
surveillance for stage III colon cancer, post op and adjuvant chemo
PE + CEA q 3-6m; CT chest, abd, pelv q1y for 3-5y; colonoscopy 1y after resection the q3-5y
when is exchange transfusion or RBC transfusion indicated in sickle cell disease?
acute management of stroke and acute chest syndrome.
most common forms of cutaneous T-cell non-Hodgkin lymphoma.
Mycosis fungoides (affects skin) and Sézary syndrome (affects skin and blood)
treatment for progressing mycosis fungoides/Sézary syndrome.
alemtuzumab (anti-CD52)
What is the Mentzer index?
MCV/RBC; <13 = β-thalassemia.
treatment of High-risk, early-stage lesions bladder cancer
BCG immunotherapy (intravesicular)