Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
56 Cards in this Set
- Front
- Back
52 yo patient presents with, fatigue, lymphadenopathy, hepatosplenomegaly, cytopenia, proliferative centers, ocular involvement,
positive CD5, CD19, CD20, CD22, CD23; Negative: CD10 and Cyclin D1; diagnosis? |
Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
|
|
51 yo male Patient presents with fatigue, lymphadenopathy, hepatosplenomegaly, greater than 5000 small round lymphocytes that are disrupted, autoimmunity towards erythrocytes or platelets, and hypogammuglobulinemia,
Diagnosis? |
Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
|
|
59 yo patient present with lymphadenopathy, hepatosplenomegaly, no proliferation centers, small irregular lymphocytes, a leukemia phase, GI polyposis,
Positive: CD5, Cyclin D1, CD19, CD20, CD22 negative: CD10, BCL-6, and CD23 Diagnosis? |
Mantle Cell Lymphoma
|
|
62 yo Patient presents with lymphadenopathy, hepatosplenomegaly, GI tract polyposis, walkdeyer's ring, alph4beta7 receptor and t(11;14)
Diagnosis? |
Mantle Cell Lymphoma
|
|
54yo Patient presents with lymphadenopathy, closed packed poorly formed neoplastic follicles without mantle zones, leukemic phase, waldeyer's ring involvement,
Positive: CD10, CD19, CD20, CD22, BCL-6 Negative: CD5, Cycl D1; diagnosis? |
Follicular lymphoma
|
|
55 yo Patient presents with centrocytes and 8/HPF of centroblasts, diagnosis? be specific:
|
Grade 2 Follicular Lymphoma
|
|
15 yo patient presents with head and neck lymphoma appearance, skin involvement, waldeyer's ring, GI tract,
Positive: CD10, CD19, CD20, CD22, BCL-6 Negative: Cyc D1, BCL-2, CD5, diagnosis? |
Follicular Lymphoma
|
|
63 yo patient presents with:
;arge transformed lymphocyte cells (2x small lymph), centroblastic, immunoblastic, anaplastic, positive: CD19, CD20, CD22 negative: CD10, CD5 Diagnosis? |
Diffuse Large B-cell Lymphomas (primary or secondary)
|
|
60 yo patient presents with t(14;18), 3q27, c-MYC rearrangements, diagnosis?
|
Diffuse Large B-cell lymphomas
|
|
Patient presents with CNS lymphomas, testicular involvement,
Positive CD19, CD20, CD22 negative: CD10, CD5, prior history of having MALT lymphoma, diagnosis? |
diffuse large B cell lymphoma secondary!
|
|
19 yo patient from a low income family, might have had earlier EBV infection, presents with abdominal mass, illeocecal, ovary, but no lymph node lymphoma involvement,
Diagnosis? |
Burkitt Lymphoma - Sporadic
|
|
5 yo patient from equatorial africa presents with jaw, omentum, and kidney, but NO lymph node lymphoma involvement
diagnosis? |
Burkitt Lymphoma - Endemic
|
|
35 yo presents with medium sized blasts with sharp lipid vacuoles and a starry sky appearance,
Diagnosis? |
Burkitt Lymphoma
|
|
Patient presents with
Positive: CD10, BCL6, CD19, CD20, CD22 Negative: TdT, CD5, BCL-2, CD23, CD34 KI-67 proliferation Index: 100% t(8;14) diagnosis? |
Burkitt Lymphoma
|
|
Patient presents with single tumor with regional lymph node involvement, two lympho node regoins same side of diaphragm, tumor in ovary and kidney same side,
diagnosis, be specific? |
Stage II: Burkitt's Lymphoma
|
|
53 yo Patient presents with pancytopenia, splenomegaly, infections and vasculitis, marrow friend egg appearance cells,
diagnosis? |
Hairy Cell Leukemia
|
|
Patient presents with splenomegaly, marrow has dry tap, lymph nodes and liver involvement,
Positive: CD103, CD22, CD25, CD11c, Cyc D1, CD19, CD20, annexin A positive, with strong TRAP stain Negative: CD5, CD10, CD23 Diagnosis? |
Hairy Cell Leukemia
|
|
63 yo Patient presents with, lymphadenopathy, waldenstrom macroglobulinemia, hyperviscosity, increase in mast cells, rouleauex formations,
diagnosis? |
Lymphoplasmacytic Lymphoma
|
|
64 yo patient presents with cryoglobulinemia, neuropathy, coagulopathy,
positive: CD19, CD20, CD22 negative: CD5, CD10, diagnosis? |
Lymphoplasmacytic Lymphoma
|
|
72 yo patient presetns with monoclonal serum protein, hypercalcemia, renal insufficiency, anemia, and bone pain,
diagnosis? |
Plasma Cell myeloma
|
|
African american former farmer presents with bence jones proteins, hypogammaglobulinemia, with active hematopoiesis in flat bones, vertebrae, ribs and clavicle
diagnosis? |
Plasma Cell Myeloma
|
|
71 yo african american cosmetologists presents with m-component positive, detectable serum spke in IgA and IgG,
Positive: CD38, CD20, CD56 and negative surface Ig; Diagnosis? |
Plasma Cell Myeloma
|
|
Patient presents with skin plaques, medium sized T cell with cerebriform nuclei, pautrier microabscesses (collection of mycosis of T-cell in the epidermal)
diagnosis? |
Mycosis Fungiodes
|
|
Adult male presents with skin with erythroderma,early lymph node involvement and minimal blood involvment, with cerebriform cells, diagnosis, be specific:
|
Mycosis Fungiodes - stage III
|
|
61 yo male presents with erythroderma, lymphadenopathy, circulating tumor cells in blood, and alopceia, diagnosis?
|
Sezary Syndrome
|
|
60 yo male patient presents with cerebriform nuclei, lutzner cells,
Positive: CD2, CD3, CD5, CD4, CLA, Skin homing receptor CCR4, Negative: CD7, CD8, ALK-protein increased CD4/CD8 ratio>10:1 diagnosis? |
Sezary Syndrome
|
|
58 yo patient presents with previous history of human T-cell leukemia virus, from japan, pleomorphic cells, (high nuclear/cytoplasmic ratio), leukemic phase - eosinophils in particular, pautrier like microabscess, hypercalcemia
diagnosis, be specific: |
Adult T cell Leukemia/Lymphoma - Acute
|
|
57 yo patient presents with adenopathy without leukemic phase, cutaneous lesions, flower cels
diagnosis, be specific: |
Adult T cell Leukemia: Lymphomatous
|
|
56 yo patient from central africa presents with pleomorphic an dflower cells, exfoliative skin rash, increased wbcs with atypical lymphocytes in blood, diagnosis, be specific?
|
Adult T cell Leukemia: chronic
|
|
58 yo patient presents with normal wbcs with >5% circulating tumor cells, skin and lung disease, morphologic variants in lymphocytes,
positive: CD2, CD3, CD5, CD4, CD25 negative: CD7, CD8, ALK diagnosis, be specific |
Adult T cell leukemia: Smoldering
|
|
28 yo patient presents with B cymptoms, lymphadenopathy, lymph node, BM, and soft tissue involvement, cells are large, kidney bean nucleaus, eosinophilic hoffregions, abundant cytoplasm, and they are concentrated around vessels ,
diagnosis, be specefic: |
Anaplastic Large Cell Lymphoma - Primary Systemic type
|
|
31 yo presents with B symptoms, lymphadenopathy, skin involvement, multinucleated wreath cells,
positive: CD2, CD4, CD5, CD30, Anaplastic large cel lymphoma kinase negative CD3, CD7, CD8, EBV diagnosis, be specific: |
Anaplastic Large Cell Lymphoma - Primary Cutaneous Type
|
|
Patient presents with large cell pleomorphic and abundant cytoplasm, with cytotoxic granule associated proteins:
TIA-1 Granzyme B Perforn t(2;5), diagnosis? |
Anaplastic Large Cell Lmphoma
|
|
42 yo patient presents with cervical, axillary, inguinal lymph node association, L and H type cells (scattered polymorphous large cells with folded/multilobated nucleus and scant cytoplasm),
positive CD45, CD20, OCT-2 and BOB.1 Negative: CD3, CD15, CD30, EBER diagnosis? |
Nodular Lymphocyte Predominant
|
|
35 yo Patient presents with popcorn cells, and large spherical follicular dendritic meshworks, BCL-6 translocation, lympho nodes, splenic, celiac, and paraaortic nodes all involved, diagnosis, be specific?
|
Stage III - 2 : Nodular Lymphocyte Predominant
|
|
14 yo Patient presents with mediastinal, bulky disease, thickened capsule, collagen bands surrounding nodule, lacunar cells, necrosis, increased EL2, 5, 10, TGF-beta, Eotaxin
diagnosis? |
Nodular Sclerosis - Hodgkin Lymphoma
|
|
38 yo patient presents with B symtoms, lymphadenopathy, mononuclear RS cells, with epithelioid histiocytes granulmas like clusters as background cells, increased cytokines,
diagnosis? |
Mixed Cellularity - Hodgkin Lymphoma
|
|
32 yo patient presents with history of EBV, mediastinal disease, bulky disease, eccentric small regressed germinal centers, capsule not thickened, scattered RS cells, resemble LP cells, small lymphocytes predominantly in background, essentially absent eosinophils
Diagnosis? |
Lymphocyte Rich
Differential: Nodular Lymphocyte Predominant HL |
|
37 yo Patient presents with B symptoms, EBV, abdominal and retroperitoneal lymph nodes involved, small lymphocytes depleted, diffuse interstitial fibrosis pattern,
diagnosis? |
Lymphocyte Depleted
|
|
Patient presents with marrow failure, >20% blasts, very primitive cells,
MOP, SBB, and NSE negative, CD13, CD33, and CD34 positive, primitive cells, Diagnosis? |
Acute Myeloid Leukemia, M0 - Minimal Differentiation
|
|
46 yo patient presents with marrow failure, >20% blasts, most non-erythroid, and few are PMN/s with auer rods,
Positive: MPO, SBB Negative: NSE Immunophenotype: CD13, CD33, CD34, cMPO diagnosis? |
Acute Myeloid Leukemia, M1 - Myeloid without maturation
|
|
Patient presents with >20% blasts, >10% of these are PMN's, and <20% are monocytic w/ auer rods, neutrophil dysplasia,
Positive: MPO, SBB, CD13, CD33, CD34, CD15, cMPO Negative: NSE Diagnosis? |
Acute Myeloid Leukemia, M2 - myeloid with maturation
|
|
Patient presents with marrow failure, >20% blasts,
Positive: MPO, SBB, CD13, CD33, CD34, CD14, CD4, CD11b/c, CD36 Diagnosis? |
Acute Myeloid Leukemia, M4 - Myelomonocytic
CD13, 33, 34 - myeloblasts CD14, 4, 11b/c, 36 - monoblasts |
|
55 yo Patient presents with bleeding in gingival, and CNS disease, blasts >20% including promonocytes
Diagnosis? |
Acute Myeloid Leukemia, M5b - Monocytic
|
|
5yo patient presents with CNS disease, blast >20% including promonocytes,
positive: NSE Negative: MPO, SBB Immuno: CD13, 33, 14, 4, 11b/c, 36 Diagnosis? |
AML: M5a, Monoblastic
|
|
Patient presents with anemia, and normoblastemia, myeloblasts >20%,
Positive: MPO, SBB Negative: NSE Immunophenotype CD13, 33, glycophorin A, Heme A Diagnosis? |
AML: M6, Erythroleukemia
|
|
Patient presents with PAS positive red cells, anemia,
Negative: MPO, SBB, NSE Immunohenotype: glycophorin A, Heme A Diagnosis? |
M6b, Pure Erythroid
|
|
Patient presents with bleeding in skin and gingival, and CNS disease, dry trap
Positive: PAS Negative MPO, SBB Immunophenotype: cCD41, cCD61, CD13, CD33 Diagnosis? |
AML: M7, Megakaryoblastic
|
|
25 yo Patient presents with t(8;21)(q22;q22) genetic workup, diagnosis?
|
AML with AML1/ETO translocation presenting like M2 - Myeloid with maturation, even if <20% blasts
|
|
Patient presents with DIC, genetic workup is: t(15;17)(q22;q12)
Diagnosis? |
Acute Promyelocytic Leukemia:presents like M3 -
PML/RAR-alpha translocation, RARalpha - retinoic acid receptor (17) and PML - promyelocytic leukemia gene (15) |
|
Patient presents with marrow failure, auer rods present, atypical eosinophils, increased monocytes,
Positive MPO, SBB Weak positive: NSE inv(16)(p13q22) Diagnosis? |
AML: CBFbeta/MYH11 translocation presents like a M4e
|
|
Patient presents with
positive: CD13, 33, cMPO, CD14, 4, 11b/c, 64 and t(16;16)(p13;q22) Diagnosis? |
AML: CBF-Beta/MYH11 translocation presents as an M4,
|
|
Patient presents with DIC, myeloid sarcoma, and t(9;11)(p22q23)
Diagnosis? |
AML: MLLT3/MLL translocation presents as a M5,
|
|
16 yo patient presents with lymphadenopathy, fatigue, rash,
Immunophenotype: TdT, HLA-CR, CD19, CD10, CD22 positive: NSE negative: MPO, SBB diagnosis? |
precursor B lymphoblastic leukemia/lymphoma
|
|
11 yo presents with lymphadenopathy, fatigure, hepatosplenomegaly, t(9;22)
positive: NSE negative: MPO, SBB Diagnosis? |
precursor B lymphoblastic leukemia/lymphoma
t(9;22) - BRC:ABL, can also have t(v;11q23) - MLL, t(1;19)PBX/E2A hypodiploid, hyperdiploid, pseudodiploid |
|
45 yo presents with CNS, Spleen, liver, and mediastinal mass..
Positive NSE, TdT, CD1a/2/3/4/5/7/8 Negative MPO, SBB Diagnosis? |
Precursor T Lymphoblastic leukemia/lymphoma
|