uoc pathology lab spring 2011

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    MD PhD

    , , 2011

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    :

    Gastrointestinal system

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    1CASE 1

    GASTRIC CANCER

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    CASE 1

    GASTRIC CARCINOMAA

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    CASE 1

    GASTRIC CARCINOMAB

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    CASE 1

    GASTRIC CARCINOMAC

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    2 CROHNCASE 2

    CROHN DISEASE

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    CASE 2

    CROHN DISEASEA

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    CASE 2

    CROHN DISEASEB

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    CASE 2

    CROHN DISEASEC

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    CASE 2

    CROHN DISEASED

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    3CASE 3

    ULCERATIVE COLITIS

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    CASE 3

    ULCERATIVE COLITISA

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    CASE 3

    ULCERATIVE COLITISB

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    CASE 3

    ULCERATIVE COLITISC

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    4 CASE 4

    COLON ADENOMA

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    CASE 4

    COLON ADENOMAA

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    CASE 4

    COLON ADENOMAB

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    CASE 4

    COLON ADENOMAC

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    5 CASE 5

    COLON CARCINOMA

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    CASE 5

    COLON CARCINOMAA

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    CASE 5

    COLON CARCINOMAB

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    CASE 5

    COLON CARCINOMAC

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    6

    KCASE 6

    CIRRHOSIS

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    CASE 6

    CIRRHOSISA

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    CASE 6

    CIRRHOSISB

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    CASE 6

    CIRRHOSISC

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    7

    CASE 7

    HEPATOCELLULAR

    CARCINOMA

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    CASE 7

    HEPATOCELLULAR

    CARCINOMA

    A

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    CASE 7

    HEPATOCELLULAR

    CARCINOMA

    B

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    CASE 7

    HEPATOCELLULAR

    CARCINOMA

    C

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    :

    -Wingo PA et al.: Long-term trends in cancer in the United States, 1930-1988.

    Cancer 97:3133, 2003.-Sands BE: Inflammatory bowel disease: past, present, and future.Journal of Gastroenterology 42:16,2007.

    -Jean Marx, et al. BIOMEDICINE: Puzzling Out the Pains in the Gut

    Science 315, 33, 2007.

    -Su L et al.: Targeted epithelial tight junction dysfunction causes

    immune activation and contributes to development of experimental colitis.Gastroenterology 136:551, 2009.

    -Shen L et al.: Integrated genetic and epigenetic analysis identifies

    three different subclasses of colon cancer.PNAS 104:18654, 2007.

    -Hahn W, Weinberg R: Rules for making cancer cells.

    New England Journal of Medicine 347:1593, 2002.-Wood LD et al: The genomic landscapes of human breast and colorectal cancers

    Science, 318(5853):1108, 2007.

    -Schuppan D, Afdhal NH: Liver cirrhosis.

    Lancet 371:838, 2008.

    -Llovet JM et al.: Design and endpoints of clinical trials in hepatocellular carcinoma

    New England Journal of Medicine 359:378, 2008.

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    Respiratory system

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    1

    CASE 1

    LUNG SQUAMOUS CELLCARCINOMA

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    CASE 1

    SQUAMOUS CELL CARCINOMAA

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    BCASE 1SQUAMOUS CELL CARCINOMA

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    CCASE 1SQUAMOUS CELL CARCINOMA

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    2

    CASE 2

    Lung adenocarcinoma

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    CASE 2

    Lung adenocarcinomaA

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    BCASE 2Lung adenocarcinoma

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    CCASE 2Lung adenocarcinoma

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    3

    CASE 3

    SMALL CELL CARCINOMA

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    CASE 3

    SMALL CELL CARCINOMAA

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    BCASE 3SMALL CELL CARCINOMA

    C S 3

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    CCASE 3SMALL CELL CARCINOMA

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    4

    CASE 4

    MESOTHELIOMA

    CASE 4

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    CASE 4

    MESOTHELIOMAA

    CASE 4

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    CASE 4MESOTHELIOMA

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    :

    -Jemal A et al.: Cancer statistics, 2008.

    CA Caner J Clin 58:71, 2008.-Hoffmann D. et al.:The biologic significance of tobacco-specific N-nitrosamines:Smoking and adenocarcinoma of the lung.

    Critical Reviews in Toxicology 26:199, 1996.

    -el-Tokry M et al.: Significant changes in the distribution of histologic types

    of lung cancer.: a review of 4928 cases.

    Cancer 65:2361, 1990.-Pershagen G. et al.: Residential radon exposure and lung cancer in Sweden.New England Journal of Medicine 330:159, 1994.

    -Herbst RS et al.: Molecular origins of cancer: Lung Cancer.

    New England Journal of Medicine 359:1367, 2008.

    -Patel AM et al: Paraneoplastic syndromes associated with lung cancer.

    Annual Reviews in Medicine 54:73, 2003.-Greillier L, Astoul P: Mesothelioma and asbestos-related pleural diseases.Respiration 76:1, 2008.

    -Rivera Z et al.: The relationship between simian virus 40 and mesothelioma.Current Opinion in Pulmonary Medicine 14:316, 2008.

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    -

    Genitourinary system

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    1

    CASE 1

    RENAL

    CLEAR CELL CARCINOMA

    CASE 1

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    CASE 1

    RENAL CLEAR CELL CARCINOMA

    CASE 1

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    CASE 1

    RENAL CLEAR CELL CARCINOMA

    CCASE 1

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    CCASE 1RENAL CLEAR CELL CARCINOMA

    CCASE 1

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    CCASE 1RENAL CLEAR CELL CARCINOMA

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    2

    CASE 2

    LOW GRADETRANSITIONAL CELL CARCINOMA

    CASE 2 A

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    CASE 2

    Low grade transitional cell carcinomaA

    BCASE 2

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    BCASE 2Low grade transitional cell carcinoma

    CCASE 2

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    CCASE 2Low grade transitional cell carcinoma

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    3

    CASE 3

    HIGH GRADETRANSITIONAL CELL CARCINOMA

    ACASE 3

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    ACASE 3High grade transitional cell carcinoma

    CASE 3

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    CASE 3High grade transitional cell carcinoma

    CCASE 3

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    CCASE 3High grade transitional cell carcinoma

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    4

    CASE 4

    SEMINOMA

    CASE 4 A

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    CASE 4

    SEMINOMAA

    BCASE 4

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    BCASE 4SEMINOMA

    CCASE 4

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    CCASE 4SEMINOMA

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    5

    CASE 5

    TESTIS TERATOMA

    ACASE 5

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    ACASE 5TESTIS TERATOMA

    BCASE 5

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    BTESTIS TERATOMA

    CCASE 5

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    CTESTIS TERATOCARCINOMA

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    6

    CASE 6

    LOW GRADEPROSTATE CARCINOMA

    ACASE 6

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    ALOW GRADE PROSTATE CARCINOMA

    BCASE 6

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    BLOW GRADE PROSTATE CARCINOMA

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    7

    CASE 7

    HIGH GRADEPROSTATE CARCINOMA

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    CASE 7

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    HIGH GRADE PROSTATE CARCINOMA

    CCASE 7

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    CHIGH GRADE PROSTATE CARCINOMA

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    :

    -Cohen HT, McGovern FJ.: Renal cell carcinoma.

    New England Journal of Medicine 353:2477, 2005.

    -Eble JN et al.: The World Health Organization classification of tumors of the urinarysystem and male genital system.

    Lyon, IARC Press, 2004.

    -Epstein JI et al.: The World Health Organization/International Society

    of Urotogical Pathology consencus classification of urothelial (transitional cell)

    neoplasms of the urinary bladder.

    Americal Journal of Surgical Pathology 22:1435, 1998.

    -Bosl GJ, Motzer RJ.: Testicular germ cell cancer.

    New England Journal of Medicine 337:242, 1997.

    -Nelson WG et al.: Prostate cancer.

    New England Journal of Medicine 349:366, 2003.

    -Kumar-Sinha C, et al: Recurrent gene fusions in prostate cancer.

    Nature Reviews Cancer 8:497, 2008.

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    Breast-gynecological system

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    1

    CASE 1

    ENDOMETRIAL CARCINOMA

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    CASE 1

    E d t i l C i

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    Endometrial Carcinoma

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    2

    CASE 2

    SIMPLE

    ENDOMETRIAL HYPERPLASIA

    CASE 2

    Si l E d t i l H l iA

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    Simple Endometrial HyperplasiaA

    BCASE 2Si l E d t i l H l i

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    BSimple Endometrial Hyperplasia

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    3

    CASE 3

    COMPLEX ENDOMETRIAL

    HEPERPLASIA

    ACASE 2C l E d t i l H l i

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    Complex Endometrial Hyperplasia

    BCASE 2C l E d t i l H l i

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    Complex Endometrial Hyperplasia

    DCASE 2C l E d t i l H l i

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    Complex Endometrial Hyperplasia

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    4

    CASE 4

    SEROUSCYSTADENOCARCINOMA

    OF THE OVARI

    CASE 4

    Ovarian Serous CarcinomaA

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    Ovarian Serous Carcinoma

    CASE 4Ovarian Serous Carcinoma

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    Ovarian Serous Carcinoma

    CASE 4

    Ovarian Serous CarcinomaC

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    Ovarian Serous Carcinoma

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    5

    CASE 5

    UTERINE LEIOMYOMA

    ACASE 5Uterine Leiomyoma

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    Uterine Leiomyoma

    CASE 5Uterine Leiomyoma

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    Uterine Leiomyoma

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    ACASE 6High Grade CIN

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    High Grade CIN

    CASE 6High Grade CIN

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    High Grade CIN

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    7

    CASE 7

    FIBROCYSTIC DISEASE

    OF THE BREAST

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    CASE 8Breast Papilloma

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    Breast Papilloma

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    CASE 9

    DUCTAL BREAST CARCINOMA

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    CCASE 9Ductal Breast Carcinoma

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    DCASE 9Ductal Breast Carcinoma

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    10

    CASE 10

    LOBULAR BREAST CARCINOMA

    ACASE 10Lobular Breast Carcinoma

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    BCASE 10Lobular Breast Carcinoma

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    :

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    -Schiffman M et al.: Human papillomavirus and cervical cancer.

    Lancet, 370:890, 2007.-Cutts PT et al.: Human papillomavirus and HPV vaccines: a review.

    Bull World Health Organization 85:719, 2007.

    -Di Cristofano A, Elllenson LH: Endometrial carcinoma.Annual Review in Pathology 2:57, 2007.

    -Ligon AH, Morton CC: Leiomyomata: treatabllity and cytogenetic studies.Human Reproduction update 7:8, 2008.

    -Bell DA: Origins and molecular pathology of ovarian cancer.

    Modern Pathology, 18:S19, 2005.

    -Stingl J, Caldas C: Molecular heterogeneity of breast carcinomas and the cancer

    stem cell hypothesis.

    Nature Reviews Cancer 10:791, 2007.

    -Yager JD, Davidson NE: Estrogen carcinogenesis in breast cancer.

    New England Journal of Medicine 354:270, 2006.-Burstein HJ et al.: Ductal carcinoma in situ of the breast.

    New England Journal of Medicine 350:1430, 2004.

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    Lymphoid system

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    1

    / -

    CASE 1

    SMALL LYMPHOCYTIC

    LYMPHOMA/LEUKEMIA

    CASE 1

    SMALL LYMPOCYTIC LYMPHOMA/LEUKEMIAA

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    CCASE 1SMALL LYMPOCYTIC LYMPHOMA/LEUKEMIA

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    2

    () CASE 2

    FOLLICULAR LYMPHOMA

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    CASE 2FOLLICULAR LYMPHOMA

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    BCASE 3DIFFUSE LARGE B-CELL LYMHOMA

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    4

    HODGKINCASE 4

    CLASSICAL

    HODGKIN LYMPHOMA

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    CASE 4CLASSICAL HODGKIN LYMPHOMA

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    CCASE 4CLASSICAL HODGKIN LYMPHOMA

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    :

    -Mebius DP: Organogenesis of lymphoid tissues.Nature Reviews Immunology 3:292, 2003.

    -Harris NL. et al.: World Health Organization classification of neoplastic diseasesof the hematopoietic and lymphoid tissues:

    Report of the Clinical Advisory Committee meeting-Airlie House,

    Virginia, November 1997.

    Journal of Clinical Oncology 17:3835, 1999.

    -Tsimberidou AM, Keating MJ: Richters transformation in chroniclymphocytic leukemia.Seminars in Oncology 33:250, 2006.

    -Kuppers R.: Prognosis in follicular lymphoma- its in the microenviroment.

    New England Journal of Medicine 351:2152, 2004.

    -Re D et al.: Molecular pathogenesis of Hodgkins lymphoma .

    Journal of Clinical Oncology 237:6379, 2005.

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    ACASE 1Squamous Cell Carcinoma

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    CASE 1

    Squamous Cell CarcinomaB

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    CCASE 1Squamous Cell Carcinoma

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    2

    CASE 2

    BASAL CELL CARCINOMA

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    3

    CASE 3

    MELANOCYTIC NEVUS

    ACASE 3Melanocytic Nevus

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    CCASE 3Melanocytic Nevus

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    CASE 4

    MelanomaA

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    CASE 4Melanoma

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    5

    CASE 5

    LEIOMYOSARCOMA

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    CASE 5Leiomyosarcoma

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    ACASE 6Leiomyoma

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    ACASE 7Myxoid Liposarcoma

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    CASE 7Myxoid Liposarcoma

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    8

    CASE 8

    SCHWANNOMA

    ACASE 8Schwannoma

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    P ll k PM t l Hi h f f BRAF t ti i i

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    -Pollock PM et al.: High frequency of BRAF mutations in nevi.Nature Genetics 33:19, 2003.

    -Chib L: The genetics of malignant melanoma: lessons from mouse and man.Nature Reviews Cancer 3:559, 2003.

    -Rubin AI et al.: Basal-cell carcinoma.New England Journal of Medicine 353:2262, 2005.

    -Alam M, Ratner D: Cutaneous squamous-cell carcinoma.New England Journal of Medicine 344:975, 2001.

    -Mitelman F et al.: The impact of translocations and gene fusions on cancer causation.Nature Reviews Cancer 7:233, 2007.

    -Riggi N et al.: Sarcomas: genetics, signaling, and cellular origins.Part I:

    The fellowship of TET.

    Journal of Pathology 213:4, 2007.

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    : -

    CNS- Endocrine system

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    1

    CASE 1MENINGIOMA

    ACASE 1Meningioma

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    CASE 1

    Meningioma

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    CCASE 1Meningioma

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    2

    CASE 2

    LOW GRADE

    GLIOMA

    CASE 2

    Low Grade GliomaA

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    CASE 2High Grade Glioma

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    4

    CASE 4

    NODULAR GOITER

    CASE 4

    Nodular GoiterA

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    5

    CASE 5

    LYMPHOCYTIC THYROIDITIS

    (HASHIMOTO)

    ACASE 5Lymphocytic Thyroiditis

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    CASE 5Lymphocytic Thyroiditis

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    6

    CASE 6

    THYROID

    PAPILLARY CARCINOMA

    ACASE 6Thyroid Papillary Carcinoma

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    CASE 6Thyroid Papillary Cell Carcinoma

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    7

    CASE 7

    THYROID

    FOLLICULAR CARCINOMA

    ACASE 7Thyroid Follicular Carcinoma

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    BCASE 7Thyroid Follicular Carcinoma

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