Ne Oplasia Revi Ew Plu s

Embed Size (px)

Citation preview

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    1/166

    NE OPLASIA REVI EWE OPLASIA REVI EW

    Pluslu s9-18-20099-18-2009

    T. DavisT. Davis

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    2/166

    1. A new test for prostate1. A new test for prostatecancer (PC) is developed.cancer (PC) is developed. 90%0% of menof men wi th PCi th PC test positive.test positive.80%0% of menof men without PCithout PC testtest

    negative.negative.2. In a population of 1000 men,2. In a population of 1000 men,30% (300 men) have the30% (300 men) have the

    disease (the prevalence is 30%).disease (the prevalence is 30%).Calculate sensitivity, specificityCalculate sensitivity, specificityand PPV.and PPV.

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    3/166

    Sen sit ivit y a nden sit ivit y a nd

    speci ficit ypeci ficit y90% sensitivity90% sensitivity90% of 1000 or 90090% of 1000 or 900

    would be thewould be the trueru e positivesositives10% of 1000 or 10010% of 1000 or 100would be thewould be the falsealseneg at iv eseg at iv es

    80% specificity80% specificity80% of 1000 or 80080% of 1000 or 800

    would be thewould be the trueru enega tivesega tives20% of 1000 or 20020% of 1000 or 200would be thewould be the falsealsepos it ivesos it ives

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    4/166

    PPVPV (predictive value of a +)(predictive value of a +)

    with a prevalence of 30%with a prevalence of 30%410 men have a positive test: 270 TP410 men have a positive test: 270 TP(90%x300) and 140 FP (20%x700)(90%x300) and 140 FP (20%x700)

    PPV= TP/FP+TPPPV= TP/FP+TPPPV= 270 / 270 + 140PPV= 270 / 270 + 140

    270/410 or about 66%270/410 or about 66%

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    5/166

    Ca ncer P recu rsor L es ion sa ncer P recu rsor L es ion s

    ________ ________ Atyp. Hyp. Breast Atyp. Hyp. Breast

    _______ _______ Endom. HyperplasiaEndom. Hyperplasia

    _________ _________

    Gastric metaplasiaGastric metaplasia(Helicobacter)(Helicobacter)

    ___________ ___________

    Sq. Cell CA Sq. Cell CA __________ __________

    Adeno CA colon Adeno CA colon ___________ ___________ Esoph. Adeno CA Esoph. Adeno CA

    _____________ _____________

    Adeno CA liver Adeno CA liver

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    6/166

    Actinic keratosis Actinic keratosis Atyp. Hyp. Breast Atyp. Hyp. BreastUlcerative ColitisUlcerative ColitisEndom. HyperplasiaEndom. Hyperplasia

    Esoph. MetaplasiaEsoph. Metaplasia(Barretts)(Barretts)Gastric metaplasiaGastric metaplasia

    (Helicobacter)(Helicobacter)

    Sq. Cell CA Sq. Cell CA Ductal CA Ductal CA

    Adeno CA colon Adeno CA colon Adeno CA endom. Adeno CA endom.

    Esoph. Adeno CA Esoph. Adeno CA

    Gastric Adeno CA Gastric Adeno CA

    Adeno CA liver Adeno CA liver

    Ca ncer P recu rsor L es ion sa ncer P recu rsor L es ion s

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    7/166

    Ca ncer P recu rsor L es ion sa ncer P recu rsor L es ion s

    Actinic keratosis Actinic keratosis

    __________ __________ Ulcerative ColitisUlcerative Colitis __________ __________

    Esoph. MetaplasiaEsoph. Metaplasia(Barretts)(Barretts)

    ___________ ___________

    CirrhosisCirrhosis

    ___________ ___________

    Ductal CA Ductal CA ___________ ___________ Adeno CA endom. Adeno CA endom.

    _____________ _____________

    Gastric Adeno CA Gastric Adeno CA __________ __________

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    8/166

    Actinic keratosis Actinic keratosis Atyp. Hyp. Breast Atyp. Hyp. BreastUlcerative ColitisUlcerative ColitisEndom. HyperplasiaEndom. Hyperplasia

    Esoph. MetaplasiaEsoph. Metaplasia(Barretts)(Barretts)Gastric metaplasiaGastric metaplasia

    (Helicobacter)(Helicobacter)

    Sq. Cell CA Sq. Cell CA Ductal CA Ductal CA

    Adeno CA colon Adeno CA colon Adeno CA Adeno CA

    endom.endom.Esoph. Adeno CA Esoph. Adeno CA Gastric Adeno CA Gastric Adeno CA

    Adeno CA liver Adeno CA liver

    Ca ncer P recu rsor L es ion sa ncer P recu rsor L es ion s

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    9/166

    Precu rs or s ( 2)recu rs or s ( 2)

    ____________ ____________

    Sq.Sq.Dysplasia/cervix,Dysplasia/cervix,lung/larynxlung/larynx

    ______________ ______________

    Adeno CA Adeno CA

    ___________ ___________

    Adeno CA colon Adeno CA colon

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    10/166

    Precu rs or s ( 2)recu rs or s ( 2)

    Scar in lungScar in lung

    Sq.Sq.Dysplasia/cervix,Dysplasia/cervix,lung/larynxlung/larynx

    Adenomatous Adenomatouspolyppolyp

    Adeno CA Adeno CA

    Ss. Cell CA Ss. Cell CA

    Adeno CA colon Adeno CA colon

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    11/166

    Precu rs or s ( 2)recu rs or s ( 2)

    Scar in lungScar in lung

    ____________ ____________

    Adenomatous Adenomatouspolyppolyp

    ____________ ____________

    Ss. Cell CA Ss. Cell CA

    _____________ _____________

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    12/166

    Precu rs or s ( 2)recu rs or s ( 2)

    Scar in lungScar in lung

    Sq.Sq.Dysplasia/cervix,Dysplasia/cervix,lung/larynxlung/larynx

    Adenomatous Adenomatouspolyppolyp

    Adeno CA Adeno CA

    Ss. Cell CA Ss. Cell CA

    Adeno CA colon Adeno CA colon

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    13/166

    Malig nan t Tu mo rs a ndalig nan t Tu mo rs a nd

    En docrin op athiesn docrin op athies _________ _________ ___________ ___________

    ___________ ___________ ____________ ____________ Insulin/hypoglycemiInsulin/hypoglycemi

    ADH/hypoNa+ ADH/hypoNa+Erythropeitin/>HctErythropeitin/>Hct

    Small Cell, Med. CA Small Cell, Med. CA ChorioCA/testisChorioCA/testis

    SC CA/lungSC CA/lungMed CA/thyroidMed CA/thyroidIslet cellIslet cell

    Small CellSmall CellRenal Cell,Renal Cell,Hepatocellular CA Hepatocellular CA

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    14/166

    Malig nan t Tu mo rs a ndalig nan t Tu mo rs a nd

    En docrin op athiesn docrin op athies ACTH/Cushings ACTH/CushingsHCG/gynecomastiaHCG/gynecomastiaPTH/hyperCa++PTH/hyperCa++Calcitonin/hypoCa+Calcitonin/hypoCa+

    Insulin/hypoglycemiInsulin/hypoglycemi ADH/hypoNa+ ADH/hypoNa+Erythropeitin/>HctErythropeitin/>Hct

    Small Cell, Med. CA Small Cell, Med. CA ChorioCA/testisChorioCA/testisSquaC CA/lungSquaC CA/lungMed CA/thyroidMed CA/thyroid

    ___________ ___________ __________ __________ _____________ _____________

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    15/166

    Malig nan t Tu mo rs a ndalig nan t Tu mo rs a nd

    En docrin op athiesn docrin op athies ACTH/Cushings ACTH/CushingsHCG/gynecomastiaHCG/gynecomastiaPTH/hyperCa++PTH/hyperCa++Calcitonin/hypoCa+Calcitonin/hypoCa+

    Insulin/hypoglycemiInsulin/hypoglycemi ADH/hypoNa+ ADH/hypoNa+Erythropeitin/>HctErythropeitin/>Hct

    _________ _________ ___________ ___________ ____________ ____________ ___________ ___________

    Islet cellIslet cellSmall CellSmall CellRenal Cell,Renal Cell,

    Hepatocellular CA Hepatocellular CA

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    16/166

    Malig nan t Tu mo rs a ndalig nan t Tu mo rs a nd

    En docrin op athiesn docrin op athies ACTH/Cushings ACTH/CushingsHCG/gynecomastiaHCG/gynecomastiaPTH/hyperCa++PTH/hyperCa++Calcitonin/hypoCa+Calcitonin/hypoCa+

    _________ _________ _________ _________ ____________ ____________

    Small Cell, Med. CA Small Cell, Med. CA ChorioCA/testisChorioCA/testisSquaC CA/lungSquaC CA/lungMed CA/thyroidMed CA/thyroid

    Islet cellIslet cellSmall CellSmall CellRenal Cell,Renal Cell,

    Hepatocellular CA Hepatocellular CA

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    17/166

    The f oll owi ng im ag e ishe f oll owi ng im ag e is

    mos t c/w wh ic h ma lign anc yos t c/w wh ic h ma lign anc y

    A. Medullary Carcinoma of Thyroid A. Medullary Carcinoma of ThyroidB. Small cell carcinoma of LungB. Small cell carcinoma of LungC. Sq. Cell Carcinoma of LungC. Sq. Cell Carcinoma of Lung

    D. Metastatic melanomaD. Metastatic melanomaE. Renal Cell AdenocarcinomaE. Renal Cell Adenocarcinoma

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    18/166

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    19/166

    An s. C, SCC o f L ungn s. C, SCC o f L ung

    These tumors frequently make aThese tumors frequently make aparathormone-like substanceparathormone-like substance

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    20/166

    Anaplasianaplasia = __ _____ ____ ______ __= __ _____ ____ ______ __

    Anaplasia is considered a hallmark of Anaplasia is considered a hallmark of ______________ ______________ .. Anaplastic features include: Anaplastic features include:

    - ?- ???

    ?

    - Undi ffere nt iat ed, po orl y di ffere nti at ed,Undi ffere nt iat ed, po orl y di ffere nti at ed,high gradeig h gr ade

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    21/166

    Anaplasianaplasia = L ack of diffe rentia ti on= L ack of diffe rentia ti on

    Anaplasia is considered a hallmark of Anaplasia is considered a hallmark of malignant transformation malignant transformation ..

    Anaplastic features include: Anaplastic features include:- Cellular/nuclear pleomorphism- Cellular/nuclear pleomorphism

    - Increased nuclear-cytoplasmic ratio- Increased nuclear-cytoplasmic ratio- Nuclear hyperchromasia (increased DNA content)- Nuclear hyperchromasia (increased DNA content)

    - Large nucleoli- Large nucleoli

    - Und iffer ent iat ed , po orly dif fer ent iat ed ,Undifferentiated, poorly differentiated,hig h g radeig h g rade

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    22/166

    GR AD ING TU MORSR AD ING TU MORS

    __________ tumors only __________ tumors onlyLook at: ? And ?Look at: ? And ?

    Grades I-III/IV (higher grades areGrades I-III/IV (higher grades aremore __________)more __________)Important for some tumors: breast,Important for some tumors: breast,

    prostate, endometrium, astocytomasprostate, endometrium, astocytomasDysplasias of the cervix are graded Dysplasias of the cervix are graded Based on microscopic featuresBased on microscopic features

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    23/166

    GR AD ING TU MORSR AD ING TU MORS

    Malignant tumors onlyMalignant tumors onlyDifferentiation and mitotic rateDifferentiation and mitotic rate

    Grades I-III/IV (higher grades areGrades I-III/IV (higher grades aremore anaplastic)more anaplastic)Important for some tumors: ?, ?, ?, ?Important for some tumors: ?, ?, ?, ?

    Dysplasias of the cervix are graded Dysplasias of the cervix are graded Based on microscopic featuresBased on microscopic features

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    24/166

    GR AD ING TU MORSR AD ING TU MORS

    Malignant tumors onlyMalignant tumors onlyDifferentiation and mitotic rateDifferentiation and mitotic rate

    Grades I-III/IV (higher grades areGrades I-III/IV (higher grades aremore anaplastic)more anaplastic)Important for some tumors: breast,Important for some tumors: breast,prostate, endometrium, astocytomasprostate, endometrium, astocytomasDysplasias of the cervix are graded Dysplasias of the cervix are graded Based on microscopic featuresBased on microscopic features

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    25/166

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    26/166

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    27/166

    SP

    SP

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    28/166

    Squamous cell carcinoma with squamous pearls (SP)

    SP

    SP

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    29/166

    SP

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    30/166

    SP

    Squamous Pearls (SP)

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    31/166

    *

    *

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    32/166

    *

    *

    Intercellular bridges (*)

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    33/166

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    34/166

    Anaplastic rhabdomyosarcoma

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    35/166

    STAGI NG TU MORSTAGI NG TU MORS

    How far has the tumor spreadHow far has the tumor spreadMalignant tumors onlyMalignant tumors only?, ?, ??, ?, ?Staging often involves: theStaging often involves: thePathologist, radiology or otherPathologist, radiology or otherimaging, lab tests (tumor markers)imaging, lab tests (tumor markers)CISIS is referred to asis referred to as __ ___ __ ____ ___ __ ___

    TAGI NG TUMORS

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    36/166

    STAGI NG TUMORSTAGI NG TUMORS

    How far has the tumor spreadHow far has the tumor spreadMalignant tumors onlyMalignant tumors onlyTumor size (Tumor size ( T), lymph node (), lymph node ( N))involvement, distant metastases (involvement, distant metastases ( M))Staging often involves: theStaging often involves: thePathologist, radiology or otherPathologist, radiology or otherimaging, lab tests (tumor markers)imaging, lab tests (tumor markers)CISIS is referred to asis referred to as Sta ge Zerota ge Zero

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    37/166

    METASTA SISETASTA SIS

    LIVER: (portal circulation)LIVER: (portal circulation) ______________ ______________ LUNG: breast, stomach, sarcomasLUNG: breast, stomach, sarcomas

    BONE: 3BONE: 3rdrd

    most frequent site for ??;most frequent site for ??;lung, breast, prostate, kidney, thyroid;lung, breast, prostate, kidney, thyroid;PROSTATE to bone gives osteoblasticPROSTATE to bone gives osteoblasticlesions on Xray and high serumlesions on Xray and high serumalkaline phosphatasealkaline phosphatase

    ADRENAL: most common ADRENAL: most common ____________ ____________

    AS A S SETASTA SIS

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    38/166

    METASTA SISETASTA SIS

    LIVER: (portal circulation) GI tractLIVER: (portal circulation) GI tractand pancreas; lung, breast,and pancreas; lung, breast,melanomasmelanomas

    LUNG: ?, ?, ?LUNG: ?, ?, ?BONE: 3BONE: 3 rdrd most frequent site formost frequent site formetastases; ?, ?, ?, ?, ?; PROSTATE tometastases; ?, ?, ?, ?, ?; PROSTATE tobone gives _____________ on Xraybone gives _____________ on Xrayand high serum ______________ and high serum ______________

    ADRENAL: most common endocrine ADRENAL: most common endocrinesitesite

    METASTA SISETASTA SIS

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    39/166

    METASTA SISETASTA SIS

    LIVER: (portal circulation) GI tractLIVER: (portal circulation) GI tractand pancreas; lung, breast,and pancreas; lung, breast,melanomasmelanomas

    LUNG: breast, stomach, sarcomasLUNG: breast, stomach, sarcomasBONE: 3BONE: 3 rdrd most frequent site formost frequent site formetastases; lung, breast, prostate,metastases; lung, breast, prostate,kidney, thyroid; PROSTATE to bonekidney, thyroid; PROSTATE to bonegives osteoblastic lesions on Xray andgives osteoblastic lesions on Xray andhigh serum alkaline phosphatasehigh serum alkaline phosphatase

    ADRENAL: most common endocrine ADRENAL: most common endocrine

    sitesite

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    40/166

    Neop las ia Ca seeop las ia Ca se

    A 38-y.o. male has a family history of A 38-y.o. male has a family history of colectomies performed between agescolectomies performed between ages

    30 and 40. The slide shows the total30 and 40. The slide shows the totalcolectomy specimen from this patient.colectomy specimen from this patient.

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    41/166

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    42/166

    Familial polyposis

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    43/166

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    44/166

    Tubular adenomas (adenomatous polyps)

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    45/166

    AC

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    46/166

    Adenomatous Change (AC)

    AC

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    47/166

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    48/166

    Carcinomain situ invasive

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    49/166

    CO LON CANC ERO LON CANC ER

    Grading is helpful/not very helpfulGrading is helpful/not very helpfulSTAGING: predicts _________ STAGING: predicts _________ TNMTNMRobbins Table 17-11Robbins Table 17-11

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    50/166

    CO LON CANC ERO LON CANC ER

    Grading is not very helpfulGrading is not very helpfulSTAGING: predicts clinical outcomeSTAGING: predicts clinical outcomeTNMTNMRobbins Table 17-11Robbins Table 17-11

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    51/166

    Tu mor Siz e ( T)u mor Siz e ( T)

    Tis- ???Tis- ???T1- ____________ T1- ____________ T2- ___________ T2- ___________ T3- ___________ T3- ___________ T4- ______________ T4- ______________

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    52/166

    Tu mor Size ( T)u mor Size ( T)

    Tis- insitu; not through the muscularisTis- insitu; not through the muscularismucosamucosa

    T1- invades submucosaT1- invades submucosaT2- into but not through theT2- into but not through themuscularis propriamuscularis propria

    T3- through muscularis propriaT3- through muscularis propriaT4- invades adjacent organsT4- invades adjacent organs

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    53/166

    ??? Staging System

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    54/166

    TNM Staging System

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    55/166

    Lymph Nodes ( N)ymph Nodes ( N)

    N0- ??N0- ??N1- ??N1- ??N2- ??N2- ??

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    56/166

    Lymph Nodes ( N)ymph Nodes ( N)

    N0- no nodes involvedN0- no nodes involvedN1- 1-3 regional LNsN1- 1-3 regional LNsN2- 4+ regional LNsN2- 4+ regional LNs

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    57/166

    Dis tant Met astas es (M)is tant Met astas es (M)

    M0- ??M0- ??M1- ??M1- ??

    *note*noteTx, Nx, Mx- can/cannot be assessedTx, Nx, Mx- can/cannot be assessed

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    58/166

    Dis tant Met astas es (M)is tant Met astas es (M)

    M0- no distant metastasisM0- no distant metastasisM1- distant mets presentM1- distant mets present

    *note*noteTx, Nx, Mx- cannot be assessedTx, Nx, Mx- cannot be assessed

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    59/166

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    60/166

    An swer : C, in activ ationn swer : C, in activ at ion

    of AP Cf APCThis disorder is autosomal dominantThis disorder is autosomal dominantwith the APC supressor gene onwith the APC supressor gene on

    chromosome 5.chromosome 5.

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    61/166

    CO LON CANC ERO LON CANC ER

    OTHER OTHER 50% of colorectal carcinomas show ?? 50% of colorectal carcinomas show ??

    mutations; 50% of adenomas > 1cm showmutations; 50% of adenomas > 1cm show ________ mutations ________ mutations _________ can be used to follow patients _________ can be used to follow patientsafter surgery- tumor monitoringafter surgery- tumor monitoringDeeply infiltrating tumors causeDeeply infiltrating tumors cause_______________________ and ???? appearanceand ???? appearance

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    62/166

    CO LON CANC ERO LON CANC ER

    OTHER OTHER 50% of colorectal carcinomas show ras 50% of colorectal carcinomas show ras

    mutations; 50% of adenomas > 1cm alsomutations; 50% of adenomas > 1cm alsoshow ras mutationsshow ras mutationsCEA (carcinoembryonic Ag) can be used toCEA (carcinoembryonic Ag) can be used tofollow patients after surgery- tumorfollow patients after surgery- tumormonitoringmonitoringDeeply infiltrating tumors causeDeeply infiltrating tumors causedes mop la si aes mop la si a and apple core/ napkin-ring and apple core/ napkin-ring

    appearanceappearance

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    63/166

    ????

    ?????

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    64/166

    Normal

    Adenocarcinoma

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    65/166

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    66/166

    Tumor: napkin ring lesionNormal, pretty!

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    67/166

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    68/166

    Na me th e m ost c om mo na me th e m ost c om mo n

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    69/166

    Na me th e m ost c om mo na me th e m ost c om mo nhuma n tum or su presso ruma n tum or su presso r

    gen es a nd p ro to onc ogeneen es a nd p ro to onc ogene(RESPECTIVELY)RESPECTIVELY)

    A. P53 and RB A. P53 and RBB. P53 and RASB. P53 and RAS

    C. RB and RASC. RB and RASD. APC and P53D. APC and P53E. APC and RBE. APC and RB

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    70/166

    An swer : B, P 53 a nd R ASn swer : B, P 53 a nd R AS

    P53 is the tumor supressor geneP53 is the tumor supressor genemutated in over 50% of humanmutated in over 50% of human

    tumors. The mutation prevents DNA tumors. The mutation prevents DNA repair and inhibits apoptosis. The pointrepair and inhibits apoptosis. The pointmutation in the proto-oncogene RASmutation in the proto-oncogene RAS

    allows cell proliferation (GTP signalallows cell proliferation (GTP signaltransduction) and is seen 30+% of transduction) and is seen 30+% of human tumorshuman tumors

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    71/166

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    72/166

    Wha t tu mo r m ar kers ar eha t tu mo r m ar kers ar e

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    73/166

    Wha t tu mo r m ar kers ar eha t tu mo r m ar kers ar eusef ul in ma na gement o fsef ul in ma na gement o f

    colon cancer?olon cancer? A. CEA is used to monitor tumor A. CEA is used to monitor tumorrecurrencerecurrenceB. CEA is used as a screening test forB. CEA is used as a screening test forcolon cancercolon cancerC. CEA is used as a confirmation test if C. CEA is used as a confirmation test if the test for occult blood is positivethe test for occult blood is positive

    D. High PSA in serum is diagnosticD. High PSA in serum is diagnosticE. High AFP in serum is diagnosticE. High AFP in serum is diagnostic

    An swer : A, u sed ton swer : A, u sed to

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    74/166

    An swer : A, u sed to,mon it or t umoron it or t umor

    recu rre nceecu rre nceCEA is not specific for colon cancerCEA is not specific for colon cancerand not a sensitive test. CEA levels areand not a sensitive test. CEA levels are

    determined pre- and post-surgery. Thedetermined pre- and post-surgery. TheCEA level should fall to near zero. If CEA level should fall to near zero. If the level falls and then increases, thethe level falls and then increases, the

    patient may receive chemotherapy forpatient may receive chemotherapy forthe recurrence.the recurrence.

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    75/166

    Tu mor Ma rk er su mor Ma rk er s

    ManagementManagementDetection (staging)Detection (staging)

    Diagnosis (screening)- PSA andDiagnosis (screening)- PSA andCA 125CA 125

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    76/166

    Markersarkers

    ? - colon, pancreas, stomach, lung,- colon, pancreas, stomach, lung,breast, (19% smokers, 3% gen. pop.)breast, (19% smokers, 3% gen. pop.)

    ?-- hepatocellular, germ cellhepatocellular, germ cell(>500ng/ml)(>500ng/ml)??-?- 80% non-mucinous80% non-mucinous ovarian CA ovarian CA

    ??- pancreatic CA (80%)??- pancreatic CA (80%)

    M kk

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    77/166

    Markersarkers

    CEAEA- colon, pancreas, stomach, lung,- colon, pancreas, stomach, lung,breast, (19% smokers, 3% gen. pop.)breast, (19% smokers, 3% gen. pop.)

    AFP-FP- hepatocellular, germ cellhepatocellular, germ cell(>500ng/ml)(>500ng/ml)CA 125 -A 125 - 80% non-mucinous80% non-mucinous ovarianovarian

    CA CA CA 19-9- pancreatic CA (80%)CA 19-9- pancreatic CA (80%)

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    78/166

    Marker s ( 2)arker s ( 2)

    PSA- (?? ng/ml normal) (> ?? ng/mlPSA- (?? ng/ml normal) (> ?? ng/mlhighly suspicious); also ??? elevationhighly suspicious); also ??? elevation

    in prostate CA assoc. with bonein prostate CA assoc. with bonemetastasis (osteoblastic)metastasis (osteoblastic)HCG- ?, ?HCG- ?, ?

    M k ( 2)k ( 2)

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    79/166

    Marker s ( 2)arker s ( 2)

    PSA- (0-4 ng/ml normal) (>10 ng/mlPSA- (0-4 ng/ml normal) (>10 ng/mlhighly suspicious); also AlkPhoshighly suspicious); also AlkPhos

    elevation in prostate CA assoc. withelevation in prostate CA assoc. withbone metastasis (osteoblastic)bone metastasis (osteoblastic)HCG- gestational trophoblasticHCG- gestational trophoblastic

    tumors, testicular tumorstumors, testicular tumors

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    80/166

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    81/166

    L

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    82/166

    Benign breast ducts and lobules

    L

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    83/166

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    84/166

    Fibroadenoma

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    85/166

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    86/166

    Fibroadenoma of breast

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    87/166

    C

    C

    CN

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    88/166

    C

    C

    CN

    Intraductal carcinoma with cribbiforming (C) and comedonecrosis (CN)

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    89/166

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    90/166

    Invasive CA

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    91/166

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    92/166

    Mammogram shows a mass and Ca**

    Stellate

    tumor

    BR EA ST CAR CI NO MAR EA ST CAR CI NO MA

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    93/166

    BR EA ST CAR CI NO MAR EA ST CAR CI NO MAGRADINGRADING

    Bloom and RichardsonBloom and Richardson

    ?? (1-3)?? (1-3)?? (1-3)?? (1-3)?? (1-3)?? (1-3)

    Total score 3-5: Grade ITotal score 3-5: Grade ITotal score 6,7: Grade IITotal score 6,7: Grade IITotal score 8,9: Grade IIITotal score 8,9: Grade III

    BR EA ST CAR CI NO MAR EA ST CAR CI NO MA

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    94/166

    BR EA ST CAR CI NO MAR EA ST CAR CI NO MAGRADINGRADING

    Bloom and RichardsonBloom and Richardson

    Tubules present (1-3)Tubules present (1-3)Nuclear atypia (1-3)Nuclear atypia (1-3)Mitoses (1-3)Mitoses (1-3)

    Total score 3-5: Grade ITotal score 3-5: Grade ITotal score 6,7: Grade IITotal score 6,7: Grade IITotal score 8,9: Grade IIITotal score 8,9: Grade III

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    95/166

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    96/166

    BR EA ST CAR CI NO MAR EA ST CAR CI NO MA

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    97/166

    STAGI NGTAGI NG

    Stage 0 (in situ or CIS): 5-year 92%Stage 0 (in situ or CIS): 5-year 92%Stage I. (4 LN+): 5-year 46%Stage IV. Distant mets: 5-year 13%Stage IV. Distant mets: 5-year 13%

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    98/166

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    99/166

    Invasive (infiltrating) ductal carcinoma with lymphatic invasion

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    100/166

    BR EA ST CAR CI NO MAR EA ST CAR CI NO MA

    OTHER OTHER Estrogen receptor (+): tumor is stimulatedEstrogen receptor (+): tumor is stimulatedby ?? and can be treated with the ?? This isby ?? and can be treated with the ?? This ispalliation.palliation.HER-2 Neu amplification: by immunostainingHER-2 Neu amplification: by immunostainingor FISH. If HER-2 Neu is amplified (20%),or FISH. If HER-2 Neu is amplified (20%),the patient can be treated with ?? This isthe patient can be treated with ?? This isvery expensive and tends to be used in highvery expensive and tends to be used in highgrade/high stage lesions that are ??grade/high stage lesions that are ??

    BR EA ST CAR CI NO MAR EA ST CAR CI NO MA

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    101/166

    BR EA ST CAR CI NO MAR EA ST CAR CI NO MA

    OTHER OTHER Estrogen receptor (+): tumor is stimulatedEstrogen receptor (+): tumor is stimulatedby estrogen and can be treated with theby estrogen and can be treated with the

    anti-estrogen tamoxifen. This is palliation. anti-estrogen tamoxifen. This is palliation.HER-2 Neu amplification: by immunostainingHER-2 Neu amplification: by immunostainingor FISH. If HER-2 Neu is amplified (20%),or FISH. If HER-2 Neu is amplified (20%),the patient can be treated with Herceptin.the patient can be treated with Herceptin.This is very expensive and tends to be usedThis is very expensive and tends to be usedin high grade/high stage lesions that arein high grade/high stage lesions that areHER-2 Neu positive.HER-2 Neu positive.

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    102/166

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    103/166

    ER (+)

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    104/166

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    105/166

    HER-2 Neu (+)

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    106/166

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    107/166

    d l

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    108/166

    HPV an d Cer vica l Ca ncerPV an d Cer vica l Ca ncer

    HPV DNA types ? And ?: condylomaHPV DNA types ? And ?: condylomaHPV ?, ?, ? others: carcinomaHPV ?, ?, ? others: carcinoma

    Viral protein _____ acts via Viral protein _____ acts viaretinoblastoma gene proteinretinoblastoma gene protein

    Viral protein E6 acts via ___________ Viral protein E6 acts via ___________

    Proliferation is stimulated andProliferation is stimulated andapoptosis is inhibitedapoptosis is inhibited

    HPV an d Cer vica l Ca ncerPV an d Cer vica l Ca ncer

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    109/166

    HPV an d Cer vica l Ca ncerPV an d Cer vica l Ca ncer

    HPV DNA types 6 and 11: condylomaHPV DNA types 6 and 11: condylomaHPV 16, 18, 13 others: carcinomaHPV 16, 18, 13 others: carcinoma

    Viral protein E7 acts via Viral protein E7 acts viaretinoblastoma gene proteinretinoblastoma gene protein

    Viral protein E6 acts via to P53 (TP53). Viral protein E6 acts via to P53 (TP53).

    Proliferation is stimulated andProliferation is stimulated andapoptosis is inhibitedapoptosis is inhibited

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    110/166

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    111/166

    Squamous metaplasia

    Endocervical glands

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    112/166

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    113/166

    Normal epithelium shows maturation at the surface

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    114/166

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    115/166

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    116/166

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    117/166

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    118/166

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    119/166

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    120/166

    ? ??

    ?? ??

    koilocyte

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    121/166

    Normal Low Grade

    Moderate Severe/CIS

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    122/166

    ?

    ?

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    123/166

    Koilocytes (K)

    K

    K

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    124/166

    ??

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    125/166

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    126/166

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    127/166

    Invasive squamous cell CA

    Wha t i s the m ost s ensi ti veha t i s the m ost s ensi ti vete st f or hi gh gr ad ee st f or hi gh gr ad e

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    128/166

    te st f or hi gh gr ad ee st f or hi gh gr ad e

    dy sp las ia of the c ervix ?y sp las ia of the c ervix ? A. Pap smear A. Pap smear

    B. HPV DNA test for high risk typesB. HPV DNA test for high risk typesC. HPV test for DNA type 16C. HPV test for DNA type 16D. HPV test for DNA type 18D. HPV test for DNA type 18E. HPV serum antibodies to DNA typeE. HPV serum antibodies to DNA type1616

    HP V DNA is m ost s ensi ti veP V DNA is m ost s ensi ti ve

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    129/166

    HP V DNA is m ost s ensi ti veP V DNA is m ost s ensi ti ve

    te st f or Hi gh G ra dee st f or Hi gh G ra dedysplasiaysplasia

    Pap smear 55%Pap smear 55%HPV DNA 95%HPV DNA 95%

    LUNG CANCE RUNG CANCE R

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    130/166

    LUNG CANCE RUNG CANCE R

    ?, ?, and ?: can be cured by surgery if ?, ?, and ?: can be cured by surgery if caught early (

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    131/166

    Large cell carcinoma, adenocarcinomaLarge cell carcinoma, adenocarcinomaand squamous cell carcinoma: can beand squamous cell carcinoma: can becured by surgery if caught earlycured by surgery if caught early(

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    132/166

    Large cell carcinoma, adenocarcinomaLarge cell carcinoma, adenocarcinomaand squamous cell carcinoma: can beand squamous cell carcinoma: can becured by surgery if caught earlycured by surgery if caught early(

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    133/166

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    134/166

    Normal

    CIS

    Squamous CA

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    135/166

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    136/166

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    137/166

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    138/166

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    139/166

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    140/166

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    141/166

    ??

    ??

    ?? ??

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    142/166

    keratin

    Nuclear molding

    Squamous Cell Carcinoma Small Cell Carcinoma

    ?? ??

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    143/166

    ?? ??

    Squamous CA Adeno CA

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    144/166

    Small cell undifferentiated carcinoma Large cell CA

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    145/166

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    146/166

    Small Cell Carcinoma

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    147/166

    ??

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    148/166

    Normal esophagus

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    149/166

    ??

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    150/166

    Barretts syndrome

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    151/166

    Para neop last icara neop lasticS dd

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    152/166

    Syndromesyndromes Acanthosis Acanthosisnigricansnigricans

    Eaton-LambertEaton-LambertOsteoarthropathyOsteoarthropathySeborrheicSeborrheic

    keratosiskeratosisMigratoryMigratorythrombophlebitisthrombophlebitis

    (Tro ssea s)(Tro ssea s)

    Adeno CA Adeno CA (gastric)(gastric)

    Small Cell CA Small Cell CA Bronchogenic CA Bronchogenic CA Gastric CA Gastric CA

    Pancreatic CA Pancreatic CA

    Para neop last icara neop lasticS dd

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    153/166

    Syndromesyndromes Acanthosis Acanthosisnigricansnigricans

    ______________ ______________ OsteoarthropathyOsteoarthropathy

    ___________ ___________

    MigratoryMigratorythrombophlebitisthrombophlebitis(Trousseaus)(Trousseaus)

    _____________ _____________

    Small Cell CA Small Cell CA ___________ ___________ Gastric CA Gastric CA

    ______________ ______________

    Para neop last icara neop lasticS dd

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    154/166

    Syndromesyndromes Acanthosis Acanthosisnigricansnigricans

    Eaton-LambertEaton-LambertOsteoarthropathyOsteoarthropathySeborrheicSeborrheic

    keratosiskeratosisMigratoryMigratorythrombophlebitisthrombophlebitis

    (T )(T )

    Adeno CA Adeno CA (gastric)(gastric)

    Small Cell CA Small Cell CA Bronchogenic CA Bronchogenic CA Gastric CA Gastric CA

    Pancreatic CA Pancreatic CA

    PARA NEO PLASTI CARA NEO PLASTI CSYNDROMESYNDROMES

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    155/166

    SYNDROMESYNDROMESSmall Cell CA Small Cell CA

    __________ __________

    Carcinoid tumorCarcinoid tumor(lung or liver(lung or liverusually)usually)

    _________ _________

    PTH-likePTH-like(Hypercalcemia)(Hypercalcemia)

    _____________ _____________

    PARA NEO PLASTI CARA NEO PLASTI CSYNDROMESYNDROMES

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    156/166

    SYNDROMESYNDROMESSmall Cell CA Small Cell CA

    Squamous cellSquamous cellCA CA hypercalcemiahypercalcemia

    Carcinoid tumorCarcinoid tumor(lung or liver(lung or liverusually)usually)

    ACTH ACTH(Cushings); ADH(Cushings); ADH(iADH)(iADH)PTH-likePTH-like(Hypercalcemia)(Hypercalcemia)

    Serotonin,Serotonin,bradykininbradykinin(Carcinoid(Carcinoid

    d )syndrome)

    PARA NEO PLASTI CARA NEO PLASTI CSYNDROMESYNDROMES

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    157/166

    SYNDROMESYNDROMES _____________ _____________

    Squamous cellSquamous cellCA CA hypercalcemiahypercalcemia

    ____________ ____________

    ACTH ACTH(Cushings); ADH(Cushings); ADH(iADH)(iADH)

    __________ __________

    Serotonin,Serotonin,bradykininbradykinin(Carcinoid(Carcinoid

    d )d )

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    158/166

    Vir uses a nd Ca ncerir uses a nd Ca ncer(RNA)RNA)

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    159/166

    (RNA)RNA) _____________ _____________

    HTLV-1HTLV-1

    HepatocellularHepatocellular

    ____________ ____________

    Vir uses a nd Ca ncerir uses a nd Ca ncer(RNA)RNA)

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    160/166

    (RNA)RNA)HCVHCV

    HTLV-1HTLV-1

    HepatocellularHepatocellular

    T-cell leukemia/T-cell leukemia/lymphomalymphoma

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    161/166

    Vir uses a nd Ca ncerir uses a nd Ca ncer(RNA)RNA)

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    162/166

    (RNA)RNA)HCVHCV

    HTLV-1HTLV-1

    HepatocellularHepatocellular

    T-cell leukemia/T-cell leukemia/lymphomalymphoma

    Vir uses a nd Ca ncerir uses a nd Ca ncer(DNA)DNA)

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    163/166

    (DNA)DNA) _________ _________

    HBV (

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    164/166

    (DNA)DNA)EBV t(8;14)EBV t(8;14)

    HBV (

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    165/166

    (DNA)DNA)EBV t(8;14)EBV t(8;14)

    ___________ ___________

    ____________ ____________ HPV 18 (E7/RB)HPV 18 (E7/RB)

    ___________ ___________

    ___________ ___________ Hepatocellular CA Hepatocellular CA

    SC CA cervix, anusSC CA cervix, anus __________ __________ Kaposis sarcoma inKaposis sarcoma in

    AIDS AIDS

    Vir uses a nd Ca ncerir uses a nd Ca ncer(DNA)DNA)

  • 8/14/2019 Ne Oplasia Revi Ew Plu s

    166/166

    (DNA)DNA)EBV t(8;14)EBV t(8;14)

    HBV (