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    Intr cti n

    Classificati n

    Epi emi logyand emographics

    athology Ris factors

    Symptoms and Signs

    Investigations Staging

    Treatment

    References

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    When cancer of theWhen cancer of theoesophagusoesophagus becomesbecomes

    symptomatic, it is alreadysymptomatic, it is alreadythree minutes untilthree minutes untilmidnightmidnight

    Julius L. Stoller

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    6th most common cancer in the world.

    Black/White: 5/1

    Male/Female: 5/1 Men have esophageal cancer 3-5 times

    more often than women

    The mean age at diagnosis is 60 year

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    BENIGNTUMORS MALIGNANT TUMOURS

    Epithelial

    apillomas

    esenchymal Leiomyomas

    Hemangiomas

    Lymphangiomas

    Fi romas Lipomas

    yxomas

    Ne rofi romas

    Epithelial (carcinoma)

    Sarcoma

    Carcino-sarcoma

    Metastatic

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    CL SSIFICATIONCLASSIFICATION--

    (a)(a) SquamousSquamous cell carcinomacell carcinoma (60%)(60%) (b)(b) AdenocarcinomaAdenocarcinoma (40 %)(40 %)

    (c) Rare types(c) Rare types::1.Mucoepidermoid carcinoma,

    2.Adenoid cystic carcinoma,3.Small cell carcinoma,

    4.undifferentiated carcinoma

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    Divides the EJs tumor

    1. EJs-1

    2. EJs-2

    3. EJs-3

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    Ris factors- Tabaco smoking Excessive alcohol consumption Nutritionaldeficiency(iron,vit.A) oor dentalhygiene

    Long term use of spicy foodandhot drinks Fungal contaminationof food Obesity Fresh fruits andvegetables are protective Occuapational exposure of asbestos,combustion product

    re-existing conditions---- Achalasia (3-5%) Barrets esophagus Chronic reflux esophagitis Caustic burns Tylosis

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    Human papilloma virus HPV serotype16 was identified in 9 percent of resection specimens

    from 70 Chinese patients with esophageal SCC.

    Controversial, but HPV has got some protectivevalue in case of adenocarcinoma.

    Keratosis palmaris et

    plantaris(tylosis) rare disease associatedwith hyperkeratosis of the palms of the hands andsoles of the feet and a high rate of esophageal SCC.

    AD

    Mapped on ch band 17q25

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    NEJM,2003NEJM,2003NEJM,2003

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    Upper third: 20%

    Middle third- 30%

    Lower third: 50%

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    Histologically, characterizedby invasive sheetsof cells that run together andare polygonal,oval,or spindle-shaped withadistinct or

    ragged stromal-epithelial interface.

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    AA-- Cauliflower type(Cauliflower type(fungatingfungating) (60%):) (60%):

    BB-- Ulcerative type :Ulcerative type : raised everted edge-

    necrotic floor- indurated base

    CC--Annular typeAnnular type :: more common in

    lower 1/3.

    Pattern of GrowthPattern of Growth

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    A 5-year survivalof 70% is associated with thepolypoid tumor compared withaless than15%5-year survival for allother types

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    Arises from the superficialanddeepglands

    of the esophagus, mainly in the lower third

    of the esophagus, especiallynear thegastroesophageal junction

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    Mayhave one of three origins:

    Malignant degenerationof metaplasticcolumnar epithelium (Barrett's mucosa)

    Heterotopic islands of columnar

    epithelium

    The esophageal submucosal glands

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    Anaplastic small cell (oat cell) carcinomaarisein the esophagus from same argyrophilic cellsfound in the lung.

    Adenoid cystic esophageal carcinoma

    Primary malignant melanomaof esophagus

    Carcinosarcoma, features of SSCand malignant

    spindle cell sarcoma.

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    Progressive dysphagia - 87-95 % Weight loss Sialorrhea (Hypersalivation) Regurgitation Pain (Odynophagia) Halitosis Dehydration

    RespiratoryProductive coughingHoarsenessDyspnea

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    Difficulty in swallowingDifficulty in swallowing

    Dysphagia in male > 50 years > 2 wks isconsidered cancer esophagus untill

    proved otherwise

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    Usuallyno signs

    Evidence of weight loss

    Cervical LAM

    Other signs of dissemination

    Hepatomegaly

    Jaundice

    Cardiac arrhytmias

    Ascites

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    (1)(1) Direct:Direct: ((main methodmain method):): to the surrounding

    (2)(2) LymphaticLymphatic:: mainly inadownwarddirection.

    Cervical esophagus lower deep cervical L.N.

    Thoracic esophagus para-oesophageal & tracheo-bronchial lymph nodes

    Abdominal esophagus lymphnodes along the lessercurvature of the stomach coeliac axis L.N.

    (3) Blood (rare):(3) Blood (rare):

    Liver,lung,bone,brain

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    Obstruction

    Perforation

    Pulmonary- Pneumonia,lungabscess,

    Esophago-tracheal/bronchial fistula

    - Cardiovascular- Bleeding, myo-pericardial met,S C syndrome

    Neural-Rec. Laryngeal,vagal,phrenic nerveinvolvement,

    Claude Bernard Horner syndrome

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    HematologicalEx.

    Barium swallow

    CT Scan

    MRI

    PET

    Endoscopy

    Esophagoscopy(biopsy)

    EndoscopicUS

    Bronchoscopy

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    - Non invasive methodof detectingprimary,nodal,distant metastases &locally recurrenttumor

    - The technique estimates areaof highglucose

    metabolism (the tumor) by measurement of theuptake of radiotracer (Flurodeoxyglucose FDG).

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    Lugol's iodide reacts with the glycogen

    components of normal squamous mucosa to

    produce a greenish brown color, while

    neoplastic tissue is depleted of glycogen andremains unstained

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    Relief fromdysphagia

    Long dysphagia free

    interval Relief from pain

    Improved quality oflife

    Improved long-termsurvival

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    Surgery

    Chemotherapy

    Radiotherapy

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    SURGERY----

    Most effective treatment

    Overall resectability50%

    Operative mortality5-10% Lymphnode involvement % 80

    Routes

    Trans-thoracic

    Thoraco-abdominal Transhiatal

    Lapassistedoesophagectomy

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    Mainlydepends onlocationof tumor

    CERVICAL Lesion-pharyngogastrostomyanastomosis is preferred.

    UPPEROesophagus-Tri Incisional approach

    MIDDLEOesophagus-Tri/Ivor Lewis

    LOWEROesophagus-Tri/Ivor

    Lewis/Transhiatol approach

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    Stomach

    Lt colon

    Rt colon

    Jejunum

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    Anastomotic leak,

    Anastomotic stricture,

    Recurrent laryngealnerve palsy,

    Respiratory complication,

    Bleeding,

    Chyle leak,

    Impaired conduit emptying

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    UnresectabilityCriterias----

    Tracheo-esophageal fistula

    Hoarseness

    Tumor> 10 cm

    Malignant pleural effusion

    Claude Bernard Horner syndrome

    Paralysis of diaphragm Invasionof surrounding structures

    Distant metastases

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    RT/CT

    Dilation withbougie

    Atkinson

    Souttar Tube

    Procter-Livingstone

    Self expanding metalstents(SEMS)

    Photodynamic therapy (PDT)

    Surgery-Bypass procedure(Retro/presternal colonic by-pass)

    Feedinggastrostomy orjejunostomy

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    Pt withM-1disease have a median survivalof 6to12 months.

    Inpt without systemic metastases,a complete R0resection is best.

    Pt withanR1(positive microscopic margin) orR2(gross left behind) resectionhave survivalsimilar to those pt havingM1disease.

    After surgery: 5-year overall survival

    10-20

    1-year survival 70%

    2-year30%

    5-year20%

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    Cisplatin 75 mg/m2 bolus givenover 30 min withadequate prehydration,mannitol andantimetics onday1,

    5-FU1000 mg/m2/daygivenas continiousinfusiononday1 through4,

    Cycle repeated every28days,

    Four cycles planned-first 2 withRT,last 2 withoutRT.

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    1. Multiple field technique-1.8Gy/day withtarget upto 50.4Gy.

    2.Highdose target volume-14.4Gy/day with

    target upto 64.8Gy.

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    1.Bailey& Loves short practice of surgery,2.Sabiston text bookof surgery,

    3.Maingot AbdominalOperation,

    4.Devita,Hellman&Rosenbergs cancer principal&practice of oncology,

    5.Lee McGregors synopsis of surgicalanatomy,

    6.Dx/Rxupper gastrointestinal malignancies:

    cancer of the stomach& esophagus-Dr.ManishA.Shah,

    7.Schwartz's Principles of Surgery

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