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CERVICAL LYMPHADENOPATHY OF UNKNOWN PRIMARY (C L U P)

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Title: CERVICAL LYMPHADENOPATHY OF UNKNOWN PRIMARY (C L U P)


1
CERVICAL LYMPHADENOPATHY OF UNKNOWN PRIMARY (C L
U P)
  • Dr. MOHAMMED ZAKARIA
  • CLINICAL ONCOLOGIST
  • MD, DMRT (LONDON)
  • JORDANIAN BOARD
  • MEMBER OF THE ROYAL COLLEGE OF RADIOLOGISTS
    (LONDON)

2
CERVICAL LYMPHADENOPATHY OF UNKNOWN PRIMARY (C L
U P)
  • Lymphadenopathy enlargement of a single or a
    group of regional lymph nodes of various etiology
  • Lymphatic spread is characteristic of EPITHELIAL
    TUMOURS, its frequency is proportional to the
    histological grading.

M. ZAKARIA PRSENTATIONS
3
THE LYMPHOID SYSTEM Comprises
  • Lymph capillaries (minute vessels) which commence
    blindly in tissue space and empty their lymph
    into certain veins.
  • The lymph nodes are small solid masses of
    lymphoid tissue into which the lymph vessel pour
    the lymph.
  • They are small, oval, or bean shaped bodies
    situated in the course of lymph vessels so that
    the lymph passes on its way to the blood through
    the L.N
  • 3 Main parts A - HILUS, B CORTEX,
  • C - MEDULLA

M. ZAKARIA PRSENTATIONS
4
THE LYMPHOID SYSTEM
  • (NATURAL DRAINING MECHANISM)
  • Provides the most common way for spread of
    carcinomas.
  • The extent of L.N involvement is of great
    prognostic significance following surgical
    removal of tumour
  • The process of TUMOUR SPREAD via lymphatic
    channels may be RETROGRADE or ORTHOGRADE

M. ZAKARIA PRSENTATIONS
5
  • Involvement of lymph nodes causes obstructive
    lymphadenopathy with alternative collateral
    pathways
  • Fixed nodes are associated with an advanced
    primary lesion.
  • Fixed nodes on one side of the neck have BETTER
    PROGNOSIS than mobile bilateral neck nodes


  • DOBBIEHENK1985

M. ZAKARIA PRSENTATIONS
6
The process of tumour spread to L.N
  • Stretching of the walls of lymphatic vessels
    creates gaps between the lining endothelial cells
    which leads to negative pressure in the lumen.
  • while the interstitial pressure is positive

M. ZAKARIA PRSENTATIONS
7
LYMPHATIC SPREAD
  • The natural history of lymphatic metastasis is of
    progressive proximal spread with involvement of
    successive groups of regional lymph nodes.
  • DOBBIE HENK 1985




M. ZAKARIA PRSENTATIONS
8
Nodal Regions of the Neck
  • CERVICAL
  • JUGULAR
  • PREAURICULAR
  • SUBDIGASTRIC
  • JUGULODIGASTIC
  • SUPRA CLAVICULAR

M. ZAKARIA PRSENTATIONS
9
(No Transcript)
10
CAUSES OF L. Ns ENLARGEMENT IN THE NECK
  • INFLAMMATORY AND REACTIVE
  • A-None SPECIFIC REACTIVE HYPERPLASIA
  • B-SPECIFIC DUE TO INFLAMMATION
  • -MALIGNANT CAUSES

M. ZAKARIA PRSENTATIONS
11
NONE MALIGNANT CAUSES OF L.N ENLARGEMENT IN THE
NECK ..1
  • None SPECIFIC REACTIVE HYPERPLASIA
  • A- Acute infection tonsillitis
  • B-Chronic infection fibrosis of the node
  • C-Reactive hyperplasia which can also be
    recognized in L.N draining malignant tumours
    (sinus histocytosis)
  • D-collagen disease
  • E-Drugs (antiepileptic)
  • A D THOMSON R E COTTON

M. ZAKARIA PRSENTATIONS
12
NONE MALIGNANT CAUSES OF L.N ENLARGEMENT IN THE
NECK ..2
  • INFLAMMATORY REACTIVE.1
  • SPECIFIC DUE TO INFLAMMATIONS
  • A-Bacterial T B, BRUCELLOSIS
  • B-Viral infectious mononucleosis ,measles
  • C-clamidial cat scratch disease.
  • D-fungal Histoplasmosis, Plastomycosis
  • A.D THOMSON COTTON

M. ZAKARIA PRSENTATIONS
13
NONE MALIGNANT CAUSES OF L.N ENLARGEMENT IN THE
NECK ..3
  • INFLAMMATORY REACTIVE.2
  • PARASITIC TOXOPLASMOSIS, FILARIASIS,
  • TRYPANOSOMIASIS, LEISHMANIASIS.
  • OTHER SARCOIDOSIS, DERMATOPATHIC
    LYMPHADENOPATHY.
  • A D THOMSON, R E COTTON

M. ZAKARIA PRSENTATIONS
14
MALIGNANT CAUSES OF L.N ENLARGEMENT.1
  • LEUKEMIA'S (CLL)
  • LYMPHOMAS
  • A- HODGKINS DISEASE
  • B-NON HODGKINS LYMPHOMAS
  • C-BURKITT'S LYMPHOMA
  • OTHER N H L
  • 1- SEZARY SYNDROME
  • ERYTHRODERMA GENERALISED L. N ENLARGEMENT (T
    CELL)
  • 2-IMMUNOBLASTIC SARCOMA (RAPIDLY Fatal)
  • 3-MALIGNANT HISTIOCYTOSIS (RAPIDLY FATAL)

She did not let me have photograph of her normal
looking neck post RT
M. ZAKARIA PRSENTATIONS
15
SECONDARY TUMOURS METASTASIZING TO NECK NODES
  • THE MOST COMMON HISTOLOGIC DIAGNOSES OF THE
    INVOLVED NODES WERE
  • Squamous cell carcinomas 62
  • Undifferentiated ca 28
  • Glandular of salivary gland origin 10
  • Halnan ,Fletcher, Moss text books

M. ZAKARIA PRSENTATIONS
16
METASTATIC NECK NODES..1
  • COMMON PRIMARY SITES
  • 1 -NASOPHARYNX
  • 2 -OROPHARYNX
  • 3-VALLECULA
  • 4-BASE OF TONGUE ORAL TONGUE
  • 5-TONSIL FAUCIAL ARCH
  • 6-ORAL CAVITY,
  • 7-FLOOR OF THE MOUTH
  • 8-SOFT PALATE

M. ZAKARIA PRSENTATIONS
17
METASTATIC NECK NODES..2
  • LARYNX
  • ARYEPIGLOTTIC FOLD
  • EPIGLOTTIS
  • HYPOPHARYNX
  • PYRIFORM FOSSA.
  • LIP
  • ORBIT
  • CHEEK
  • SKIN OF THE FACE

M. ZAKARIA PRSENTATIONS
18
METASTATIC NECK NODES
  • MAXILLARY ANTRUM
  • SALIVARY GL .(PAROTID)
  • CERVICAL ESOPHAGUS
  • THYROID
  • LUNG
  • PEDIATRIC SOFT TISSUE SARCOMAS OF HN

M. ZAKARIA PRSENTATIONS
19
CLINICALLY VE L.N ON ADMISSION TO M .D. ANDERSON
HOSPITAL
643 patients
NASOPHARYNX
TONSIL
BASE OF TONGUE
HYPOPHARYNX
OROPHARYNX
OROPHARYNX
SUPRA GLOTTIC LARYNX
SOFT PALATE
RETROMOLAR TRIANGLE
ORAL TONGUE
FLOOR OF MOUTH
M. ZAKARIA PRSENTATIONS
20
L.N. GROUPS INVOLVED ON ADMISSION TO M. D
.ANDERSON HOSPITAL
M. ZAKARIA PRSENTATIONS
21
Other Epithelial tumours of GLANDULAR STRUCTURE
WHICH CAUSE NECK NODE ENLARGEMENT
  • TUMOURS OF SALIVARY GLANDS
  • THYROID
  • CERVICAL OESOPHAGUS SUPR .CLAV
  • STOMACH SUPRA CLAV .L.N
  • PROSTATE CERVICAL L.N

M. ZAKARIA PRSENTATIONS
22
CONTRALATERAL L.N. INVOLVEMENT OF SELECTED HEAD
NECK SQUAMOUS .C. CA
M. ZAKARIA PRSENTATIONS
23
METASTATIC ADENOCARCINOMA TO CERVICAL L.N FROM
OCCULT PRIMARY SITE
  • RETROSPECTIVE ANALYSIS AT THE MIDDLESEX HOSPITAL
    (LONDON) 1987
  • THE COMMONEST SINGLE SITE WAS THE
  • JUGULODIGASTRIC NODE
  • ARISING FROM ONE OF THE FOLLOWING
  • BREAST
  • THYROID
  • OVARY
  • STOMACH
  • PROSTATE

M. ZAKARIA PRSENTATIONS
24
THE PRIMARY SITE MAY REMAIN UNDISCOVERED IN UP TO
10 OF CASES (1)
  • IN SOME PATIENTS WITH SECONDARY ADENOCARCINOMA,
    OR SQUAMOUS CELL CARCINOMA
  • THE PROGNOSIS FOR THESE PATIENTS IS HOPELESS (2)
  • IF CLINICAL EXAM INVESTIGATIONS HAVE FAILED TO
    IDENTIFY THE PRIMARY SITE THEN EXTENSIVE
    INVESTIGATIONS
  • ARE RARELY JUSTIFIABLE (3)
  • 1JOSSE ET al 1979, (2)NORDBOTRUM et al (3)
    STEWART, TATERS, WOODS AND FOX 1989

M. ZAKARIA PRSENTATIONS
25
DISCUSSION1
  • A VERY CAREFUL EXAMINATION OF ALL SITES OF
    POSSIBLE PRIMARY IS MANDATORY
  • 10 OF CASES WITH CERVICAL LYMPHADENOPATHY, THE
    PRIMARY SITE MAY REMAIN UNDISCOVERED
  • THERE IS ALSO THE POSSIBILITY OF GETTING
    HISTOLOGICALLY NEGATIVE RESULTS IN ALL EXAMINED
    PRIMARIES.

M. ZAKARIA PRSENTATIONS
26
DISCUSSION.2
  • OCCASIONALLY A NODE IN THE NECK MAY BE THE ONLY
    CLINICAL EVIDENCE OF Ca THYROID OR OTHER PRIMARY.
  • HISTOLOGICAL EXAMINATION OF THE CERVICAL L.N
    SHOULD INDICATE THE PRIMARY SITE.
  • POINTON CLEAVE 1990

M. ZAKARIA PRSENTATIONS
27
DIAGNOSIS.1
  • HISTORY
  • CLINICAL EXAMINATION
  • MULTIPLE BIOPSIES BEARING IN MINED THAT THE
    FALSE NEGATIVE RATE IS 14 to 2 0.8
  • EXAMPLE SQUAMOUS CELL CARCINOMA OF THE FLOOR OF
    THE MOUTH.
  • POINTON CLEAVE 1990

M. ZAKARIA PRSENTATIONS
28
DIAGNOSIS2
  • AT M. D. ANDERSON HOSPITAL 114 PATIENTS HAD
    DIRECT EXAMINATION UNDER G. A , PALPATION OF
    MUCOSAL SURFACES OF THE UPPER RESPIRATORY AND
    ALIMENTARY TRACTS.
  • 62 PTS SQ C CA,28 UNDIF .CA, 10 SAL. GLAND
    ORIGIN, 14 PTS REMAINED WITH UNKNOWN HIS.
  • BIOPSIES WERE PERFORMED ON ANY ABNORMAL MUCOSAL
    SURFACE
  • RANDOM BIOPSIES ARE USUALLY TAKEN FROM BASE OF
    TONGUE, TONSILS AND PYRIFORM SINUSES.

M. ZAKARIA PRSENTATIONS
29
DIAGNOSIS3
  • SIMPLE SOFT TISSUE VIEWS OF THE NECK
  • CT SCAN HAS LIMITED VALUE IN THE ASSESSMENT OF
    CLINICALLY ACCESSIBLE NODES.
  • US MAY BE OF SOME VALUE IN EXPERIENCED HANDS FOR
    THE DETECTION OF DEEP SEATED ACCESSIBLE NODES ,
    THEN
  • CONFIRMATION CAN BE ATTEMPTED BY NEEDLE
    ASPIRATION.

M. ZAKARIA PRSENTATIONS
30
DIAGNOSIS4
  • F N A (FINE NEEDLE ASPIRATION) IS MANDATORY BUT
    THERE IS A LOT OF CONTROVERSY REGARDING
  • WHO SHOULD DO IT
  • WHEN SHOULD IT BE DONE
  • FALSE POSITIVE
  • FALSE NEGATIVE RESULTS

M. ZAKARIA PRSENTATIONS
31
DIAGNOSIS..5
  • FNA FINE NEEDLE ASPIRATION CYTOLOGY1
  • IS A DIAGNOSTIC METHOD OF ENLARGED ACCESSIBLE
    LYMPH NODES.
  • IT IS AN OUT PATIENT PROCEDURE
  • THE DIAGNOSTIC ACCURACY OF F N A IS INFLUENCED BY
    A VARIETY OF FACTORS
  • SITE
  • SIZE
  • FIBROSIS
  • NUMBER OF PUNCTURES MADE
  • CYTOLOGICAL PREPARATION

M. ZAKARIA PRSENTATIONS
32
DIAGNOSIS6
  • F N A .2
  • FAILURE TO OBTAIN A REPRESENTATIVE ASPIRATION IS
    CONSIDERED TO BE RESPONSIBLE FOR MOST FALSE
    NEGATIVE DIAGNOSES.
  • HALNAN

M. ZAKARIA PRSENTATIONS
33
DIAGNOSIS7
  • F N A 3
  • BETSIL HADJDU IN 1980 REVIEWED 361 PTS WHO HAD
    FNA CYTOLOGY OF ACCESSIBLE L.N
  • 62 OF THE TOTAL WERE HARD NODES
  • BETSIL HADJDU 1980

OF RESULTS OF FNA
M. ZAKARIA PRSENTATIONS
34
DIAGNOSIS8
  • F N A4
  • A NEGATIVE REPORT FOR MALIGNANCY CAN NOT BE
    REGARDED AS DIAGNOSTIC SO OTHER INVESTIGATIONS
    ARE APPROPRIATE.

M. ZAKARIA PRSENTATIONS
35
METASTATIC NODES ON PRESENTATION FOR EACH T STAGE
  • THEREFORE
  • THE INCIDENCE OF METASTATIC L.N
  • INCREASES PROPORTIONALLY AS T INCREASES

M. ZAKARIA PRSENTATIONS
THE INCIDENCE OF METASTATIC NODES ON
PRESENTATION FOR EACH T STAGE
36
STAGING 1210 PATIENTS PRESENTED WITH CERVICAL
LYMPHADENOPATHY. THE DISTRIBUTION OF L.N
INVOLVEMENT WAS AS FOLLOWS
M. ZAKARIA PRSENTATIONS
OF PTS WITH CERVICAL LYMPHADENOPATHY
37
STAGING ACCORDING TO LYMPH NODE SIZE..2
  • N1single ipsilateral L.N 3 cm or less.
  • N2A single ipsilateral L.N gt3 cm but less lt than
    6 cm.
  • N2Bmultiple ipsilateral L.N not gt 6 cm.
  • N2Cbilateral or contralateral L.N gt6 cm.
  • N3metastasis in a L.N gt 6 cm.
  • ROBERT VP HUTTER 1992 (MANUAL FOR STAGING OF
    CANCER)

M. ZAKARIA PRSENTATIONS
38
TREATMENT POLICY1
  • IN study of large number of head neck tumors
  • VERONICI concluded the following.
  • PTS FALL IN 3 MAIN CLINICAL GROUPS
  • 1 No clinical evidence of involved L.N.
  • HE treated the primary tumors elective
    radical neck dissection Vs RT to whole neck
    Equal survival rate and remission.
  • 2 IN MOBILE DISCRETE NODES(N1N2) in block RT
    to primary tumour neck RT
  • 3 - FIXED NODES N3 best treated by RT

M. ZAKARIA PRSENTATIONS
39
O.K. THAT WAS VERONICI TREATMENT, BUT WHAT IS THE
CURRENT TREATMENT
  • 1 -No clinical evidence of involved L.N.
  • RT to primary whole neck/- adjuvant
    Cisplatinum containing regime chemotherapy
  • 2 -In mobile discrete (N1N2) RT to primary
    whole neck Cisplatinum containing regime
    chemotherapy.
  • 3 -FIXED NODES N3 best treated by RT CT
  • (primary and whole neck) chemotherapy

M. ZAKARIA PRSENTATIONS
40
Treatment options1
  • We must understand and accept the TREATMENT of
    caner must be multidisciplinary
  • The concept of combined clinics must be accepted
    and practiced i.e.
  • Combined ONCOLOGY- ENT Clinic So the patient must
    be seen by these two disciplines before , during
    treatment , and follow up jointly.

M. ZAKARIA PRSENTATIONS
41
Treatment options2
  • Usually the treatment of choice starts by Surgery
    either to
  • 1 removal of the tumour totally or
  • 2 - debulk the tumour or
  • 3 - at least taking biopsy.

M. ZAKARIA PRSENTATIONS
42
Treatment options3
  • CURATIVE Radiotherapy 6000 -7000 cGy IN 30 -35
    fractions over 6 -7 weeks to the primary without
    irradiating heavily the surrounding normal
    structures.
  • RT to neck nodes 5000 cGy in 25 fractions over 5
    weeks avoiding the spinal cord and boost the
    residual tumour in the nodes by Electron beam
    which treats superficial and less deep lesions.
  • or just palliative treatment to comfort the pt
    for short period of time.

M. ZAKARIA PRSENTATIONS
43
The role of chemotherapy in head neck cancer
with or without cervical Lymphadenopathy
  • Chemotherapy Chemotherapy in head neck cancer
    with or without cervical Lymphadenopathy was
    introduced in late 1990s and gave very promising
    results in term of tumour remission and survival
    and cervical node regression.
  • Now Cisplatinum based chemotherapy is considered
    one important treatment option in head neck
    cancer.
  • The incidence of recurrence rates are much less
    when adding Chemotherapy to the usual Surgery and
    Radiotherapy.

M. ZAKARIA PRSENTATIONS
44
Treatment options4
  • Chemotherapy 3- 6 courses either pre or post RT
  • B M C
  • BLEOMYCIN 10 UNITS IM DAYS 1,8,15
  • METHOTREXATE IM 40 mg/m2 days 1 and15
  • CISPLATINUM50 mg/m2 50 mg/m2 iv on day 4 repeat
    every 21 days
  • C F Cisplatin-FLUOROURACIL
  • Cisplatin100 mg/m2 iv day 1
  • FLUOROURACIL1000mg by continuous iv infusion for
    96 hours repeat every 3 weeks

M. ZAKARIA PRSENTATIONS
45
THE RESULTS OF CHEMOTHERAPY in head neck
cancer with or without cervical Lymphadenopathy
  • Survival rates have increased dramatically
  • Recurrence rates in the primary tumour and
    Cervical Lymphadenopathy are now much less than
    before.
  • Cisplatinum based chemotherapy has changed the
    results of treatment as compared with the trials
    using high dose Methotrexate by Strong et al
    in1998.

M. ZAKARIA PRSENTATIONS
46
RADIOTHERAPY RESULTS
M. ZAKARIA PRSENTATIONS
47
RADIOTHERAPY RESULTS
M. ZAKARIA PRSENTATIONS
48
THANK YOU
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