The Role of FNAB (Fine Needle Aspiration
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Transcript of The Role of FNAB (Fine Needle Aspiration
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1853 : James paget cell aspiratesfrom breast cancer
1904 : Greig and gray
trypanosomesfrom lymph node
1921 : Guthriemalignant lymphomafrom lymph node
1930 : Martin and Ellis diagnose a varietyof swellingin memorial hospital in NewYork
FKUI : begin 1989
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Distinguish benign from malignant lesions
Classify neoplasms and others
pathologic processes
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The patient
Minimal pain and post aspiration discomfort
Anesthesia is rarely necessary Can be used in high risk patients
Usually an outpatients procedure
Save time and hospitalization
Rapid alleviation of anxiety
More time to adjust to other procedures
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Clinical management Easily repeated
Allows sampling of multiple area with minimal trauma
Minimal disturbance of tissue planes for the solepurpose of diagnosis
Confirm malignancy of a nodule, but leaves it intactto monitor therapy by clinical examination or byrepeated aspiration
Therapeutic for some masses ( cysts and abscesses) Does not require extensive training of physicians
Quick feedback help in training and planning otherinvestigative procedures
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The laboratory
Simple, inexpensive equipment
Excellent cell preservation due to rapidfixation
Allows studies requiring freshly harvested cells
material can be obtained for other
examination ( microbiology, moleculartechnique, cytogenetic studies, enzymaticassay, stem cell culture etc)
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Marked hemorrhagic diathesis increasesthe risk of a significant hemorrhagic
Highly vascular tumors
Aneurysm or a vascular malformation
Deep organ(specific for each organ) severe cough, bullous emphysema,
pulmonary hypertension, respiratory failurein the case of lung aspiration
Liversevere jaundice, suspicious ofhemangioma or hydatid disease
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1. Superficial organ/ nodule Lymph node
Thyroid
Breast
Salivary gland
Others nodule
2.Deep organ by imaging guidance liver
Intraabdominal mass
Unpalpable mass
etc
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FNAB
DEFINITIVE
DIAGNOSIS ?Depend on :
- Organ- disease (diagnosis)
- need ancillary technique ( Imunocytochemistry,
molecular technique, etc )
- consensus
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Dawson et al (1998) : excellent result inbreast cancer diagnosis(35 y.o or younger)
Cohen et al (1987) and Ljung et al (2001) :correct diagnosis in 97% - 98% of patients
Stahl (1996) : suggested that asking thepatient to indicate the location of the lesionis more reliable than actual palpation
Procedures may be used : Palpable lesion ( solid, cystic)
Non-palpable lesion ( mammography, USG, MRIetc)
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Smear or cell block suitable for
ancillary examination
ER,PR, Ki-67 (proliferation factor), HER-2 Limitation of FNAB
Result of FNA is atypical or suspicious :
the procedure should be repeated,
another opinion or
The lesion should be excised for histopatologicexamination
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Protokol penatalaksanaan pasien (National Cancer Institute ConsensusConference on the uniform approach to breast FNAB )
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PENYEBAB DIAGNOSIS FALSE-NEGATIVE Kegagalan mendapatkan sampel yang
representative, berhubungan langsung dengan
karakteristik tumor (size, lokasi, derajat fibrosis,tipe histologik, diferensiasi), faktor tehnik
Kegagalan pengenalan sel ganas,berhubungan dengan pengalaman ahlipatologi
PENYEBAB DIAGNOSIS FALSE-POSITIVE Interpretasi yang kurang tepat pada lesi atipik
Preparasi slide buruk
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INSUFISIENSI /UNSATISFACTORY( NOTREPRESENTATIVE)
NEGATIVE (BENIGN LESION) INCONCLUSIVE (SUSPICIOUS)
POSITIVE FOR MALIGNANCY
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Invasiveductal
carcinoma
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FNAB accepted by head-neck surgeon asan excellent
Zaijcek, 1974 ; Batsakis et al, 1992; Boccato et
al 1992 primary methods of evaluatingspace occupying lesion of the salivary glands
FNA of salivary glands : Is the mass of salivary gland origin ?
If the mass is of salivary gland origin, is it neoplastic ornon-neoplastic ?
If the mass neoplastic, is it benign or malignant ?
If the mass is malignant, is it primary or metastatic ?
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Diagnosis of FNAB :
Influences management of the patients
(Zaijcek,1974;Kocjan et al ,1990; Orell, 1995) For example :
Benign lesion/neoplasms : surgicalintervention may be delayed or modified
Malignant neoplasms : prompt surgicaltreatment or irradiation
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Significant complication rare Kern (1998) : postaspiration necrosis in a case
of warthins tumor
Layfield et al (1992) : necrosisin a case ofpleomorphic adenoma Stephens et al (1999) : xantogranulomatous
following FNA of Warthins tumors Li et al (2000) and Mukunyadzi et al (2000)
review the histology Salivary glands lesionspreviously samples by FNAB : Infarction, necrosis, hemorrhage, inflammmation,
granulation tissue
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The primary objective :
Select the case :
Require surgery for neoplastic
Inflammmatory abnormality followed
clinically or treated medically
Aspiration biopsy
25 gauge needle
Larger caliber needles NOTRECOMMENDED (bleeding)
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Adequate/inadequate
Benign non neoplastic lesion
Cellular follicular lesion Hurtle cell neooplasm
Suspicious neoplasm
Malignant
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Adequacy of aspiration biopsy :
Six clusters of epithelial cells
Some centers do not agree case withpure colloid goiter ??
Depent of type of lesion (cystic or solid)
Ground glass appearance
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Ground glass appearance
PAPILLARY CARCINOMA OF THE THYROID
COURTESY OF PROF. SHOTARO MAEDA, NMS
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FOLLICULAR CARCINOMA OF THE THYROID
COURTESY OF PROF.S HOTARO MAEDA, NMS
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Triple diagnosis :
1. Clinical diagnosis
2. Radiology diagnosis3. Cytology/Histopathology diagnosis
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COURTESY OF PROF.S HOTARO MAEDA, NMS
GIANT CELL TUMOR OF THE BONE
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GIANT CELL TUMOR OF THE BONE
COURTESY OF PROF.S HOTARO MAEDA, NMS
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FNAB OF THE LUNG
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Janes and Spiro, AJRCCM 2007
ESTS, Deleyn P , Eur Cardio T Surg 2007 ACCP, Detterbeck F, Chest 2007
COURTESY OF DR. MAUD VESSELIC, LUMC
Radial vs Linear Endosonography (2)
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Radial vs Linear Endosonography (2)
COURTESY OF DR. MAUD VESSELIC, LUMC
Scopes and Ultrasound Processor
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Scopes and Ultrasound Processor
COURTESY OF DR. MAUD VESSELIC, LUMC
Transesopfageale echografie + naald punctie
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Transesopfageale echografie + naald punctie
COURTESY OF DR. MAUD VESSELIC, LUMC
Small cell lung carcinoma
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Small cell lung carcinoma
Syncytial group with nuclear molding and paranuclear cytoplasmic globules(so-called blue bodies)
Cells showing increasd cytoplasma that may be mistaken for non-small
cell carcinoma
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Immediately put the slide (after makesmear) into alcohol fixative 95% -96%minimally 30 minutes.
A part of slides let in the air until dry ( ifpossible use hairdryer or fan to makedry fast )
Dont forget to write down the patientlabel on the slide
Send to laboratory with form andcompletely clinical data
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