Dr.AEBEENA BABU
PG –FIRST MDS
DEPT OF ORAL AND MAXILLOFACIAL PATHOLOGY
 Biopsy is the removal of tissue from the living organism for the
purpose of microscopic examination and diagnosis
 Surgical biopsy
Incisional biopsy
Excisional biopsy
Punch biopsy
 Fine needle aspiration cytology(FNAC)& CT guided FNAC
 Exfoliative cytology
 Brush biopsy
 Frozen section biopsy
 Endoscopic biopsy
 Cone biopsy
 Core needle biopsy
 Suction assisted core needle biopsy
 Laser biopsy
Lesion is totally excised for histological evaluation- Excisional
biopsy
Done in case of small lesions
Excised tissue is then processed and histologically analyzed
under microscope to determine the true nature of the tissue
 Small section of the tissue is removed from a lesion for the purpose of
histological evaluation is known as incisional biopsy.
 Indicated :
1)Lesion is too large to excise initially without knowing the exact diagnosis.
2)lesion is of such a nature that the total excision would be irrational
 Punch biopsy is useful in obtaining tissue samples from the skin and mucous
membrane
 Frequently by dermatologists and oral pathologists.
 Helps in removing tissue samples from a variety of lesions
eg: Oral cancers and pre cancers
Vesiculobullous lesions
Moles, Small lumps etc
 Surgical biopsy and removes the tissue which is cylindrical or cone shaped
 Advantage – large sample of the tissue
 Done by aspirating needle from inside a lesion
 Commonly performed in cases in glandular cystic lesion
 How its done???
Needle is inserted into the lesion
Vaccum is created so that the tissue samples are sucked in to syringe
Sample is used to prepare a smear and seen under microscope
Same as FNAC
 Needle is inserted to the target lesion
 Needle is advanced within the deeper cell layer to remove the
core tissue
 Needle has a cutting tip that helps in removing tissue
 Core biopsy syringe is attached to a suction associated with vaccum
device
 Performed in order to get an immediate histological report of the
lesion
 The tissue is obtained from a lesion and the fresh tissue is quickly
frozen at about -70 degree Celsius in liquid nitrogen or dry ice.
 The frozen tissue is then sectioned in a refrigerated microtome and
then stained and diagnosed
 Disadvantage: Slide cannot be preserved for future references .
Photomicrographs of the slide are taken
Used to collect cells from the surface as well as sub surface
layer of the suspected lesion for microscopic examination.
A round stiff brush is rotated vigorously at a particular
site of the lesion until bleeding starts, which ensure a
sufficiently deep sample
Smear is prepared from the sample and scanned under
microscope to detect any abnormal cells.
The area of the wound from where the biopsy will be taken is
cleaned first.
 The area is anesthetized.
The most representative site of the wound is identified.
 A section of tissue from the identified site of wound (or sometimes
the entire wound) is removed.
The tissue is cleaned and put into 10 percent formalin solution for
fixation.
 The biopsy site is sutured after achieving hemostasis.
 The biopsy specimen is sent to the histopathologist for diagnosis
after labeling it properly.
Before the biopsy, specimen should be properly labeled in the following
manners.
 Mention the name, age and sex of the patient.
 Mention the date and time of biopsy.
 Mention the type of biopsy, the site from where it is obtained and the
nature of the tissue (e.g. bone tissue or soft tissue, etc.).
 Mention the brief clinical, radiological and other relevant features of
the lesion (if any).
 Mention the provisional diagnosis.
 A negative report should not be considered final, especially if it is
totally
unexpected than what was thought earlier.
 Biopsy should be repeated, if there is any doubt regarding the
diagnosis.
 If further investigations are required, e.g. histochemistry,
immunohistochemistry,
tissue culture or animal inoculation, etc. should be done.
 Specimen obtained from unrepresentative site of the lesion.
 Damaged or improperly fixed specimen. •
 Specimen of insufficient depth.
 Microscopic features are too difficult to interpret as in poorly
differentiated lesions.
 Lesion with non-specific histological findings, e.g. aphthous ulcer.
 Exfoliative cytology is the microscopic study of cells obtained from
the surface of an organ or lesion after suitable staining.
Herpes simplex.
 Herpes zoster
Pemphigus vulgaris
Pemphigoid
Squamous cell carcinoma
 Aphthous ulcer
 Candidiasis
 First ,surface of the lesion is cleaned by removing all the debris and mucins, etc.
 Gentle scrapping is done on the surface of the lesion with a metal cement spatula
or a moistened tongue blade for several times.
 Materials present on the surface of the lesion are adhered or collected at the
border of the instrument.
 Collected material is then evenly spread over a microscopic slide and is fixed
immediately with either 95 percent alcohol or equal parts of alcohol and ether.
 Slide is then air-dried and is stained by a special stain called PAP stain
(papanicolaou stain).
 Not a substitute for surgical biopsy.
 Anesthesia is not required in this technique
 It is a quick, simple, painless and bloodless procedure.
 It helps to check the false-negative biopsy cases
 Special procedures like immunohistochemistry can be performed in
exfoliative cytology samples.
 Helpful in follow up detection of recurrent cancer cases.
 Helps in screening a large number of lesions, which do not look like
cancers clinically.
biopsy in oral lesions bbbbbbbbbbbbbpptx

biopsy in oral lesions bbbbbbbbbbbbbpptx

  • 1.
    Dr.AEBEENA BABU PG –FIRSTMDS DEPT OF ORAL AND MAXILLOFACIAL PATHOLOGY
  • 2.
     Biopsy isthe removal of tissue from the living organism for the purpose of microscopic examination and diagnosis
  • 3.
     Surgical biopsy Incisionalbiopsy Excisional biopsy Punch biopsy  Fine needle aspiration cytology(FNAC)& CT guided FNAC  Exfoliative cytology  Brush biopsy  Frozen section biopsy  Endoscopic biopsy  Cone biopsy  Core needle biopsy  Suction assisted core needle biopsy  Laser biopsy
  • 4.
    Lesion is totallyexcised for histological evaluation- Excisional biopsy Done in case of small lesions Excised tissue is then processed and histologically analyzed under microscope to determine the true nature of the tissue
  • 6.
     Small sectionof the tissue is removed from a lesion for the purpose of histological evaluation is known as incisional biopsy.  Indicated : 1)Lesion is too large to excise initially without knowing the exact diagnosis. 2)lesion is of such a nature that the total excision would be irrational
  • 8.
     Punch biopsyis useful in obtaining tissue samples from the skin and mucous membrane  Frequently by dermatologists and oral pathologists.  Helps in removing tissue samples from a variety of lesions eg: Oral cancers and pre cancers Vesiculobullous lesions Moles, Small lumps etc
  • 10.
     Surgical biopsyand removes the tissue which is cylindrical or cone shaped  Advantage – large sample of the tissue
  • 11.
     Done byaspirating needle from inside a lesion  Commonly performed in cases in glandular cystic lesion  How its done??? Needle is inserted into the lesion Vaccum is created so that the tissue samples are sucked in to syringe Sample is used to prepare a smear and seen under microscope
  • 13.
    Same as FNAC Needle is inserted to the target lesion  Needle is advanced within the deeper cell layer to remove the core tissue  Needle has a cutting tip that helps in removing tissue
  • 15.
     Core biopsysyringe is attached to a suction associated with vaccum device
  • 16.
     Performed inorder to get an immediate histological report of the lesion  The tissue is obtained from a lesion and the fresh tissue is quickly frozen at about -70 degree Celsius in liquid nitrogen or dry ice.  The frozen tissue is then sectioned in a refrigerated microtome and then stained and diagnosed  Disadvantage: Slide cannot be preserved for future references . Photomicrographs of the slide are taken
  • 17.
    Used to collectcells from the surface as well as sub surface layer of the suspected lesion for microscopic examination. A round stiff brush is rotated vigorously at a particular site of the lesion until bleeding starts, which ensure a sufficiently deep sample Smear is prepared from the sample and scanned under microscope to detect any abnormal cells.
  • 18.
    The area ofthe wound from where the biopsy will be taken is cleaned first.  The area is anesthetized. The most representative site of the wound is identified.  A section of tissue from the identified site of wound (or sometimes the entire wound) is removed. The tissue is cleaned and put into 10 percent formalin solution for fixation.  The biopsy site is sutured after achieving hemostasis.  The biopsy specimen is sent to the histopathologist for diagnosis after labeling it properly.
  • 19.
    Before the biopsy,specimen should be properly labeled in the following manners.  Mention the name, age and sex of the patient.  Mention the date and time of biopsy.  Mention the type of biopsy, the site from where it is obtained and the nature of the tissue (e.g. bone tissue or soft tissue, etc.).  Mention the brief clinical, radiological and other relevant features of the lesion (if any).  Mention the provisional diagnosis.
  • 20.
     A negativereport should not be considered final, especially if it is totally unexpected than what was thought earlier.  Biopsy should be repeated, if there is any doubt regarding the diagnosis.  If further investigations are required, e.g. histochemistry, immunohistochemistry, tissue culture or animal inoculation, etc. should be done.
  • 21.
     Specimen obtainedfrom unrepresentative site of the lesion.  Damaged or improperly fixed specimen. •  Specimen of insufficient depth.  Microscopic features are too difficult to interpret as in poorly differentiated lesions.  Lesion with non-specific histological findings, e.g. aphthous ulcer.
  • 23.
     Exfoliative cytologyis the microscopic study of cells obtained from the surface of an organ or lesion after suitable staining.
  • 24.
    Herpes simplex.  Herpeszoster Pemphigus vulgaris Pemphigoid Squamous cell carcinoma  Aphthous ulcer  Candidiasis
  • 25.
     First ,surfaceof the lesion is cleaned by removing all the debris and mucins, etc.  Gentle scrapping is done on the surface of the lesion with a metal cement spatula or a moistened tongue blade for several times.  Materials present on the surface of the lesion are adhered or collected at the border of the instrument.  Collected material is then evenly spread over a microscopic slide and is fixed immediately with either 95 percent alcohol or equal parts of alcohol and ether.  Slide is then air-dried and is stained by a special stain called PAP stain (papanicolaou stain).
  • 27.
     Not asubstitute for surgical biopsy.  Anesthesia is not required in this technique  It is a quick, simple, painless and bloodless procedure.  It helps to check the false-negative biopsy cases  Special procedures like immunohistochemistry can be performed in exfoliative cytology samples.  Helpful in follow up detection of recurrent cancer cases.  Helps in screening a large number of lesions, which do not look like cancers clinically.