PRACTICE

BRITISH DENTAL JOURNAL VOLUME 196 NO. 6 MARCH 27 2004 329

Oral biopsies: methods and applications
R. J. Oliver
1
P. Sloan
2
and M. N. Pemberton
3
Biopsies are an important diagnostic tool for the diagnosis of lesions ranging from simple periapical lesions to malignancies.
Planning prior to performing a biopsy is essential. It will be beneficial to the receiving pathologist in reaching a helpful and
meaningful diagnosis, and therefore ultimately and more importantly, to the patient. This paper presents an updated view of
biopsies and discusses some of the potential problems with biopsy technique and specimens and how to overcome them.
1
Lecturer in Oral Surgery,
2
Professor of Oral Pathology,
3
Consultant in Oral Medicine, Oral and Maxillofacial
Sciences, University Dental Hospital of Manchester, Higher
Cambridge Street, Manchester M15 6FH
Correspondence to: Dr. Richard Oliver, University Dental
Hospital of Manchester, Higher Cambridge Street,
Manchester, M15 6FH
E-mail: [email protected]
Refereed Paper
doi:10.1038/sj.bdj.4811075
Received 05.12.02; Accepted 07.07.03
British Dental Journal 2004; 196: 329333
A biopsy is often the only way to diagnose
oral lesions and diseases and as with most
procedures there is often more than one
method of undertaking the surgery suc-
cessfully. Whatever the method used, how-
ever, the aim is to provide a suitably repre-
sentative sample for the pathologist to
interpret, while minimising perioperative
discomfort for the patient. An unsuitable,
unrepresentative sample is of no use to the
pathologist, clinician or most importantly
the patient who would be ill served by an
unnecessary repeat procedure. Although
most biopsies are performed in hospitals, a
recent study has shown that many general
dental practitioners felt able to perform
biopsies but lacked some of the necessary
skills.
1
The purpose of this article is to
review those skills, to discuss new develop-
ments in this area, and to highlight some of
the potential pitfalls that may occur in tak-
ing a biopsy and methods available to
avoid them. The authors feel it will be of
value to both general dental practitioners
and junior hospital staff. Problems related
to specific areas will be covered including
apical lesions and those associated with the
dental hard tissues. Mucosal and soft tissue
biopsies together with general points
regarding techniques and fixation will also
be discussed.
SPECIFIC TISSUES
Apical lesions and those associated with
the dental hard tissues
Many apical lesions are submitted routine-
ly from general dental practice as well as
hospitals following periradicular surgery.
The majority of the lesions are inflammato-
ry in origin, most commonly periapical
granulomas or radicular cysts. Less com-
monly, other odontogenic cysts present at
the apex, namely nasopalatine duct cyst or
of greater significance the odontogenic
keratocyst. Less frequently still, odonto-
genic tumours may present at such a site.
Bone lesions such as Langerhans cell histi-
ocytosis, giant cell granuloma and myelo-
ma may also present in this way. Rarely,
malignant metastatic deposits or even
intraosseous squamous cell carcinoma can
occur at this site.
2
The value of routinely
examining apical lesions has recently been
questioned,
3
however, the resulting corre-
spondence has all been strongly in support
of submitting material; one respondent
4
cited that the non-submission of material
often leads to a failure to diagnose and the
situation regarding periapical lesions is no
different, no matter how rare such
instances occur.
For diagnosis, the excised material
needs to be fixed to stop tissue autolysis
prior to the sample reaching the pathology
laboratory. The solution of choice to do this
is 10% neutral buffered formalin fixative (a
4% solution of formaldehyde). This can
easily be obtained on request from most
pathology laboratories together with a sup-
ply of request forms and specimen pots. In
a recent survey,
1
many practitioners
appeared unaware of these facilities and as
such pathology laboratories may need to
consider advertising their services more
widely. It should be noted that some labo-
ratories might levy a nominal charge for
such services.
Some clinicians submit apical lesions on
gauze which has been placed in formalin
solution. However, if the volume of forma-
lin in the container is not great enough, the
gauze tends to absorb most of the formalin
leaving the specimen dry and unfixed.
Although not essential, it is desirable to
inform the pathologist if bone is included
in the specimen.
Occasionally, it is necessary to examine
the dental hard tissues, most often to rule
out an abnormality of dentine or enamel.
Biopsies of different tissue types and sites require specific techniques.
Correct handling of biopsy specimens is crucial.
The chosen site for a mucosal biopsy is dependent upon the disease/lesion.
Written consent is advised for all biopsies.
I N BRI E F
VERIFIABLE
CPD PAPER
06p329-333.qxd 23/02/2004 10:43 Page 329
PRACTICE
330 BRITISH DENTAL JOURNAL VOLUME 196 NO. 6 MARCH 27 2004
As with most other tissues submitted for
routine examination, teeth should also be
submitted in 10% neutral buffered formalin
fixative. A mineralised sample, such as
bone or tooth may require decalcification
before it can be processed. The time for the
decalcification will vary according to the
size and consistency of the specimen as
well as the methods employed by a particu-
lar laboratory, but it should be borne in
mind that it can be a matter of weeks
before a histopathology report is available.
Mucosal biopsies
Biopsy technique for the sampling of
mucosal biopsies can be critical. If a
tumour or premalignant disease is suspect-
ed, or when widespread mucosal disease is
suspected, we would strongly advocate the
biopsy being undertaken in a hospital set-
ting following appropriate referral; such
lesions should not be biopsied in general
dental practice. Such biopsies should be
performed by the clinician who is going to
initiate the treatment. Some of the follow-
ing section is, therefore, for information for
general dental practitioners and of more
relevance to junior hospital staff.
Simple excisional biopsies of polyps or
epulides are suitable for general dental
practice, and can be both diagnostic and
curative at the same time. Before embark-
ing on a biopsy the question of what the
biopsy is being taken for must be answered
(Table 1). The provisional clinical diagno-
sis is especially important in guiding the
technique and tissue handling to be used
(Table 2).
Suspected malignancy
If the reason for the biopsy was to exclude
malignancy in a long-standing ulcer, a
biopsy of the ulcer to include some adja-
cent clinically normal epithelium would be
desirable. If the lesion is a carcinoma this
allows confirmation that it is arising from
the overlying epithelium rather than from a
deeper structure or from a metastasis from
a different site. It also allows the invasive
front to be examined which can yield use-
ful prognostic information.
5
The centre of
larger tumours should be avoided as this is
often necrotic and will not yield diagnostic
material. A recent study has demonstrated
that cytokeratins were present in the
peripheral blood of two out of ten patients
15 minutes after the incisional biopsy of an
oral squamous cell carcinoma, thereby
demonstrating that there was dissemina-
tion of cancer cells which may result in
metastasis.
6
These authors suggested that
chemotherapeutic drugs should be admin-
istered prior to biopsy to minimise the risk
of metastasis in such patients. However, the
incidence of blood borne metastasis in
relation to oral cancer is low, but this area
merits further investigation.
Mucocutaneous lesions
Biopsies are commonly taken to confirm
the clinical diagnosis of lichen planus,
lichenoid reactions or other similar muco-
cutaneous conditions. To aid in the histo-
logical diagnosis of such lesions, an area of
non-erosive lesional tissue should be cho-
sen. Sampling of an erosive area will often
show non-specific inflammatory changes
associated with ulceration and will not aid
in the diagnosis. Adjacent normal tissue is
not generally required for such lesions.
Similarly for suspected vesiculobullous
disorders, the site of the biopsy should be
adjacent to bulla where the epithelium is
still intact. For these lesions it is desirable
also for the laboratory to receive a fresh
specimen of tissue in addition to a formalin
fixed one to allow direct immunofluores-
cence (see later regarding fresh specimens).
When desquamative gingivitis is present,
the biopsy should be taken from the most
intact area of mucosa which is often the
attached gingiva; an elliptical area of
mucosa is incised and carefully dissected
from the underlying periosteum with a
Mitchell's trimmer.
Precancerous lesions
For the precancerous lesions of leukoplakia
and erythroplakia, the adequate and correct
sampling of lesions may prove more diffi-
cult. It is now well recognised that lesions
showing a non-homogenous or speckled
appearance and lesions of erythroplakia
are potentially more serious with a gener-
ally higher incidence of dysplasia and
malignant transformation.
7
These areas, if
present, should be the site of choice for
biopsy. If the lesion is extensive or there are
numerous erythematous regions it may be
prudent to biopsy more than one area.
Handling of mucosal biopsies
Care should be exercised when handling
mucosal biopsy specimens as they can be
particularly prone to damage. Sometimes
specimens can be rendered of little diag-
nostic value due to poor handling which
produce a crush artefact in histological
section. There are various methods avail-
able to reduce traumatic damage to the
specimens.
A popular method is to place a suture
within the mucosa that is to be removed,
and hold the ends of the suture in an
artery forcep or sometimes tie a loose knot
above the mucosa, while undertaking the
biopsy. A tight knot close to the specimen,
however, is to be avoided as it may result
in the tissue being crushed. The use of
such a suture can aid the biopsy procedure
by providing traction and preventing
unwanted movement of tissue when tak-
ing a biopsy from mobile structures such
as the tongue. It also helps the pathologist
to orientate the biopsy sample for section-
ing. The traditional technique using
toothed tissue forceps to grasp the speci-
men is acceptable providing care is taken
and the area grasped is away from the
main site of interest.
The punch biopsy technique is an alter-
native to the traditional incisional biopsy.
8
Essentially the punch comprises a circular
blade attached to a plastic handle. Diame-
ters of two to ten millimetres are available.
This removes a core of tissue the base of
which can be simply and atraumatically
released using curved scissors. Alternative-
ly, the specimen can be lifted from the
mucosal surface and the base undermined
with a scalpel. Care should be taken if aspi-
ration is being used to prevent the speci-
men being sucked away. The resultant
wound may not require suturing if using
the smaller diameter punches. This tech-
nique is described and reviewed in detail by
Table 1 Points to consider prior to mucosal biopsy
1. Why is biopsy being taken? Eg to confirm a mucosal disease such as lichen
planus or to exclude malignancy.
2. What information is required from the pathologist? Eg is the lesion
completely excised.
3. Is the biopsy to exclude malignancy? Therefore take the biopsy from the edge
of the lesion
4. Is the biopsy incisional or excisional? Eg For excisional biopsies a margin of
surrounding normal tissue will be required.
5. Will the specimen be required to be orientated? This is important for excisional
biopsies so that if residual tumour is left or the excision is close to the
margin, the surgeon knows where to perform a re-excision if necessary.
6. Is a fresh specimen required? For vesiculobullous lesions these are often
required for direct immunofluorescence. They are also used if a rapid diagnosis
is required.
06p329-333.qxd 27/02/2004 10:19 Page 330
PRACTICE
BRITISH DENTAL JOURNAL VOLUME 196 NO. 6 MARCH 27 2004 331
Lynch and Morris.
9
Punch biopsies have
been shown to have fewer artefacts than
conventional incisional biopsies,
10
although
Kerwala
11
argued that careful handling
using a suture during an incisional biopsy
would also produce minimal artefacts.
A case has been reported of surgical
emphysema following an intra-oral punch
biopsy caused by the patient sneezing
shortly after the procedure.
12
The use of
punch biopsies does require the receiving
laboratory to be familiar with the handling
of such specimens. If in doubt, contact the
laboratory prior to performing the biopsy.
Also, it is generally safer to use the larger
diameter punches to avoid handling prob-
lems both clinically and in the laboratory.
This is especially true when material for
both formalin-fixed and frozen processing
is required, such as in the diagnosis of
vesiculobullous disorders.
Generally when performing a mucosal
biopsy an adequate depth of tissue should
be obtained to include the epithelium and a
few millimetres of underlying lamina pro-
pria. Traditional incisional biopsies are in
the shape of an ellipse, the length of which
should be approximately three times the
width.
13
The site of the biopsy may determine
which of the above techniques are possible.
For example, palatal and gingival sites do
not generally allow adequate biopsies
using the punch biopsy technique, and
access to some sites such as the lingual
gingivae may be impossible using this
technique.
Orientation of biopsies
The majority of mucosal biopsies are inci-
sional, however, occasionally small
lesions may be excised encompassing
diagnosis and treatment in one operation.
If malignancy is suspected, the biopsy
should be of sufficient depth and have a
surrounding margin to ensure adequate
clearance. In case the lesion was not com-
pletely excised it should be orientated.
This can be achieved by placing a suture
at one known margin, for example the
anterior or superior margin. This would
enable the pathologist to confidently
indicate the precise location of any resid-
ual tumour. The same applies for surgical
resection specimens.
A technique new to the oral cavity but
established for other bodily sites is that of
the brush biopsy. Essentially a hybrid of
fine needle aspiration biopsy and exfolia-
tive cytology, this technique uses a small
brush to sample cells from all the layers of
the epithelium. Only one large study from
the United States has yet been published
but they claimed a high sensitivity and
specificity using the technique to detect
dysplasia.
14
SOFT TISSUE BIOPSIES
Biopsies of the soft tissues are a less common
procedure. Indications include the diagnosis
of granulomatous conditions such as Crohn's
disease and the diagnosis of salivary lesions.
In the case of the former, an incisional biopsy
of adequate depth is required. Punch biopsies
can sometimes be used but their depth of
penetration is often limited.
When performing labial gland biopsies
in the diagnosis of Sjgren's syndrome, a
minimum of five minor salivary gland lob-
ules should be obtained. The lower lip is the
site of choice and care should be taken to
minimise trauma to adjacent glandular tis-
sue which is not being removed. Addition-
ally, minimal sharp dissection of the area
should be performed to lessen the chance
of sensory nerve damage.
Mucocoeles arise from the blockage and
subsequent rupture of minor salivary gland
ducts. It is important when excising such
lesions to remove the associated minor
salivary glands to help prevent recurrence.
As with labial gland biopsies, care should
be exercised to minimise trauma to adja-
cent tissues. Mucocoeles are extremely
uncommon in the upper lip, so swellings in
this site should be treated as minor salivary
gland tumours, until proved otherwise, and
carefully and completely excised.
For palatal swellings which are suspect-
ed salivary tumours, incisional biopsies
should be as deep as possible and down to
bone if appropriate after due attention to
the position of the palatal vessels and
nerves. This is due to the anatomy of the
region as lesions can be a considerable
depth beneath the mucosa and so a superfi-
cial biopsy may give a false negative result.
Vascular lesions, haemangiomas for
example, should be approached with cau-
tion. Incisional biopsies should never be
performed. Smaller lesions obviously with-
in the soft tissues can safely be excised.
Larger lesions, particularly those affecting
the lip are best ablated with either laser or
cryosurgery. The disadvantage of these
techniques is the lack of material for histo-
logical examination.
For the diagnosis of extra-oral soft tis-
sue swellings the techniques of fine needle
aspiration cytology (FNAC) and fine needle
cutting biopsy (FNCB) are advocated in
certain situations. These techniques are
specialised and the reader is directed
towards other publications for details of
FNAC
15
and FNCB
16
techniques. The for-
mer is often best performed by or under the
guidance of an experienced cytologist.
FIXATION AND TRANSPORT
Ensure the specimen is placed in an ade-
quate volume of fixative, this should be at
least ten times the volume of the specimen.
Avoid the use of gauze to place the speci-
Table 2 Guidelines for an appropriate biopsy
Clinical diagnosis Type of biopsy Suitable for general
dental practice
Chronic ulcer or Incisional biopsy of No, urgent referral
squamous cell carcinoma margin of ulcer to hospital
Leukoplakia/erythroplakia Incisional or punch No, referral to hospital
biopsy of worst area
consider multiple
biopsies if extensive
lesion
Mucosal lichen planus Incisional biopsy of a Only very experienced
representative area practitioners
Bullous lesions Incisional or punch No, referral to hospital
(pemphigus pemphigoid, biopsy of unaffected
etc) mucosa close to bulla or
erosion plus fresh tissue
specimen
Granulomatous diseases Deep incisional biopsy No, referral to hospital
(Crohn's, orofacial plus fresh sample to
granulomatosis, microbiology if infective
ulcerative colitis, TB) agent suspected
Mucocoele Careful excision biopsy Yes, with care
Fibroepithelial polyp, Excision biopsy Yes
pyogenic granuloma,
epulis
Minor salivary gland Palate: deep incisional No, urgent referral
tumour biopsy to hospital
Upper lip: excisional
biopsy
Major salivary gland FNAC/FNCB (Seek No, urgent referral
tumour advice) to hospital
06p329-333.qxd 23/02/2004 10:50 Page 331
PRACTICE
332 BRITISH DENTAL JOURNAL VOLUME 196 NO. 6 MARCH 27 2004
men onto as it merely absorbs the fixative
and can make separation of the specimen
from the gauze difficult. The fixative
should be 10% neutral buffered formalin
which has a pungent and distinct odour.
Occasionally, formalin is further diluted
with water by ancillary staff or specimens
are placed in alternative solutions such as
saline or water which results in poor fixa-
tion and artefactual change. Formalin fixes
specimens by forming intermolecular
bridges between proteins and cross-links
between protein end-groups.
17
If this
process does not occur, soon after removal
from the body the specimen will undergo
autolysis rendering the tissues progressively
undecipherable histologically.
A disadvantage of the protein cross-link-
ing produced by formalin is that the speci-
men is rendered unsuitable for immunofluo-
rescent antibody staining. The diagnosis of
vesiculobullous autoimmune disorders is
aided by direct immunofluorescence of peri-
lesional tissue which requires fresh material
that can be immediately frozen. Most other
immunohistochemical methods used in
diagnosis can now be performed on fixed
tissue with the use of antigen retrieval.
18
The
other main situation where fresh tissue is
processed is when frozen sections are used to
examine surgical margins perioperatively.
Again the specimen should be delivered to
the laboratory fresh in a sterile universal
container or petri-dish. Prior to taking the
specimen at operation, it is both advisable
and courteous to telephone the laboratory to
ensure technical support and a pathologist
are available.
Sometimes it is necessary to send patho-
logical specimens through the post to the
laboratory. Both the tissue and the formalin
in which it is placed are potentially harmful
to those handling the specimen. Precise
details of the regulations governing the
posting of pathological specimens will be
available from the laboratory or the Post
Office. Most of the regulations are common
sense and apply to the packaging of the
specimen. The primary container in which
the specimen is placed with the formalin
should be tightly sealed and wrapped in
sufficient absorbent material to absorb the
fixative if leakage occurs. Paper towels or
cotton wool are suitable for this purpose.
The wrapped container should then be
placed in a sealed plastic bag which should
then be placed in a rigid outer container
which is capable of being secured by adhe-
sive tape. Specific cardboard boxes with
full-depth lids or grooved polystyrene con-
tainers are available for this purpose. A
further outer padded bag is recommended
which should be labelled PATHOLOGICAL
SPECIMEN FRAGILE WITH CARE and
the name and address of the sender should
be clearly displayed. Recent correspon-
dence in this journal has highlighted the
fact that oral pathology services do not get
any part of the fee paid to the GDP for the
biopsy.
19
Occasionally, specimens are required for
electron microscopy, these should ideally
be fixed in glutaraldehyde, but formalin is
an acceptable alternative; again this will
require some pre-arrangement. Specimens
for cytogenetics may be required to con-
firm genetic changes in rare tumours (for
example, synovial sarcoma), these should
be submitted in universal transport medi-
um which has been stored at 4C.
GENERAL POINTS
Local anaesthesia should be administered
deep to or in a field around the proposed
biopsy site. A regional block can also be
used although the haemostatic effect of the
adrenaline within the anaesthetic solution
will be lost. Sampling of tissues at the site
of the local anaesthetic will produce arte-
factual tissue oedema or distortion. For
example bulla formation in gingival tissue
or oedema which may lead to confusion in
the diagnosis of Crohn's disease or orofa-
cial granulomatosis where interstitial oede-
ma is one of the diagnostic features.
The biopsy should be planned before local
anaesthetic is administered. Major vessels
and nerves should be avoided and to min-
imise the risk of damage to smaller struc-
tures, incisions should be made parallel to
their expected position. For example, in the
palate, incisions should run parallel to the
palatal nerves (ie antero-posteriorly) rather
than across the nerves (medio-laterally).
Attention to the surgical technique will
minimise the introduction of artefacts into
the tissues which can hinder pathological
diagnosis or even render the specimen
non-diagnostic. Some such artefacts have
been mentioned above and others are
detailed elsewhere.
20
Fulguration artefact
is an important problem induced during
electrosurgical or laser cutting of tissue.
The resulting effect of a layer of carbonised
tissue, a zone of thermal necrosis and a
zone of tissue exhibiting thermal damage
makes histopathological interpretation
more difficult.
21
As such these methods of
cutting should not be used for diagnostic
incisional biopsies.
Consideration should also be given to
healing of the biopsy site. It has been sug-
gested that punch biopsies can be left
unsutured.
9
Conventional incisional biop-
sies are usually closed. The traditional use
of silk is now being replaced by resorbable
sutures such as polyglactin, formulations
of which exist which resorb more rapidly
(Vicryl Rapide, Ethicon Ltd, Edinburgh).
The supply of catgut (manufactured from
bovine intestine) sutures for human use in
the UK has recently ceased because there
are acceptable synthetic alternatives avail-
able although there is no evidence that
there is any risk to human health.
22
A non-
eugenol-containing periodontal dressing
(Coe-PakTM, GC America Inc.) can be used
for covering gingival biopsy sites. Where
large palatal biopsies are planned, the
securing of a periodontal dressing under-
neath a denture or pre-constructed acrylic
base plate can be helpful.
Label the specimen container with the
patients name, date of birth, date of biop-
sy and the site of the biopsy together with
the hospital number if appropriate. The
site of the biopsy is especially important
if there are specimens from more than
one site in an individual patient. If more
than one specimen has to be placed in the
same container, they must be clearly
marked, which is most readily done by
means of sutures; do not rely on describ-
ing the shapes of the pieces of tissue sub-
mitted because when they are fixed this
will probably have altered. For mucosal
disease it is desirable for the pathologist
to know details of the factors outlined in
Table 3. Accompanying information such
as this will enable a more comprehensive
interpretation of the specimen, in turn,
producing a more meaningful and useful
report to the clinician.
Adequate clinical history supplied on the
request form relevant to the suspected diag-
nosis is essential to enable the pathologist to
provide a useful and meaningful diagnosis.
Additionally, on the request form, it is desir-
able to have previous biopsy numbers to
enable comparison to be made if necessary.
For example, to comment on the progres-
sion or regression of a dysplastic lesion.
It is advised that all patients give
informed written consent to having a
biopsy as it is an unusual procedure for
Table 3 Information to accompany mucosal biopsies
1. Patient demographic data
2. Description of the clinical appearance of the lesion and suspected diagnosis
3. The site of the biopsy
4. The relationship of the lesion to restorations, particularly amalgam
5. A detailed drug history
6. Medical history including blood dyscrasias
7. Smoking and alcohol consumption
06p329-333.qxd 23/02/2004 10:50 Page 332
PRACTICE
BRITISH DENTAL JOURNAL VOLUME 196 NO. 6 MARCH 27 2004 333
patients particularly in general dental
practice (Dental Protection, personal com-
munication). It would be appropriate to
include on the consent form the indication
for the biopsy and details of possible risks
involved with biopsy procedures. These
risks are mostly site related; paraesthesia
can be induced in the lips or the tongue,
swelling and bruising can result from pro-
cedures in the tongue, lips and buccal
mucosa, and procedures in the floor of the
mouth can lead to submandibular or sub-
lingual duct damage. Removal of muco-
coeles from the lip carries the risk of fur-
ther gland damage and recurrence. Kearns
et al.
23
reported a recent study into pain
experience following oral mucosal biop-
sies. They concluded that most patients did
not experience significant pain post-oper-
atively and those that did were controlled
adequately with analgesics; most patients'
pain reduced after 3 days. It is important to
give the standard post-operative oral sur-
gery instructions to the patient.
CONCLUSIONS
When considering biopsy a little forward
planning and thought can greatly
improve the diagnostic value obtained.
Careful handling of the tissue and prompt
appropriate fixation will enable a confi-
dent histological diagnosis to be reached.
Inadequate care at any stage could result
in a non-diagnostic biopsy and may
necessitate the patient having a repeat
procedure with its ensuing physical and
psychological morbidity.
1. Diamanti N, Duxbury A J, Ariyaratnam S, Macfarlane T
V. Attitudes to biopsy procedures in general dental
practice. Br Dent J 2002; 192: 588-592.
2. Lavery K, Blomquist J E, Awty M D, Stevens P J.
Squamous cell carcinoma arising in a dental cyst. Br
Dent J 1987; 162: 259-260.
3. Walton R E. Routine histopathologic examination of
endodontic periradicular surgical specimens-is it
warranted. Oral Surg Oral Med Oral Pathol Oral Radiol
Endod 1998; 86: 505
4. Baughman R A. To biopsy or not. (Letter). Oral Surg
Oral Med Oral Pathol Oral Radiol Endod 1999; 87:
644-645.
5. Bnkfalvi A, Piffko J. Prognostic and predictive factors
in oral cancer: the role of the invasive tumour front.
J Oral Pathol Med 2000; 29: 291-298.
6. Kinsukawa J, Suefuji Y, Ryu F, Noguchi R, Iwamoto O,
Kameyama T. Dissemination of cancer cells into
circulation occurs by incisional biopsy of oral
squamous cell carcinoma. J Oral Pathol Med 2000;
29: 303-307.
7. Speight P M, Morgan P R. The natural history and
pathology of oral cancer and precancer. Comm Dent
Health 1993; 10 (Suppl 1): 31-41.
8. Eisen D. The oral mucosal punch biopsy. Report of 140
cases. Arch Dermatol 1992; 128: 815-817.
9. Lynch D P, Morris L F. The mucosal punch biopsy:
indications and technique. J Am Dent Assoc 1990;
121: 145-149.
10. Moule I, Parsons P A, Irvine G H. Avoiding artefacts in
oral biopsies: the punch biopsy versus the incisional
biopsy. Br J Oral Maxillofac Surg 1995; 33: 244-247.
11. Kerawala C J. Incisional biopsy: reducing artefact. Br J
Oral Maxillofac Surg 1995; 33: 396.
12. Staines K, Felix D H. Surgical emphysema: an unusual
complication of punch biopsy. Oral Diseases 1998; 4:
41-42.
13. Golden D P, Hooley J R. Oral mucosal biopsy
procedures. Excisional and incisional. Dent Clin North
Am1994; 38: 279-300.
14. Sciubba J J. Improving detection of precancerous and
cancerous oral lesions. Computer-assisted analysis of
the oral brush biopsy. J Am Dent Assoc 1999; 130:
1445-1457.
15. Orell S R, Sterrett G F, Waters M N, Whitaker D.
Manual and Atlas of Fine Needle Aspiration Cytology.
Edinburgh and London: Churchill Livingstone, 1986.
16. Southam J C, Bradley P F, Musgrove B T. Fine needle
cutting biopsy of lesions of the head and neck. Br J
Oral Maxillofac Surg 1991; 29: 219-222.
17. Pearse A G E. The chemistry and practice of fixation. In
Pearse A G E (Ed) Histochemistry. Theoretical and
applied. Edinburgh: Churchill Livingstone, 1980:
97-158.
18. Shi S R, Cote R J, Taylor C R. Antigen retrieval
immunohistochemistry: past, present, and future.
J Histochem Cytochem1997; 45: 327-343.
19. Odell E W, Morgan P R. Practitioner biopsy services.
(Letter). Br Dent J 2002; 193: 182.
20. Margarone J E, Natiella J R, Vaughan C D. Artefacts in
oral biopsy specimens. J Oral Maxillofac Surg 1985;
43: 163-172.
21. Krause L S, Cobb C M, Rapley J W, Kilroy W J, Spencer
P. Laser irradiation of bone. I. An in vitro study
concerning the effects of the CO2 laser on oral
mucosa and subadjacent bone. J Periodontol 1997;
68: 872-880.
22. Medical Devices Agency. Catgut sutures-cessation of
supply. 2001. http://www.medical-devices.gov.UK/
catgutsutures.htm
23. Kearns H P O, McCartan B E, Lamey P-J. Patients' pain
experience following oral mucosal biopsy under local
anaesthesia. Br Dent J 2001; 190: 33-35.
ONLINE SUBMISSIONto the British Dental Journal
The British Dental Journal at www.bdj.co.uk is pleased to be able to offer its authors the option
to submit their manuscripts online.
Authors from anywhere in the world can quickly and easily enter their contact details into
an online form, and attach their manuscript files, either as separate text and graphics, or as
an integrated file.
Author files will be automatically converted into a PDF (Portable Document Format) file,
which can be approved by the author on screen prior to submission. Submissions will be
promptly acknowledged by e-mail. Editors and referees will then view the PDF on the
website cutting out the time that manuscripts traditionally spend in the postal system.
Authors who, for whatever reason, are unable to submit online can also benefit from the
timeliness of electronic peer review. Authors are encouraged to submit their manuscripts on
disk, or if necessary hard copy submissions can be converted into PDF files using high-
quality scanners.
Making use of online submission and electronic peer review will enable us to speed up the
review process, providing a better and more efficient service to authors.
For further information about submitting your paper electronically please e-mail:
[email protected]
06p329-333.qxd 27/02/2004 10:20 Page 333