Sabato 27 ottobre 2012 - Pacini Editore
Sabato 27 ottobre 2012 - Pacini Editore
Sabato 27 ottobre 2012 - Pacini Editore
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COmuNiCaziONi ORali<br />
general dental practitioners, who, although experts in their own<br />
field, had no specialist training in oncology nor specific competence<br />
in the sector of Oral Medicine and Pathology. The training<br />
session lasted about 90 minutes and included the use of visual<br />
aids, such as photographs and a video, so as to provide them with<br />
the notions necessary to carry out the sampling correctly. At the<br />
end of the session, each dentist was given a detailed leaflet with<br />
a description of the sampling technique and 5 kits. The kits contained<br />
all the material required to carry out the sampling, which<br />
was to be done on the first five consecutive patients with oral cavity<br />
lesions of the mucosa during their routine practise. Each kit<br />
had: 1 disposable dermatological curette, 7mm in diametre, (Acu-<br />
Dispo Curette®, Acuderm Inc., Ft. Lauderdale, FL, USA); 1 fixing<br />
vial with Thin Prep® (Cytic Corporation, Marlborough, MA,<br />
USA); 1 form with patient details e.g. anagraphic data, medical<br />
anamnesis including the use of alcohol and/or tobacco, the site,<br />
colour dimension and symptomatology of the lesions, the time<br />
of onset, whether or not anaesthesia had been used for sampling<br />
and diagnostic suspicion. The operative protocol recommended<br />
that sampling be carried out only in the presence of lesions of<br />
epithelial origin i.e. patches, papules, plaques, verrucous lesions,<br />
erosions and ulcers.<br />
The dentist was taught to hold the curette tangential to the lesion<br />
surface so as to avoid cutting rather than scraping and to continue<br />
scraping until such times as an adequate amount of tissue fragments<br />
had been obtained, with visible uniform slight bleeding on<br />
the whole surface area of the lesion being sampled. The curette<br />
was then to be placed into the fixing vial and shaken to free<br />
the fragments. As a rule, no local anaesthesia, topical sprays,<br />
or emulsions/creams should be used to avoid lubrication of the<br />
lesion surface, which would reduce scraping efficacy when collecting<br />
fragments, except in particularly symptomatic cases, or on<br />
patient request. The micro-biopsies are then embedded in paraffin,<br />
cut with a microtome, stained with haematoxylin-eosin and<br />
subjected to histological examination by an expert pathologist.<br />
The sample is classified on the basis of the histological evaluation:<br />
ADEQUATE in the presence of a representative strip of<br />
epithelium (at least 100 non-superficial cells), or INADEQUATE<br />
when only horny material is present (anucleated cells).<br />
Results. A total of 50/75 dentists, who took part in the training<br />
session, took part in the study. Between February 2009 and September<br />
2011, 152 micro-biopsies were sent for evaluation, from<br />
sampling carried out on a total of 132 patients, 72 males and 60<br />
females (M:F = 1.2:1) average age 53.6 years (25-88).<br />
There were 140/152 adequate samples (92.1%) and 110/140<br />
(78.5%) had a visible basal membrane (110/140). Whilst 12/152<br />
(7.9%) were inadequate. The data obtained in this study showed<br />
that the number of adequate samples obtained in non-expert<br />
hands were superimposable on those obtained by personnel<br />
expert in the field i.e. 92.1% and 96.3% respectively; p = 0.167.<br />
The inadequate samples showed no statistically significant difference<br />
on the basis of the type of lesion (p = 0.320), or the<br />
lesion site (p = 0.740). The first-level micro-biopsy examination<br />
355<br />
result was confirmed in all cases that were referred for a 2 nd<br />
level diagnostic test (scalpel biopsy). A histological diagnosis of<br />
dysplasia was made in 10/140 micro-biopsy samples (7.1%) and<br />
one carcinoma (0.7%). There were no relevant complications and<br />
anaesthesia was used in 18.4% of cases.<br />
Conclusions/Summary. We demonstrated that the micro-biopsy<br />
technique in expert hands is minimally invasive with a high sensitivity<br />
(97.65%) and high negative predictive value (97.33%)<br />
(Navone et al., 2008). Therefore, we hypothesized its use as a<br />
first level diagnostic test for dentists on the field. The innovative<br />
research reported herein aimed at evaluating the feasibility of<br />
such a hypothesis and demonstrated that a brief training session<br />
sufficed to enable dentists who, although experts in their own<br />
field, had no specific oncological training, to provide adequate<br />
samples for histological examination through an economical,<br />
user-friendly and well accepted first level test. Moreover, to<br />
the best of our knowledge, for the first time, this study obtained<br />
valuable information as to the number and type of oral mucosal<br />
lesions that put the dentist into difficulty when making a differential<br />
diagnosis in everyday practise. The most common lesions<br />
sampled were patches, papules, plaques, rather than erosions/<br />
ulcers, most likely due to the fact that the latter heal quickly once<br />
the source of the problem has been identified and modified e.g.<br />
ill-fitting prosthesis or other factors tied to dental issues. Taken<br />
as a whole, the lesions sampled and referred for histology had<br />
relevant oncological characteristics with 7.8% having a definite<br />
diagnosis of dysplasia or carcinoma, absolutely not to be underestimated.<br />
Indeed, these data have demonstrated for the first time<br />
how important the dentist’s role can be in providing early data on<br />
these types of potentially fatal lesions. Last, but not least, these<br />
data show how the first level micro-biopsy diagnostic test is able<br />
to select a small group of patients to be sent for further evaluation<br />
allowing professionals working in an important health-care sector<br />
to treat their patients with state-of-the-art technology. Moreover,<br />
thanks to the follow-up of all the negative cases, future data will<br />
provide information as to the presence of any false-negative cases<br />
at the 1 st level test. The adoption of this strategy could, hopefully,<br />
make a contribution in reducing the percentage of late diagnosis<br />
in oral mucosal squamous cell carcinoma.<br />
references<br />
Lingen MW, Kalmar JR, Karrison T, et al. Critical evaluation of diagnostic<br />
aids for the detection of oral cancer. Oral Oncol 2008;44:10-22.<br />
Navone R, Pentenero M, Gandolfo S. Liquid-based cytology in oral cavity<br />
squamous cell cancer. Current opinion in otolaryngology & head and<br />
neck surgery 2011;19:77-81.<br />
Navone R, Pentenero M, Rostan I, et al. Oral potentially malignant lesions:<br />
first-level micro-histological diagnosis from tissue fragments<br />
sampled in liquid-based diagnostic cytology. J Oral Pathol Med<br />
2008;37:358-63.<br />
Pentenero M, Carrozzo M, Pagano M, et al. Oral mucosal dysplastic<br />
lesions and early squamous cell carcinomas: underdiagnosis from<br />
incisional biopsy. Oral diseases 2003;9:68-72.<br />
Pentenero M, Navone R, Motta F, et al. Clinical features of microinvasive<br />
stage I oral carcinoma. Oral diseases 2011;17: 298-303.