Ameloblastoma of The Jaw and Maxillary Bone: Clinical Study and Report of Our Experience
Ameloblastoma of The Jaw and Maxillary Bone: Clinical Study and Report of Our Experience
Ameloblastoma of The Jaw and Maxillary Bone: Clinical Study and Report of Our Experience
Ameloblastoma of the jaw and maxillary bone: clinical study and report of our experience
Di Cosola M, Turco M, Bizzoca G, Tavoulari K, Capodiferro S, Escudero-Castao N, Lo Muzio L. Ameloblastoma of the jaw and maxillary bone: clinical study and report of our experience. Av. Odontoestomatol 2007; 23
(6): 367-373.
INTRODUCTION
The ameloblastoma is a relatively rare dental tumor,
described for the first time by Broca in 1868, and so
denominated by Churchill in 1934.
According to Larsonn and Almeren (1), its
incidence is 0,6 cases per million, while Shear and
Singh (2) found an incidence of 0.31 cases per
million in a white population of Witwatersrand in
South Africa. Between 1975 and the beginning of
the 80, the concept that the ameloblastoma exists
in three different clinical/histopatological forms was
accepted (3-4): solid-multicystical, unicystical and
peripheral.
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Fig. 1.
Site distribution
9 cases were located in the jaw and 1 in the upper
maxilla. The ratio between the upper maxilla and jaw
was 9:1. In 7 cases the ameloblastoma was located
in the posterior third of the maxillary bones,
including the area of the molar teeth and the
structures distal to them. In 3 cases the tumor was
found in the anterior and /or middle part of the
368 /AVANCES EN ODONTOESTOMATOLOGA
Fig. 2.
Fig. 3.
Fig. 4.
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dical surgery also includes marginal resection, segmental or total resection of the mandible with wide
margins.
The analysis of the first group (6 patients) showed 3
cases of recurrences. The average time between the
treatment and the recurrences was 3,5 years (range
4 months-10 years).
2 of the 3 recurrences were treated again with
conservative therapy.
In one case the treatment of the recurrence consisted
in the resection of the jaw without continuity of the
inferior edge and a bone autograft, which has not
recurred.
In the second group of solid ameloblastomas the 2
patients were treated with radical surgery.
In this group the only case of recurrence was observed
after 5 years, in spite of the resection of the jaw with
solution of continuity of the inferior edge the
recurrence was diagnosed and treated with a surgical
extension of the borders.
The third group with unicystic ameloblastomas, is
composed of 2 patients with an initial conservative
treatment.
The unicystic ameloblastomas recurred in average
after 3.5 years.
There was one recurrence in this group. It was
possible to reconstruct the following therapeutic
history: first treated with conservative therapy,
recurred for the second time and a jaw resection with
solution of continuity of the inferior edge was
necessary but successful.
Clinical and histological factors of risk for
recurrence
The first group (cases 1-6) had 3 recurrences out of
a total of 6 with dimensions greater than 2 cm at the
moment hospitalisation and 1 recurrences had
dimensions inferior than 2 cm at the time of
hospitalisation. In the second group (cases 7-8), 1
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We believe that for the diagnostic phase the instrumental examinations (X-RAY, CT or MRT) are
essential; while intralesional byopsies are inefficient
because they don t offer a whole vision of the tumor
and could lead to diagnostic error. Therefore we think
that it is advisable, considering: the site and extention,
of the lesion, age and general conditions of the
patient, to remove the lesion in a conservative manner
in a first surgical step and according to the histolgical
aspect evaluate a possible radical resection.
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