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Multiple Sclerotic masses of the jaws
T. Saini, BDS, MS, Dip ABOMR,
N.O. Nartey, BDS, MSc, MRC(C)
College of Dentistry, King Saud University, P.O. Box 60169, Riyadh 11545, Saudi Arabia.
Multiple sclerotic masses of the jaws
commonly occur in middle aged black females. A plethora of terminologies to
describe these entities exist, it is speculated that the phenomenon is due to
low grade infection or dysplastic changes of osseous tissue. Familial history
has been noticed in some cases. Radiographically, the masses appear as
multiple, dense, and globular radropacities with a radioiucent rim. This
criterion may be used to distinguish the masses from chronic diffuse sclerosing
osteomyelitis. Secondary infection leading to sequestration is a common
complication.
Multiple sclerotic masses restricted to the alveolar
ridges of the jaws present a diagnostic challenge to the clinician.
Controversies exist concerning the nomenclature of such lesions. It is doubtful
if the masses appear because of separate disease processes, or as a result of
varying manifestations of a singular fibrosseous dysplasia. There are no
definitive histological criteria for recognition of such lesions. The
radiological changes are non-specific. The familial history of occurrence may
be contributory in delineating some of the lesions. This condition does not
exhibit extragnathic skeletal involvement and there is no change in the blood
chemistry of patients with multiple sclerotic masses.
One of the conditions known to produce multiple sclerotic
masses in the jaws is chronic diffuse sclerosing osteomyelitis.1 The sclerotic masses have been attributed to
low grade infection such as chronic periodontitis. Radiographically, the
margins of the sclerotic masses are indistinguishable from the normal adjacent
bone. Waldron et al2 described a condition with a similar appearance
having cemental rather than osseous tissue. They called the lesion "sclerotic
cemental masses of the jaws". Shafer3 mentioned
that both osseous and cemental tissues can be recognized in such a lesion. He
stated that the existing similarity between the two lesions may indicate two
ramifications of a single disease process.
A third condition has been described by Melrose et al.4 They recommended a new descriptive term
"Florid osseous dysplasia" to encompass the exuberant cemento-osseous
dysplastic changes. They noticed a concomitant occurrence of simple bone cysts
in 40% of a series of 34 cases. Shafer3 stated that the so-called florid osseous
dysplasia virtually presents the same clinical, radiographical, and
histological findings as the diffuse sclerosing osteomyelitis.
Gigantiform cementoma is another condition which
demonstrates multiple sclerotic masses in the jaws.5 It is analogous to periapical cemental
dysplasia. This condition is hereditary and a positive family history usually
establishes the diagnosis. Sedano et al6 described a condition termed autosomal
dominant cemental dysplasia which presents multiple cemental masses in the
jaws. The condition was detected in ten members of a single family and
segregated as autosomal dominant. They referred to another condition which
exhibited similar cemental masses and familial tendency. The salient feature of
this condition was generalized osteoporosis of extragnathic bones, which had a
tendency to fracture.
Sclerotic masses in the jaws are usually asymptomatic but
may produce slight expansion of the cortical plate in some cases. Chronic
osteomyelitis leading eventually to sequestration of the masses may occur. Four
cases with sclerotic masses in the jaws, which were diagnosed at King Saud
University College of Dentistry, are reported in this study (Table 1).
Radiographic features and their implication in differential diagnosis are
discussed.
Case 1 :
A 51-year-old Saudi female was referred to the Oral
Diagnosis Clinic for routine dental examination. Clinical examination revealed
gingival recession, supragingival calculus deposition and severe periodontitis.
Panoramic radiographic examination revealed multiple dense
globular radiopacities surrounded by irregular radiolucent rims [Fig. 11. The
opacities were localized to the entire height of the alveolar processes of the
maxilla and the mandible. The bony architecture of the intervening areas were
normal. A retained root of the maxillary left second molar was noted. The
retained root was surrounded by a radiopaque lesion.
Under local anesthesia, the retained root was extracted
and the opaque material was curetted and submitted for histopathological
examination. Radiographically, a tentative diagnosis of multiple
cemento-osseous dysplasia was made.
Laboratory investigations did not indicate any changes in
serum calcium, phosphate or alkaline phosphatase levels from the normal.
Histological examination revealed a mixture of mature and immature trabeculae
with osteoblastic seams. Fibrous tissue surrounding the trabeculae demonstrated
mild chronic inflammatory reaction. The condition was diagnosed as florid
osseous dysplasia.
Case 2:
A 38-year-old black female reported to the Emergency
Clinic with acute pain in the left second mandibular molar area. Clinical
examination revealed gross carious involvement of all the teeth. Moderate to
severe periodontitis was noticed.
Panoramic X-ray examination revealed multiple discrete
radiopacities of about one- centimeter diameter localized to the entire body of
the mandible bilaterally [Fig. 2a]. Each opacity was surrounded by a thin
radiolucent rim, The lamina dura circumscribing the teeth was intact and there
was no evidence of root resorption. No bony expansion was noticed. Extragnathic
radiographic examination was negative. A tentative clinical diagnosis of
multiple cemento-osseous dysplasia was made.
Under local anesthesia, the first and second right
mandibular molars were extracted and healing was uneventful. One year
radiographic follow up did not show any change in the dimension or texture of
the opacities [Fig. 2b].
Case 3 :
A 40-year-old black female patient presented to the Oral
Diagnosis Clinic for routine dental check up. The clinical examination revealed
moderate periodontitis and badly decayed maxillary incisors.
Panoramic X-ray examination showed multiple, dense
radiopaque masses, each about a centimeter in diameter, distributed bilaterally
in the molar areas of the mandible [Fig. 3a]. The masses had a lucent margin
and a definite corticated rim. The right second mandibular molar was extracted
because of severe mobility. The socket was curetted and submitted for
histopathological examination. No bony expansion of the jaws was noticed.
Radiographic examination of the skull was negative.
Microscopic examination of the curetted socket tissue
showed small aggregates of fibrous tissue stroma with interspersed irregular
bony trabeculae. Osteoid tissue was seen along the borders of some trabeculae.
Viable osteocytes were seen. A diagnosis of fibrosseous lesion was made. One
year follow up did not show any changes in the radiopaque masses [Fig. 3b].
There was normal filling of the extraction socket with fine bony trabeculae
[Fig. 3b].
Case 4 ;
A 47-year-old black female presented to the Emergency
Clinic with a diffuse swelling localized to the edentulous right alveolar ridge
in the maxillary molar area. The clinical examination revealed slight buccal
and palatal expansion of the cortical plates in the right maxilla. The patient
depicted severe periodontitis.
Panoramic X-ray examination showed multiple dense and
discrete radiopacities of five-millimeter diameter in the maxillary molar area
[Fig. 4a]. The radiopacities were surrounded by irregular, ill-defined,
radiolucent areas. The surrounding bone showed massive condensing osteitis
resembling the so-called ground glass appearance. The panoramic radiograph also
demonstrated solitary osteosclerotic lesion in the left mandibular first molar
area. A radiolucent area with central opacity was noted in the right mandibular
first molar area. Extragnathic radiographic examination proved negative.
Laboratory investigation indicated nothing of
significance. Under antibiotic
cover and local anesthesia, the radiopaque lesions in
the maxillary molar area were curetted. Histological examination revealed bony
sequestra surrounded by granulation tissue.
It was diagnosed as a fibrosseous lesion with secondary infection.
Healing was uneventful [Fig. 4b].
A number of terminologies to describe multiple sclerotic
masses of jaws are used. It seems that these terms connote a single disease
process. The more descriptive term, multiple cemento-osseous masses of jaws,
encompasses all such lesions. A consensus about the origin of these masses does
not exist. Blashke7 reported that the
cemento-osse-ous masses form as a result of a reactive response from the cells
in, or near, the periodontal ligament spaces. All cases in this study showed
moderate to severe periodontitis with many grossly carious teeth. The role of
low grade infection to stimulate an osteoblastic response may be suspected. The
incidence of periodontitis is usually very high in middle-aged patients, and it
may be a concomitant affliction rather than indicating a cause and effect
relationship. Radiographically, the reactive sclerosis of the bone in chronic
diffuse sclerosing osteomyelitis does not exhibit a radiolucent rim or globular
texture as seen in these masses. Waldron et al2 considered multiple cemento-osseous masses to
be an exuberant form of periapical cemental dysplasia. They stated that the
masses may represent part of the spectrum of benign fibrosseous lesions of
periodontal ligament origin. The clinical, radiographical, and histological
appearances of the masses closely resemble those of periapical cemental
dysplasia. The masses are analogous to cemental dysplasia in its predilection
for middle-aged black females as was also noticed in the present study. Lucas8 suspected the masses to be hamartomous in
nature. The incidence of masses found in the older patients negates this
hypothesis. According to Puniamoorthy,9 sclerotic masses of the jaws as a disease may
be an exaggerated form
of hypercementosis resulting from continued growth of cemental remnants left
behind after the removal of associated teeth. He added that the familial nature
of this condition, such as gigan-tiform cementoma, has not been proven.
Familial occurrence in the present series could not be established.
Radiographically, the lesions can be divided into two
groups based upon the appearance of the margin of the opacities. Conditions
like chronic diffuse sclerosing oseteomyelitis do not demonstrate radiolucent
rims. The adjacent bone may show gradual transition from dense opacity to a
ground glass appearance transitioning into normal bone. The entity described,
as multiple cemental masses, show similar border. On the other hand, the
lesions, like gigantiform cementoma and florid osseous dysplasia, are
characterized by discrete globular dense radiopaque masses surrounded by a thin
radiolucent rim of regular width. The surrounding bone shows normal
architecture. In the absence of infection, the radiographic appearance does not
show any change even after a period of one year as seen in three of the cases
present in this study.
Multiple radiopaque masses described as cotton wool
appearance may occur in Paget's disease. Although Paget's disease of bone is
more commonly seen in older patients, it is characterized by extragnathic
involvement and specific changes in blood chemistry. The masses in Paget's
disease do not have a radiolucent rim and the involved bones show expansion. On
rare occasions, multiple radiopacities can also result in jaws from metastatic
breast or prostate carcinoma.
Cemento-osseous masses are usually asymptomatic unless
complicated by supervening infection. Secondary osteomyelitis with
sequestration is known to occur in these patients. Treatment of carious teeth
and prevention of periodontal disease will prevent the infection from gaining
entrance into the area.
In the authors' opinion, the term cemento-osseous masses
should be restricted to the conditions of the jaws which appear
radiographically as multiple globular radiopacities delineated from the normal
bone by a regular radiolucent margin. The term chronic diffuse sclerosing
osteomyelitis should be used to refer to generalized condensing osteitis of the
jaws where the margins of the lesions merge imperceptibly with the surrounding
normal bone.
- Bell WH. Sclerosing osteomyelitis of tnte mandible and maxilla.
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Shafer WG, Hine MK, Levy BM. A textbook of oral pathology. 4th ed.
Philadelphia:WB
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Melrose RJ, Abrams AM, Mills BG. Florid osseous dysplasia. Oral
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Agazzi C, Belloni L. Gil odontomi duri dei mascellari, Arch Hoi
Otol LXIV (Suppl XVI) 1953;64:5.
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Sedano HO, Kuba R, Gorlin RJ. Autosomal dominant cemental
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Goaz PW, White SC. Oral radiology. In Blashke DD ed. Diseases of
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Mosby Co, 1982:529.
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Lucas RB. Pathology of tumors of the oral tissues. 4th ed,
Edinburgh:Churchill Livingstone, 1984:104.
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