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Benign connective tissue tumors 4/certified fixed orthodontic courses by Indian dental academy
1. INDIAN DENTAL ACADEMYINDIAN DENTAL ACADEMY
Leader in continuing DentalLeader in continuing Dental
EducationEducation
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2. At the end of the lecture students should be able to
Describe clinical features , histopathological features
and treatment of –
1. Myxoma
2. Neurofibroma
3. Neurilemoma
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3. Abundant myxoid ground substance
(mucopolysaccharides, mainly hyaluronic acid)
True neoplasm made of tissue resembling primitive
mesenchyme
Benign lesion, does not metastasize
Frequently infiltrates adjacent tissues
Intraoral soft tissue myxoma- extremely rare
Cases occurring in jaw bones- commonly are
odontogenic myxomas
Myxoma
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4. Histopathlogical Features-
Loose-textured tissue with delicate reticulin fibers
Mucoid material probably hyaluronic acid
Varying nos. of stellate cells & occasional spindle
cells interspersed throughout
No encapsulation
May invade into surrounding tissue
Myxoma
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7. Benign tumor of nerve tissue origin
derived from cells that form nerve sheath
Seen either
◦ As a solitary lesion- similar except absence of
hereditary factors, unknown etiology
◦ As a part of Neurofibromatosis- Autosomal
Dominant trait
Neurofibroma
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8. Clinical Features-
Hereditary disease, Autosomal dominant trait,
No gender predilection, cosmetic problems,
Risk of malignant transformation
Discrete, non-ulcerated nodules or Diffuse masses of
tissue
Buccal mucosa, palate, alveolar ridge, tongue
Macroglossia due to diffuse involvement of tongue
Occasionally located centrally within jaw bones
Neurofibroma
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10. Histopathological Features-
May or may not be well circumscribed
Interlacing bundles of spindle-shaped cells often with
wavy nuclei
Cells are associated with delicate collagen bundles
variable amounts of myxoid matrix
Numerous mast cells
In plexiform neurofibroma- distorted masses of
myxomatous peripheral nerve tissue still within
perineural sheath
Neurofibroma
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12. Treatment-
Solitary neurofibroma- surgical excision
For neurofibromas associated with
Neurofibromatosis- surgical removal only for
functional or cosmetic purpose
Neurofibroma
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13. Benign neural neoplasm of Schwann cell origin
Neurites are not a component of tumor as in
neurofibroma
Clinical Features-
Occurs at any age, no gender predilection
Slow growing lesion, arises in association with a
nerve trunk
Usually painless unless causes pressure on adjacent
nerve
Few mm to several cm in size
Neurilemoma
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14. Oral Manifestations-
Tongue- most common site for oral neurilemomas
Can occur anywhere in mouth
Single circumscribed nodule of varying size
Can occur centrally within jaw bones
◦ commonly in mandible- arising from mandibular
nerve
◦ May cause destruction of bone with cortical plate
expansion
Neurilemoma
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16. Histopathological Features-
Usually encapsulated
2 microscopic patterns in varying amounts
Antoni type A
◦ Streaming fascicles of spindle-shaped Schwann
cells
◦ Cells often form a palisaded arrangement around
central acellular,
◦ eosinophilic areas called verocay bodies
◦ Verocay bodies consist of reduplicated basement
membrane & cytoplasmic processes
Neurilemoma
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18. Antoni type B-
◦ Less cellular & less organized
◦ Spindle cells arranged randomly within a loose
myxomatous stroma
No neurites, but degenerative changes can be seen
Treatment & Prognosis-
Surgical excision
Recurrence uncommon
No malignant transformation
Neurilemoma
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19. Clinical features , histopathological features and
treatment of –
Myxoma
Neurofibroma
Neurilemoma
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