Oral Pathology – NON ODONTOGENIC TUMOURS
Read the complete lesson in an organized slide-by-slide format. This topic contains 23 learning sections from the source presentation.
LESSON CONTENTS — 23 SECTIONS
NON ODONTOGENIC TUMOURS
FIBROMA
An elevated lesion of normal colour with a smooth surface.
It can either be sessile or penduculated.
The size of the tumour varies from small to several cm in diameter.
The lesion is prone to traumatisation and ulceration due to its projection over the surface.
Described as a well defined, slow growing tumour affecting all ages but mostly in the 3rd, 4th and 5th decades.
Common sites for its occurrence include the gingiva, buccal mucosa, tongue,lips and palate.
On palpation, the lesion is either soft and spongy or firm.
OSSIFYING FIBROMA
A benign neoplasm characterized by replacement of normal bone by fibrous tissue of varying amount of newly formed bone or cementum like material.
Common in female
Affect the mandible molar premolar region
Occurs commonly in 3rd to 4th decade of life
It presents as a painless slow growing expansible lesion
Swelling when it grows big causing facial assymetry
Displacement of teeth can be noticed
Radiological features
Well circmscribed radioluscency with varying degree of calcification.
Sclerotic margins
Bowing of the inferior boarder of the mandible
Image
FIBROUS HYPERPLASIA
Benign overgrowth of the fibrous connective tissue.
A result id chronic irritation or trauma
Forms of fibrous hyperplasia
Fibrous epulis
Pregnancy epulis
Peripheral giant cell glanuloma
Pyogenic granuloma
Fibrous epulis
common present as a pedunculated mass, firm of consistency with similar colour od adjacent gingiva.
Most arise between 11- 40 years
Pregnancy epulis
Presents as a soft, deep reddish purple swelling, extensively ulcerated
Bleeding occurs spontenously or due to minor trauma
Arise around first trimester
Regress after delivery
Peripheral giant cell granuloma
Less common
Present as dark red pedunculated commonly ulcerated
Peak incidence in male is 2nd decade whike in female 5th decade of life
Common in mandible than maxilla
Arise anywhere on gingiva or alveolar mucosa
Pyogenic granuloma
Aries on the gingiva, tongue, buccal and labial mucosa
Initiated by trauma or irritation
Hyperplastic granulation tissue
Treatment include excision
Removal of the irritant
May recur but has no malignant potential
ANGIOMAS
An Angioma is a tumour, the cells of which tend to form blood or lymph vessels.
Capillary Hemangiomas are composed of a stroma containing many small capillary blood vessels.
Large cavernous hemangiomas microscopically contain large endothelium-lined vascular spaces engorged with blood.
Hemagiomas and lymphagiomas
Hemangioma
considered to be benign tumours of infancy that are characterized by rapid growth phase with endothelial proliferation followed by gradual involution.
They are not recognized at birth appear within 8 weeks of life
Occur in 5-10% of 1 year old children
Female: male 3:1
Clinical presentation
Common loaction is in the head and neck, which accounts for 60% of all hemangiomas cases.
80% occurs as single lesion the rest 20% of the affected patient will have multiple lesions.
A pale macule with thread like telangiectasias may be noted on the skin.
During the first few weeks of life the tumours will rapid development that occur faster than the infact overall growth.
Deeper tumors may be slightly raised with bluish hue
Superficial tumors of the skin appear raised with bright red color, they are firm rubbery on palpation and blood can not be evacuated by applying pressure.
Deeper tumors may be slightly raised with bluish hue
The prolifeative phase usually last 6-10 month and begins to involute.by 5 years most of hemangioma show complete resolution
Some resolve with no complication but changes like atrophy, scarring,wrinkling or telangectasis
Slide 14
Treatment
Observations as they resolve
Pharmacological therapy eg systemic corticosteroids may reduce the size
Sclerotherapy for smaller lesion
Surgery after sclerotherapy
LYMHAGIOMA
benign harmatomatous tumor of lymphahtic vessel.
Developmental malformation that arise from sequestration of lymphatic tissues that do not communicate noramally with the rest of the lymphatic vessels.
Types of lymphagioma
Lymphangioma simplex / capillary lymphangioma: consist of small, capillary sized vessel
Cavernous lympangioma: composed of larger dilated lypmphatic system
Cystic lymphangioma/ cystic hygroma: exhibit large, macroscopic cystic space
Clinical features.
lymphangioma have a marked predilection for the head and neck which accounts for 50-75% of all cases
About half of lesions are noted at birth and around 90% develop by 2 years of age.
Oral lymphagioma may occur at various site but most frequent anterior two third of the tongue, appear as macroglossia.
Lesions are soft, fluctuant mass.
Slide 19
Treatment
Surgical excision, total removal may not be possible.
There are chances of recurence
Sclerotheray doesn’t respond well but some cases used,
LIPOMA
Lipoma is benign tumor of fat.
Most occur on the trunk and proximal portions of extremities.
Lipoma in the oral and facial regions are less frequent
Lipoma is a benign, slow-growing tumor composed of mature fat cells located beneath the oral mucosa.
Clinical features
Oral lipomas are soft, smooth surfaced nodular masses that can sessile or pedunculated
Tumors are asymptomatic and often noted after many ears or month
Buccal mucosa and vestibule are the most common intraoral site
It is encountered in adults, rare in children
Treatment: surgical excision
The overlying epithelium is so thin over the surface, that superficial b.v are readily visible. The lesion is soft to palpation.
Treatment: surgical excision
Additional Study Notes
This section is separated from the source slides to make the lesson easier to revise.
Supplementary learning: For each oral lesion or condition, revise the definition, common site, causes or associated factors, clinical appearance, important differential features, investigations where relevant, complications and general management principles within the learner’s scope.
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