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October 11, 2005

Oral Pathology II
0701441
Connective Tissue Lesions
Connective Tissue Lesions
 Fibrous lesions:
 Reactive hyperplasia: Fibrous hyperplasia or exuberant
proliferation of granulation tissue
Peripheral fibroma
Generalized gingival hyperplasia
Denture induced fibrous hyperplasia
 Neoplasms: heterogeneous that form complex collection of
disease
Myxoma
Fibrosarcoma
Connective Tissue Lesions
“Fibrous Lesions”
 Peripheral fibroma
 Etiology: Reactive (secondary to overexuberant repair)
 Origin: Connective tissue of the submucosa
 Clinical features:
Predilection for young adults
Female>male
Location: commonly at the gingiva anterior to molars
Similar in color to the surrounding tissue
Connective Tissue Lesions
“Fibrous Lesions”

Peripheral Odontogenic fibroma
Connective Tissue Lesions
“Fibrous Lesions”
 Focal fibrous hyperplasia:
 It is common in frequently
traumatized area
Connective Tissue Lesions
“Fibrous Lesions”
 Peripheral fibroma
 Histopathology:
Focal fibrous hyperplasia: Highly collagenous and relatively
avascular
Mild to moderate inflammatory cell infiltrate
Subtypes:
Peripheral ossifying fibroma
Peripheral odontogenic fibroma
Giant cell fibroma
 Differential diagnosis: Pyogenic granuloma & peripheral giant
cell granuloma
 Treatment: Local excision
Connective Tissue Lesions
“Fibrous Lesions”
 Peripheral Ossifying Fibroma
Connective Tissue Lesions
“Fibrous Lesions”
 Generalized gingival hyperplasia:
 Definition: Overgrowth of the gingiva
 Etiology:
Non-specific: Response to chronic inflammation
associated with local factor
Hormonal changes (imbalance)
Drugs (Phenytoin, Cyclosporine, Nifidipine)
Leukemia
Connective Tissue Lesions
“Fibrous Lesions”
 Generalized gingival hyperplasia:
 Clinical features: Increase in the bulk of free and attached gingiva.
 Stippling is lost
 Color: red to blue
 Associated inflammation: non-specific factors & hormonal imbalance
appears more inflamed than drug induced hyperplasia

 Histopathology:
 Abundance in collagen
 Increased number of fibroblasts
 Various degree of chronic inflammation
 Increased capillaries (hormonal)
 Immature & atypical white blood cells with leukemic type
Connective Tissue Lesions
“Fibrous Lesions”
Gingival fibromatosis
Connective Tissue Lesions
“Fibrous Lesions”
 Generalized gingival hyperplasia:
 Treatment: Attentive oral hygiene is necessary
 Gingivoplasty or gingivectomy in combination with prophylaxis
Connective Tissue Lesions
“Fibrous Lesions”
 Denture-induced fibrous hyperplasia
 Etiology: Chronic trauma produced by an ill-fitting denture
 Clinical features: Occurs in the vestibular mucosa
Overexuberant fibrous connective tissue reparative
response
Painless folds of fibrous tissue
 Treatment: Surgical excision is usually required
Epulis Fissuratum
Connective Tissue Lesions
“Fibrous Lesions”
 Neoplasms:
 Myxoma: Benign proliferation of spindle cells
 Clinical features: It is a soft neoplasms composed of
gelatinous material
Slow growing
Asymptomatic
Location: Palate
Occurs at any age

Soap bubble multilocular area
Connective Tissue Lesions
“Fibrous Lesions”
 Myxoma:
 Histopathology:
 Not encapsulated (may exhibit
infiltration into surrounding soft tissue)
 Dispersed stellate & spindle-shaped fibroblasts
 Loose myxoid stroma
Connective Tissue Lesions
“Fibrous Lesions”
 Myxoma:
 Treatment: Surgical excision
 Recurrence is not uncommon
Pluripotential Mesenchymal Stem Cells
Connective Tissue Lesions
“Fibrous Lesions”
 Fibrosarcoma: It is a malignant spindle
cell tumor showing interlacing fascicular
pattern
 Clinical features
Can arise in bone
Young adults most commonly affected
It is considered as infiltrative neoplasms
Connective Tissue Lesions
“Fibrous Lesions”
 Fibrosarcoma:
 Histopathology:
Collagen sparse
Frequent mitotic figures
Ill defined periphery
Connective Tissue Lesions
“Fibrous Lesions”
Treatment of Fibrosarcoma


Wide surgical excision
 Recurrence is not uncommon
 Metastasis is infrequent
 5 years survival rate is 3050%
Vascular Lesion
 Reactive & Congenital Lesions
 Lymphangioma
 Etiology:
 It is regarded as congenital lesion
 Appears within the first 2 decades of life
 Clinical features:
 Painless nodular, vesicle like swelling
 Crepitant sound
 Tongue is the most common
intraoral site
Vascular Lesion
 Histopathology:
 Endothelium-lined lymphatic channels
 Eosinophilic lymph that occasionally
include red blood cells
 Lymphatic channels directly adjacent
to overlying epithelium

 Treatment: Surgical removal but because
of lack of encapsulation, recurrences are
common
Vascular lesion
 Neoplasms:
 Angiosarcoma
 It is a neoplasm of endothelial cell origin
 Scalp is the usual location
 The lesion consists of an unencapsulated
proliferation of endothelial cells enclosing
irregular luminal spaces
 It has an aggressive clinical course and
poor prognosis
Neural lesions
 Reactive lesion:
 Traumatic neuroma:
 Etiology: It is caused by injury of peripheral nerve
 Oral surgery procedure
 Local anesthetic injection
 Accident
 Clinical features:
 Pain
 Wide age range
 Mental foramen is the most common location
Neural lesion
 Traumatic neuroma (Cont.)
 Histopathology:
 Bundles of nerves admixed
with dense collagenous fibrous
tissue
 Treatment: Surgical excision
Neural Lesion
 Neoplasms:
 Granular cell tumors
 Etiology: It is an uncommon benign tumor of unknown cause
 The granular cell that make this tumor is believed to originate
from Schwann cells
 Clinical features:
 Wide age range
 Tongue is the most common location
 Uninflamed asymptomatic mass
 < 2 cm in diameter
 Overlying epithelium is intact
Neural lesion
 Neoplasms:
 Granular cell tumors
 Histopathologically:
 Unencapsulated sheets of
 large polygonal cells with pale
granular or grainy cytoplasm
 Pseudoepitheliomatous hyperplasia

 Treatment: Surgical removal
Neural lesion
 Neoplasms:
 Schwannoma:
 Etiology: It is derived from schwann cells
 Clinical features:
 It is an encapsulated submucosal mass
 Asymptomatic lump
 Occurs at any age
 Tongue is the most common location
 Bony lesion produce a well-defined
radiolucent lesion
 Slow growing but may undergoe
a sudden increase (hemorrhage)
Neural lesion
 Neoplasms:
 Schwannoma:
 Histopathology:
 Spindle cells either organized
(palisaded waves) or
haphazardly distributed
 Treatment: Surgical excision
Neural lesion
 Neoplasms:
 Neurofibroma:
 It mat appear as solitary or multiple lesions
 Etiology: - Solitary type is unknown
- Neurofibromatosis is inherited
 Clinical features: Solitary type
 Uniflamed asymptomatic submucosal mass
 Location: Tongue, vestibule & buccal mucosa
Neural lesion
Neurofibroma
Neural lesion
 Neurofibroma:
 Clinical features: Neurofibromatosis:
 Multiple
 Café-au-lait macules
 Bone abnormalities (cortical erosion
or medullary resorption)
 Central nervous system changes
 Pain or parasthesia may be seen
 Malignant degeneration into
neurogenic sarcoma is seen in
5% to 15%
Neurofibromatosis

(JADA, 1988)
Neural lesion
 Neurofibroma:
 Histopathology:
 Spindle-shaped cells in connective
tissue matrix
 It may be well circumscribed or blended
into surrounding connective tissue
 Mast cells are scattered
 Immunohistochemistry with S-100 is a
useful tool to confirm diagnosis
 Treatment: Surgical excision for solitary lesion

Lack of encapsulation
Neural lesion
 Malignant peripheral nerve sheet tumor
 The cell of origin is believed to be the schwann cells and
possibly other nerve sheath cells
 It appears as expansile mass (soft tissue)
 Asymptomatic
 Dilation of the mandibular canal (bone)
 Pain or parasthesia
Neural lesion
 Malignant peripheral nerve sheet tumor
 Histopathologically:
 Abundant spindle cells
 Mitotic figures
 Nuclear pleomorphism
 Treatment: Wide surgical exicion
 Recurrence is common
 Metastases are frequently seen
Muscle Lesions
 Neoplasms (Leiomyoma & leiomyosarcoma):
 Smooth muscle neoplasms are relatively common
 They may arise anywhere in the body

 Leiomyoma
 Leiomyomas are commonly arise in the
muscularis of the gut and uterus
 Oral leiomyoma is slow growing &
asymptomatic submucosal masses
 Appears in the tongue, hard palate
or buccal mucosa
Spindle cells
 Appears at any age

Pterygo-mandibular space
Muscle Lesions
 Leiomyoma
 Histopathology:
 Immunohistochemical demonstration of actin and
desmin protein expression can confirm diagnosis

Obvious vascular origin

Vascular leiomyoma

Limited & uniform proliferation
around each of the vascular spaces
Muscle Lesions
 Neoplasms
 Leiomyosarcoma
 It is commonly arise in the retroperitoneum,
mesentery, or subcutaneous and deep tissue
of the limbs
 It may appear at any age
 Immunohistocemistry can be a valuable
diagnostic tool
 Treatment: wide surgical excision
 Metastasis is not uncommon

Blunt ended nuclei
Muscle Lesions
 Rhabdomyoma:
 Predilection for the soft tissues
of the head and neck
Floor of the mouth, soft palate,
tongue & buccal mucosa
 Mean age: 50 years (children to older adults)
 Asymptomatic
 Well defined submucosal mass Well demarcated but
unencapsulated
 The neoplastic cells mimic their
normal counterpart (adult)
Large eosinophilic granular cell
with peripheral nuclei
Muscle Lesions
 Rhabdomyosarcoma:
 When occurs in head and neck is
primarily found in children
 It is a rapidly growing mass
 May cause pain and parasthesia
 Common location: Tongue and soft palate
Muscle Lesions
Rhabdomyosarcoma
 Histopathology:
 Embryonal type (children) consists
of primitive round cells in which
striations are rarely found
 Immunohistochemistry demonstrates
desmin, actin and myogenin
Muscle Lesions
Rhabdomyosarcoma
 Treatment: Combination of surgery,
radiation and chemotherapy
 Survival rate incraese from 10% to 70%

with this aggressive treatment approach
Fat Lesion
 Lipoma:
 Location: Buccal mucosa, tongue
& floor of the mouth
 Asymptomatic, yellowish submucosal mass
 Overlying epithelium is intact
 Superficial blood vessels are usually evident
Fat Lesion
 Lipoma:
 Well circumscribed, lobulated mass
of mature fat cells
Fat Lesion
 Lipomyosarcoma:






It is a lesion of adulthood
It may occur at any site
Slow growing (mistaken for a benign process)
Treatment: surgery or radiation
Prognosis is fair to good

Well differentiated

Myxoid type
Mumps




It is an acute viral sialadenitis affecting primarily the parotid
glands
Etiology & pathogenesis:



Paramyxovirus, incubation period is 2-3 weeks
Transmission is by direct contact with salivary droplets

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Connective tissue lesions

  • 1. October 11, 2005 Oral Pathology II 0701441 Connective Tissue Lesions
  • 2. Connective Tissue Lesions  Fibrous lesions:  Reactive hyperplasia: Fibrous hyperplasia or exuberant proliferation of granulation tissue Peripheral fibroma Generalized gingival hyperplasia Denture induced fibrous hyperplasia  Neoplasms: heterogeneous that form complex collection of disease Myxoma Fibrosarcoma
  • 3. Connective Tissue Lesions “Fibrous Lesions”  Peripheral fibroma  Etiology: Reactive (secondary to overexuberant repair)  Origin: Connective tissue of the submucosa  Clinical features: Predilection for young adults Female>male Location: commonly at the gingiva anterior to molars Similar in color to the surrounding tissue
  • 4. Connective Tissue Lesions “Fibrous Lesions” Peripheral Odontogenic fibroma
  • 5. Connective Tissue Lesions “Fibrous Lesions”  Focal fibrous hyperplasia:  It is common in frequently traumatized area
  • 6. Connective Tissue Lesions “Fibrous Lesions”  Peripheral fibroma  Histopathology: Focal fibrous hyperplasia: Highly collagenous and relatively avascular Mild to moderate inflammatory cell infiltrate Subtypes: Peripheral ossifying fibroma Peripheral odontogenic fibroma Giant cell fibroma  Differential diagnosis: Pyogenic granuloma & peripheral giant cell granuloma  Treatment: Local excision
  • 7. Connective Tissue Lesions “Fibrous Lesions”  Peripheral Ossifying Fibroma
  • 8. Connective Tissue Lesions “Fibrous Lesions”  Generalized gingival hyperplasia:  Definition: Overgrowth of the gingiva  Etiology: Non-specific: Response to chronic inflammation associated with local factor Hormonal changes (imbalance) Drugs (Phenytoin, Cyclosporine, Nifidipine) Leukemia
  • 9. Connective Tissue Lesions “Fibrous Lesions”  Generalized gingival hyperplasia:  Clinical features: Increase in the bulk of free and attached gingiva.  Stippling is lost  Color: red to blue  Associated inflammation: non-specific factors & hormonal imbalance appears more inflamed than drug induced hyperplasia  Histopathology:  Abundance in collagen  Increased number of fibroblasts  Various degree of chronic inflammation  Increased capillaries (hormonal)  Immature & atypical white blood cells with leukemic type
  • 10. Connective Tissue Lesions “Fibrous Lesions” Gingival fibromatosis
  • 11. Connective Tissue Lesions “Fibrous Lesions”  Generalized gingival hyperplasia:  Treatment: Attentive oral hygiene is necessary  Gingivoplasty or gingivectomy in combination with prophylaxis
  • 12. Connective Tissue Lesions “Fibrous Lesions”  Denture-induced fibrous hyperplasia  Etiology: Chronic trauma produced by an ill-fitting denture  Clinical features: Occurs in the vestibular mucosa Overexuberant fibrous connective tissue reparative response Painless folds of fibrous tissue  Treatment: Surgical excision is usually required
  • 14. Connective Tissue Lesions “Fibrous Lesions”  Neoplasms:  Myxoma: Benign proliferation of spindle cells  Clinical features: It is a soft neoplasms composed of gelatinous material Slow growing Asymptomatic Location: Palate Occurs at any age Soap bubble multilocular area
  • 15. Connective Tissue Lesions “Fibrous Lesions”  Myxoma:  Histopathology:  Not encapsulated (may exhibit infiltration into surrounding soft tissue)  Dispersed stellate & spindle-shaped fibroblasts  Loose myxoid stroma
  • 16. Connective Tissue Lesions “Fibrous Lesions”  Myxoma:  Treatment: Surgical excision  Recurrence is not uncommon
  • 18. Connective Tissue Lesions “Fibrous Lesions”  Fibrosarcoma: It is a malignant spindle cell tumor showing interlacing fascicular pattern  Clinical features Can arise in bone Young adults most commonly affected It is considered as infiltrative neoplasms
  • 19. Connective Tissue Lesions “Fibrous Lesions”  Fibrosarcoma:  Histopathology: Collagen sparse Frequent mitotic figures Ill defined periphery
  • 20. Connective Tissue Lesions “Fibrous Lesions” Treatment of Fibrosarcoma  Wide surgical excision  Recurrence is not uncommon  Metastasis is infrequent  5 years survival rate is 3050%
  • 21. Vascular Lesion  Reactive & Congenital Lesions  Lymphangioma  Etiology:  It is regarded as congenital lesion  Appears within the first 2 decades of life  Clinical features:  Painless nodular, vesicle like swelling  Crepitant sound  Tongue is the most common intraoral site
  • 22. Vascular Lesion  Histopathology:  Endothelium-lined lymphatic channels  Eosinophilic lymph that occasionally include red blood cells  Lymphatic channels directly adjacent to overlying epithelium  Treatment: Surgical removal but because of lack of encapsulation, recurrences are common
  • 23. Vascular lesion  Neoplasms:  Angiosarcoma  It is a neoplasm of endothelial cell origin  Scalp is the usual location  The lesion consists of an unencapsulated proliferation of endothelial cells enclosing irregular luminal spaces  It has an aggressive clinical course and poor prognosis
  • 24. Neural lesions  Reactive lesion:  Traumatic neuroma:  Etiology: It is caused by injury of peripheral nerve  Oral surgery procedure  Local anesthetic injection  Accident  Clinical features:  Pain  Wide age range  Mental foramen is the most common location
  • 25. Neural lesion  Traumatic neuroma (Cont.)  Histopathology:  Bundles of nerves admixed with dense collagenous fibrous tissue  Treatment: Surgical excision
  • 26. Neural Lesion  Neoplasms:  Granular cell tumors  Etiology: It is an uncommon benign tumor of unknown cause  The granular cell that make this tumor is believed to originate from Schwann cells  Clinical features:  Wide age range  Tongue is the most common location  Uninflamed asymptomatic mass  < 2 cm in diameter  Overlying epithelium is intact
  • 27. Neural lesion  Neoplasms:  Granular cell tumors  Histopathologically:  Unencapsulated sheets of  large polygonal cells with pale granular or grainy cytoplasm  Pseudoepitheliomatous hyperplasia  Treatment: Surgical removal
  • 28. Neural lesion  Neoplasms:  Schwannoma:  Etiology: It is derived from schwann cells  Clinical features:  It is an encapsulated submucosal mass  Asymptomatic lump  Occurs at any age  Tongue is the most common location  Bony lesion produce a well-defined radiolucent lesion  Slow growing but may undergoe a sudden increase (hemorrhage)
  • 29. Neural lesion  Neoplasms:  Schwannoma:  Histopathology:  Spindle cells either organized (palisaded waves) or haphazardly distributed  Treatment: Surgical excision
  • 30. Neural lesion  Neoplasms:  Neurofibroma:  It mat appear as solitary or multiple lesions  Etiology: - Solitary type is unknown - Neurofibromatosis is inherited  Clinical features: Solitary type  Uniflamed asymptomatic submucosal mass  Location: Tongue, vestibule & buccal mucosa
  • 32. Neural lesion  Neurofibroma:  Clinical features: Neurofibromatosis:  Multiple  Café-au-lait macules  Bone abnormalities (cortical erosion or medullary resorption)  Central nervous system changes  Pain or parasthesia may be seen  Malignant degeneration into neurogenic sarcoma is seen in 5% to 15%
  • 34. Neural lesion  Neurofibroma:  Histopathology:  Spindle-shaped cells in connective tissue matrix  It may be well circumscribed or blended into surrounding connective tissue  Mast cells are scattered  Immunohistochemistry with S-100 is a useful tool to confirm diagnosis  Treatment: Surgical excision for solitary lesion Lack of encapsulation
  • 35. Neural lesion  Malignant peripheral nerve sheet tumor  The cell of origin is believed to be the schwann cells and possibly other nerve sheath cells  It appears as expansile mass (soft tissue)  Asymptomatic  Dilation of the mandibular canal (bone)  Pain or parasthesia
  • 36. Neural lesion  Malignant peripheral nerve sheet tumor  Histopathologically:  Abundant spindle cells  Mitotic figures  Nuclear pleomorphism  Treatment: Wide surgical exicion  Recurrence is common  Metastases are frequently seen
  • 37. Muscle Lesions  Neoplasms (Leiomyoma & leiomyosarcoma):  Smooth muscle neoplasms are relatively common  They may arise anywhere in the body  Leiomyoma  Leiomyomas are commonly arise in the muscularis of the gut and uterus  Oral leiomyoma is slow growing & asymptomatic submucosal masses  Appears in the tongue, hard palate or buccal mucosa Spindle cells  Appears at any age Pterygo-mandibular space
  • 38. Muscle Lesions  Leiomyoma  Histopathology:  Immunohistochemical demonstration of actin and desmin protein expression can confirm diagnosis Obvious vascular origin Vascular leiomyoma Limited & uniform proliferation around each of the vascular spaces
  • 39. Muscle Lesions  Neoplasms  Leiomyosarcoma  It is commonly arise in the retroperitoneum, mesentery, or subcutaneous and deep tissue of the limbs  It may appear at any age  Immunohistocemistry can be a valuable diagnostic tool  Treatment: wide surgical excision  Metastasis is not uncommon Blunt ended nuclei
  • 40. Muscle Lesions  Rhabdomyoma:  Predilection for the soft tissues of the head and neck Floor of the mouth, soft palate, tongue & buccal mucosa  Mean age: 50 years (children to older adults)  Asymptomatic  Well defined submucosal mass Well demarcated but unencapsulated  The neoplastic cells mimic their normal counterpart (adult) Large eosinophilic granular cell with peripheral nuclei
  • 41. Muscle Lesions  Rhabdomyosarcoma:  When occurs in head and neck is primarily found in children  It is a rapidly growing mass  May cause pain and parasthesia  Common location: Tongue and soft palate
  • 42. Muscle Lesions Rhabdomyosarcoma  Histopathology:  Embryonal type (children) consists of primitive round cells in which striations are rarely found  Immunohistochemistry demonstrates desmin, actin and myogenin
  • 43. Muscle Lesions Rhabdomyosarcoma  Treatment: Combination of surgery, radiation and chemotherapy  Survival rate incraese from 10% to 70% with this aggressive treatment approach
  • 44. Fat Lesion  Lipoma:  Location: Buccal mucosa, tongue & floor of the mouth  Asymptomatic, yellowish submucosal mass  Overlying epithelium is intact  Superficial blood vessels are usually evident
  • 45. Fat Lesion  Lipoma:  Well circumscribed, lobulated mass of mature fat cells
  • 46. Fat Lesion  Lipomyosarcoma:      It is a lesion of adulthood It may occur at any site Slow growing (mistaken for a benign process) Treatment: surgery or radiation Prognosis is fair to good Well differentiated Myxoid type
  • 47. Mumps   It is an acute viral sialadenitis affecting primarily the parotid glands Etiology & pathogenesis:   Paramyxovirus, incubation period is 2-3 weeks Transmission is by direct contact with salivary droplets