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Vascular Anomalies
Dr. Shahzad Hussain
BDS, FCPS (Resident)
Nishtar Institute Of Dentistry, Multan
SNDENTALCARE.Co
Outline
 What are Vascular Anomalies?
 Hemangioma
 Rendu Osler Weber Disease
 Sturge Weber syndrome
 Lymphangioma
 Cystic Hygroma
Basic Cell biology
• On basis of cell kinetics, there are two
major types of vascular anomalies:
• Hemangiomas: lesions demonstrating
endothelial hyperplasia.
• Vascular Malformations : lesions with
normal endothelial turnover.
Classification
Hemangioma
• The word "hemangioma" comes from the
Greek haema-, "blood"; angeio , "vessel"; -
oma , "tumor".
• A hemangioma is a benign and usually self-involuting
tumor of the endothelial cells that line blood vessels,
and is characterised by increased number of normal
or abnormal vessels filled with blood.
• May be present at Birth or arise during early childhood.
Hemangioma
• Mostly within Skin
• May be relatively large, covering large skin,
Which are termed as birthmarks.
• Mostly invoulate by the time of puberty.
• Those hemangiomas that do not invoulate are
called hemartomas.
How we Classify Hemangioma?
Capillary Hemangioma
• occur in superficial layer of skin.
• most common type of hemangioma.
• made up of small capillaries that are
normal in size and diameter, but high in
number.
• Because of their proximity to the surface
of the skin, capillary hemangiomas are
typically brighter red in color.
Cavernous Hemangioma
• In contrast with a capillary hemangioma,
a cavernous hemangioma is made up of
larger blood vessels that are dilated.
• The blood vessels are not as closely
packed as in a capillary hemangioma
• the spaces (or "caverns") between them
are filled with blood
Intra Muscular Hemangioma
• Arise any where in the soft tissue of head &
neck
• Spongy Texture on palpation
• Usually deep seated
• Seen on the tongue and lips
Clinical Features Of Hemangioma
• Usually raised
• Often Multinoduler
• No sex prediction
• Blenching on compression
• May Arise in any site but most commonly arise
in tongue
Anteriovenous Malformation
• Occur in head & neck
• Central Mandibular
• 1: more in female Childs
• 2: painless, slow expansion
• 3:bruit on auscultation
• 4:spontanious hemorrhage on aspiration or prick.
• 5: small Multilocular radiolucency termed as worm
hole
• 6: Rarely subjected to biopsy due to excessive
bleeding.
• Diagnosed with imaging studies such as Doppler
angiography or time-lapse angiography.
Port wine Stain
• Unique type of hemangioma
• Usually unilateral
• Follow One, two or All division of trigeminal
nerve.
• Purplish, Diffuse, Maccular and sharply
demarcated from the adjacent skin.
True Hemangioma
• Benign vascular tumor
• Under capillary or venous pressure
• Identical to ordinary hemangioma of Soft
tissues
• May Expand the bone
• Multilocular appearance
• No detectable Bruit
Histopathology
• Hemangioma are characterized by
Multiple small capillary channel (
Capillary Hemangioma) or Large tortuous
dilated (cavernous hemangioma)
vascular spaces packed with
erythrocytes.
Micro-photograph of the capillary hemangioma, showing
multiple vessels with RBCs occluding the lumen and
inflammatory cells uniformly distributed
Capillary Hemangioma
(Histopathology)
• Closely packed endothelial lined channels
typify the capillary Hemangioma.
• Fibrous Stroma not present.
• Well formed capillaries present throughout
but there may be a foci of prolifirating
endothelial cells that does not make a lumen.
• DD: Pyogenic granuloma
Cavernous Hemangioma
(Histopathology)
• Large, irregular shaped, dilated endothelial
lined channels of variable size that are
separated by mature fibrous stroma and
contain large aggregates of erythrocytes.
• Lack a muscular coat as a rule!!
• Central hemangiomas are of cavernous
type.
Histopathology
Treatment
• Left untreated in childhood
• Cosmetic reasons may require surgical
removal.
• Sclerosing agents
•Multilocular
Radiolucency that
yield blood upon
aspiration ?? DD?
• 1: Central Hemangioma
• 2:Anurysmal bone Cyst
• 3:Central AV malformation
• Treatment of choice is induced embolization
admisntered through feeder vessels.
• Bilateral vascular supply may further complicate
the treatment plan.
• Tooth extraction may cause death due to
excessive bleeding
HEREDITARY HEMORRHAGIC
TELANGIECTASIA
(Rendu Osler Weber disease)
• Autosomal dominant trait
• Thought to be due to mutations in
Transferring Growth Factor (TGF)-beta
signaling
Clinical features
Telangiectasia
Epistaxis
GI bleeding
Basic Mechanism
post-capillary venules get enlarge and
connect to enlarging arterioles, thus
forming direct arteriolar-venular
connections
Sturge-Weber syndrome
(encephalotrigeminal angiomatosis)
• Syndrome characterized by
• 1:Intracranial Hemangioma(Parralle
Radiopaque Lines termed as TRAMLINE
CALCIFICATIONS)
• 2: Epilepsy
• 3: Port wine Stain
LYMPHANGIOMA
• Lymphangiomas are benign tumours of lymphatic
vessels
• shows as a focal superficial lesion in the oral
cavity and as a massive diffuse lesion of the neck
(cystic Hygroma)
Features
• Arise during childhood
• No sex prediction
• Two major types in the head & neck region
• 1: Self limiting in the oral cavity
• 2: Cystic hygroma in the lateral neck in
Clinical Features
• Oral mucosal in the tongues of child
• May invoulate or persist at puberty
• Racemose appearing grape like cluster which
is yellowish and soft.
• Lips are second most common site.
Treatment of lymphangioma
• Various methods have been reported for the
treatment of Lymphangiomas.
Procedures such as
• 1)Surgical excision
• 2)Radiation therapy,
• 3)Cryotherapy,
Histopathology
• Stratifi ed squamous epithelium of tongue beneath
which dilated lymphatic vessels filled with lymph are
seen along with chronic inflamatory cells
CYSTIC HYGROMA
• known as cystic lymphangioma
• macrocystic lymphatic malformation
• congenital multiloculated lymphatic lesion
• can arise anywhere
• classically found in the left posterior triangle
of the neck and armpits. This is the most
common form of lymphangioma.
Cystic Hygroma
Vascular anomalies
Vascular anomalies

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Vascular anomalies

  • 1. Vascular Anomalies Dr. Shahzad Hussain BDS, FCPS (Resident) Nishtar Institute Of Dentistry, Multan SNDENTALCARE.Co
  • 2. Outline  What are Vascular Anomalies?  Hemangioma  Rendu Osler Weber Disease  Sturge Weber syndrome  Lymphangioma  Cystic Hygroma
  • 3. Basic Cell biology • On basis of cell kinetics, there are two major types of vascular anomalies: • Hemangiomas: lesions demonstrating endothelial hyperplasia. • Vascular Malformations : lesions with normal endothelial turnover.
  • 5. Hemangioma • The word "hemangioma" comes from the Greek haema-, "blood"; angeio , "vessel"; - oma , "tumor". • A hemangioma is a benign and usually self-involuting tumor of the endothelial cells that line blood vessels, and is characterised by increased number of normal or abnormal vessels filled with blood. • May be present at Birth or arise during early childhood.
  • 6. Hemangioma • Mostly within Skin • May be relatively large, covering large skin, Which are termed as birthmarks. • Mostly invoulate by the time of puberty. • Those hemangiomas that do not invoulate are called hemartomas.
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  • 8. How we Classify Hemangioma?
  • 9. Capillary Hemangioma • occur in superficial layer of skin. • most common type of hemangioma. • made up of small capillaries that are normal in size and diameter, but high in number. • Because of their proximity to the surface of the skin, capillary hemangiomas are typically brighter red in color.
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  • 12. Cavernous Hemangioma • In contrast with a capillary hemangioma, a cavernous hemangioma is made up of larger blood vessels that are dilated. • The blood vessels are not as closely packed as in a capillary hemangioma • the spaces (or "caverns") between them are filled with blood
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  • 14. Intra Muscular Hemangioma • Arise any where in the soft tissue of head & neck • Spongy Texture on palpation • Usually deep seated • Seen on the tongue and lips
  • 15. Clinical Features Of Hemangioma • Usually raised • Often Multinoduler • No sex prediction • Blenching on compression • May Arise in any site but most commonly arise in tongue
  • 16. Anteriovenous Malformation • Occur in head & neck • Central Mandibular • 1: more in female Childs • 2: painless, slow expansion • 3:bruit on auscultation • 4:spontanious hemorrhage on aspiration or prick. • 5: small Multilocular radiolucency termed as worm hole • 6: Rarely subjected to biopsy due to excessive bleeding. • Diagnosed with imaging studies such as Doppler angiography or time-lapse angiography.
  • 17. Port wine Stain • Unique type of hemangioma • Usually unilateral • Follow One, two or All division of trigeminal nerve. • Purplish, Diffuse, Maccular and sharply demarcated from the adjacent skin.
  • 18. True Hemangioma • Benign vascular tumor • Under capillary or venous pressure • Identical to ordinary hemangioma of Soft tissues • May Expand the bone • Multilocular appearance • No detectable Bruit
  • 19. Histopathology • Hemangioma are characterized by Multiple small capillary channel ( Capillary Hemangioma) or Large tortuous dilated (cavernous hemangioma) vascular spaces packed with erythrocytes.
  • 20. Micro-photograph of the capillary hemangioma, showing multiple vessels with RBCs occluding the lumen and inflammatory cells uniformly distributed
  • 21. Capillary Hemangioma (Histopathology) • Closely packed endothelial lined channels typify the capillary Hemangioma. • Fibrous Stroma not present. • Well formed capillaries present throughout but there may be a foci of prolifirating endothelial cells that does not make a lumen. • DD: Pyogenic granuloma
  • 22. Cavernous Hemangioma (Histopathology) • Large, irregular shaped, dilated endothelial lined channels of variable size that are separated by mature fibrous stroma and contain large aggregates of erythrocytes. • Lack a muscular coat as a rule!! • Central hemangiomas are of cavernous type.
  • 24. Treatment • Left untreated in childhood • Cosmetic reasons may require surgical removal. • Sclerosing agents
  • 26. • 1: Central Hemangioma • 2:Anurysmal bone Cyst • 3:Central AV malformation • Treatment of choice is induced embolization admisntered through feeder vessels. • Bilateral vascular supply may further complicate the treatment plan. • Tooth extraction may cause death due to excessive bleeding
  • 27. HEREDITARY HEMORRHAGIC TELANGIECTASIA (Rendu Osler Weber disease) • Autosomal dominant trait • Thought to be due to mutations in Transferring Growth Factor (TGF)-beta signaling
  • 32. Basic Mechanism post-capillary venules get enlarge and connect to enlarging arterioles, thus forming direct arteriolar-venular connections
  • 33. Sturge-Weber syndrome (encephalotrigeminal angiomatosis) • Syndrome characterized by • 1:Intracranial Hemangioma(Parralle Radiopaque Lines termed as TRAMLINE CALCIFICATIONS) • 2: Epilepsy • 3: Port wine Stain
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  • 36. LYMPHANGIOMA • Lymphangiomas are benign tumours of lymphatic vessels • shows as a focal superficial lesion in the oral cavity and as a massive diffuse lesion of the neck (cystic Hygroma)
  • 37. Features • Arise during childhood • No sex prediction • Two major types in the head & neck region • 1: Self limiting in the oral cavity • 2: Cystic hygroma in the lateral neck in
  • 38. Clinical Features • Oral mucosal in the tongues of child • May invoulate or persist at puberty • Racemose appearing grape like cluster which is yellowish and soft. • Lips are second most common site.
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  • 41. Treatment of lymphangioma • Various methods have been reported for the treatment of Lymphangiomas. Procedures such as • 1)Surgical excision • 2)Radiation therapy, • 3)Cryotherapy,
  • 42. Histopathology • Stratifi ed squamous epithelium of tongue beneath which dilated lymphatic vessels filled with lymph are seen along with chronic inflamatory cells
  • 43. CYSTIC HYGROMA • known as cystic lymphangioma • macrocystic lymphatic malformation • congenital multiloculated lymphatic lesion • can arise anywhere • classically found in the left posterior triangle of the neck and armpits. This is the most common form of lymphangioma.