Vascular Lesions Flashcards

(41 cards)

1
Q

Congenital vascular lesions

A

Lymphangioma and hemangioma

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2
Q

Neoplasm vascular lesion

A

Angiosarcoma and kaposi sarcoma

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3
Q

Benign vascular lesion composed of a localized collection of dilated lymphatic channels

A

Lymphangioma

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4
Q

Presents as painless, nodular, vesicle like swellings when superficial or as submucosal masses when located deeper

Diagnosed within the first two decades of life

A

Lymphangioma

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5
Q

Location of intraoral lymphangioma

And extraoral lymphangioma

A

Tongue most common
Palate, buccal mucosa gingiva and lips

Skin and subcutaneous tissues

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6
Q

Lymphangioma of the lip may cause a ____

A

Macrocheilia (permanent swelling of the lip)

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7
Q

A diffuse soft tissue swelling that may be life threatening because it involves vital structures of the neck

A

Lymphangioma of the neck

Aka

Cystic hygroma, hygroma colli or cavernoius lymphangioma

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8
Q

Histopathological feature

Variably sized, irregular, this walled fluid - filled spaces are lined by lymphatic epithelium ad surrounded by a stroma of fibrous, smooth muscle and adipose tissue along with lymphocytes

A

Lymphangioma

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9
Q

Histopathological feature of lymphagioma

A

Variably sized, irregular, this walled fluid - filled spaces are lined by lymphatic epithelium ad surrounded by a stroma of fibrous, smooth muscle and adipose tissue along with lymphocytes

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10
Q

IHC profile of lymphangioma

A

D2-40 (podoplanin, transmembrane mucoprotein)

CD31, SMA on walls of lymphatic vessels

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11
Q

Treatment for lymphangiooma

A

Surgical excision

Recurrence are common die to its non-encapsulated nature

Pwede pd sclerotherapy

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12
Q

Etiology of kaposi sarcoma

A

Human herpersivrus 8

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13
Q

The lesion consists of an unencapsulated proliferation of anaplastic endothelial cells enclosing irregular luminal spaces

A

Angiosarcoma

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14
Q

Benign vasular lesion/ tumor

Abnormal endothelial cell proliferation

A

Hemangioma

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15
Q

Subtype of hemangioma:

Proliferation of capillaries with plump endothelial cells in a fibromyxoid stroma, arranged in lobules

A

Lobullar capillary hemangioma

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16
Q

Subtype of hemangioma

Multiple, large cystic, thin-walled, blood filled spaces lined by endothelial cells and separated by scant connective tissue stroma

A

Cavernous hemangioma

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17
Q

Essential diagnostic criteria

Polypoid, lobular circumscribed nastomosing network of capillaries

Plump endothelial cells

Fibroymxoid stroma arranged in one or more lobules

18
Q

Treatment for hemangioma

A

Excision

45% recurrence, more common in children if not completely eradicated

M,ay regress spontaneously

19
Q

Two vascular malformationt that was introduced in the topi

A

Struge weber syndrome (encephalotrigeminal angiomatosis)

And

Rendu-osler weber syndrome (hereditary hemorrhagic telangiectasia)

20
Q

Malignant neoplasm that represents the morphological and iHC features of endothelial cells and unknown origin

21
Q

Usual location or amgiosarcomas

A

Scalp

Occasionally in maxillary sinus and oral cavity

22
Q

Unencapsulated prliferation of anaplastic endothelial cells enclosing irregular luminal spaces

Has an aggressive clinical course and a poor prognosis

23
Q

Non specific, general signs and symptoms of enlarging tumor

Invasion of vital structures and bone erosion

5th decade = male

39mm

24
Q

Less than 15mm in size __

More than 39mm in size

A

<15 mm hemagioma

39mm > angiosarcoma

25
Histologic features Anastomosing vascular space line by atypical endothelial cells; infiltrative growth; endothelial multilayering; marked nuclear atypia; brisk mitotic activity
Angiosarcoma
26
IHC for angiosarcoma
ERG transcription factor - most commonly used CD34, CD31
27
40% reoccur 60% overall srvival rate Metastasis spread most commonly to the lungs, liver, spleen and bone
Angiosarcoma
28
Also of endothelial origin but known to be caused by the human herpesvirus 8 (HHV8)
Kaposi sarcoma
29
Locally agressive vascular endothelial proliferation assciated with HHV-8 Immunocompromised, AIDS related
Kaposi sarcoma
30
Multiple reddish to purple macules that progress into plaques or nodules, which may ulcerate
Kaposi sarcoma
31
Etiologic agent for kaposi sarcome
Herpesvirus Aids
32
Kaposi sarcoma that is predominntly in older men living in the mediterranean basin
Classic type kaposi sarcoma
33
Kaposi sarcoma that apears multifocal reddish brown nodules primarily in the skin of the lower extremities , organ may also be affected Indolent course and only a fair prognosis
Classic type kaposi sarcoma
34
Was identified in africa, where it is considered endemic Seen in extremities of blacks Most commonly affected organ is the skin
Endemic type of kaposi sarcoma
35
Kaposi sarcoma seen in patients with immunodeficiency status, includes with organ transplants and commonly associated with AIDS
Immunodeficiency type of kaposi sarcoma
36
Hypercellular foci containing bland-appearing spindle cells, ill-defined vascular channels and extravasated RBC
Kaposi sarcoma
37
IHC for kaposi sarcoma
CD31, CD34 and factor VIII-related antigen will identify endothelial cell derived tumors
38
DD of kaposi
Hemangioma Erythroplakia Melanoma Pyogenic granuloma
39
Treatment of kaposi
Highly active antiretroviral therapy (HAART)
40
Small, slit like vascular spaces with extravasated RBC Mildly atypical cell with surrounding bland spindle cells Lymphocytic infiltrate is present Unencapsulated infiltrating fascicles of spondle cells with atypia and mitoses
Kaposi sarcoma
41
Extraoral; unilateral epixstasis Oral: solitary, red hemorrhagic papule
Hemangioma