DISORDERS OF PRIMARY HEMOSTASIS Flashcards

1
Q

occurs when small blood vessels leak blood under the skin

A

PURPURA

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2
Q

measure 4-10mm in diameter

A

PURPURA

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3
Q

purpura spots are less than 4 mm in diameter, they are called

A

PETECHIAE

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4
Q

measures less than 2mm

A

petechiae

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5
Q

Pinpoint non-blanching spots

A

petechiae

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6
Q

small bruise cause by blood leaking from broken blood vessels into the tissues of the skin or mucous membranes

A

Ecchymosis (Raccoon eyes)

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7
Q

excessive bleeding that requires medical or physical intervention

A

Hemorrhage

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8
Q

recurrent, chronic bruising in multiple locations

A

purpura

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9
Q

Disorders of vessels and their supporting tissues.

A

Vascular Disorders

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10
Q

Diagnosis is often based on medical history and is made by ruling out other sources of bleeding disorders.

A

Vascular Disorders

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11
Q

Vascular malformation involves vessels throughout the body, which are dilated and disorganised. It is characterised by the presence of widespread telangiectatic lesions of the skin and mucous membrane

A

Hereditary Hemorrhagic Telangiectasia (Rendu-Osler-Weber Syndrome)

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12
Q

Lesions develop on the tongue, lips,
palate, face, and hands.

A

Hereditary Hemorrhagic Telangiectasia (Rendu-Osler-Weber Syndrome)

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13
Q

Tumor of the vessel

A

Hemangioma-Thrombocytopenia Syndrome (kasabach merrit syndrome)

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14
Q

Bleeding diathesis

A

Petechiae
Purpura

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15
Q

malformations include

A

Giant cavernous hemangioma

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16
Q

Giant cavernous hemangioma

A

tumor in the blood vessel

17
Q

More severe than Eccymosis

A

hematoma

18
Q

caused by a broken blood vessel that was damaged by surgery or an injury.

A

hematoma

19
Q

More severe than Eccymosis

A

hematoma

20
Q

autosomal dominant disorder characterized by hyperdistensible joints and fragile skin

A

ehlers-danlos syndrome/cutis hyperelastica

21
Q

autosomal dominant genetic disorder due to mutation of the gene

A

marfan

22
Q

resulting in abnormalities in connective tissues and risk for bleeding and bruising

A

MARFAN SYDROME

23
Q

autosomal dominant genetic disorder due to mutation of the gene (FBN1) resulting in abnormalities in connective tissues and risk for bleeding and bruising

A

MARFAN SYNDROME

24
Q

An autosomal recessive disorder affecting elastic fiber of connective tissue of skin and arteries

A

Pseudoxanthoma Elasticum / Gröenblad-Strandberg

25
Q

rare autosomal dominant disorder

A

osteogenesis imperfecta

26
Q

known as simple purpura or devil’s pinches result of skin fragility

A

primary purpura

27
Q

seen in older individuals or in individuals undergoing corticosteroid therapy; purpuric lesions occur on the hand and arms.

A

senile purpura