CLIPP 21: 6 y/o male with bruising Flashcards

1
Q

List 4 general causes of petechiae/purpura

A

Trauma
Platelet deficiency or dysfunction (e.g. immune-mediated thrombocytopenia, bone marrow infiltration or suppression, malignancy)
Coagulation abnormalities (e.g. hereditary or acquired clotting-factor deficiencies)
Vascular fragility (e.g., immune-mediated vasculitis)
-or-
Combinations of the above

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2
Q

List long differential for bruising (petechiae/ purpura) and leg pain

A
Coagulation disorders
HSP
ITP
Leukemia
Viral infection
Bacterial endocarditis
Meningococcal septicemia
RMSF
SLE
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3
Q

What is HSP?

A

HSP is a self-limited, IgA-mediated, small vessel vasculitis that typically involves the skin, GI tract, joints, and kidneys.

Often presents in an otherwise well appearing child with bruising and leg pain (due to arthritis).

In roughly 50% of cases, a URI precedes the diagnosis of HSP.

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4
Q

Can viruses cause a petechial rash?

A

Yes, particularly enteroviruses

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5
Q

Describe the rash pattern in RMSF

A

The rash of RMSF is often petechial, and starts on the extremities before moving centrally.

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6
Q

Lymph nodes > what size are concerning for disease?

A

> 2cm

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7
Q

Palpable lymph nodes where are concerning for lymphoma?

A

Supraclavicular

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8
Q

What is lymphadenitis?

A

Infection of the lymph node itself

Characterized by Tenderness, warmth, fluctuance, overlying erythema or edema suggest local infection or infection of the node itself

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9
Q

Major general causes of hepatomegaly (5)?

A

Hepatomegaly may occur as a result of inflammation (e.g., viral hepatitis), infiltration (e.g., leukemia/lymphoma), accumulation of storage products (e.g., glycogen-storage disease), congestion (e.g., congestive heart failure) or obstruction (e.g., biliary atresia).

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10
Q

Most frequent cause of splenomegaly in children?

A

Epstein-Barr virus
Cytomegalovirus
Bacterial sepsis
Endocarditis

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11
Q

Two systemic inflammatory diseases that can cause splenomegaly?

A

LSE

Juvenile idiopathic arthritis

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12
Q

Common cause of hemolysis and splenomegaly?

A

Sickle cell disease

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13
Q

Hallmark of HSP?

A

Non-thrombocytopenic purpura

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14
Q

Signs and symptoms of HSP?

A

1/3 present with renal involvement –> hematuria
Arthritis/arthralgias (mostly knees and ankles) in 75%
Colicky abdominal pain; 50% may develop GI bleeds with guiac positive stool
2/3rds with URI

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15
Q

Treatment for HSP?

A

Controversial role of corticosteroids

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16
Q

HSP with low platelet count?

A

ITP

17
Q

What causes ITP?

A

ITP is caused by the binding of an antiplatelet antibody to the platelet surface, leading to removal and destruction of platelets in the spleen and liver. It is the most common cause of isolated thrombocytopenia in otherwise healthy children.

18
Q

Classic presentation of intussiception

A

Paroxysms of severe abdominal pain with inconsolable crying
Passage of “currant jelly” stool containing blood and mucus
Palpation of a “sausage-shaped” mass in the right abdomen

19
Q

Classic diagnosis and treatment of intussusception?

A

Air or barium enema

20
Q

Recurrence rate of HSP?

A

30%

21
Q

Incidence of ALL peaks at what age?

A

4 years old