OnlineMedEd: Rheumatology - "Other Connective Tissue" Flashcards

1
Q

Scleroderma results from _____________.

A

collagen deposition (everything gets stiffer)

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2
Q

Review CREST syndrome (limited cutaneous systemic scleroderma –LCSS).

A
  • Calcinosis (HTN?)
  • Raynaud’s
  • Esophageal dysmotility (unrelenting GERD)
  • Sclerodactyly (tense fingers)
  • Telangiectasia (GI bleed, IDA)
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3
Q

What are the diffuse manifestations of scleroderma (diffuse cutaneous systemic scleroderma –DCSS)?

A
  • Intrinsic lung disease
  • Constrictive pericarditis
  • Sclerodermal renal crisis
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4
Q

How can you treat CREST?

A

There are no DMARDs, but you can manage symptoms:
• Sclerodactyly –penicillamine
•Esophageal dysmotility –PPIs, Nissen
•Raynaud’s –CCBs

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5
Q

True or false: steroids can be used in sclerodermal crises.

A

False

Steroids can precipitate a renal crisis in scleroderma.

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6
Q

How do you treat sclerodermal renal crises?

A

ACE inhibitors

It is unusual to give an ACEi in the setting of a rising creatinine, but this works.

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7
Q

What antibody is seen in diffuse scleroderma?

A

Anti-scl70 (aka anti-topoisomerase)

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8
Q

Sjögren’s is caused by _________________.

A

lymphoplasmocytic destruction of the exocrine glands

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9
Q

Review the signs and symptoms of Sjögren’s.

A
  • Keratoconjunctivitis sicca (dry eyes)
  • Xerostomia (dry mouth)
  • Parotid swelling
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10
Q

Describe the diagnosis of Sjögren’s.

A

1st: ANA, RF positive
2nd: Ro, La antibodies
3rd: Schirmer test positive

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11
Q

What is the usual cause of death in Sjögren’s?

A

Trick question: nothing

Those with Sjögren’s are generally only symptomatically managed and do not have complications.

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12
Q

There are three autoimmune myositis disorders: ______________.

A

dermatomyositis, polymyositis, and inclusion-body myositis

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13
Q

How do you diagnose inflammatory myopathies?

A
  • CK
  • EMG
  • Biopsy
  • Anti-Jo and anti-Jo antibodies
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