Polymyositis and dermatomyositis laboratory findings: Difference between revisions

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* Severe dermatomyositis rash without significant lung involvement 
* Severe dermatomyositis rash without significant lung involvement 
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|Anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMGCR)
|Anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMGCR)
|immune-mediated necrotizing myopathies
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* Statin-associated necrotizing autoimmune myopathy (SANAM)
* Statin-associated necrotizing autoimmune myopathy (SANAM)

Revision as of 16:04, 5 April 2018

Polymyositis and dermatomyositis Microchapters

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Sadaf Sharfaei M.D.[2]

Overview

An elevated/reduced concentration of serum/blood/urinary/CSF/other [lab test] is diagnostic of [disease name].

OR

Laboratory findings consistent with the diagnosis of [disease name] include [abnormal test 1], [abnormal test 2], and [abnormal test 3].

OR

[Test] is usually normal for patients with [disease name].

OR

Some patients with [disease name] may have elevated/reduced concentration of [test], which is usually suggestive of [progression/complication].

OR

There are no diagnostic laboratory findings associated with [disease name].

Laboratory Findings

  • Laboratory findings consistent with the diagnosis of polymyositis and dermatomyositis include:[1]

Myositis-specific autoantibodies

Autoantibody Effect Association Percentage
Histidyl-tRNA synthetase (anti-Jo-1)
  • Myositis
  • Interstitial lung disease
  • Mechanic’s hands
  • Arthritis
  • Antisynthetase syndrome
  • Flare up in spring
  • Epstein-Barr virus (EBV), adenovirus, and influenza infection
Chromodomain helicase DNA binding protein 4 (Mi-2)
  • Severe dermatomyositis rash without significant lung involvement 
  • Severe dermatomyositis rash without significant lung involvement 
Signal recognition particle (anti-SRP)
  • Flare up in fall
Alanyl-tRNA synthetase (PL-12)
  • Epstein-Barr virus (EBV), adenovirus, and influenza infection
Transcriptional intermediary factor 1-gamma (TIF-1γ)
  • Cancer-associated myositis
  • Juvenile dermatomyositis
Nuclear matrix protein (NXP-2)
  • Cancer-associated myositis
  • Juvenile dermatomyositis
Anti-small ubiquitin-like modifier activating enzyme (anti-SAE)
  • Cancer-associated myositis
Anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMGCR)
  • Statin-associated necrotizing autoimmune myopathy (SANAM)
6%

References

  1. Adler BL, Christopher-Stine L (February 2018). "Triggers of inflammatory myopathy: insights into pathogenesis". Discov Med. 25 (136): 75–83. PMID 29579414.