Stevens-Johnson syndrome laboratory findings

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

Overview

SJS is mainly diagnosed through the clinical skin findings. However, a skin biopsy is helpful in making the definitive diagnosis. Other tests are done to either rule out the superimposed bacterial infection, measure disease severity or detect the causative agent or organism. Tests include CBC, BMP, Blood cultures, ESR, CRP, IL-6, ELISA for virus detection among others.

Laboratory Findings

Skin Biopsy is the only study that can make the definitive diagnosis of SJS. Other Lab tests are done to detect superimposed bacterial infection or in cases of severe or extensive skin involvement that is more commonly seen in TEN as compared to SJS.

The first Step after suspicion of SJS is identifying and discontinuing the offending agent.

Following tests are done[1][2]:

  • Skin Biopsy (Urgent Frozen section): Lesional Biopsy and Perilesional Biopsy
  • Direct immunofloresence: Negative
  • Complete Blood Count:
    • Anemia and Lymphopenia are seen frequently[4]
    • Abnormal blood counts can be seen in case of superimposed bacterial infections
  • Metabolic Panel: Electrolyte disturbances, glucose, BUN, Cr, total protein, albumin (reduced), ALT, AST (increased) - abnormalities seen in cases of extensive disease with dehydration, bacteremia, Hypovolemic shock and Multiorgan failure
  • Bacterial and fungal cultures - taken from blood, mucosal surfaces
  • CRP, ESR, TNF-alpha, IL-6: Levels are typically elevated
  • Bronchoscopy: May be needed to detect mucosal lesions
  • HSV-IgM
  • Mycoplasma IgM
  • ELISA-to detect other causative viruses (HAV, HBV, HCV, HIV, EBV, Rubella)

References

  1. Wetter DA, Camilleri MJ (2010). "Clinical, etiologic, and histopathologic features of Stevens-Johnson syndrome during an 8-year period at Mayo Clinic". Mayo Clin Proc. 85 (2): 131–8. doi:10.4065/mcp.2009.0379. PMC 2813820. PMID 20118388.
  2. Çekiç Ş, Canıtez Y, Sapan N (2016). "Evaluation of the patients diagnosed with Stevens Johnson syndrome and toxic epidermal necrolysis: a single center experience". Turk Pediatri Ars. 51 (3): 152–158. doi:10.5152/TurkPediatriArs.2016.3836. PMC 5047364. PMID 27738400.
  3. French LE (2006). "Toxic epidermal necrolysis and Stevens Johnson syndrome: our current understanding". Allergol Int. 55 (1): 9–16. doi:10.2332/allergolint.55.9. PMID 17075281.
  4. Roujeau JC, Chosidow O, Saiag P, Guillaume JC (1990). "Toxic epidermal necrolysis (Lyell syndrome)". J Am Acad Dermatol. 23 (6 Pt 1): 1039–58. PMID 2273103.

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