Munchausen by proxy syndrome mimicking systemic autoinflammatory disease: case report and review of the literature

Pediatr Rheumatol Online J. 2017 Apr 5;15(1):19. doi: 10.1186/s12969-017-0152-6.

Abstract

Background: Systemic autoinflammatory diseases (SAIDs) represent a growing number of monogenic, polygenic or multifactorial disorders that are often difficult to diagnose.

Case presentation: Here we report a patient who was initially erroneously diagnosed and treated for SAID. Symptoms consisted of recurrent fever, erythematous and/or blistering skin lesions, angioedema, susceptibility to bleeding, external ear infections and reversible anisocoria in the absence of laboratory evidence of systemic inflammation. After two and a half years of extensive diagnostic work-up and multiple empirical therapies, a final diagnosis of Munchausen by proxy syndrome (MBPS) was established.

Conclusions: The diagnosis of SAID needs to be carefully reassessed if measurable systemic inflammation is missing, and MBPS should be included in the differential diagnosis.

Keywords: Autoinflammation; Differential diagnosis; Münchhausen by proxy syndrome (MBPS); Systemic autoinflammatory disease (SAID).

Publication types

  • Case Reports
  • Review

MeSH terms

  • Child, Preschool
  • Diagnosis, Differential
  • Hereditary Autoinflammatory Diseases / diagnosis*
  • Humans
  • Male
  • Munchausen Syndrome by Proxy / diagnosis*