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Pediatric Rheumatology 2017-Apr

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

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Helmut Wittkowski
Claas Hinze
Sigrid Häfner-Harms
Vinzenz Oji
Katja Masjosthusmann
Martina Monninger
Ulrike Grenzebach
Dirk Foell

Keywords

Abstract

BACKGROUND

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

METHODS

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.

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