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

被引:10
作者
Wittkowski, Helmut [1 ]
Hinze, Claas [1 ]
Haefner-Harms, Sigrid [2 ]
Oji, Vinzenz [3 ]
Masjosthusmann, Katja [2 ]
Monninger, Martina [2 ]
Grenzebach, Ulrike [4 ]
Foell, Dirk [1 ]
机构
[1] Univ Childrens Hosp Muenster, Dept Paediat Rheumatol & Immunol, Albert Schweitzer Campus 1,Bld W30, D-48149 Munster, Germany
[2] Univ Childrens Hosp Muenster, Dept Gen Pediat, Munster, Germany
[3] Univ Hosp Muenster, Dept Dermatol, Munster, Germany
[4] Univ Hosp Muenster, Dept Ophthalmol, Munster, Germany
关键词
Autoinflammation; Systemic autoinflammatory disease (SAID); Munchhausen by proxy syndrome (MBPS); Differential diagnosis; MUNCHHAUSEN SYNDROME; UNKNOWN ORIGIN; CHILD-ABUSE; FEVER; ILLNESS;
D O I
10.1186/s12969-017-0152-6
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
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.
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页数:5
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