Abstract
Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) is a rare
autosomal recessive disorder, characterised by a loss of self-tolerance to endocrine
tissues, chronic candidiasis and ectodermal disorders. APECED is associated with mutations
of a single gene, designated autoimmune regulator (AIRE). We describe a 31-year-old APECED patient with non-traumatic, cutaneous ulcers on
both forearms with features of a lupus-like panniculitis. On admission to the ICU
in September 2001, the patient suffered from a ketoacidotic, hyperglycemic coma and
adrenal crisis due to an Enterobacter-cloacae sepsis, originating from multiple, necrotising
deep cutaneous ulcers. These ulcers spontaneously developed on both forearms, some
of which were just emerging, full blown or healing with scars. Histological examination
showed signs of a scarring panniculitis and vasculitis. Immunohistochemistry and direct
immunofluorescence with characterisation of immunoglobulin and complement-factor binding
pattern revealed features of a lupus-like panniculitis. Sequence analysis of all 14
exons of the AIRE gene revealed a R257 X mutation in exon 6 resulting in a nonsense mutation at codon
257 confirming the diagnosis of APECED. Oral treatment with 60 mg/day corticosteroids
for two weeks led to complete resolution of all ulcers. In conclusion, mutations in
the AIRE gene may provide the genetic background against which additional factors can initiate
an autoimmune process. Here, autoimmune panniculitis appears to be an associated feature
of the APECED syndrome. Our findings support the use of immunosuppressive therapy
for autoimmune disease components of the APECED syndrome.
Key words
APECED - autoimmune - panniculitis - AIRE - HLA
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1 These two authors contributed equally.
Dr. Martin Füchtenbusch
3rd. Med. Dept., Endocrinology, Diabetology & Gastroenterology, Academic Hospital
München-Schwabing
Kölner Platz 1
80804 Munich
Germany
Phone: + 498930793114
Fax: + 4 98 93 08 17 33
Email: martin.fuechtenbusch@lrz.uni-muenchen.de