Granulomatous skin involvement in a patient with an unusual NOD2 mutation

The Australasian Journal of Dermatology
Ifedayo O KuyeGideon P Smith

Abstract

Blau syndrome is a rare disorder that is classically characterised by granulomatous arthritis, skin eruptions and uveitis, which occur in the absence of lung involvement. Blau syndrome has been linked to encoding mutations in the NOD-2 gene and is inherited in an autosomal dominant form. The most commonly observed mutations are missense substitutions affecting the arginine residue at position 334. The rare E600A mutation has been described as causing uveitis without skin involvement. Our patient is a 54-year-old man with an unusual heterozygous c.1799A>C(E600A) mutation, who was seen for bilateral lower extremity swelling and pain. On physical examination, he was found to have lower leg oedema with decreased hair growth on the affected area. Biopsy showed non-caseating micro-granulomas consistent with a diagnosis of Blau syndrome. The patient had excellent response to colchicine, but this was stopped because he developed elevated transaminases. Thus, we present an unusual genetic form of a rare condition and we demonstrate skin involvement in a subtype where cutaneous involvement has not hitherto been reported. In addition, the type and presentation of the skin involvement is different from that normally found in classic Blau s...Continue Reading

References

Nov 1, 1985·The Journal of Pediatrics·E B Blau
Aug 31, 2001·Nature Genetics·C Miceli-RichardJ P Hugot
Aug 14, 2012·Autoimmunity Reviews·Paolo SfrisoLeonardo Punzi
Apr 10, 2014·Arthritis Research & Therapy·Kei IkedaHiroshi Nakajima
May 31, 2014·Case Reports in Rheumatology·Krati Chauhan, Clement Michet
Aug 20, 2014·Pediatric Rheumatology Online Journal·Carine H WoutersCarlos D Rose

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