Granulomatous disease associated with NOD2 sequence variants and familial camptodactyly: An intermediate form of NOD2 -associated diseases?

Abstract Objective Nucleotide-binding oligomerization domain-containing protein-2 ( NOD 2)-associated diseases may be a spectrum of disease. We report two families who exhibited an intermediate form of Blau syndrome and NOD2 -associated autoinflammatory disease (NAID). Methods We identified two families with granulomatous disease. The clinical phenotypes and genotypes of these two families were reviewed and analyzed. Results The proband in family 1 was a white 57-year-old woman, with camptodactyly (age 6 years), inflammatory polyarthritis and dermatitis (age of 30 years), and cough, dyspnea, dry eyes, parotid gland enlargement, and fever. A computerized tomography showed mediastinal lymphadenopathy without hilar involvement, and a mediastinal lymph node biopsy revealed non-caseating granuloma. Pedigree analysis suggested autosomal dominant inheritance, and genetic testing identified a NOD2 sequence variant IVS8+158 . The proband in family 2 was a white 50-year-old woman with inflammatory polyarthritis and periarticular subcutaneous nodules. Skin biopsy showed non-necrotizing granuloma. There was a family history of camptodactyly, and genetic testing identified a NOD2 sequence variant R703C. Conclusions Both probands had granulomatous disease and autosomal dominant phenotype of familial camptodactyly coupled with the presence of the NOD2 sequence variants, IVS8+158 , and R703C. Granulomatous disease associated with NOD2 variants may be an intermediate form between Blau syndrome and NAID.