2017European Journal of DermatologyRequires access

Mixed connective tissue disease with bilateral erythematous palpebral oedema and targetoid skin lesions

Masanobu Sakaguchi, Tomoki Takeda, Takao Kodera, Kazuhiro Murakami, Masahiro Oka

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Abstract

Mixed connective tissue disease (MCTD) is a rare connective tissue disease with an autoimmune background. Clinically, it is characterised by manifestations shared with other connective tissue diseases; systemic lupus erythematosus (SLE), systemic sclerosis (SSc), and polymyositis/dermatomyositis [1, 2]. High titres of distinct serum autoantibodies to the U1 small nuclear ribonucleoprotein (RNP) are characteristic of MCTD. Several skin manifestations of MCTD are known, including Raynaud's phenomenon, [...]

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What this paper is about

Mixed connective tissue disease (MCTD) is a rare connective tissue disease with an autoimmune background. Clinically, it is characterised by manifestations shared with other connective tissue diseases; systemic lupus erythematosus (SLE), systemic sclerosis (SSc), and polymyositis/dermatomyositis [1, 2]. High titres of distinct serum autoantibodies to the U1 small nuclear ribonucleoprotein (RNP) are characteristic of MCTD. Several skin manifestations of MCTD are known, including Raynaud's phenomenon, [...]

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Available abstract

Mixed connective tissue disease (MCTD) is a rare connective tissue disease with an autoimmune background. Clinically, it is characterised by manifestations shared with other connective tissue diseases; systemic lupus erythematosus (SLE), systemic sclerosis (SSc), and polymyositis/dermatomyositis [1, 2]. High titres of distinct serum autoantibodies to the U1 small nuclear ribonucleoprotein (RNP) are characteristic of MCTD. Several skin manifestations of MCTD are known, including Raynaud's phenomenon, [...]

Key concepts: Mixed connective tissue disease, Medicine, Dermatomyositis, Polymyositis, Connective tissue disease, Pathology, Scleroderma (fungus), Connective tissue

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