Abstract
Calcinosis, Raynaud’s phenomenon, oesophageal dysmotility, sclerodactyly, telangiectasia (CREST) syndrome, a limited form of systemic sclerosis, is sometimes complicated by primary biliary cirrhosis (PBC). A 52- and 61-year-old Japanese woman with PBC–CREST overlap syndrome accompanied by Sjögren's syndrome, and Hashimoto’s thyroiditis, and Graves’ disease, respectively, are reported. They had suffered from Raynaud’s phenomena, sclerodactyly, morning stiffness, arthralgia, and sicca symptoms during these several years. They exhibited an increased level of alkaline phosphatase, γ-glutamyl transpeptidase, positive antibodies against mitochondria and centromere, and hyperglobulinemia without any cholestatic symptoms. Histological findings from liver biopsy specimens were consistent with those of PBC. Clinically, they were diagnosed as both asymptomatic PBC and incomplete CREST syndrome. Their human leukocyte antigen typing showed both DR4 and DR8 positive. The association of the four autoimmune conditions is clinically and etiologically important. Although a combination of these diseases is rare, it is of importance to keep in mind that various autoimmune diseases could occur simultaneously. Of critical importance is that an active diagnostic attitude towards them is admirable, and that early diagnosis and therapy are needed.
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Acknowledgement
We would like to thank Laurence A. Boxer, MD, Professor, University of Michigan Medical Center, Ann Arbor, MI, USA for his editorial advice on the manuscript.
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Nakamura, T., Higashi, Si., Tomoda, K. et al. Primary biliary cirrhosis (PBC)–CREST overlap syndrome with coexistence of Sjögren's syndrome and thyroid dysfunction. Clin Rheumatol 26, 596–600 (2007). https://doi.org/10.1007/s10067-005-0178-x
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DOI: https://doi.org/10.1007/s10067-005-0178-x