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DOI 10.2169/internalmedicine.4888-20

Медицинская библиотека · Internal medicine (Tokyo, Japan) · 2020

An Overlapping Case of IgG4-related Disease and Klinefelter Syndrome with Lupus-like Serological and Neurological Features: A Case Report and Literature Review.

Takanashi Satoshi, Hanaoka Hironari, Ota Yuichiro, Kaneko Yuko, Takeuchi Tsutomu

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Аннотация

A 46-year-old man with Klinefelter syndrome (KS) presented with obliterative phlebitis of the lower legs with a deteriorated renal function, and elevated serum alkaline phosphatase and ataxia levels. Examinations demonstrated tubulointerstitial nephritis, obliterative phlebitis and lymphadenopathy with IgG4+ plasma cell infiltrate and sclerosing cholangitis. Although the serological profile and central nerve system involvement were compatible for systemic lupus erythematosus (SLE), a definite diagnosis of SLE was difficult to make. IgG4-related disease (IgG4-RD) with KS was finally diagnosed, and high dose prednisolone with intravenous cyclophosphamide was initiated and thereafter the patient demonstrated a prompt improvement. This is the first known case demonstrating overlapping IgG4-RD with lupus-like serological and neurological features in a patient with KS, thus highlighting the pathogenic role with the genomic background for IgG4-RD and SLE.

Для цитирования: Takanashi Satoshi, Hanaoka Hironari, Ota Yuichiro, Kaneko Yuko, Takeuchi Tsutomu. An Overlapping Case of IgG4-related Disease and Klinefelter Syndrome with Lupus-like Serological and Neurological Features: A Case Report and Literature Review.. Internal medicine (Tokyo, Japan). 2020. DOI: 10.2169/internalmedicine.4888-20.

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