Kikuchi–Fujimoto’s disease and adult-onset Still’s disease: A rare co-occurence Kikuchi-Fujimoto-Syndrom und adulter Morbus Still: Eine seltene Koinzidenz

Sondermann W, Hillen U, Reis AC, Schimming T, Schilling B (2015)

Publication Type: Journal article

Publication year: 2015

Journal

Hautarzt Springer Verlag (Germany)

Book Volume: 66

Pages Range: 940-944

Journal Issue: 12

DOI: 10.1007/s00105-015-3652-7

Abstract

Kikuchi–Fujimoto’s disease and adult-onset Still’s disease are rare inflammatory conditions with overlapping clinical features. Adult-onset Still’s disease causes high fevers, a typical salmon-colored rash, and joint pain. The principal symptom of Kikuchi’s disease is cervical lymphadenopathy with typical histopathological features including extensive necrosis of the involved lymph nodes. Here, we report on a rare case of concurrent adult-onset Still’s disease and Kikuchi–Fujimoto syndrome in a young Caucasian patient.

Involved external institutions

Universitätsklinikum Essen DE Germany (DE)

How to cite

APA:

Sondermann, W., Hillen, U., Reis, A.C., Schimming, T., & Schilling, B. (2015). Kikuchi–Fujimoto’s disease and adult-onset Still’s disease: A rare co-occurence Kikuchi-Fujimoto-Syndrom und adulter Morbus Still: Eine seltene Koinzidenz. Hautarzt, 66(12), 940-944. https://doi.org/10.1007/s00105-015-3652-7

MLA:

Sondermann, W., et al. "Kikuchi–Fujimoto’s disease and adult-onset Still’s disease: A rare co-occurence Kikuchi-Fujimoto-Syndrom und adulter Morbus Still: Eine seltene Koinzidenz." Hautarzt 66.12 (2015): 940-944.

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