| Literature DB >> 25580788 |
Jan Šternberský, Martin Tichý1.
Abstract
Fuchs' syndrome (Stevens-Johnson syndrome without skin involvement) is a sporadically diagnosed disease. Most authors consider it to be a pure mucosal variant of Stevens-Johnson syndrome; however, some consider the syndrome a separate entity. The complete absence of cutaneous symptoms may be the reason that not all cases of Fuchs' syndrome are diagnosed and properly classified. The authors describe a case of a 22-year-old patient suffering only from mucosal symptoms, diagnosed as Fuchs' syndrome from the context of the tests performed. A Mycoplasma pneumoniae infection triggered the disease onset. Mycoplasma infection, as a trigger factor of Fuchs' syndrome in adults, has so far been described in only a few isolated cases worldwide.Entities:
Mesh:
Substances:
Year: 2014 PMID: 25580788
Source DB: PubMed Journal: Acta Dermatovenerol Croat ISSN: 1330-027X Impact factor: 1.256