[Skip to Content]
Access to paid content on this site is currently suspended due to excessive activity being detected from your IP address 54.205.150.215. Please contact the publisher to request reinstatement.
[Skip to Content Landing]
Correspondence
Aug 2012

Stevens-Johnson Syndrome Without Skin Lesions (Fuchs Syndrome): A Literature Review of Adult Cases With Mycoplasma Cause

Author Affiliations

Author Affiliations: Division of Dermatology, University of Calgary, Calgary, Alberta, Canada.

Arch Dermatol. 2012;148(8):963-964. doi:10.1001/archdermatol.2012.681

The characteristics of Stevens-Johnson syndrome (SJS) include a generalized cutaneous eruption, fever, inflamed buccal mucosa, and severe purulent conjunctivitis.1 Stevens-Johnson syndrome without skin lesions and only mucosal involvement has been described as Fuchs syndrome in Germany and is believed to be a variant of erythema multiforme majus.2 This presentation is also known as atypical SJS and Mycoplasma pneumoniae –associated mucositis when caused by a Mycoplasma infection.2 Fuchs syndrome associated with Mycoplasma pneumoniae has usually been seen in children and adolescents. To our knowledge, only 7 cases in the adult population have been reported.

First Page Preview View Large
First page PDF preview
First page PDF preview
×