Fixed Drug Eruption to Multiple Drugs: Clinical and Laboratory Investigation

1991 ◽  
Vol 30 (2) ◽  
pp. 149-151 ◽  
Author(s):  
S. Kivity
2020 ◽  
Vol 12 (1) ◽  
pp. 25-32 ◽  
Author(s):  
Michie Katsuta ◽  
Akihiko Asahina ◽  
Tetsuo Shiohara

Although hepatitis C virus (HCV) infection is often associated with extrahepatic cutaneous manifestations such as lichen planus, it is unclear whether HCV per se or HCV-specific immune responses play a pathophysiological role in the development of HCV-related cutaneous diseases. We recently treated a patient who developed parapsoriasis en plaque-like lesions after ingestion of various drugs. She showed hypersensitivity to multiple drugs after interferon therapy. Her clinical course was complicated by flares of parapsoriasis-like lesions which returned at precisely the same sites. The flares had begun within hours of ingesting nicardipine hydrochloride, amlodipine besilate, candesartan cilexetil and atenolol for the first time despite showing a low level of HCV RNA. Interestingly, the flares gradually subsided during continued treatment with these drugs while her HCV RNA level paradoxically increased: thus, there was an inverse correlation between flares and HCV RNA level. The eruptions were eventually diagnosed as fixed drug eruption, although the clinical manifestations mimicked parapsoriasis en plaque. Our results suggest that multiple drug hypersensitivity could be induced by antiviral immune responses that are cross-reactive to multiple drugs, but not by HCV per se.


1970 ◽  
Vol 101 (5) ◽  
pp. 621b-621 ◽  
Author(s):  
M. B. Brodin

2000 ◽  
Vol 62 (3) ◽  
pp. 343-345
Author(s):  
Kaoru MURATA ◽  
Atsushi HATAMOCHI ◽  
Hiroshi SHINKAI

2005 ◽  
Vol 67 (2) ◽  
pp. 141-146 ◽  
Author(s):  
Yumiko KUBOTA ◽  
Juichiro NAKAYAMA

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