Journal
CLINICAL COSMETIC AND INVESTIGATIONAL DERMATOLOGY
Volume 15, Issue -, Pages 1805-1808Publisher
DOVE MEDICAL PRESS LTD
DOI: 10.2147/CCID.S374556
Keywords
bullous pemphigoid; erythrodermic psoriasis; comorbidity
Categories
Funding
- National Natural Science Foundation of China [82103707]
- Clinical Research Plan of SHDC [SHDC2020CR1014B]
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This case report presents a rare occurrence of bullous pemphigoid (BP) in a woman with severe erythrodermic psoriasis (EP), possibly triggered by beta hemolytic streptococcus infection. This highlights the need for physicians to be attentive to the complicated condition of such patients and further study for better treatment.
Psoriasis is an immune-mediated systemic disease with multiple organs involvement, such as cardiovascular, live, gut, endocrine, and so on. Bullous pemphigoid (BP) is a rare comorbidity associated with psoriasis, while BP occurring in erythrodermic psoriasis (EP) is very rare. In this case, we reported a woman with severe EP who developed BP, in whom beta hemolytic streptococcus infection was a possible triggering factor. The complicated condition of such patients needs to draw attention of the physician and study further for better treatment.
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