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IgA nephropathy associated with erythrodermic psoriasis: A case report

RATIONALE: Cases about IgAN associated with EP are rare and the pathogenesis is poorly understood. We reported a 74-year-old Chinese male who suffered the IgAN and EP at the same time and explored a possible pathophysiologic link and points toward the possible pathogenesis. PATIENT CONCERNS: The pat...

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Detalles Bibliográficos
Autores principales: Zhang, Li, Xue, Shuai, Yu, JinYu, Si, HeNan, Xu, Ying, Li, Jia, Ma, FuZhe, Xu, ZhongGao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6531157/
https://www.ncbi.nlm.nih.gov/pubmed/31083172
http://dx.doi.org/10.1097/MD.0000000000015433
Descripción
Sumario:RATIONALE: Cases about IgAN associated with EP are rare and the pathogenesis is poorly understood. We reported a 74-year-old Chinese male who suffered the IgAN and EP at the same time and explored a possible pathophysiologic link and points toward the possible pathogenesis. PATIENT CONCERNS: The patient complained deteriorating symptoms (erythrodermia, skin pruritus, and pain) of psoriasis and obvious pitting edema on his legs. DIAGNOSIS: The patient was diagnosed as IgAN and EP concurrently according to medical history, physical examination, laboratory test, and pathology. INTERVENTIONS: Intravenous dexamethasone (5 mg/day) and oral ciclosporin (200 mg twice a day). OUTCOMES: The patient's symptoms of psoriasis and IgA nephropathy improved obviously after 11-day treatment and discharged from the hospital. LESSONS: IgAN should be considered when the patient is diagnosed as EP. The combination of dexamethasone and ciclosporin may be effective option for patients with IgAN and EP concurrently.