Coexistence of TEMPI syndrome and leukocytoclastic vasculitis successfully treated with autologous stem cell transplantation

The TEMPI syndrome is a very rare paraneoplastic syndrome associated with plasma cell dyscrasia and monoclonal gammopathy. First described in 2011, the pathophysiology of TEMPI syndrome is still unknown. Essential for diagnosis is to recognize the five clinical findings: telangiectasias, erythrocyto...

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Detalles Bibliográficos
Autores principales: Nappi, Davide, Tauber, Martina, Sykes, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9713062/
https://www.ncbi.nlm.nih.gov/pubmed/36467823
http://dx.doi.org/10.1002/jha2.561

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9713062/
https://www.ncbi.nlm.nih.gov/pubmed/36467823
http://dx.doi.org/10.1002/jha2.561

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