Abstract |
Paraneoplastic pemphigus is a life-threatening autoimmune bullous disease associated with neoplasia, generally of lymphoid origin. Immunosuppressive therapy is often disappointing and there are only a few reports of patients surviving more than 2 years. These cases were generally associated with benign neoplasms. We report here the case of a patient with paraneoplastic pemphigus associated with non-Hodgkin B-cell lymphoma who had a surprisingly good response to systemic corticosteroids and remains free of lesions more than 3 years later despite progression of her neoplasm.
|
Authors | María Isabel Martínez De Pablo, Pilar Iranzo, José Manuel Mascaró, Alex Llambrich, Manel Baradad, Carmen Herrero |
Journal | Acta dermato-venereologica
(Acta Derm Venereol)
Vol. 85
Issue 3
Pg. 233-5
( 2005)
ISSN: 0001-5555 [Print] Sweden |
PMID | 16040408
(Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't)
|
Chemical References |
- Glucocorticoids
- Prednisone
|
Topics |
- Aged
- Diagnosis, Differential
- Drug Administration Schedule
- Female
- Glucocorticoids
(administration & dosage)
- Humans
- Lymphoma, B-Cell
(complications, diagnosis, drug therapy)
- Oral Ulcer
(pathology)
- Paraneoplastic Syndromes
(complications, diagnosis, drug therapy, pathology)
- Pemphigus
(complications, diagnosis, drug therapy, pathology)
- Prednisone
(administration & dosage)
|