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Paraneoplastic pemphigus associated with non-Hodgkin B-cell lymphoma and good response to prednisone.

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.
AuthorsMaría Isabel Martínez De Pablo, Pilar Iranzo, José Manuel Mascaró, Alex Llambrich, Manel Baradad, Carmen Herrero
JournalActa dermato-venereologica (Acta Derm Venereol) Vol. 85 Issue 3 Pg. 233-5 ( 2005) ISSN: 0001-5555 [Print] Sweden
PMID16040408 (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)

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