Publication details
IgA pemphigus associated with monoclonal gammopathy completely resolved after achievement of complete remission of multiple myeloma with bortezomib, cyclophosphamide and dexamethasone regimen
| Basic information | |
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| Original title: | IgA pemphigus associated with monoclonal gammopathy completely resolved after achievement of complete remission of multiple myeloma with bortezomib, cyclophosphamide and dexamethasone regimen |
| Authors: | Zdeněk Adam, Marta Krejčí, Luděk Pour, Josef Feit, Tomáš Büchler, Roman Hájek |
| Further information | |
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| Citation: | ADAM, Zdeněk, Marta KREJČÍ, Luděk POUR, Josef FEIT, Tomáš
BÜCHLER and Roman HÁJEK. IgA pemphigus associated with
monoclonal gammopathy completely resolved after achievement of
complete remission of multiple myeloma with bortezomib,
cyclophosphamide and dexamethasone regimen. Wiener klinische
Wochenschrift, Wien: Springer, 2010, vol. 122, 9 -10, p.
311 -314. ISSN 0043 -5325.Export BibTeX |
| Original language: | English |
| Field: | Oncology and hematology |
| Type: | Article in Periodical |
| Keywords: | IgA pemphigus;bortezomib; rituximab; monoclonal gammopathy |
Monoclonal gammopathy-associated IgA pemphigus is a debilitating skin disorder with inconsistent response to treatment. A 61-year-old woman with IgA pemphigus and monoclonal gammopathy of unknown significance had been treated with bortezomib, cyclophosphamide and dexamethasone regimen, which resulted in complete and durable remission of multiple myeloma and IgA pemphigus. This suggests that bortezomib-based therapy is useful for the treatment of the rare dermatologic disorder associated with IgA gammopathy.
Related projects:
- University Research Centre - Czech Myeloma Group
- From classic prognostic markers to clinical applications in selected pharmacogenomic and pharmacoproteomic projects in multiple myeloma and monoclonal gammapathies












