Detailed Information on Publication Record
2010
IgA pemphigus associated with monoclonal gammopathy completely resolved after achievement of complete remission of multiple myeloma with bortezomib, cyclophosphamide and dexamethasone regimen
ADAM, Zdeněk, Marta KREJČÍ, Luděk POUR, Josef FEIT, Tomáš BÜCHLER et. al.Basic information
Original name
IgA pemphigus associated with monoclonal gammopathy completely resolved after achievement of complete remission of multiple myeloma with bortezomib, cyclophosphamide and dexamethasone regimen
Name in Czech
Vymizení IgA pemphigus spojeného s monoklonální gamapatií po dosažení kompletní remise mnohočetného myelomu po léčbě režimem VCD
Authors
ADAM, Zdeněk (203 Czech Republic, guarantor), Marta KREJČÍ (203 Czech Republic), Luděk POUR (203 Czech Republic), Josef FEIT (203 Czech Republic), Tomáš BÜCHLER (703 Slovakia) and Roman HÁJEK (203 Czech Republic)
Edition
Wiener klinische Wochenschrift, Wien, Springer, 2010, 0043-5325
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30200 3.2 Clinical medicine
Country of publisher
Austria
Confidentiality degree
není předmětem státního či obchodního tajemství
Impact factor
Impact factor: 0.747
RIV identification code
RIV/00216224:14110/10:00044190
Organization unit
Faculty of Medicine
UT WoS
000278954200008
Keywords (in Czech)
IgA pemphigus; bortezomib; rituximab; monoklonální gamapatie
Keywords in English
IgA pemphigus;bortezomib; rituximab; monoclonal gammopathy
Změněno: 10/8/2010 12:05, Jitka Firešová
V originále
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.
In Czech
V publikaci je popsán případ 61 leté pecientky s IgA pemfigem a monoklonální gamapatií a výslekdy léčby režimem bortezomib, cyclophosphamid a dexamethasone, po němž došlo k úplnému vymyzení IgA pemfingu.
Links
LC06027, research and development project |
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MSM0021622434, plan (intention) |
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