Abstract:
:We report on a patient affected by multicentric Castleman's disease who developed an acute immunohemolytic anemia due to warm antibody. The clinical course was characterized by refractoriness to the steroidal treatment and by a dramatic improvement of the hematological and objective picture following combination chemotherapy (CHOP regimen). The possible existence of a link between the lymphoproliferative syndrome and the immunological derangement is also discussed.
journal_name
Haematologicajournal_title
Haematologicaauthors
Liberato NL,Bollati P,Chiofalo F,Filipponi M,Poli Msubject
Has Abstractpub_date
1996-01-01 00:00:00pages
40-43issue
1eissn
0390-6078issn
1592-8721journal_volume
81pub_type
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