Autoimmune hemolytic anemia in multicentric Castleman's disease.

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

Haematologica

journal_title

Haematologica

authors

Liberato NL,Bollati P,Chiofalo F,Filipponi M,Poli M

subject

Has Abstract

pub_date

1996-01-01 00:00:00

pages

40-43

issue

1

eissn

0390-6078

issn

1592-8721

journal_volume

81

pub_type

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