Idiopathic CD4+ lymphocytopenia and systemic vasculitis.

Abstract:

:The syndrome defined as "idiopathic CD4 lymphocytopenia' (ICL) is a rare disease of unknown aetiology, often associated with severe depression of immune defences and the occurrence of opportunistic infections. A case is reported wherein a severe immunodeficiency syndrome with persistent idiopathic CD4+ lymphopenia developed in a woman suffering from systemic microscopic polyarteritis; no signs of HIV 1/2 or HTLV I/II infection were evident. The patient died of widespread opportunistic infections. The association of ICL with vasculitis has never been reported until now. A link between the two diseases cannot be ruled out.

journal_name

J Intern Med

authors

Bordin G,Ballaré M,Paglino S,Ravanini P,Dulio D,Malosso MC,Boldorini R,Monteverde A

doi

10.1046/j.1365-2796.1996.447785000.x

subject

Has Abstract

pub_date

1996-07-01 00:00:00

pages

37-41

issue

1

eissn

0954-6820

issn

1365-2796

journal_volume

240

pub_type

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