Mycobacterial Infection: A Difficult and Late Diagnosis in Stem Cell Transplant Recipients
Identifieur interne : 00A844 ( Main/Exploration ); précédent : 00A843; suivant : 00A845Mycobacterial Infection: A Difficult and Late Diagnosis in Stem Cell Transplant Recipients
Auteurs : C. Cordonnier [France] ; R. Martino [Espagne] ; P. Trabasso [Brésil] ; T. K. Held [Allemagne] ; H. Akan [Turquie] ; M. S. Ward [Australie] ; K. Fabian [Hongrie] ; A. J. Ullmann [Allemagne] ; N. Wulffraat [Pays-Bas] ; P. Ljungman [Suède] ; E. P. Alessandrino ; J. Pretnar [Slovénie] ; J. Gmür [Suisse] ; R. Varela [Espagne] ; A. Vitek [République tchèque] ; S. Sica [Italie] ; M. Rovira [Espagne]Source :
- Clinical Infectious Diseases [ 1058-4838 ] ; 2004-05-01.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Cellule souche, Homme, Information.
English descriptors
- KwdEn :
Abstract
The Infectious Diseases Working Party of the European Blood and Marrow Transplant Group conducted a survey to obtain information about the frequency, presentation, and treatment of mycobacterial infection (MBI) in stem cell transplant (SCT) recipients. Among 29 centers, MBI was diagnosed in 0.79% of 1513 allogeneic and 0.23% of 3012 autologous SCT recipients during 1994–1998 a median of 160 days after transplantation. The mean interval between first symptoms and diagnosis was 29 days and was still longer for patients with atypical MBI or recipients of corticosteroid therapy. The prevalence of MBI was highest among those who received matched unrelated or mismatched STCs from related donors. Of 31 patients, 20 had tuberculosis, 8 had atypical MBI, and 3 had diagnoses based on histological findings only. Five patients (16%) died, all of whom had received an allogeneic SCT. Because of the increased numbers of unmatched donors and transplantation programs in countries with a high prevalence of tuberculosis, constant vigilance is required to early detect MBI in SCT recipients.
Url:
DOI: 10.1086/383307
Affiliations:
- Allemagne, Australie, Brésil, Espagne, France, Hongrie, Italie, Pays-Bas, République tchèque, Slovénie, Suisse, Suède, Turquie
- Berlin, Bohême centrale, Hongrie centrale, Latium, Rhénanie-Palatinat, Svealand, Utrecht (province), Île-de-France
- Berlin, Budapest, Créteil, Mayence, Prague, Rome, Stockholm, Utrecht
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- to stream PascalFrancis, to step Corpus: 004B69
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Le document en format XML
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Allogeneic system</term>
<term>Atypical</term>
<term>Autologous system</term>
<term>Bone marrow</term>
<term>Corticosteroid</term>
<term>Diagnosis</term>
<term>Europe</term>
<term>Hematopoietic cell</term>
<term>Homograft</term>
<term>Homotransplantation</term>
<term>Human</term>
<term>Information</term>
<term>Mycobacterial infection</term>
<term>Prevalence</term>
<term>Recipient</term>
<term>Stem cell</term>
<term>Survey</term>
<term>Symptomatology</term>
<term>Treatment</term>
<term>Tuberculosis</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Atypique</term>
<term>Cellule hématopoïétique</term>
<term>Cellule souche</term>
<term>Corticostéroïde</term>
<term>Diagnostic</term>
<term>Enquête</term>
<term>Europe</term>
<term>Homme</term>
<term>Homogreffe</term>
<term>Homotransplantation</term>
<term>Information</term>
<term>Moelle osseuse</term>
<term>Mycobactériose</term>
<term>Prévalence</term>
<term>Receveur</term>
<term>Symptomatologie</term>
<term>Système allogénique</term>
<term>Système autologue</term>
<term>Traitement</term>
<term>Tuberculose</term>
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<front><div type="abstract">The Infectious Diseases Working Party of the European Blood and Marrow Transplant Group conducted a survey to obtain information about the frequency, presentation, and treatment of mycobacterial infection (MBI) in stem cell transplant (SCT) recipients. Among 29 centers, MBI was diagnosed in 0.79% of 1513 allogeneic and 0.23% of 3012 autologous SCT recipients during 1994–1998 a median of 160 days after transplantation. The mean interval between first symptoms and diagnosis was 29 days and was still longer for patients with atypical MBI or recipients of corticosteroid therapy. The prevalence of MBI was highest among those who received matched unrelated or mismatched STCs from related donors. Of 31 patients, 20 had tuberculosis, 8 had atypical MBI, and 3 had diagnoses based on histological findings only. Five patients (16%) died, all of whom had received an allogeneic SCT. Because of the increased numbers of unmatched donors and transplantation programs in countries with a high prevalence of tuberculosis, constant vigilance is required to early detect MBI in SCT recipients.</div>
</front>
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