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Late-onset Pneumocystis jirovecii pneumonia in solid organ transplant recipients
被引:26
|作者:
Perez-Ordono, L.
[1
]
Hoyo, I.
[1
]
Sanclemente, G.
[1
]
Ricart, M. J.
[2
]
Cofan, F.
[2
]
Perez-Villa, F.
[3
]
Puig de la Bellacasa, J.
[4
]
Moreno, A.
[1
]
Cervera, C.
[1
]
机构:
[1] Univ Barcelona, Dept Infect Dis, Hosp Clin Barcelona, Barcelona, Spain
[2] Univ Barcelona, Hosp Clin Barcelona, Renal Transplant Unit, Barcelona, Spain
[3] Univ Barcelona, Hosp Clin Barcelona, Heart Transplant Unit, Barcelona, Spain
[4] Univ Barcelona, Hosp Clin Barcelona, Ctr Int Hlth Res CRESIB, CDB,Dept Microbiol, Barcelona, Spain
关键词:
Pneumocystis jirovecii;
PCP;
late-onset opportunistic infection;
solid organ transplantation;
lymphopenia;
rituximab;
CARINII-PNEUMONIA;
RITUXIMAB THERAPY;
IMMUNOCOMPROMISED PATIENTS;
CYTOMEGALOVIRUS-INFECTION;
RISK-FACTORS;
REJECTION;
PROPHYLAXIS;
PREVENTION;
SIROLIMUS;
D O I:
10.1111/tid.12184
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Anti-Pneumocystis prophylaxis is recommended for at least 6-12months after solid organ transplantation, as most cases of Pneumocystis jirovecii pneumonia (PCP) occur during the first year post transplantation. Herein, we report 4 cases of late-onset PCP (>1year post transplant). PCP appeared in a range of 50-68months post transplant. Two cases had history of humoral rejection episodes treated with rituximab, and the other 2 had low CD4+ T-cell count (<200 cells/mm(3)) at the time of diagnosis. All 4 patients survived. In conclusion, although the number of cases is low, we must be aware of the possibility of late-onset PCP in solid organ transplant patients. The role of previous use of rituximab or persistent CD4+ T-cell lymphopenia should be addressed in future studies.
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页码:324 / 328
页数:5
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