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A renal transplant recipient with pulmonary tuberculosis and visceral leishmaniasis: Review of superimposed infections and therapy approaches

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Ersoy, Alparslan
Güllülü, Mustafa
Usta, Mehmet
Özçelik, Tülay
Yılmaz, E.
Uzaslan, Esra Kunt
Vuruşkan, Hakan
Yavuz, Mahmut
Oktay, Bülent
Dilek, Kamil

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Dustri-Verlag

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Visceral leishmaniasis (VL) is an acute or subacute disease that is almost invariably fatal if untreated. It is a rare disease in renal transplant recipients and frequently reported together with other infectious agents. A 39-year-old renal transplant patient was admitted to hospital for elective coronary surgery. In the post-operative period, he developed spiking fever and non-productive cough and his general condition deteriorated. While he was taking medication for nonspecific pneumonia, a cavitary lesion occurred in his lung, and he had the diagnosis of pulmonary tuberculosis and antituberculous treatment was started. Despite treatment, his fever continued. As the patient developed pancytopenia and splenomegaly, a bone marrow aspiration was done. Evaluation of bone marrow aspirate indicated Leishmania parasites. He was successfully treated with a more intensive liposomal amphotericin (L-AmB). Complete cure was achieved during follow-up period of 10 months without clinical relapse. In the existence of fever and long-standing pancytopenia, VL should be suspected although the patient had another proved infection and did not live or visit an endemic area. L-AmB usage can be safely preferred for treatment of selected renal transplant recipients with VL as first-line therapy.

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Kidney transplantation, Visceral leishmaniasis, Pulmonary tuberculosis, Liposomal amphotericin treatment, Liposomal amphotericin-B, Fatal leishmaniasis, Unexplained fever, Graft recipient, Rare cause, Kala-azar, Patient, Ketoconazole, Allopurinol, Antimoniate, Urology and nephrology

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Ersoy, A. vd. (2003). “A renal transplant recipient with pulmonary tuberculosis and visceral leishmaniasis: Review of superimposed infections and therapy approaches”. Clinical Nephrology, 60(4), 289-294.

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