Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/26301
Title: A renal transplant recipient with pulmonary tuberculosis and visceral leishmaniasis: Review of superimposed infections and therapy approaches
Authors: Uludağ Üniversitesi/Tıp Fakültesi/Nefroloji Bilim Dalı.
Uludağ Üniversitesi/Tıp Fakültesi/Hematoloji Bilim Dalı.
Uludağ Üniversitesi/Tıp Fakültesi/Enfeksiyon Hastalıkları ve Klinik Mikrobiyoloji Anabilim Dalı.
Uludağ Üniversitesi/Tıp Fakültesi/Göğüs Hastalıkları Anabilim Dalı.
Uludağ Üniversitesi/Tıp Fakültesi/Üroloji Anabilim Dalı.
0000-0002-0710-0923
Ersoy, Alparslan
Güllülü, Mustafa
Usta, Mehmet
Özçelik, Tülay
Yılmaz, E.
Uzaslan, Esra Kunt
Vuruşkan, Hakan
Yavuz, Mahmut
Oktay, Bülent
Dilek, Kamil
Yurtkuran, Mustafa
AAH-5054-2021
AAI-1004-2021
35612977100
6602684544
7005030712
7005424333
57224424133
8761653500
6507328150
7006244754
6602172127
56005080200
7003389525
Keywords: 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
Issue Date: Oct-2003
Publisher: Dustri-Verlag
Citation: 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.
Abstract: 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.
URI: http://hdl.handle.net/11452/26301
ISSN: 0301-0430
Appears in Collections:Scopus
Web of Science

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