scholarly journals Delayed and Overlooked Diagnosis of an Unusual Opportunistic Infection in a Renal Transplant Recipient: Visceral Leishmaniasis

2010 ◽  
Vol 34 (4) ◽  
pp. 183-185 ◽  
Author(s):  
Aysegul ZUMRUTDAL ◽  
Ertugrul ERKEN ◽  
Tuba TURUNC ◽  
Sule COLAKOGLU ◽  
Yusuf Ziya DEMIROGLU ◽  
...  
2002 ◽  
Vol 18 (4) ◽  
pp. 187-191 ◽  
Author(s):  
Marina Valente ◽  
Massimo Marroni ◽  
Claudio Sfara ◽  
Daniela Francisci ◽  
Lisa Malincarne ◽  
...  

Objective To report a case of visceral leishmaniasis treated with liposomal amphotericin B (LAB) after probable failure with amphotericin B lipid complex (ABLC). Case Summary A 62-year-old white renal transplant recipient was admitted for pyrexia, hepato-splenomegaly, and pancytopenia. Leishmania amastigotes were detected from bone marrow aspirate and in circulating blood monocytes and neutrophils. The patient, who weighed 56 kg, received ABLC at a starting dose of 200 mg/d (3.6 mg/kg of body weight per day) for 13 days, achieving a total dose of 2,600 mg (46 mg/kg) without clinical improvement. The patient was switched to 100 mg/d (1.8 mg/kg) of LAB for 10 days, after which a dose of 250 mg (4.5 mg/kg) was repeated on days 17,24,31, and 38. Twenty-four hours after the first dose of LAB, the patient showed an excellent clinical response. On the following days, there was a progressive increase in hemoglobin concentration and leukocyte and platelet counts. Three months later, the patient was asymptomatic. Discussion Although treatment with ABLC appears to be effective for the treatment of Indian patients with visceral leishmaniasis, experience with immunocompromised patients is limited. This is the first case of a renal transplant recipient in which ABLC was used to treat visceral leishmaniasis without remarkable efficacy, but with infusion-related adverse effects perhaps due to the use of higher doses. Conclusions A randomized comparative trial is needed to compare LAB with ABLC in the treatment of visceral leishmaniasis in patients who have received kidney allografts.


1991 ◽  
Vol 6 (10) ◽  
pp. 736-738 ◽  
Author(s):  
V. Kher ◽  
A. K. Ghosh ◽  
A. Gupta ◽  
P. Arora ◽  
T. N. Dhole

1996 ◽  
Vol 16 (4) ◽  
pp. 358-360 ◽  
Author(s):  
Raj K. Sharma ◽  
Ratan Jha ◽  
Pradeep Kumar ◽  
Vijay Kher ◽  
Amit Gupta ◽  
...  

2018 ◽  
Vol 102 ◽  
pp. S661 ◽  
Author(s):  
Elizete Keitel ◽  
Rosana Mussoi Bruno ◽  
Helen Zanetti ◽  
Gisele Meinerz ◽  
Lazaro Pereira Jacobina ◽  
...  

1992 ◽  
Vol 2 (12) ◽  
pp. S264
Author(s):  
N E Tolkoff-Rubin ◽  
R H Rubin

The risk of opportunistic infection in the renal transplant recipient is determined by the interaction between two factors: the epidemiologic exposures the individual encounters within the community and the hospital and a complex function termed the net state of immunosuppression. There are two general categories of opportunistic fungal infection in this patient population: (1) disseminated primary or reactivation infection with one of the geographically restricted systemic mycoses (histoplasmosis, coccidioidomycosis, blastomycosis, and paracoccidioidomycosis) and (2) opportunistic infection with fungal species that rarely cause invasive infection in the normal host (Aspergillus species, Candida species, Cryptococcus neoformans, and the Mucoraceae), with these last usually being acquired within the hospital environment. Newly available azole compounds, fluconazole and itraconazole, are exciting new alternatives to amphotericin in the treatment of at least some of these infections. The three most important forms of opportunistic bacterial infections are those due to Listeria monocytogenes, Nocardia asteroides, and a variety of mycobacterial species. Clinical diseases with these first two are effectively prevented by low-dose trimethoprim-sulfamethoxazole prophylaxis. There are two cardinal therapeutic rules to be followed by clinicians in dealing with these infections: prevention is better than treatment; when treatment is required, however, the major determinant of the success of therapy is the rapidity with which the diagnosis is made and effective therapy is initiated.


2013 ◽  
Vol 23 (6) ◽  
pp. 892-893 ◽  
Author(s):  
Sedef Yücel ◽  
Deren Özcan ◽  
Deniz Seçkin ◽  
Adil M. Allahverdiyev ◽  
Fazilet Kayaselçuk ◽  
...  

1998 ◽  
Vol 18 (2) ◽  
pp. 171-171 ◽  
Author(s):  
Francisco Gómez Campderá ◽  
Juan Berenguer ◽  
Fernando Anaya ◽  
Marisa Rodriguez ◽  
Fernando Valderrábano

1986 ◽  
Vol 13 (3) ◽  
pp. 301-303 ◽  
Author(s):  
Jose M. Aguado ◽  
Fernando Bonet ◽  
Juan J. Plaza ◽  
Antonio Escudero

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