2011
DOI: 10.1097/qco.0b013e32834a8ba1
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Recent advances in post-kala-azar dermal leishmaniasis

Abstract: The incidence of PKDL is reducing in India after introduction of miltefosine and amphotericin B for treatment of visceral leishmaniasis. It remains higher in Bangladesh and in Sudan. Parasite burden is higher in nodular and papular forms of PKDL compared to the macular form of the disease. The demonstration of Leishmania DNA in peripheral blood buffy coat and in skin specimens can help to diagnose 40-75% clinically suspected PKDL individuals. An initial cure rate of 95% has been achieved with miltefosine for t… Show more

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Cited by 38 publications
(40 citation statements)
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“…PKDL or dermal leishmanoid11 is a condition in which dermal lesions can be heavily parasitized in a subset of patients successfully treated for VL, and it occurs mainly in India and Sudan in patients infected by L. donovani 13,14. They remain asymptomatic for months to years and then develop a progressive proliferation of parasites within the skin, giving rise to diffuse macular, maculopapular, or nodular lesions 13.…”
Section: Pathogenesismentioning
confidence: 99%
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“…PKDL or dermal leishmanoid11 is a condition in which dermal lesions can be heavily parasitized in a subset of patients successfully treated for VL, and it occurs mainly in India and Sudan in patients infected by L. donovani 13,14. They remain asymptomatic for months to years and then develop a progressive proliferation of parasites within the skin, giving rise to diffuse macular, maculopapular, or nodular lesions 13.…”
Section: Pathogenesismentioning
confidence: 99%
“…The patient has an irregular fever, anemia, and leukopenia; hepatosplenomegaly and bone marrow suppression are characteristic (see above); and HIV coinfections often produce atypical presentations 11–13. Rates of PKDL vary regionally, arising within 6 months in up to 50% of treated VL patients in parts of Sudan, but within 2–3 years in only approximately 5%–10% of patients in India 1214…”
Section: Diagnosismentioning
confidence: 99%
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“…Although PKDL in Sudan can appear concurrently with, or sometimes in the absence of, VL, in general the disease is highly uncommon in patients who have not yet presented with VL and received treatment. Thus, certain therapies are actually considered a significant risk factor for developing the disease [10]. Because the therapies often restore or boost the patient’s inflammatory T helper 1 (Th1) immune response, PKDL is widely accepted as being an immunologically mediated disease (Box 2).…”
Section: Post-kala-azar Dermal Leishmaniasismentioning
confidence: 99%
“…Persistence of a mixed cellular immune response characterized by high levels of IL-10 and IFNγ after complete treatment of VL is associated with development of PKDL. 52 Therefore, immunoprophylaxis during the treatment of VL so as to enhance Th 1 cellular immune responses along with a well-tuned immunoregulatory response to infection may prevent the development of PKDL after treatment of VL. This is supported by the findings of the study in Sudan in which PKDL treatment was substantially improved by adding alum/alum + BCG vaccine to the conventional treatment with SSG.…”
Section: Prevention Of Pkdlmentioning
confidence: 99%