Skip to main content
. 2016 Nov 22;110(7-8):326–329. doi: 10.1080/20477724.2016.1258163

Table 1.

The clinical features, diagnosis, and treatment outcome of cases

Diagnostic method
Case Age (year) Sex P/H VL Past Treatment history Fever Spleen size (cm) Liver size (cm) Lesion Type BMA/SA Skin smear rK39 Treatment outcome*
1 25 F No _ Yes 1 1 M, P BM+ 4ve + 3ve + ve Cured
2 20 M Yes SAG Yes 1 1 M,P BM+ 4ve + 2ve + ve Cured
3 14 M No _ Yes 6 2 M BM+ 3ve + 2ve + ve Cured
4 50 M Yes Mil. Yes 4 1 M BM+ 2ve + 4ve + ve Cured
5 36 M Yes SAG Yes 5 2 M SA+ 4ve + 1ve + ve Cured
6 40 M Yes Mil. Yes 8 4 M,P,N SA+ 3ve + 2ve + ve Cured
7 15 M No _ Yes 5 1 M SA+ 3ve + 1ve + ve Cured
8 18 F No _ Yes 14 1 M SA+ 4ve + 1ve + ve Cured
9 25 F yes SAG Yes 10 2 M,P SA+1ve + 4ve + ve Cured

Notes: BMA: Bone marrow aspiration, SA: Splenic aspiration, P/H: Past history, VL: Visceral Leishmaniasis, PKDL: Post-kala-azar dermal leishmaniasis, SAG: Sodium antimony gluconate, SDA: Single-dose AmBisome, Mil.: Miltefosine PS: Parasitic score, M: Macular, P: Papular, N: Nodular, M: Male, F: Female.

*

Each case was first treated for VL with single-dose AmBisome (10 mg/kg) and followed by Miltefosine (2.5 mg/kg/daily) 50 mg twice a day for 12 weeks for PKDL.