Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Janki Bisht"'
Autor:
Janki Bisht, Akshay Prasad
Publikováno v:
INTERNATIONAL JOURNAL OF SCIENTIFIC RESEARCH. :1-3
The purpose of this study is to compare between the efficacy of Bleomycin and Sodium tetra decyl sulphate as intralesional sclerotherapy for lymphangioma. Materials and methods- This prospective study was done between Jan 2018 to Jan 2020. Total of 3
Autor:
Uttara Chatterjee, Janki Bisht, Suvrendu Kar, Avijit Mitra, Ram Narayan Das, Banhisikha Kanjilal, Moupali Ghosh
Publikováno v:
Diagnostic Cytopathology. 46:1064-1067
Adrenocortical carcinoma (ACC) is a rare tumour, which sometimes affects pediatric age group. Fine needle aspiration cytology (FNAC) is a rarely performed technique in adrenal cortical tumours. There is sparse literature available describing the cyto
Autor:
Indranil Das, Ram Narayan Das, Janki Bisht, Bibhas Saha Dalal, Banhishikha Kanjilal, Uttara Chatterjee
Publikováno v:
Diagnostic Cytopathology. 45:761-765
Clear cell sarcoma of kidney (CCSK) is a rare aggressive malignant renal neoplasm with a high metastatic potential. Its outcome has however, improved with the advent of doxorubicin based neoadjuvant chemotherapy. Here, we present two cases of CCSK in
Autor:
Janki Bisht, Ram Narayan Das, Manoj Kumar Chaudhuri, Mamata Guha Mallick, Uttara Chatterjee, Goutam Bera, Chhanda Datta, Prafulla Kumar Mishra
Publikováno v:
Diagnostic Cytopathology. 44:823-827
Congenital mesoblastic nephroma (CMN) is a rare pediatric renal neoplasm, occurring most commonly in the first few months of life, with a favourable clinical outcome. Accurate pre-operative cytological diagnosis of this entity is important as pre-ope
Autor:
Indranil, Das, Ram Narayan, Das, Bibhas Saha, Dalal, Janki, Bisht, Banhishikha, Kanjilal, Uttara, Chatterjee
Publikováno v:
Diagnostic cytopathology. 45(8)
Clear cell sarcoma of kidney (CCSK) is a rare aggressive malignant renal neoplasm with a high metastatic potential. Its outcome has however, improved with the advent of doxorubicin based neoadjuvant chemotherapy. Here, we present two cases of CCSK in