Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Manoj Kumar Chaudhuri"'
Autor:
Manoj Kumar Chaudhuri, Chhanda Datta, Uttara Chatterjee, Sandip Chatterjee, Shubhamitra Chaudhuri, Debashis Chakrabarty, Priyanka Maity Chaudhuri
Publikováno v:
Diagnostic Cytopathology. 45:270-273
Tanycytic ependymoma is a rare variant of ependymoma which has a predilection for the spinal cord. It is a WHO grade II tumour with favourable outcome. Although squash cytology of ependymoma is well described, there is sparse literature available on
Autor:
Uttara Chatterjee, Sugato Banerjee, Prafulla Kumar Mishra, Moumita Sengupta, Manoj Kumar Chaudhuri, Shabnam Parvin
Publikováno v:
Journal of Pediatric Surgery. 51:1072-1077
Background Gastric teratoma is a rare entity comprising less than 1% of germ cell tumors of childhood. We present a series of seven gastric teratomas with a review of literature. Objective To study the demographic profile, clinicopathological feature
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:
Priyanka Maity, Chaudhuri, Shubhamitra, Chaudhuri, Debashis, Chakrabarty, Sandip, Chatterjee, Chhanda, Datta, Manoj Kumar, Chaudhuri, Uttara, Chatterjee
Publikováno v:
Diagnostic cytopathology. 45(3)
Tanycytic ependymoma is a rare variant of ependymoma which has a predilection for the spinal cord. It is a WHO grade II tumour with favourable outcome. Although squash cytology of ependymoma is well described, there is sparse literature available on
Autor:
Uttara Chatterjee, Chhanda Datta, Prafulla Kumar Mishra, Moumita Sengupta, Sugato Banerjee, Manoj Kumar Chaudhuri, Paromita Roy, Nelofar Islam, Soutrik Das
Publikováno v:
Journal of pediatric surgery. 51(11)
Purpose Adrenocortical tumors (ACTs) are rare in pediatric age group. Pediatric ACTs behave differently from their histologically similar adult counterparts and Weiss criteria often cannot accurately predict their clinical behavior. Wieneke et al. pr
Autor:
Dilip Dutta, Sandip Chatterjee, Ranajoy Ghosh, Shatavisha Dasgupta, Uttara Chatterjee, Manoj Kumar Chaudhuri
Publikováno v:
Neurology India. 64:1365