Primary melanocytic tumours of the uterine cervix are rare. These include blue nevi and malignant melanoma. Blue nevi are benign melanocytic lesions which occur as incidental finding. Primary cervical melanomas are ra...Primary melanocytic tumours of the uterine cervix are rare. These include blue nevi and malignant melanoma. Blue nevi are benign melanocytic lesions which occur as incidental finding. Primary cervical melanomas are rare mucosal melanomas with aggressive behaviour. In small biopsies, they can mimic poorly differentiated carcinomas. Here we present the cases of melanocytic tumours reported from our institute during the last 6 years展开更多
Post transplantation lymphoproliferative disorder is a lymphoid/plasmacytic proliferation that develops as a consequence of immunosuppression in a recipient of a solid organ/bone marrow/stem cell allograft. The incide...Post transplantation lymphoproliferative disorder is a lymphoid/plasmacytic proliferation that develops as a consequence of immunosuppression in a recipient of a solid organ/bone marrow/stem cell allograft. The incidence reported in literature in post liver transplant patients is 1% - 2%. This case was of a 16-year-old boy who underwent liver transplantation for fulminant hepatic failure and subsequently developed PTLD. Morphologically and immunohistochemically, it was Hodgkin’s lymphoma like PTLD, which was the least common type reported in literature.展开更多
文摘Primary melanocytic tumours of the uterine cervix are rare. These include blue nevi and malignant melanoma. Blue nevi are benign melanocytic lesions which occur as incidental finding. Primary cervical melanomas are rare mucosal melanomas with aggressive behaviour. In small biopsies, they can mimic poorly differentiated carcinomas. Here we present the cases of melanocytic tumours reported from our institute during the last 6 years
文摘Post transplantation lymphoproliferative disorder is a lymphoid/plasmacytic proliferation that develops as a consequence of immunosuppression in a recipient of a solid organ/bone marrow/stem cell allograft. The incidence reported in literature in post liver transplant patients is 1% - 2%. This case was of a 16-year-old boy who underwent liver transplantation for fulminant hepatic failure and subsequently developed PTLD. Morphologically and immunohistochemically, it was Hodgkin’s lymphoma like PTLD, which was the least common type reported in literature.
