Background: Post-transplant lymphoproliferative disorder (PTLD) is a complication of solid organ and allogeneic hematopoietic stem cell transplantation (HSCT); following autologous HSCT only rare cases of PTLD have been reported. Here, a case of Hodgkin's disease (HD), as unusual presentation of PTLD after autologous HSCT for malignant glioma is described. Case presentation: 60-years old man affected by cerebral anaplastic astrocytoma underwent subtotal neurosurgical excision and subsequent high-dose chemotherapy followed by autologous HSCT. During the post HSCT course, cranial irradiation and corticosteroids were administered as completion of therapeutic program. At day + 105 after HSCT, the patient developed HD, nodular sclerosis type, with polymorphic HDlike skin infiltration. Conclusion: The clinical and pathological findings were consistent with the diagnosis of PTLD.
Zambelli, A., Lilleri, D., Baldanti, F., Scelsi, M., Villani, L., Da Prada, G. (2005). Hodgkin's disease as unusual presentation of post-transplant lymphoproliferative disorder after autologous hematopoietic cell transplantation for malignant glioma. BMC CANCER, 5(1) [10.1186/1471-2407-5-109].
Hodgkin's disease as unusual presentation of post-transplant lymphoproliferative disorder after autologous hematopoietic cell transplantation for malignant glioma
Zambelli, Alberto;
2005
Abstract
Background: Post-transplant lymphoproliferative disorder (PTLD) is a complication of solid organ and allogeneic hematopoietic stem cell transplantation (HSCT); following autologous HSCT only rare cases of PTLD have been reported. Here, a case of Hodgkin's disease (HD), as unusual presentation of PTLD after autologous HSCT for malignant glioma is described. Case presentation: 60-years old man affected by cerebral anaplastic astrocytoma underwent subtotal neurosurgical excision and subsequent high-dose chemotherapy followed by autologous HSCT. During the post HSCT course, cranial irradiation and corticosteroids were administered as completion of therapeutic program. At day + 105 after HSCT, the patient developed HD, nodular sclerosis type, with polymorphic HDlike skin infiltration. Conclusion: The clinical and pathological findings were consistent with the diagnosis of PTLD.| File | Dimensione | Formato | |
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