Polymorphic PTLD
نویسندگان
چکیده
منابع مشابه
PTLD risk and IFNG polymorphisms
First, we would like to thank Thomas and colleagues for their interest in our work, their provision of additional data, and their commentary regarding genotyping studies and clinical posttransplantation lymphoproliferative disorder (PTLD). A central component of our prospective preclinical study using the human peripheralblood leukocyte severe combined immunodeficient (hu PBL SCID) mouse model ...
متن کاملTreatment of PTLD with rituximab or chemotherapy.
Information regarding treatment of post-transplant lymphoproliferative disease (PTLD) beyond reduction in immunosuppression (RI) is limited. We retrospectively evaluated patients receiving rituximab and/or chemotherapy for PTLD for response, time to treatment failure (TTF) and overall survival (OS). Thirty-five patients met inclusion criteria. Twenty-two underwent rituximab treatment, with over...
متن کاملPTLD Burkitt Lymphoma in a Patient with Remote Lymphomatoid Granulomatosis
Posttransplant lymphoproliferative disorder (PTLD) is a potentially fatal complication of solid organ transplantation. The majority of PTLD is of B-cell origin, and 90% are associated with the Epstein-Barr virus (EBV). Lymphomatoid granulomatosis (LG) is a rare, EBV-associated systemic angiodestructive lymphoproliferative disorder, which has rarely been described in patients with renal transpla...
متن کاملPost Transplantation Lymphoproliferative Disorder (PTLD) Presenting as Biliary Duct Obstruction
After adult liver transplantation (LT), post-transplant lymphoproliferative disorder (PTLD) is an uncommon but serious complication of immunosuppression (IMS) in presence of an acute or latent EBV infection. The clinical presentation of this disease is aspecific, and, after LT, it may mimic anastomotic bile duct stricture. We report the cases of 2 adult patients who developed, 3 months and 8 ye...
متن کاملPolymorphic cutaneous sarcoidosis: A case report
Sarcoidosis (Besnier-Boeck-Schaumann disease) is a multisystem disease of unknown etiology with various cutaneous presentations. It is characterized by the presence of non-caseating ‘naked’ granulomas in the affected tissue. We report a case of polymorphic cutaneous sarcoid in a 39-year-old immunocompetent male. He was visited at our outpatient department with multiple asymptomatic red colored ...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Atlas of Genetics and Cytogenetics in Oncology and Haematology
سال: 2018
ISSN: 1768-3262
DOI: 10.4267/2042/68903