نتایج جستجو برای: lymphoproliferative disorder

تعداد نتایج: 601094  

ژورنال: Hormozgan Medical Journal 2011
Abdi, N, Mohammadi, K, Molavi, M.A, Nazemi, A.M,

Introduction: Chediak-Higashi syndrome is a rare autosomal recessive disorder that characterized by severe immunodeficiency. It is also associated with a lymphoproliferative disorder termed the accelerated phase with lymphocytic infiltration of the major organ of the body. Case Report: The patients was a 1-year old boy with intermittent fever, anorexia, malaise. On physical examination h...

2018
Faisal Inayat Ghias Ul Hassan Ghias Un Nabi Tayyab Muhammad Wasif Saif

Post-transplantation lymphoproliferative disorders (PTLDs) are lymphoid proliferations or lymphomas that are the second most common tumors in adult transplant recipients. Most cases of PTLD are attributed to Epstein-Barr virus, which induces B-cell proliferation and occurs in the setting of severe immunosuppression after solid organ or bone marrow transplantation. The disorder is seen in 1-3% o...

Journal: :Journal of the College of Physicians and Surgeons--Pakistan : JCPSP 2010
Raana Akhtar Noshin Wasim Yusuf Shahzada Khalid Iram Nadeem Rahat Sarfaraz Muhammad Imran

Posttransplantation lymphoproliferative disorders (PTLD) are lymphoid proliferations or lymphomas that develop as a result of immunosuppression in recipients of solid organs and bone marrow allografts. The disorder is seen in 1-2% of renal transplant recipients with a variable time period of presentation and is usually seen within the first year following transplantation. We report a case of B-...

Journal: :Journal of immunology 2009
Cristel Archambaud Amandine Sansoni Michael Mingueneau Elisabeth Devilard Georges Delsol Bernard Malissen Marie Malissen

Mutant mice in which tyrosine 136 of linker for activation of T cells (LAT) was replaced with a phenylalanine (Lat(Y136F) mice) develop a lymphoproliferative disorder involving polyclonal CD4 effector T cells that produce massive amounts of IL-4 and trigger severe Th2 inflammation. Naive CD4 T cells can themselves produce IL-4 and thereby initiate a self-reinforcing positive regulatory loop tha...

Journal: :Blood 1987
W J Miller R S Shapiro R Gonzalez-Sarmiento J H Kersey

Chronic myelocytic leukemia (CML) may display a lymphoproliferative phase (lymphoid blast crisis) that is generally of B cell phenotype. Since lymphoproliferative disorders may occur following bone marrow transplantation (BMT), it may be difficult to distinguish posttransplant relapse of CML lymphoid blast crisis from de novo lymphoproliferation. Lymphoid blast crisis cells from a patient with ...

Journal: :iranian red crescent medical journal 0
bita geramizadeh department of pathology, shiraz university of medical sciences, iran +98-711-6474331, [email protected]; department of pathology, shiraz university of medical sciences, iran +98-711-6474331, [email protected] sama nikeghbalian department of hepatobiliary surgery, transplant research center, shiraz university of medical sciences, iran seyed mohsen dehghani department of pediatrics, shiraz university of medical sciences, iran ali bahador department of pediatric surgery, transplant research center, shiraz university of medical sciences, iran heshmatollah salahi department of surgery, transplant research center, shiraz university of medical sciences, iran

post-transplant lymphoproliferative disorder is a lymphocyte proliferating disease, usually of b cell origin, and rarely of t cell. involvement of liver itself in liver transplant recipients as the primary organ is not common. herein we report our experience in two patients who primarily presented in the allografted liver, both of whom were promptly diagnosed after liver biopsy and treated succ...

Journal: :Pediatrics 2001
M H Collins K T Montone A M Leahey R L Hodinka K E Salhany D A Belchis J E Tomaszewski

OBJECTIVES Posttransplant lymphoproliferative disorder (PTLD) causes significant morbidity and mortality, is related to Epstein-Barr virus (EBV) infection, and is more common in children than in adults. We reviewed autopsies of children who died with PTLD to compare postmortem with antemortem PTLD histology, to assess the extent of PTLD, to document associated pathology, and to identify cause o...

Journal: :Arquivos brasileiros de cardiologia 2006
Paulo Manuel Pêgo Fernandes Estela Azeka Vicente Odoni Jader Joel Machado Junqueira Gabriella Paiva Bento Vera Aiello Miguel Barbero-Marcial

Immunosuppressive therapy for transplanted patients exposes them to a high risk of developing posttransplantation lymphoproliferative disorders (PTLD). We report the case of a child undergoing heart transplantation at seven months of age who developed PTLD at nine years of age, diagnosed by resection of a pulmonary nodule.

Journal: :Haematologica 1994
R Invernizzi

A 65-year-old male patient was admitted who had been suffering for some months from weakness and sensory alterations of the legs, with difficulty in walking. At physical examination pallor, hepatomegaly and splenomegaly (6 cm below the costal margin) were found; there was no lymphadenopathy. Laboratory findings showed anemia (Hb 8.3 g/dL), leucocytosis (WBC 42.3u10/L), normal platelet count (23...

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