Results 41 to 50 of about 1,106,155 (263)
Does breast implant-associated ALCL begin as a lymphoproliferative disorder?
Breast implant-associated anaplastic large cell lymphoma (BIA-ALCL) has been included as a provisional entity in the revised version of the World Health Organization Classification of Tumors of Haematopoietic and Lymphoid Tissue.
Inghirami G. +3 more
core +1 more source
Increased Pediatric Head and Neck Abscesses Following the COVID‐19 Pandemic
This study evaluated the impact of the COVID‐19 pandemic on pediatric head and neck abscesses at two tertiary care centers. Overall head and neck abscess incidence increased more than threefold in the post‐pandemic period compared with the pre‐pandemic period, with increases observed across all major abscess subtypes.
Marco DiBlasi +4 more
wiley +1 more source
A case of posttransplant lymphoproliferative disorder
Posttransplant lymphoproliferative disorders (PTLDs) are life-threatening complications of solid-organ and bone marrow transplantations leading to a high mortality. PTLD represents a heterogeneous group of lymphoproliferative diseases.
G S Chowdhary +2 more
doaj +1 more source
An aggressive extranodal NK-cell lymphoma arising from indolent NK-cell lymphoproliferative disorder
Indolent NK-cell lymphoproliferative disorder, also known as chronic natural killer (NK) cell large granular lymphocytosis (leukemia), is a very rare entity in the World Health Organization (WHO) Classification of Tumors of Hematopoietic & Lymphoid ...
Weiss, Lawrence M. +3 more
core +1 more source
Abstract Objective To evaluate differences in clinicopathological characteristics, treatment strategies, and oncological outcomes between preoperatively diagnosed and undiagnosed major salivary gland cancers (MSGCs). Study Design Retrospective cohort study. Setting A single tertiary academic hospital. Methods Surgically confirmed MSGCs between 2012 and
Dongbin Ahn +4 more
wiley +1 more source
Post-transplant lymphoproliferative disorder (PTLD) is a heterogeneous spectrum of lymphoproliferative disorders that can develop in the setting of immunosuppression following transplant.
Taylor Viggiano +4 more
doaj +1 more source
Diagnosis and Management of Prenatal Hereditary Pyropoikilocytosis
ABSTRACT Hereditary pyropoikilocytosis (HPP) is a severe hemolytic anemia caused by variants in SPTA1, SPTB, and EPB41. These weaken horizontal interactions in the erythrocyte cytoskeleton, causing membrane fragmentation and splenic sequestration. It will readily cause fetal anemia and often hydrops fetalis. Prenatal diagnosis requires first ruling out
Connor Hartzell +6 more
wiley +1 more source
Case of a young girl with marked bone marrow plasmacytosis
Marked plasmacytosis in the bone marrow is a rare finding in young people. If present it is secondary to an underlying disease condition. Castleman disease is a rare form of lymphoproliferative disorder. Due to its rarity, it is not frequently considered
V. C. Panditha Gunwardena +4 more
doaj +1 more source
Case series: Kikuchi‐Fujimoto disease with diagnostic overlap
Kikuchi‐Fujimoto disease (KFD) is a rare, self‐limiting necrotizing lymphadenitis that poses significant diagnostic challenges due to its overlap with tuberculosis, systemic lupus erythematosus (SLE), and malignancy. We present four cases highlighting distinct diagnostic complexities: KFD mimicking tuberculosis with concomitant latent TB infection and ...
Ecem Kalemoglu +6 more
wiley +1 more source
Posttransplant Lymphoproliferative Disorder With Lung Involvement in a Renal Transplant Recipient
Posttransplant lymphoproliferative disorder is one of the most important complications of solid-organ transplant in terms of malignancy. Here, we report a case of Epstein-Barr-virus-negative posttransplant lymphoproliferative disorder of T-cell type ...
AKYÜREK, NALAN +7 more
core +2 more sources

