Results 41 to 50 of about 6,197,685 (170)

Possible roles of Epstein-Barr virus in Castleman disease

open access: yesJournal of Cardiothoracic Surgery, 2009
Background Complete resection seemed to be curative in patients with Castleman disease of any location but the disease is likely to be reactive in its pathogenesis. The relation between Epstein-Barr virus and Castleman disease has not been elucidated. We
Liu Hung-Chang   +3 more
doaj   +1 more source

Early tocilizumab and outcomes in acute necrotizing encephalopathy

open access: yesDevelopmental Medicine &Child Neurology, EarlyView.
Early tocilizumab and outcome in acute necrotising encephalopathy. Aim To evaluate the timing and safety of tocilizumab in acute necrotizing encephalopathy (ANE). Method This was a multicentre retrospective study evaluating outcomes (modified Rankin Scale [mRS]) in children with ANE treated with tocilizumab. A logistic regression model determined a cut‐
Velda X Han   +14 more
wiley   +1 more source

CASTLEMAN DISEASE – A RARE CASE REPORT

open access: yes, 2018
<p>Castleman disease (CD) is a rare disease of lymph nodes and related tissues.It was first described by Dr. Benjamin Castleman in the 1950s. It is also known as Castleman’s disease, giant lymph node hyperplasia<em>, </em ...
Dr.Manaswinee Sahoo*, Dr Sunil Kumar Agarwalla, Dr.Soumya Ranjan Samal & Dr.Upasna Jhunjhunwala
core   +1 more source

Examining the Interaction of Genes and Epidemiology on Castleman Disease [PDF]

open access: yes, 2022
Castleman Disease is a rare disorder in which a person experiences an overgrowth of cells in the lymph nodes. Research on Castleman Disease is, at the moment, very elementary due to the lack of patient population size and previous research.
Sarabia, Julia   +5 more
core   +1 more source

Castleman disease. A rare clinical case of retroperitoneal tumor localization in an elderly patient

open access: yesActa Biomedica Scientifica, 2023
Castleman disease is an extremely rare benign disease of the lymphatic system with an estimated incidence of 1–9 cases per 1,000,000. Its etiology remains unknown; interleukin 6 (IL-6) plays an important role in pathogenesis.
M. B. Polyanskiy   +3 more
doaj   +1 more source

Charting the course of Sjögren's disease: A historical analysis of scientific progress

open access: yesEuropean Journal of Oral Sciences, EarlyView.
Abstract Sjögren's disease (SjD) bears the name of the Swedish ophthalmologist Henrik Sjögren. His 1933 doctoral thesis on keratoconjunctivitis sicca ignited interest, yet much remains under debate. SjD is an autoimmune disorder that primarily affects the exocrine glands, particularly the salivary and lacrimal glands, leading to a dryness of the eyes ...
Diego Ustárroz Cantali   +3 more
wiley   +1 more source

When idiopathic retroperitoneal fibrosis mimics Castleman disease: a challenging differential diagnosis

open access: yes, 2022
Idiopathic retroperitoneal fibrosis (I-RPF) can occur either in the spectrum of IgG4-related disease or as a non-IgG4-related form. I-RPF, especially the IgG4-related forms, can sometimes mimic clinically and/or histologically Castleman disease; to ...
Paolo Graziano   +7 more
core   +1 more source

Comparison of intestinal histopathological changes following teclistamab, BCMA‐directed CAR T, CD19‐directed CAR T and rituximab therapies

open access: yesHistopathology, EarlyView.
This is a retrospective review of intestinal tract biopsies from patients treated with various cellular immunotherapies (BCMA and CD19‐directed CAR T, teclistamab and rituximab therapies). We found distinct but overlapping histologic patterns across treatment groups, with lamina propria plasma cell depletion, crypt apoptotic bodies and active ...
Olivia J Leung   +7 more
wiley   +1 more source

Idiopathic multicentric Castleman disease: A case report

open access: yesAsian Journal of Medical Sciences
Castleman disease is a rare disease affecting lymph nodes and is considered a non-clonal lymphoproliferative disorder. It has variable clinical presentation and is divided into clinical and histopathological subtypes.
Anna John , Sheima R Das
doaj   +1 more source

Single‐centre analysis of severe Coombs‐positive autoimmune haemolytic anaemia in an HIV‐endemic population

open access: yesHIV Medicine, EarlyView.
Abstract Introduction Human immunodeficiency virus (HIV) is a rare cause of autoimmune haemolytic anaemia (AIHA) which requires prompt diagnosis and treatment. We compared clinical and laboratory findings in AIHA patients with and without HIV. Methods We included adults with severe AIHA (haemoglobin ≤8 g/dL) diagnosed at a tertiary academic centre ...
Kathleen O. De John   +4 more
wiley   +1 more source

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