Results 41 to 50 of about 2,889 (110)
Neutrophils acquire extracellular fatty acids or adipocyte‐derived lipids and store them as triglycerides, polarizing into a lipid‐laden phenotype. Lipid‐laden neutrophils are found in the peripheral blood of HFD‐fed mice and patients with MASLD. These neutrophils release extracellular vesicles enriched with triglycerides and microRNAs that deliver ...
Sanjeeb Shrestha +10 more
wiley +1 more source
General anesthesia in a patient with multicentric Castleman's disease: a case report [PDF]
Castleman's disease (CD) is a rare lymphoproliferative disorder of undetermined etiology. Unicentric Castleman's disease is confined to a single lymph node; it is usually asymptomatic though sometimes has local manifestations related to mass effects.
Hee Won Son +5 more
doaj +1 more source
Cytoplasmic aggregation of TDP‐43 is a common pathological feature in amyotrophic lateral sclerosis, frontotemporal lobar degeneration, and Alzheimer's disease with TDP‐43 pathology. This study reports that wild‐type PDI slows down phase separation of TDP‐43 through direct interaction with TDP‐43.
Jia‐Qi Liu +14 more
wiley +1 more source
Castleman's disease in an adolescent
Castleman’s disease is a clinic-pathological entity of unknown etiology with non–neoplastic lymph node hyperplasia. It is extremely rare and can be found in patients of all age groups.
Ujjwala Singh +3 more
doaj +1 more source
Castleman’s disease: A report of two cases at a tertiary hospital in Northern Tanzania
Castleman’s disease is a rare lympho-proliferative disease entity characterized by variable clinical presentations, distinctive histological manifestations, and prognosis. Its incidence and etiology are unclear.
Alex Mremi +4 more
doaj +1 more source
ABSTRACT Refractory oral erosions or polymorphous eruptions should prompt evaluation for paraneoplastic pemphigus, particularly when associated with mediastinal masses. Early tumor excision, multidisciplinary care, and vigilant monitoring for bronchiolitis obliterans are essential to improve outcomes in Castleman disease–associated paraneoplastic ...
Ayaan Sohail, Jessica Evans, Mika Tabata
wiley +1 more source
Immunophenotypic characteristics of plasma cells in POEMS syndrome
Abstract To analyze the immunophenotypic characteristics of plasma cells in patients with polyneuropathy, organomegaly, endocrinopathy, myeloma protein, and skin changes (POEMS) syndrome. This retrospective study included patients with POEMS syndrome hospitalized in the Department of Hematology, Huashan Hospital, from September 2017 to August 2025 ...
Zhenhua Wang +6 more
wiley +1 more source
ABSTRACT The Kaposi Sarcoma herpesvirus (KSHV) causes Kaposi sarcoma (KS), primary effusion lymphoma, a lymphoproliferative disease (KSHV‐multicentric Castleman's disease), and a cytokine inflammatory syndrome (KICS). These diseases occur more frequently, though not exclusively, among people living with HIV or other types of immune dysregulation. While
Julian Naipauer +10 more
wiley +1 more source
Unusual Presentation of Abdominal Castleman's Disease
Castleman's disease is a rare lymphoproliferative disorder of uncertain origin. We report an unusual presentation of Castleman's disease in the transverse mesocolon that mimicked a vascular gastrointestinal stromal tumour and review the literature ...
W.L.E. Chuwa, H.S. Ong
doaj +1 more source
Multisystem IgG4‐RD can closely mimic metastatic malignancy and should be considered when thoracic and extrapulmonary mass‐forming lesions coexist. Timely biopsy confirmation is essential to avoid misdiagnosis and treatment delay. ABSTRACT IgG4‐related disease (IgG4‐RD) is a multisystem fibroinflammatory condition that can mimic metastatic malignancy ...
Ho Young Lee, Juyeon Kang
wiley +1 more source

