Results 51 to 60 of about 6,197,685 (170)

Castleman disease [PDF]

open access: yes, 2005
Castleman disease or giant lymph node hyperplasia, is a rare disorder that is located most commonly in the visceral mediastinum. We report a Castleman disease represented with hilar lymph node hyperplasia. Diagnosis and treatment of this rare disorder is

core  

Castleman Disease

open access: yes, 2018
HIV-negative Castleman disease has been associated with autoimmune disease, collagen vascular disorders, pulmonary arterial hypertension, and ...
Zhou, Jing, Hu, Amanda, Cohn, Jason E
core   +1 more source

AustrAIHANZ – consensus guidelines on the investigation and management of autoimmune haemolytic anaemia in Australia and New Zealand

open access: yesInternal Medicine Journal, EarlyView.
Abstract Autoimmune haemolytic anaemia is a rare immune‐mediated disorder leading to accelerated red cell destruction and anaemia. There is considerable clinical heterogeneity, with some patients barely requiring intervention, while others experience fulminant haemolysis and experience mortality rates as high as 30% with severe anaemia and end‐organ ...
Philip Choi   +9 more
wiley   +1 more source

Lumps, Bumps, and Diagnostic Stumps: A Case Report of IgG4‐Related Disease

open access: yesClinical Case Reports, Volume 14, Issue 11, November 2026.
ABSTRACT IgG4‐related disease and idiopathic multicentric Castleman disease are rare conditions that can present with overlapping features, complicating diagnosis and delaying proper treatment.
Michael Miller   +4 more
wiley   +1 more source

Castleman disease of childhood: A case report

open access: yes, 2001
Giant lymph node hyperplasia (Castleman disease) is uncommon in children and rare in infancy. A 9-month-old girl with a left cervical mass, was followed up for six months.
Filiz Bolat   +4 more
core   +1 more source

A Rare Lymphoproliferative Disease: Castleman Disease

open access: yesTurkish Journal of Hematology, 2021
Castleman disease is a rare lymphoproliferative disease also known as angiofollicular lymph node hyperplasia. It is classified as hyaline vascular and plasmacytic variants histologically but characteristics of both types can coexist.
Eren Gündüz   +3 more
doaj   +1 more source

Neutrophils: Heterogeneity, Biology, Diseases, and Therapeutic Strategies

open access: yesMedComm, Volume 7, Issue 11, November 2026.
Neutrophils exhibit remarkable functional plasticity and play dual roles in tissue protection and disease progression. This review summarizes their key biological functions and highlights the shift from conventional broad‐spectrum interventions to neutrophil‐based drug delivery systems.
Yibing Zhang   +4 more
wiley   +1 more source

POEMS Syndrome: 2026 Update on Diagnosis, Risk‐Stratification, and Management

open access: yesAmerican Journal of Hematology, Volume 101, Issue 10, Page 2632-2651, October 2026.
ABSTRACT Disease Overview POEMS syndrome is a life‐threatening syndrome due to an underlying plasma cell neoplasm. The major criteria for the syndrome are polyneuropathy, clonal plasma cell disorder (PCD), sclerotic bone lesions, elevated vascular endothelial growth factor, and the presence of Castleman disease.
Angela Dispenzieri
wiley   +1 more source

2007-2008 Charles Castleman (Violin) [PDF]

open access: yes, 2007
Charles Castleman Master Class (October 7, 2007 ...
Lin, Tao, Castleman, Charles
core  

Myasthenia gravis with Castleman disease: A case report with review of literature

open access: yesIndian Journal of Pathology and Microbiology
Myasthenia gravis is an autoimmune disorder caused by the formation of autoantibodies directed against the synapses of neuromuscular junction. It is most commonly associated with other non-thymomatous lesions. Castleman disease is one of them, which is a
Sujit Nandy   +3 more
doaj   +1 more source

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