Results 1 to 10 of about 24,360 (218)

Grading of Castleman Disease Histopathology with an Attention-Based Multiple Instance Learning Model [PDF]

open access: yesDiagnostics
Background/Objectives: Castleman disease is a rare cytokine-driven lymphoproliferative disorder in which lymph node histopathology provides key diagnostic information.
Muir J. Morrison   +29 more
doaj   +2 more sources

A Review of Genetic Abnormalities in Unicentric and Multicentric Castleman Disease

open access: yesBiology, 2021
Simple Summary Castleman disease is a rare hematopoietic disorder with a broad spectrum of clinical presentations. Different subtypes have been described based on how many lymph nodes are involved, histologic appearance, and associated viral infections ...
Kaushik Sridhar   +2 more
exaly   +2 more sources

Case report: A rare case of retroperitoneal mixed type unicentric Castleman disease [PDF]

open access: yesFrontiers in Oncology
ObjectiveTo enhance the understanding, diagnosis, and management of retroperitoneal mixed type unicentric Castleman disease.MethodsThis report describes a case of retroperitoneal mixed type unicentric Castleman disease managed at our institution.
Jiajie Zhang   +5 more
doaj   +2 more sources

Case of a young girl with marked bone marrow plasmacytosis

open access: yesSri Lanka Journal of Medicine, 2021
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

A national, multicenter, retrospective study of Castleman disease in China implementing CDCN criteria

open access: yesThe Lancet Regional Health - Western Pacific, 2023
Summary Background Castleman disease (CD) is a group of rare and heterogenous lymphoproliferative disorders including unicentric CD (UCD), human herpesvirus-8(HHV-8)-associated multicentric CD (HHV8-MCD), and HHV-8-negative/idiopathic multicentric CD ...
Lu Zhang   +41 more
semanticscholar   +1 more source

A model for crowdsourcing high-impact research questions for Castleman disease and other rare diseases

open access: yesOrphanet Journal of Rare Diseases, 2023
Background There are approximately 10,000 rare diseases that affect around 30,000,000 individuals in the U.S.A., most of which do not have an FDA-approved treatment.
Ania Korsunska   +3 more
doaj   +1 more source

Idiopathic multicentric Castleman disease: An update in diagnosis and treatment advances.

open access: yesBlood reviews, 2023
Idiopathic multicentric Castleman disease (iMCD) is a rare disease, and it is likely underdiagnosed because of the heterogeneity of clinical manifestations and laboratory findings.
E. Lang, F. van Rhee
semanticscholar   +1 more source

Unicentric form of Castleman´s disease, pitfalls of diagnosis and surgical treatment

open access: yesFrontiers in Oncology, 2023
Background Castleman´s disease is an extremely rare heterogenous lymphoproliferative pathology with a mostly benign behavior. It is a localized or generalized lymph node enlargement of an unknown aetiology.
J. Moláček   +9 more
semanticscholar   +1 more source

Castleman disease

open access: yesNature Reviews Disease Primers, 2021
Castleman disease (CD), a heterogeneous group of disorders that share morphological features, is divided into unicentric CD and multicentric CD (MCD) according to the clinical presentation and disease course.
A. Carbone   +7 more
semanticscholar   +1 more source

The application of a multidisciplinary approach in the diagnosis of Castleman disease and Castleman‐like lymphadenopathies: A 20‐year retrospective analysis of clinical and pathological features

open access: yesBritish Journal of Haematology, 2023
Castleman disease (CD) comprises a group of rare and heterogeneous haematological disorders, including unicentric (UCD) and multicentric (MCD) forms, the latter further subdivided into HHV8‐MCD, POEMS‐MCD and idiopathic‐MCD (iMCD).
S. Pelliccia   +20 more
semanticscholar   +1 more source

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