Results 41 to 50 of about 24,360 (218)

Doppler findings In castleman disease - A rare case

open access: yesIndian Journal of Radiology and Imaging, 2006
Castleman′s disease is a rare, benign disease of unknown cause that induces reactive lymph node hyperplasia. It has two histologic subtypes: hyaline vascular and plasma cellular. A definitive diagnosis necessitates tissue biopsy.
S Raniga   +4 more
doaj   +1 more source

Expert Perspective: Diagnosis and Treatment of Castleman Disease

open access: yesArthritis & Rheumatology
Castleman disease (CD) is a major diagnostic challenge for rheumatologists. Unicentric CD (UCD) involves one enlarged lymph node region, whereas multicentric CD (MCD) involves multiple enlarged lymph node regions.
Lu-Ke Y. C. Chen   +2 more
semanticscholar   +1 more source

Multicentric Castleman disease and the evolution of the concept

open access: yesPathologica, 2021
Summary The term multicentric Castleman disease (MCD) encompasses a spectrum of conditions that share some overlapping clinicopathological manifestations.
Ting Zhou   +3 more
semanticscholar   +1 more source

Idiopathic multicentric Castleman disease (iMCD)-idiopathic plasmacytic lymphadenopathy: A distinct subtype of iMCD-not otherwise specified with different clinical features and better survival

open access: yesBritish Journal of Haematology
Idiopathic multicentric Castleman disease (iMCD) is subclassified into iMCD‐thrombocytopenia, anasarca, reticulin fibrosis, renal dysfunction, organomegaly (TAFRO) and iMCD‐not otherwise specified (NOS) according to the Castleman Disease Collaborative ...
Yu-Han Gao   +6 more
semanticscholar   +1 more source

Bilateral orbital Castleman disease: Building castles around the eye

open access: yesIndian Journal of Ophthalmology. Case Reports
Castleman disease is a rare, benign, clinicopathological entity associated with lymphoproliferation. Orbital Castleman disease is an even rarer condition, with multicentric involvement of the orbit being exceptionally uncommon. We report the case of a 61-
Anna Kurian Mullasseril   +5 more
doaj   +1 more source

Castleman disease mimicking an adrenal tumor: A case report

open access: yesUrology Case Reports, 2022
Castleman disease is a benign complex lymphoproliferative disease. The most common site is the mediastinum. In this paper, we present a case of Castleman disease in the adrenal gland, as a very rare region.A 29-year-old woman was referred to our clinic ...
Robab Maghsoudi   +3 more
doaj   +1 more source

International, evidence-based consensus treatment guidelines for idiopathic multicentric Castleman disease.

open access: yesBlood, 2018
Castleman disease (CD) describes a group of heterogeneous hematologic disorders with characteristic histopathological features. CD can present with unicentric or multicentric (MCD) regions of lymph node enlargement.
Fritz Van Rhee   +41 more
semanticscholar   +1 more source

Castleman disease: A single-center case series

open access: yesInternational journal of surgery case reports, 2021
Highlights • Castleman disease is an overgrowth of lymphatic cells, usually in the chest or abdomen.• Multicentric Castleman disease affects lymphatic cells throughout the body.• HHV-8 and HIV have been associated with multicentric Castleman disease ...
K. Pribyl   +7 more
semanticscholar   +1 more source

Unicentric Castleman Disease and Pheochromocytoma [PDF]

open access: yes, 2022
Castleman disease is an uncommon and heterogenous lymphoproliferative disorder which is classified as unicentric or multicentric depending on the number of lymph nodes involved. Each type has a different clinical presentation,
Maia, Rosana   +9 more
core   +1 more source

A Rare Case of Castleman Variant of POEMS Syndrome

open access: yesJournal of the Indian Academy of Geriatrics
POEMS syndrome is a rare multisystemic disease, characterized by polyneuropathy, organomegaly, endocrinopathy, monoclonal protein, and skin changes. The presence of polyneuropathy and monoclonal plasma cell proliferation is mandatory for the diagnosis of
Gevesh Chand Dewangan   +3 more
doaj   +1 more source

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