Results 31 to 40 of about 6,363 (176)

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

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

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

CT of Castleman disease in the mediastinum

open access: yesRadiology Case Reports, 2023
Castleman disease is a rare lymphoproliferative disease commonly occurring as a benign localized mass of lymph nodes in the mediastinum. Given that Castleman disease presents as asymptomatic or through non-specific thoracic symptoms, detection is ...
Elias Lugo-Fagundo, BS   +3 more
doaj   +1 more source

Overview of Castleman disease [PDF]

open access: yesBlood, 2020
AbstractCastleman disease (CD) describes a group of at least 4 disorders that share a spectrum of characteristic histopathological features but have a wide range of etiologies, presentations, treatments, and outcomes. CD includes unicentric CD (UCD) and multicentric CD (MCD), the latter of which is divided into idiopathic MCD (iMCD), human herpes virus-
David C. Fajgenbaum, Angela Dispenzieri
openaire   +2 more sources

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

Localized Plaques on the Scalp as Initial Presentation of Multicentric Plasmacytic Castleman Disease

open access: yesClinical, Cosmetic and Investigational Dermatology, 2022
Heng Zhang, Kun Li, Jianzhong Zhang, Xue Chen Department of Dermatology, Peking University People’s Hospital, Beijing, People’s Republic of ChinaCorrespondence: Xue Chen, Department of Dermatology, Peking University People’s Hospital, # 11.
Zhang H, Li K, Zhang J, Chen X
doaj  

Retroperitoneal Castlemans Disease associated with Paraneoplastic Pemphigus

open access: yesHematology/Oncology and Stem Cell Therapy, 2014
Paraneoplastic pemphigus is a rare dermatologic condition that can occur as a paraneoplastic manifestation of lymphoproliferative disorders, visceral malignancies, Castleman disease and thymomas.
Naseer A Choh   +5 more
doaj   +1 more source

Castleman's Disease of the Neck

open access: yesActa Otorrinolaringologica (English Edition), 2007
Castleman's disease is an uncommon benign lymphoid disorder usually found in the mediastinum (70 %) which is thought to be due to antigenic hyperstimulation of unknown origin. Two histological subtypes may be found in relation to two different clinical patterns with clinical and therapeutic implications.
Enrique, Coscarón Blanco   +4 more
openaire   +4 more sources

Castleman disease of plasma cell type accompanied with bronchiolitis obliterans: a case report and review of the literature

open access: yesJournal of Medical Case Reports, 2023
Background Castleman disease, also known as giant lymph node hyperplasia or angiofollicular lymph node hyperplasia, is a highly heterogeneous clinicopathological entity that belongs to the family lymphoproliferative disorders.
Qingyuan Zhu, Shuiyou Wang
doaj   +1 more source

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