Results 11 to 20 of about 26,630,094 (175)

Castleman′s disease: Hyaline vascular type

open access: yesMedical Journal of Dr. D.Y. Patil University, 2014
Castleman′s disease is a rare disease of lymph node with two identified forms, the hyaline vascular type and plasma cell type. It presents as localized or systemic lymphadenopathy or even as extranodal mass and may give rise to several differential ...
Srikanth Shastry, Anandam Gadda
doaj   +2 more sources

Cytodiagnosis of Castleman′s disease: A diagnostic challenge

open access: yesMuller Journal of Medical Sciences and Research, 2016
Castleman′s disease (CD) is an uncommon cause of solitary or multiple lymphadenopathy, which may be a target for fine-needle aspiration (FNA). Because of its rarity and lack of adequate literature available on its cytomorphological findings, the ...
Muktha R Pai   +2 more
doaj   +2 more sources

Retinal vein occlusion during flare of multicentric Castleman's disease

open access: yesClinical Ophthalmology, 2013
Igor Kozak,1,2 Erin G Reid31King Khaled Eye Specialist Hospital, Riyadh, Kingdom of Saudi Arabia; 2University of California San Diego, Jacobs Retina Center at the Shiley Eye Center, La Jolla, CA, USA; 3University of California San Diego, Moores Cancer ...
Kozak I, Reid EG
doaj   +1 more source

A rare association of Castleman′s disease and nephrotic syndrome

open access: yesSaudi Journal of Kidney Diseases and Transplantation, 2011
Castleman′s Disease (CD) is an uncommon and poorly understood disorder of lymph node hyperplasia of unknown etiology. This entity belongs to the atypical lymphoproliferative disorders, a heterogeneous group of diseases characterized by a hyperplastic ...
I Tazi   +3 more
doaj   +1 more source

Castleman’s disease in the HIV-endemic setting

open access: yesCancer Management and Research, 2018
Esam-Rajab Mahroug,1 Candice Sher-Locketz,1 Minodora-Silvia Desmirean,2,3 Emmanuel-Akinola Abayomi,1,4 Ciprian Tomuleasa,3,5,6 Ravnit Grewal1,7 1Division of Haematology, Department of Pathology, University of Stellenbosch, Tygerberg Academic Hospital ...
Mahroug E   +5 more
doaj   +1 more source

Rethinking Common Diagnoses: Idiopathic Multicentric Castleman Disease Presenting as TAFRO Syndrome: A Case Report. [PDF]

open access: yesClin Case Rep
ABSTRACT Idiopathic multicentric Castleman disease (TAFRO subtype) can mimic common differentials. High suspicion is required for chronic systemic symptoms and generalized lymphadenopathy. As fine‐needle aspiration is often non‐diagnostic, early excisional biopsy is important.
Rohatgi D   +3 more
europepmc   +2 more sources

POEMS Syndrome: 2026 Update on Diagnosis, Risk-Stratification, and Management. [PDF]

open access: yesAm J Hematol
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.
Dispenzieri A.
europepmc   +2 more sources

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

open access: yesClin Case Rep
ABSTRACT IgG4‐related disease and idiopathic multicentric Castleman disease are rare conditions that can present with overlapping features, complicating diagnosis and delaying proper treatment.
Miller M   +4 more
europepmc   +2 more sources

Castleman’s Disease- A Case Report

open access: yesBangabandhu Sheikh Mujib Medical University Journal, 2012
Castleman’s disease(CD) is a heterogeneous group of lymphoproliferative disorders of uncertain cause presenting with lymphadenopathy. It is histologically and prognostically distinct from malignant lymph-node hyperplasia.
Md. Ismail Patwary   +5 more
doaj   +1 more source

Castelman´s disease of the neck: a case report and literature review

open access: yesThe Pan African Medical Journal, 2020
Castleman’s disease is a rare pathology, poorly understood. It is considered as a lymphoproliferative disorder, described for the first time in 1954, which may be confused with other causes of lymphadenopathy.
Amel El Korbi   +8 more
doaj   +1 more source

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