Results 11 to 20 of about 6,197,685 (170)

Unicentric Castleman′s disease in the orbit: A case report

open access: yesIndian Journal of Ophthalmology, 2015
A 53-year-old man presented with a palpable mass on the left lower eyelid and occasional diplopia. Under suspicion of orbital lymphoma, an excisional biopsy was performed, and histopathology revealed Castleman′s disease.
Dongwan Kang   +3 more
doaj   +2 more sources

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

Persistent or recurrent Castleman′s disease - Look out for a lurking lymphoma!

open access: yesIndian Journal of Medical and Paediatric Oncology, 2011
Castleman′s disease, a rare condition of uncertain etiology clinically presents in isolated form or as a multicentric disease. The multicentric form can develop malignancies such as Kaposi′s sarcoma or lymphomas.
Shalinee Rao   +4 more
doaj   +2 more sources

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

open access: yesClinical Case Reports, Volume 14, Issue 10, October 2026.
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.
Divita Rohatgi   +3 more
wiley   +2 more sources

Idiopathic Multicentric Castleman Disease Associated With Seronegative Erosive Chronic Polyarthritis: A Diagnostic Challenge [PDF]

open access: yesClinical Case Reports, Volume 14, Issue 9, September 2026.
ABSTRACT Idiopathic multicentric Castleman disease can rarely present with systemic inflammation and erosive seronegative polyarthritis. Awareness of this association helps prevent misdiagnosis and ensures appropriate immunosuppressive management based on clinicopathological and immunohistochemical correlation.
Birahim Lo   +9 more
wiley   +2 more sources

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

Castleman Disease: An Unexpected Cause of a Solitary Pleural Mass [PDF]

open access: yesCase Reports in Radiology, 2013
Castleman disease (CD) is a rare benign lymphoproliferative disorder, the etiology of which is unclear. Clinically it may manifest as localized disease (unicentric) or disseminated disease (multicentric).
Fiachra Moloney   +3 more
doaj   +2 more sources

Immune reconstitution inflammatory syndrome, human herpesvirus 8 viremia, and HIV-associated multicentric Castleman disease

open access: yesInternational Journal of Infectious Diseases, 2016
Kaposi's sarcoma and multicentric Castleman Disease are HIV-related disease processes that are associated with human herpesvirus 8 (HHV-8) infection.
Marc O. Siegel   +3 more
doaj   +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

Minimal access surgery in Castleman disease in a child, a case report

open access: yesJournal of Pediatric Surgery Case Reports, 2015
This case report describes a child with Castleman disease. We present an overview of the disease, the investigation leading to the diagnosis, the laparoscopic approach for surgical treatment and the follow up. This rare entity must be considered in cases
Jan F. Svensson   +3 more
doaj   +2 more sources

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