Results 11 to 20 of about 4,266 (136)

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   +1 more source

Lenalidomideas a Second-line Therapy Achieves Long-term Remission in Elderly Patients with Relapsed/Refractory Multicentric Castleman's Disease:a Report of Two Cases and Literature Review [PDF]

open access: yesZhongguo quanke yixue, 2022
No standard therapy is recommended for elderly multicentric Castleman's disease (MCD) patients who failed to the first-line treatment or relapsed. Lenalidomide has been reported to be effective for relapsed/refractory MCD in foreign countries, but ...
TANG Yangming, SHI Renzhou, LAN Mei, LI Xuejun, WEN Zonghua, LU Xiaochen
doaj   +1 more source

Retroperitoneal pararenal castleman’s disease: a case report

open access: yesJournal of Pathology of Nepal, 2013
Castleman’s diseas is a rare lymphoproliferative disorder of unknown etiology. We report a 28 years old woman with solitary Castleman’s disease in the left pararenal space. This case was diagnosed preoperatively as renal cell carcinoma.
S Shrestha   +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

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   +1 more source

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

POEMS (polyneuropathy, organomegaly, endocrinopathy, M protein, skin lesions) syndrome: a South America's report POEMS (polineuropatia, organomegalia, endocrinopatia, proteína M, alterações de pele): relato sul-americano

open access: yesArquivos de Neuro-Psiquiatria, 2007
The POEMS syndrome, also known as Crow-Fukase syndrome, is an unusual systemic disorder described mainly in Asian individuals. It is characterized by the presence of (P)polyneuropathy, (O)organomegaly, (E)endocrinopathy, (M) M-protein, and (S) skin ...
Ana Claudia Celestino Leite   +3 more
doaj   +1 more source

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   +1 more source

Doença de Castleman hialino-vascular do mediastino

open access: yesRevista Portuguesa de Pneumologia, 2000
RESUMO: A doença de Castleman ou hiperplasia angiofolicular dos gânglios linfáticos, é uma entidade pouco frequente e de origem desconhecida. Dois padrões histológicos distintos foram descritos: o tipo hialinovascular e o plasmo-celular.
Ana Paula Martins, Fernando Rocha
doaj   +1 more source

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