Results 71 to 80 of about 12,522 (168)

Diagnostic challenges in patients with Castleman disease, a single center experience from Hungary

Pathology and Oncology Research
Castleman disease is a rare and atypical lymphoproliferative disorder characterized by diverse clinical manifestations. It has both unicentric and multicentric forms, the latter with further subdivisions, i.e., human herpesvirus 8-associated and ...
Boglárka Brúgós, Boglárka Brúgós, Zsófia Simon, Gábor Méhes, Árpád Illés, György Pfliegler, György Pfliegler   +6 more
doaj   +1 more source

Immunophenotypic characteristics of plasma cells in POEMS syndrome

Cytometry Part B: Clinical Cytometry, Volume 110, Issue 4, Page 266-273, July 2026.
Abstract To analyze the immunophenotypic characteristics of plasma cells in patients with polyneuropathy, organomegaly, endocrinopathy, myeloma protein, and skin changes (POEMS) syndrome. This retrospective study included patients with POEMS syndrome hospitalized in the Department of Hematology, Huashan Hospital, from September 2017 to August 2025 ...
Zhenhua Wang, Tianling Ding, Beiqian Wu, Qiang Niu, Leyao Gu, Yan Yuan, Ping Zhu   +6 more
wiley   +1 more source

Refractory Uveitis in Patient with Castleman Disease Successfully Treated with Tocilizumab

Case Reports in Ophthalmological Medicine, 2012
Although multicentric Castleman disease is a rare but life-threatening disease, eye complications are extremely uncommon. We present a case of refractory uveitis accompanied with Castleman disease successfully treated with tocilizumab.
Toshiyuki Oshitari, Fusae Kajita, Aya Tobe, Makiko Itami, Jiro Yotsukura, Takayuki Baba, Shuichi Yamamoto   +6 more
doaj   +1 more source

Quantitative analysis of a rare disease network’s international contact database and E-repository provides insights into biobanking in the electronic consent era

Orphanet Journal of Rare Diseases, 2019
Background Castleman disease (CD) describes a group of rare and poorly understood lymphoproliferative disorders that include unicentric CD (UCD), Human Herpes Virus-8 (HHV8)-associated multicentric CD (HHV8 + MCD), and HHV8-negative/idiopathic MCD (iMCD).
Alexander Suarez, Curran Reilly, David C. Fajgenbaum   +2 more
doaj   +1 more source

Update and new approaches in the treatment of Castleman disease

, 2016
Kah-Lok Chan,1 Stephen Lade,2 H Miles Prince,1,3 Simon J Harrison1,3 1Department of Haematology, 2Department of Anatomical Pathology, Peter MacCallum Cancer Centre, 3Sir Peter MacCallum Department of Oncology, The University of Melbourne, Melbourne, VIC,
Prince HM, Harrison SJ, Chan KL, Lade S
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Maladie de castleman multicentrique: A propos d’un cas [PDF]

, 2010
La maladie de Castleman est une affection rare, d’étiologie inconnue, caractérisée sur le plan histologique par une hyperplasie lymphoïde angiofolliculaire. Elle se présente sous deux formes différentes, localisée et multicentrique.
M Belcadhi, I Riahi, Bouzouita, K, M Abdelkefi, Khlif, A, I Zeglaoui, R Mani, Abdelkefi, M, Mani, R, A Khlif, Zeglaoui, I, Bellakhdher, M, Sriha, B, B Ali, Riahi, I, Belcadhi, M, B Sriha, K Bouzouita, Ali, B, M Bellakhdher   +19 more
core   +1 more source

P. F. Castleman [PDF]

, 1896
R-P of P. Castleman. 17 Mar. SR 498, 54-1, v2, 2p. [3363] or HR 1558, 54-1, v6, 2p.

core   +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

Arquivos 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, Osvaldo J.M. Nascimento, Marco Antonio Lima, Maria José Andrada-Serpa   +3 more
doaj   +1 more source

Real‐World Usage and Outcomes of Different Siltuximab Dosing Frequency in Idiopathic Multicentric Castleman Disease

American Journal of Hematology, Volume 101, Issue 8, Page 2033-2037, August 2026.
Yoshito Nishimura, Maria Santiago Estevez, Hakeem Asad, Thomas Habermann, Angela Dispenzieri   +4 more
wiley   +1 more source

Malattia di Castleman

, 2020
La malattia di Castleman, una patologia rara che può colpire tutte le età, comprende un gruppo eterogeneo di disordini linfoproliferativi che condividono le stesse caratteristiche istopatologiche.
giona fiorina, mohamed sara
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