Results 101 to 110 of about 24,360 (218)

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

Human Herpesvirus 8 Causes a Wide Spectrum of Disease in Liver Transplant Recipients and May be Donor Derived: Case Series and Systematic Review of an Emerging Challenge

Transplant Infectious Disease, Volume 28, Issue 5, September/October 2026.
Among 135 cases of post‐liver transplant HHV8 disease (4 from NSW), presentations varied, and mortality was high (44%). Donor screening was rare, and donor‐derived infection was suspected in 33%. Survival improved with mTORi, reduced immunosuppression, chemotherapy, and, for non‐KS disease, donor screening. ABSTRACT Background Human herpesvirus 8 (HHV8)
Karen M. J. Waller, Sudarshan Arvind, Simone I. Strasser, Ken Liu, Geoff W. McCaughan, David G. Bowen, Madeleine Gill, Rebecca Davis, William Rawlinson, Sacha Stelzer‐Braid, Geoff Watson, Vinay Vanguru, Tina Marinelli   +12 more
wiley   +1 more source

JW Castleman

, 1977
J.W.

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Intrapericardial pneumonectomy for unicentric hilar castleman disease.

, 2021
Introduction: The intrapulmonary involvement of Castleman disease is extremely rare with very few cases reported in the literature. Case report: We present a case of a 16-year-old male who underwent pulmonary resection for Castleman disease.
YEGEN, Gülçin, TUĞCU, Deniz, Ulker, Melike Güler, ÖZKAN, Berker, KARA, Murat   +4 more
core   +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

Recurrent PDGFRB mutations in unicentric Castleman disease

Leukemia, 2019
Castleman disease (CD) is a rare heterogeneous group of lymphoproliferative disorders that share common lymph node histopathological features [1, 2]. It can be classified into unicentric CD (UCD), HHV-8-positive multicentric CD (MCD) and HHV-8-negative ...
Zhao-Ming Li, X. Lan, Chaoping Li, Yan-Jie Zhang, Yingjun Wang, Wei-Li Xue, Lisha Lu, M. Jin, Zhiyuan Zhou, Xin-Hua Wang, Ling Li, Lei Zhang, Xin Li, Xiao-Rui Fu, Zhen-Chang Sun, Jing-Jing Wu, Xu-Dong Zhang, Hui Yu, F. Nan, Yu Chang, Jia-Qin Yan, Xiaolong Wu, Guan-Nan Wang, Dan-Dan Zhang, Yuan Zhang, K. Young, Ming-Zhi Zhang   +26 more
semanticscholar   +1 more source

Epidemiological analysis of multicentric and unicentric Castleman disease and TAFRO syndrome in Japan

Journal of Clinical and Experimental Hematopathology, 2019
Castleman disease is a polyclonal lymphoproliferative disease which is clinically classified into unicentric (UCD) and multicentric (MCD). TAFRO syndrome is a relatively new concept that partly overlaps with MCD.
Y. Masaki, H. Kawabata, Shino Fujimoto, M. Kawano, Noriko Iwaki, T. Kotani, A. Nakashima, N. Kurose, K. Takai, R. Suzuki, S. Aoki   +10 more
semanticscholar   +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

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.

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