نتایج جستجو برای: castleman disease

تعداد نتایج: 1490199  

Journal: :British journal of haematology 2005
Corey Casper

Fifty years ago, Dr Benjamin Castleman first described the unusual lymphoproliferative disorder that now bears his name. Over the subsequent decades, astute clinical and pathologic observations coupled with clever molecular biologic research have increased our understanding of the aetiology of Castleman disease (CD). This article proposes three broad CD variants based on both distinctive histop...

Journal: :Blood 2000
N Dupin T L Diss P Kellam M Tulliez M Q Du D Sicard R A Weiss P G Isaacson C Boshoff

Castleman disease (CD) is a lymphoproliferative disorder of unknown etiology that is associated with the development of secondary tumors, including B-cell lymphoma. Human herpesvirus 8 (HHV-8) (Kaposi's sarcoma-associated herpesvirus) sequences have been described in some cases of multicentric Castleman disease (MCD). Using a monoclonal antibody against an HHV-8-latent nuclear antigen, we show ...

2013
Katie Stone Emily Woods Susann M. Szmania Owen W. Stephens Tarun K. Garg Bart Barlogie John D. Shaughnessy Brett Hall Manjula Reddy Antje Hoering Emily Hansen Frits van Rhee

Multicentric Castleman Disease is largely driven by increased signaling in the pathway for the plasma cell growth factor interleukin-6. We hypothesized that interleukin-6/interleukin-6 receptor/gp130 polymorphisms contribute to increased interleukin-6 and/or other components of the interleukin-6 signaling pathway in HIV-negative Castleman Disease patients. The study group was composed of 58 pat...

Journal: :Laryngo-rhino-otologie 2022

Background Idiopathic multicentric Morbus Castleman (iMCD) is a very rare disease with broad spectrum of symptoms and complex histopathological diagnosis. An expert meeting in 2017 by Fajgenbaum et al. defined new criteria for the diagnosis iMCD. Estimations prevalence German population do not exist yet. As lymphadenopathy often occurs primarily head neck region patients are frequently referred...

Journal: :European Journal of Cardio-Thoracic Surgery 2004

Journal: :Medical Journal of Dr. D.Y. Patil University 2014

2014
O. McDonnell Melinda Morris Z. Khaleel

Localised nasopharyngeal Castleman disease has rarely been reported. We present a case involving a 23-year-old female, describe the clinical, imaging, and histopathologic features of this challenging diagnosis, and review the literature.

Journal: :International journal of clinical and experimental pathology 2015
Hang Yu Fang Yao Yue Li Jian Li Quan-Cai Cui

POEMS syndrome is a rare hematological disorder associated with plasma cell dyscrasia characterized by polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy and skin changes. Castleman disease is a lymphoproliferative disorder that can be present in POEMS patients, which can be defined as Castleman disease variant of POEMS syndrome. Herein, we described a 24-year-old male patient ...

Journal: :British journal of haematology 2015
Yujun Dong Mingyue Wang Lin Nong Lihong Wang Xinan Cen Wei Liu Sainan Zhu Yuhua Sun Zeyin Liang Yuan Li Jinping Ou Zhixiang Qiu Hanyun Ren

This study retrospectively collected the clinical and laboratory data of 114 patients with Castleman disease (CD) from a single medical centre. Clinical classification identified 62 patients (54·4%) with unicentric Castleman disease and 52 (45·6%) with multi-centric Castleman disease. Pathological classification revealed 68 cases (59·6%) of hyaline vascular variant, 16 (14·1%) mixed cellular va...

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