Results 31 to 40 of about 584,998 (146)

A rare case report of hyaline-vascular type Castleman disease in the presacral region

Frontiers in Oncology
Castleman disease (CD), also known as giant lymph node hyperplasia or angiofollicular lymph node hyperplasia, is a rare and indeterminate group of chronic lymphoproliferative disorders.
Long Chang, Shuang Wang, Jiannan Li, Zeyun Zhao, Min Wang   +4 more
doaj   +1 more source

Multicentric Castleman disease with TAFRO syndrome and Sjögren's

Clinical Case Reports, Volume 7, Issue 12, Page 2388-2392, December 2019., 2019
We describe a patient with Castleman's disease with TAFRO syndrome and concurrent Sjögren's syndrome and investigate whether the autoimmune process may have accelerated the onset of her Castleman's disease. Treated with R‐CVP therapy with remission of symptoms although there is no current standard treatment.
Zi Ying Li, Shirley Kim, SiYi Huang, Raza Mian   +3 more
wiley   +1 more source

Isolated retroperitoneal Castleman's disease: A case report and literature review

Clinical Case Reports, Volume 6, Issue 8, Page 1543-1548, August 2018., 2018
Unicentric Castleman's disease (CD) may rarely present as an isolated retroperitoneal tumor. Even experienced surgeons may misdiagnose CD because of its rarity. Surgeons should consider this disease when faced with an isolated retroperitoneal tumor. Unicentric CD is usually cured with surgical resection.
Jhen‐Hao Jhan, Ching‐Chia Li, Wen‐Jeng Wu, Hsiang‐Ying Lee   +3 more
wiley   +1 more source

Resolution of membranoproliferative glomerulonephritis complicating angiofollicular lymph node hyperplasia (Castleman's Disease)

, 1993
A novel renal complication was reported in a patient with angiofollicular lymph node hyperplasia (Castleman's Disease), who developed acute renal failure due to membranoproliferative glomerulonephritis.
Chan, TM, Wong, KL, Cheng, IKP, Chan, KW
core   +1 more source

Clinical features and outcomes in patients with human immunodeficiency virus-negative, Castleman’s disease: a single medical center study in Tunisia

Romanian Journal of Internal Medicine
Castleman’s disease (CD), known as angiofollicular lymph node hyperplasia, is an uncommon condition. The two most common histological subtypes are hyaline vascular and plasma cell.
Chabchoub Imen, Salah Raida Ben, Kallel Rim, Snoussi Mouna, Frikha Feten, Marzouk Sameh, Boudawara Tahya Sellami, Bahloul Zouhir   +7 more
doaj   +1 more source

Clinical characteristics and outcomes of Castleman disease: A multicenter study of 185 Chinese patients

Cancer Science, Volume 109, Issue 1, Page 199-206, January 2018., 2018
This multicenter study concerning the clinical features, outcomes, and prognostic factors of Castleman disease comprised the largest sample size to date and firstly demonstrated that age, splenomegaly and pretreated serum albumin level were independent prognostic factors for multicentric Castleman disease patients.
Xuanye Zhang, Huilan Rao, Xiaolu Xu, Zhihua Li, Bing Liao, Hongmei Wu, Mei Li, Xiuzhen Tong, Juan Li, Qingqing Cai   +9 more
wiley   +1 more source

Deciphering the full spectrum of Castleman diseases based on a cohort of 700 patients in a western country

British Journal of Haematology, Volume 208, Issue 6, Page 2036-2046, June 2026.
The spectrum of Castleman diseases has expanded over the past three decades. The phenotype of the diseases varies not only among the three major types but also according to the patient ancestry. Summary Under the Castleman disease (CD) eponym, three distinct diseases sharing common pathological features have been described over time.
Eric Oksenhendler, Marion Malphettes, Véronique Meignin, David Boutboul, Lionel Galicier   +4 more
wiley   +1 more source

Rituximab Monotherapy in the Management of a Rare Case of an HIV Associated Lymphoproliferative Disorder

Case Reports in Oncological Medicine, Volume 2017, Issue 1, 2017., 2017
Background. Castleman’s disease (CD), also known as angiofollicular node hyperplasia, is a rare heterogenous lymphoproliferative disorder. This disease exists as two distinct entities: a localized or unicentric CD (UCD) which has a more benign clinical course and multicentric CD (MCD) which is a systemic disease and carries a worse prognosis.
Jason Hew, Fauzia Rana, Louise Zhou, Jose I. Mayordomo   +3 more
wiley   +1 more source

Cutaneous Disorders Associated with Castleman’s Disease

Acta Dermato-Venereologica, 2019
Castleman’s disease is a rare disease of the lymph nodes and related tissues, presenting as angiofollicular or giant lymph node hyperplasia. Although various skin manifestations have been reported to occur in Castleman’s disease, a comprehensive study of
Hyo Jung Kim, Ju Hee Han, Chul Hwan Bang, Kyung Shin Park, Seok-Goo Cho, Dong Su Yoo, Kyung Moon Kim, Hyun Jung Park, Young Min Park, Jun Young Lee, Ji Hyun Lee   +10 more
doaj   +1 more source

Castleman Disease in Tunisia: A Multicenter Clinical, Prognostic, and Therapeutic Study

Advances in Hematology, Volume 2026, Issue 1, 2026.
Introduction Castleman disease is an uncommon benign lymphoproliferative condition that includes diverse clinical, biochemical, and histological variations, each characterized by unique prognoses and therapeutic approaches. The aim of our study was to characterize the clinical and paraclinical features, as well as the management approaches, of ...
Tayssir Ben Achour, Syrine Sassi, Aida Khadar, Wafa Skouri, Mariem Borgi, Maysem Jridi, Arfaoui Bilel, Aydi Zohra, Adaily Najeh, Amri Raja, Ben Abdelhafidh Nadia, Ben Abdelghni Khaoula, Ben Fraj Fatma, Ben Hssine Lamia, Boussema Fatma, Daada Syrine, Guediche Nour El Houda, Ines Chelly, Jebri Meriem, Smiti Monia, Kalyani Sen   +20 more
wiley   +1 more source