Results 111 to 120 of about 21,386 (303)

Clinical Presentation, Treatment, and Outcomes of 28 Patients With Castleman Disease: A Retrospective Analysis of an Italian Cohort

eJHaem, Volume 6, Issue 6, December 2025.
ABSTRACT Background Castleman disease (CD) encompasses a range of heterogeneous non‐clonal lymphoproliferative disorders, including unicentric (UCD), and multicentric (MCD) forms. The latter is subdivided into HHV‐8+ MCD, POEMS‐MCD, and idiopathic‐MCD, not otherwise specified (iMCD‐NOS).
Caterina Cristinelli, Michele Merli, Marco Lucioni, Manuel Gotti, Roberta Sciarra, Sara Rattotti, Federico Carpi, Gianmarco Favrin, Benedetta Bianchi, Giuseppe Neri, Marta Coscia, Marcello Gambacorta, Francesco Passamonti, Marco Paulli, Luca Arcaini   +14 more
wiley   +1 more source

Castleman Disease in China: State-of-the-art Technology Before the Era of IL-6 Targeted Therapy

Xiehe Yixue Zazhi, 2023
Castleman disease (CD) is a group of rare and heterogenous hematological diseases included in the 'Rare disease catalogue' of China. Among the different clinical subtypes of CD, idiopathic multicentric Castleman disease (iMCD) is characterized by ...
ZHANG Lu, LI Jian
doaj   +1 more source

Multicentric Castleman's disease as a cause for unclear febrile episodes in a 55-year-old HIV-infected man [PDF]

, 2018
Our case illustrates the difficulties involved in diagnosing multicentric Castleman's disease (MCD) in a human immunodeficiency virus-infected man with febrile episodes and malaise. In the absence of well-established treatment protocols, we have chosen a
Achermann, Y., Fehr, J., Lederer, H., Stenner, F., Tinguely, M.   +4 more
core  

Ühekoldelise Castlemani tõve juhtum [PDF]

, 2013
Castlemani tõbi on harva esinev lümfoproliferatiivne haigus, mis esineb kas ühekoldelise või hulgikoldelisena. Haigus on tavaliselt asümptomaatiline, mistõttu diagnoosimine on sageli keeruline ja aeganõudev.
Oeselg, Airi, Semjonov, Eero
core   +2 more sources

Spatial Transcriptomics of Patients With Kaposi Sarcoma Identifies Mechanisms of Immune Evasion

Journal of Medical Virology, Volume 97, Issue 12, December 2025.
ABSTRACT To identify the cell types that are infected with KSHV and the immune interactions in Kaposi sarcoma (KS) lesions, we performed spatial transcriptomics with seven KS skin tumors. We used a single‐cell RNA‐sequencing reference data set from healthy skin donors with a method to conduct spatially informed cell‐type deconvolution for spatial ...
Bahman Afsari, Ramya Ramaswami, Kathryn Lurain, Takanobu Tagawa, Daphne Knudsen‐Palmer, Guruswamy Mahesh, Ameera Mungale, Robert Yarchoan, Joseph Ziegelbauer   +8 more
wiley   +1 more source

Idiopathic multicentric Castleman disease: a mysterious case of generalized lymphadenopathy [PDF]

, 2023
Castleman disease is a syndrome with significant clinico-pathological overlap between malignancy, autoimmune causes and infectious etiologies.
J., Kumanan, Lakshmanan, Archana, P. N., Shoaib Nawaz, Raja, Thirumalairaj, Ramya Ananthkrishnan, Sebastian, Nikhil   +5 more
core   +2 more sources

Insufficient evidence exists to use histopathologic subtype to guide treatment of idiopathic multicentric Castleman disease

American journal of hematology/oncology, 2020
Idiopathic multicentric Castleman disease (iMCD) is a rare immunologic disorder characterized by systemic inflammation, multicentric lymphadenopathy, and organ dysfunction.
D. Fajgenbaum, David Wu, A. Goodman, R. Wong, A. Chadburn, S. Nasta, G. Srkalović, S. Mukherjee, H. Leitch, Raj K. Jayanthan, S. Ferrero, Y. Sato, S. Schey, A. Dispenzieri, É. Oksenhendler, P. Zinzani, M. Lechowicz, C. Hoffmann, N. Pemmaraju, A. Bagg, A. Fosså, M. Lim, F. Van Rhee   +22 more
semanticscholar   +1 more source

Idiopathic Multicentric Castleman Disease with Cutaneous Manifestation: Case Report [PDF]

, 2022
Christoforos Kosmıdis, Chrysi Maria Mystakidou, Georgios Koimtzis, Evanthia Papadopoulou, Vassiliki Theodorou, Nikolaos Iason Katsios, Eleni Georgakoudi, Christina Sevva, Ioannis Charalampous, Nikolaos Varsamis, Charilaos Koulouris, Christina Michael, K. Papadopoulos, Georgios Anthimidis, Sofia Baka   +14 more
openalex   +1 more source

Clinical perspectives and comparisons between immunoglobulin G4‐related disease and antineutrophil cytoplasmic antibody‐associated vasculitis

Rheumatology &Autoimmunity, Volume 5, Issue 4, Page 267-274, December 2025.
Clinical perspectives and comparisons between immunoglobulin G4‐related disease and antineutrophil cytoplasmic antibody‐associated vasculitis. Abstract Both immunoglobulin G4‐related disease (IgG4‐RD) and antineutrophil cytoplasmic antibody (ANCA)‐associated vasculitis (AAV) are systemic disorders that affect a wide range of organs.
Wenhuan Zeng, Mingxin Bai, Yanying Liu
wiley   +1 more source

Doppler findings In castleman disease - A rare case

Indian 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, C Shah, A Shrivastava, P Amin, P Patel   +4 more
doaj   +1 more source