Results 81 to 90 of about 1,394 (181)

Symptom Burden in Idiopathic Multicentric Castleman Disease: Protocol for the Development of a Novel Standardized Patient Reported Outcome Measure [PDF]

, 2023
Sudipto Mukherjee, Philip A. Powell, Jill Carlton, Clara Murukia, Antonio Adolfo Guerra Soares Brandão, Karthik Ramasamy, F. Shupo, Grace Wayi-Wayi, Karan Kanhai, Kelley Dacus, Kelly Makarounas‐Kirchmann, Anju Keetharuth   +11 more
openalex   +1 more source

Heterogeneous Presentations of iMCD: A Single‐Institution Case Series

Case Reports in Hematology, Volume 2025, Issue 1, 2025.
Background Idiopathic multicentric Castleman disease (iMCD) is a rare lymphadenopathic disorder characterized by hyperplasia of multiple lymph nodes and can be associated with a wide range of symptoms and presentations, from mild disease to life‐threatening organ failure.
Jaspreet Kaur, Anthony Sisk, Jonathan E. Zuckerman, Haifaa Abdulhaq, Kalyani Sen   +4 more
wiley   +1 more source

TAFRO syndrome associated with C3 nephropathy (an analysis of clinical experience)

Klinicist
Aim. To present a clinical case of TAFRO syndrome – a recently described subtype of idiopathic multicentric Castleman disease of unknown etiology, characterized by thrombocytopenia, anasarca, fever, reticulin fibrosis of the bone marrow and / or renal ...
I. V. Pozharov, A. O. Grigorevskaya, G. R. Setdikova, E. S. Stolyarevich   +3 more
doaj   +1 more source

Atypical clinical presentation associated with Castleman disease: a case report and review of the literature

Frontiers in Medicine
BackgroundCastleman disease (CD) is a group of rare and complicated diseases characterized by systemic inflammation, lymphadenopathy, and multiorgan involvement.
Weiwei Hu, Yuke Kong, Bianxiang Hu, Jun Ai, Peng Zhang   +4 more
doaj   +1 more source

Acrocyanosis: The Least Known Acrosyndrome Revisited With a Dermatologic Perspective

Dermatology Research and Practice, Volume 2025, Issue 1, 2025.
Background: Acrocyanosis is a functional peripheral vascular disorder, currently categorized under the canopy of acrosyndromes, i.e., a group of clinically similar and significantly overlapping vascular disorders involving the acral skin. The disorder might be primary or secondary, depending on the cause.
Deniz Demircioğlu, Emel Öztürk Durmaz, Enzo Errichetti   +2 more
wiley   +1 more source

Interleukin‐6 transcripts up‐regulation in lymph nodes from unicentric and multicentric Castleman disease

eJHaem, Volume 5, Issue 6, Page 1182-1189, December 2024.
Abstract Introduction Castleman disease (CD) represents a spectrum of heterogeneous lymphoproliferative disorders sharing peculiar histopathological features, clinically subdivided into unicentric CD (UCD) and multicentric CD (MCD) and presenting with variable inflammatory symptoms.
Marco Lucioni, Gaia Morello, Caterina Cristinelli, Sara Fraticelli, Giuseppe Neri, Erica Travaglino, Marco Minetto, Francesca Antoci, Paolo Libretti, Marcello Gambacorta, Luca Arcaini, Claudio Tripodo, Marco Paulli   +12 more
wiley   +1 more source

Chronic urticaria as a manifestation of multicentric Castleman disease treated with rituximab

JEADV Clinical Practice
We present the case of a 26‐year‐old female with chronic urticaria (CU) with systemic symptoms in whom comprehensive laboratory and imaging studies led to the diagnosis of idiopathic multicentric Castleman disease.
Osorio‐Aragón I. Yolanda, Milián‐Solís Ximena, Berumen‐Glinz Cristina, Vargas C. Estefanía, Vega‐Memije M. Elisa, Andrade‐Rojas J. Jose, Contreras‐Solis M. Fernanda, González‐Hernández Isaac   +7 more
doaj   +1 more source

HIV‐negative HHV8‐positive multicentric Castleman's disease coexistent with atypical Kaposi's sarcoma

JEADV Clinical Practice, Volume 3, Issue 5, Page 1606-1610, December 2024.
Abstract The co‐occurence of multicentric Castleman's disease (MCD) and Kaposi's sarcoma (KS) represents a rare clinical entity, mostly observed in individuals infected with the human immunodeficiency virus (HIV). Human herpesvirus 8 (HHV‐8) is attributed a crucial etiological role in both conditions. This study presents the case of a 75‐year‐old woman
Anna Scattone, Giacomo Loseto, Biagina Gisella Mennuni, Valentina Mastrandrea, Rosalba Buquicchio, Caterina Foti, Francesco Alfredo Zito, Raffaele Filotico   +7 more
wiley   +1 more source

Longitudinal, natural history study reveals the disease burden of idiopathic multicentric Castleman disease

Haematologica
Idiopathic multicentric Castleman disease (iMCD) is a rare hematologic disorder with heterogeneous presentations ranging from moderate constitutional symptoms to life-threatening multiorgan system involvement. iMCD patients present with vastly different
Mateo Sarmiento Bustamante, Sheila K. Pierson, Yue Ren, Adam Bagg, Joshua D. Brandstadter, Gordan Srkalovic, Natalie Mango, Daisy Alapat, Mary Jo Lechowicz, Hongzhe Li, Frits van Rhee, Megan S. Lim, David C. Fajgenbaum   +12 more
doaj   +1 more source

Peripheral helper-T-cell-derived CXCL13 is a crucial pathogenic factor in idiopathic multicentric Castleman disease [PDF]

, 2023
Takuya Harada, Yoshikane Kikushige, Toshihiro Miyamoto, Kazuko Uno, Hiroaki Niiro, Atsushi Kawakami, Tomohiro Koga, Koichi Akashi, Kazuyuki Yoshizaki   +8 more
openalex   +1 more source