Results 61 to 70 of about 378 (110)

A hypothesis on treatment strategy of severe multicentric Castleman disease with continuous renal replacement therapy

Journal of Cellular and Molecular Medicine, Volume 28, Issue 17, September 2024.
Abstract Castleman disease (CD) is a rare lymphoproliferative disorder, with non‐specific clinical manifestations, often delayed diagnosis and treatment, which pose a significant challenge in the present times. Patients diagnosed with this disease have poor prognosis due to the limited treatment options.
Cătălin Constantinescu, David Kegyes, Bogdan Tigu, Vlad Moisoiu, Olga Grăjdieru, Andrea Szekely, Evangelos Terpos, Ciprian Tomuleasa   +7 more
wiley   +1 more source

The application of a multidisciplinary approach in the diagnosis of Castleman disease and Castleman‐like lymphadenopathies: A 20‐year retrospective analysis of clinical and pathological features

British Journal of Haematology, Volume 204, Issue 2, Page 534-547, February 2024.
Summary Background Castleman disease (CD) comprises a group of rare and heterogeneous haematological disorders, including unicentric (UCD) and multicentric (MCD) forms, the latter further subdivided into HHV8‐MCD, POEMS‐MCD and idiopathic‐MCD (iMCD). However, according to the Castleman Disease Collaborative Network guidelines, the diagnosis of CD can ...
Sabrina Pelliccia, Evelina Rogges, Antonello Cardoni, Gianluca Lopez, Esmeralda Conte, Anna Laura Faccini, Rita De Vito, Katia Girardi, Antonella Bianchi, Ombretta Annibali, Stefano Fratoni, Daniele Remotti, Gioia De Angelis, Carla Giordano, Giovanna Palumbo, Stefania Scarpino, Flavia Del Porto, Maria Paola Bianchi, Francesca Di Gregorio, Agostino Tafuri, Arianna Di Napoli   +20 more
wiley   +1 more source

A case of idiopathic multicentric Castleman's disease with secondary autoimmune neutropenia

Respirology Case Reports, Volume 12, Issue 1, January 2024.
Thrombocytopenia and anaemia are common complications of Idiopathic multicentric Castleman's disease (iMCD)‐induced hematologic disorders, however, neutropenia associated with iMCD is rare. The association between iMCD and autoimmune neutropenia (AIN) involving anti‐neutrophil antibodies has not yet been elucidated.
Toshiki Morimoto, Takako Kawaguchi, Kei Yamasaki, Tatsuya Shingu, Hiroaki Ikegami, Hiroki Dosaka, Yuichi Murata, Yoshinori Kawabata, Kazuhiro Yatera   +8 more
wiley   +1 more source

Radiological Imaging Findings of Adrenal Abnormalities in TAFRO Syndrome: A Systematic Review

Biomedicines
This systematic review article aims to investigate the clinical and radiological imaging characteristics of adrenal abnormalities in patients with thrombocytopenia, anasarca, fever, reticulin fibrosis, renal dysfunction, and organomegaly (TAFRO) syndrome.
Ryo Kurokawa, Akira Baba, Rui Kano, Yo Kaneko, Mariko Kurokawa, Wataru Gonoi, Osamu Abe   +6 more
doaj   +1 more source

Unraveling TAFRO Syndrome: An In-Depth Look at the Pathophysiology, Management, and Future Perspectives

Biomedicines
TAFRO syndrome is a rare and aggressive inflammatory entity characterized by thrombocytopenia, anasarca, fever, renal failure, reticulin fibrosis, and organomegaly.
Juan Carlos Caballero, Nazaret Conejero, Laura Solan, Francisco Javier Diaz de la Pinta, Raul Cordoba, Alberto Lopez-Garcia   +5 more
doaj   +1 more source

T-Cells Subsets in Castleman Disease: Analysis of 28 Cases Including Unicentric, Multicentric and HHV8-Related Clinical Forms

, 2023
Castleman disease (CD) is a rare lymphoproliferative disorder that includes various clinico-pathological subtypes. According to clinical course, CD is divided into unicentric CD (UCD) and multicentric CD (MCD).
Antonio Lazzaro, Caterina Cristinelli, Deborah Marchiori, Giuseppe Neri, Luca Arcaini, Marco Lucioni, Marco Paulli, Michele Merli, Rodolfo Monaco, Sara Fraticelli, Silvia Uccella, Tiziana Borra   +11 more
core   +1 more source

Characterization of Castleman Disease Reveals Patients with Oligocentric Adenopathy and Clinicopathologic Characteristics Similar to Unicentric Castleman Disease

, 2021
Castleman disease (CD) describes a group of heterogeneous lymphoproliferative disorders with characteristic histopathology that are classified based on the number of enlarged lymph node (LN) stations, etiological drivers, and clinical phenotype.
Adam Bagg, Daisy Alapat, David C Fajgenbaum, Frits van Rhee, Gordan Srkalovic, Mary Jo Lechowicz, Megan S. Lim, Sheila K Pierson, Thomas S. Uldrick   +8 more
core   +1 more source

An unusual case of HHV-8 negative, idiopathic, multicentric Castleman disease following chronic lymphocytic leukaemia

European Journal of Case Reports in Internal Medicine
Background: Castleman disease is a rare condition characterised by polytypic lymphocytes proliferation and lymphadenopathy generally with a benign course.
Pierre-Yves Sansen, Hélène Vellemans, Julien Depaus, Caroline Fervaille, Benoit Krug, Anne Sonet, Elodie Collinge   +6 more
doaj   +1 more source

Common connective tissue disorder and anti-cytokine autoantibodies are enriched in idiopathic multicentric castleman disease patients

Frontiers in Immunology
IntroductionIdiopathic Multicentric Castleman Disease (iMCD) is a polyclonal lymphoproliferative disorder involving cytokine storms that can lead to organ failure and death.
Allan Feng, Allan Feng, Michael V. Gonzalez, Muge Kalaycioglu, Muge Kalaycioglu, Xihui Yin, Xihui Yin, Melanie Mumau, Saishravan Shyamsundar, Mateo Sarmiento Bustamante, Sarah E. Chang, Sarah E. Chang, Shaurya Dhingra, Shaurya Dhingra, Tea Dodig-Crnkovic, Jochen M. Schwenk, Tarun Garg, Kazuyuki Yoshizaki, Frits van Rhee, David C. Fajgenbaum, Paul J. Utz, Paul J. Utz   +21 more
doaj   +1 more source

TAFRO Syndrome on ¹⁸F-FDG-PET/CT: An Appealing Diagnostic Tool

Diagnostics
TAFRO syndrome (TS) is a recently recognized and heterogenous systemic disease characterized by a confluence of symptoms: thrombocytopenia (T), anasarca (A), fever (F), reticulin myelofibrosis (R), and organomegaly (O).
Ayoub Jaafari, Nadim Taheri, Sohaïb Mansour, Saïf-Eddine El Bouhali, Rachid Attou   +4 more
doaj   +1 more source