Results 61 to 70 of about 6,197,685 (170)

Castleman disease presenting as lymphadenopathy in a female with systemic lupus erythematosus: A rare case report

Clinical Case Reports, 2023
Key Clinical Message Castleman disease is an infrequent disease that affects the lymph nodes and related tissues. The condition may manifest with lymphadenopathy, characterized by the enlargement of the lymph nodes, alongside additional symptoms such as ...
Alireza Khabbazi, Amirreza Khalaji, Omid Pourbagherian, Amir Vahedi, Mehdi Jafarpour   +4 more
doaj   +1 more source

When Liver Disease Misleads the Diagnosis: Two Cases of TAFRO Syndrome With Porto‐Sinusoidal Vascular Disease

eJHaem, Volume 7, Issue 5, October 2026.
ABSTRACT Background TAFRO syndrome is a rare inflammatory disorder whose hepatic manifestations may mimic decompensated cirrhosis. Cases: We report two women with TAFRO syndrome associated with portal‐sinusoidal vascular disorder (PSVD), a rare cause of non‐cirrhotic portal hypertension. In both cases, liver biopsy excluded cirrhosis and confirmed PSVD.
Laura Dassy, Fanny Poletti, Kaoutar Hafraoui, Marie Lejeune, Joan Somja, Patrick Collins, Julien Guiot, Ivan Theate, Jo Caers, Jean Delwaide, Astrid Marot, Virginie Putzeys, Gaëlle Vertenoeil   +12 more
wiley   +1 more source

Parapancreatic Castleman disease: contrast-enhanced sonography and CT features

, 2007
Castleman disease is a rare lymphoproliferative disorder that can be classified into 3 types: hyaline-vascular, plasma cell, and mixed. We report a rare case of localized parapancreatic hyaline-vascular Castleman disease that was evaluated using contrast-
A. PADDEU, Andrea Imperatori, Carlo Fugazzola, IMPERATORI, ANDREA SELENITO, CARRAFIELLO, GIANPAOLO, G. Carrafiello, M. MANGINI, A. Imperatori, Elena Bertolotti, Gianpaolo Carrafiello, S. Uccella, FUGAZZOLA, CARLO, N. Rotolo, Antonio Paddeu, Silvia Uccella, E. BERTOLOTTI, Monica Mangini, Nicola Rotolo, UCCELLA, SILVIA, ROTOLO, NICOLA, C. Fugazzola, Luca Aiani, L. AIANI   +22 more
core   +1 more source

HHV-8-Associated Multicentric Castleman Disease, a Diagnostic Challenge in a Patient With Acquired Immunodeficiency Syndrome and Fever

Journal of Investigative Medicine High Impact Case Reports, 2022
Patients with acquired immunodeficiency syndrome (AIDS) are at an increased susceptibility to pathogens and associated malignancies which can present with a unique constellation of symptoms.
Robert Dunn MS4, Roopam Jariwal MD, Frederick Venter MD, Shikha Mishra MD, Janpreet Bhandohal MD, Everado Cobos MD, Arash Heidari MD   +6 more
doaj   +1 more source

Long‐Term Outcomes After Elective Splenectomy for Haematological Disease: A 27‐Year Single‐Centre Study

ANZ Journal of Surgery, Volume 96, Issue 10, Page 3116-3125, October 2026.
Splenectomy is a safe and effective treatment option in selected patients with haematological disease, despite declining referrals over the last 27 years in the era of targeted therapies. Outcomes are favourable when performed laparoscopically and long‐term follow‐up demonstrates sustained haematologic benefit in surviving patients.
Salil Dutt Barrett, Anthony Downhill, Douglas Greer, William Stevenson, Ian Kerridge, Chris Ward, Matthew Greenwood, Naomi Mackinlay, Luke Coyle, Thomas J. Hugh   +9 more
wiley   +1 more source

Bilateral orbital Castleman disease: Building castles around the eye

Indian Journal of Ophthalmology. Case Reports
Castleman disease is a rare, benign, clinicopathological entity associated with lymphoproliferation. Orbital Castleman disease is an even rarer condition, with multicentric involvement of the orbit being exceptionally uncommon. We report the case of a 61-
Anna Kurian Mullasseril, Ani Sreedhar, JK Ann, Dona Ann Mathew, Sajitha Abdusamad, Jophy Varghese   +5 more
doaj   +1 more source

Refractory Uveitis in Patient with Castleman Disease Successfully Treated with Tocilizumab

Case Reports in Ophthalmological Medicine, 2012
Although multicentric Castleman disease is a rare but life-threatening disease, eye complications are extremely uncommon. We present a case of refractory uveitis accompanied with Castleman disease successfully treated with tocilizumab.
Toshiyuki Oshitari, Fusae Kajita, Aya Tobe, Makiko Itami, Jiro Yotsukura, Takayuki Baba, Shuichi Yamamoto   +6 more
doaj   +1 more source

Step into action: how reminders shape engagement in fitness apps

Economica, Volume 93, Issue 372, Page 1225-1259, October 2026.
Abstract Regular exercise offers well‐documented health benefits, and mobile applications are increasingly used to promote physical activity. In this study, we conduct a large‐scale randomized controlled trial with 20,187 users of the WeWard app in France to evaluate the effectiveness of different message framings and intervention durations on app ...
Beatrice Braut, Claire Mollier, Sarah Zaccagni   +2 more
wiley   +1 more source

The Significance of cGAS‐STING Signaling in Response to Oncogenic Viruses

Cell Biochemistry and Function, Volume 44, Issue 9, September 2026.
ABSTRACT The cyclic GMP‐AMP synthase (cGAS)‐stimulator of interferon genes (STING) signaling pathway, as a key DNA sensor, plays a significant role in the regulation of innate immune responses. This pathway can be activated by sensing abnormal DNA, and is of great significance for resisting the invasion of pathogenic microorganisms and maintaining ...
Limei Guo, Li Li, Fang Wang, Wen Liu, Yan Zhang   +4 more
wiley   +1 more source

Diagnostic challenges in patients with Castleman disease, a single center experience from Hungary

Pathology and Oncology Research
Castleman disease is a rare and atypical lymphoproliferative disorder characterized by diverse clinical manifestations. It has both unicentric and multicentric forms, the latter with further subdivisions, i.e., human herpesvirus 8-associated and ...
Boglárka Brúgós, Boglárka Brúgós, Zsófia Simon, Gábor Méhes, Árpád Illés, György Pfliegler, György Pfliegler   +6 more
doaj   +1 more source