Results 51 to 60 of about 5,191,497 (165)

Castleman's disease requiring repeat surgical excision

Journal of Pediatric Surgery Case Reports, 2018
Castleman's disease is an uncommon lymphoproliferative disorder that can be found in both unicentric and multicentric forms. Although the multicentric form is typically seen in immunocompromised patients, the unicentric variety often presents as an ...
Andrew B. Nordin, Aleksander D. Nordin, Mark A. Ranalli, Brian D. Kenney   +3 more
doaj   +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

Unicentric Castleman’s Disease Masquerading Pancreatic Neoplasm [PDF]

, 2012
Castleman’s disease is a rare nonclonal proliferative disorder of the lymph nodes with an unknown etiology. Common locations of Castleman’s disease are mediastinum, neck, axilla, and abdomen.
Partha Chakraborty, Jyoti Ranjan Swain, Souvik Chatterjee, Santanu Sinha, Pritha Rakshit, Saurabh Jain   +5 more
core   +1 more source

Idiopathic Multicentric Castleman Disease Associated With Seronegative Erosive Chronic Polyarthritis: A Diagnostic Challenge

Clinical Case Reports, Volume 14, Issue 9, September 2026.
ABSTRACT Idiopathic multicentric Castleman disease can rarely present with systemic inflammation and erosive seronegative polyarthritis. Awareness of this association helps prevent misdiagnosis and ensures appropriate immunosuppressive management based on clinicopathological and immunohistochemical correlation.
Birahim Lo, Baïdy Sy Kane, Fatine Benjelloun, Mouhamed Almakhy Niang, Ibra Kaïré, Charifah Siddiki, Avotra Razafimandimby, Hamidou Deme, Cherif Mouhamed Moustapha Dial, Abdoulaye Pouye   +9 more
wiley   +1 more source

Human Herpesvirus 8 Causes a Wide Spectrum of Disease in Liver Transplant Recipients and May be Donor Derived: Case Series and Systematic Review of an Emerging Challenge

Transplant Infectious Disease, Volume 28, Issue 5, September/October 2026.
Among 135 cases of post‐liver transplant HHV8 disease (4 from NSW), presentations varied, and mortality was high (44%). Donor screening was rare, and donor‐derived infection was suspected in 33%. Survival improved with mTORi, reduced immunosuppression, chemotherapy, and, for non‐KS disease, donor screening. ABSTRACT Background Human herpesvirus 8 (HHV8)
Karen M. J. Waller, Sudarshan Arvind, Simone I. Strasser, Ken Liu, Geoff W. McCaughan, David G. Bowen, Madeleine Gill, Rebecca Davis, William Rawlinson, Sacha Stelzer‐Braid, Geoff Watson, Vinay Vanguru, Tina Marinelli   +12 more
wiley   +1 more source

Castleman’s Disease Presenting as a Tumorous Paracardiac Formation

Acta Clinica Croatica, 2016
Castleman’s disease (in the literature also known as angiofollicular hyperplasia) is a rare benign lymphoproliferative disease. Clinically, it can manifest as unicentric or multicentric disease.
Ivica Vuković, Toni Brešković, Darko Duplančić, Tonči Batinić, Ivana Štula, Cristian Bulat, Snježana Tomić   +6 more
doaj   +1 more source

Paraneoplastic Pemphigus/Paraneoplastic Autoimmune Multiorgan Syndrome Associated With Castleman Disease: Multidisciplinary Management of a Rare Life‐Threatening Syndrome

Clinical Case Reports, Volume 14, Issue 7, July 2026.
ABSTRACT Refractory oral erosions or polymorphous eruptions should prompt evaluation for paraneoplastic pemphigus, particularly when associated with mediastinal masses. Early tumor excision, multidisciplinary care, and vigilant monitoring for bronchiolitis obliterans are essential to improve outcomes in Castleman disease–associated paraneoplastic ...
Ayaan Sohail, Jessica Evans, Mika Tabata
wiley   +1 more source

Castleman’s Disease Mimetizing Pancreatic Tumor [PDF]

, 2012
Context Angiofollicular lymph node hyperplasia or Castleman’s disease is a rare clinical condition. Knowledge about etiology and physiopathology; and treatment management as well are yet to be defined.
Beron, Reinaldo Isaacs, Goldman, Suzan Menasce, Apodaca-Torrez, Franz Robert, Filho, Benedito Herani, Goldenberg, Alberto, Lobo, Edson José   +5 more
core   +1 more source

Castleman’s Disease. Association with System Scleroderma

, 2023
The article presents an observation of a rare benign lymphoproliferative disease — Castleman’s disease, with pronounced systemic symptoms. The clinical case is of interest not only for the rarity of pathology, but also for the peculiarities of clinical ...
A. V. Yagoda, D. P. Kharchenko, E. V. Bondarenko, P. V. Koroy   +3 more
core   +1 more source

HIV Infection and Opioid Treatment Enable the Engraftment of Kaposi Sarcoma‐Like Tumors Into Immunocompetent Mice

Journal of Medical Virology, Volume 98, Issue 7, July 2026.
ABSTRACT The Kaposi Sarcoma herpesvirus (KSHV) causes Kaposi sarcoma (KS), primary effusion lymphoma, a lymphoproliferative disease (KSHV‐multicentric Castleman's disease), and a cytokine inflammatory syndrome (KICS). These diseases occur more frequently, though not exclusively, among people living with HIV or other types of immune dysregulation. While
Julian Naipauer, Ezequiel Lacunza, Anuj Ahuja, Santas Rosario, Carolina Alejandra Alvarez Canete, Martin C. Abba, Ethel Cesarman, Sundaram Ramakrishnan, Enrique Mesri, Sabita Roy, Umakant Sharma   +10 more
wiley   +1 more source