Results 51 to 60 of about 26,630,094 (175)

Unicentric Castleman&Apos;S Disease Presenting With Multiple Enlarged Lymph Nodes In Mediastinum [PDF]

, 2013
A case of unicentric Castleman's disease located in the mediastinum is presented. A 20 years old male suffering from cough had an image of right hilar enlargement on chest X-ray.
Bozkanat, Erkan, Taş, Dilaver, Kartaloğlu, Zafer, Okutan, Oğuzhan, Erikçi, Alev   +4 more
core   +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

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

Castleman disease of childhood: A case report

, 2001
Giant lymph node hyperplasia (Castleman disease) is uncommon in children and rare in infancy. A 9-month-old girl with a left cervical mass, was followed up for six months.
Filiz Bolat, Derya Alabaz, Melek Ergin, Aysun Uğuz, Gülfiliz Gönlüşen   +4 more
core   +1 more source

Megaloblastic anemia with peripheral neuropathy, a misleading initial presentation in POEMS syndrome: A case report

Journal of Mahatma Gandhi Institute of Medical Sciences, 2014
POEMS (peripheral neuropathy, organomegaly, endocrinopathy, M protein, skin changes) syndrome is a rare multisystem paraneoplastic disorder that occurs in the setting of a plasma cell dyscrasia.
Iadarilang Tiewsoh, Vineeta Singh, U N Jajoo   +2 more
doaj   +1 more source

Espectro clínico de la Enfermedad de Castleman

Galicia Clínica, 2014
RESUMEN La enfermedad de Castleman(EC) es una enfermedad hematológica rara caracterizada por hiperplasia de nódulos linfoides con dos patrones histológicos y clínicos bien diferenciados: hialino-vascular que suele ser unicéntrico, de comportamiento poco ...
María Rebeca Guzmán-Fernández, Fiz Campoy-García, María Pereiro-Sánchez, José Luis Jímenez-Martínez, José Luis Sastre-Moral   +4 more
doaj   +1 more source

Lack of Differences in the Pharmacokinetics of Therapeutic Monoclonal Antibodies Between Japanese and Non‐Japanese Individuals

The Journal of Clinical Pharmacology, Volume 66, Issue 8, August 2026.
Abstract Evaluation of the pharmacokinetics (PK) of new drugs in Japanese individuals is regularly requested by the Japanese regulatory agency prior to participation in global clinical trials or for bridging approaches for regulatory approval. However, the need for PK assessments in the Japanese population may be less compelling for monoclonal ...
Paridhi Gupta, Ashish Sharma, Bernd Meibohm   +2 more
wiley   +1 more source

Neutrophils Promote Metabolic Dysfunction‐Associated Steatotic Liver Disease Through Extracellular Vesicle‐mediated Lipid Transfer

Journal of Extracellular Vesicles, Volume 15, Issue 8, August 2026.
Neutrophils acquire extracellular fatty acids or adipocyte‐derived lipids and store them as triglycerides, polarizing into a lipid‐laden phenotype. Lipid‐laden neutrophils are found in the peripheral blood of HFD‐fed mice and patients with MASLD. These neutrophils release extracellular vesicles enriched with triglycerides and microRNAs that deliver ...
Sanjeeb Shrestha, Soo‐Jung Jung, Seong‐Min Lim, Yu‐Bin Lee, Hyeung‐Wook Shin, Hoyul Lee, Hee‐Kyung Jin, Jae‐Sung Bae, Jae‐Han Jeon, Lai Guan Ng, Chang‐Won Hong   +10 more
wiley   +1 more source

Castleman’s Disease - A Rare Cause of Pyrexia of Unknown Origin (PUO): Case Report

Bangabandhu Sheikh Mujib Medical University Journal, 2010
Pyrexia of unknown origin (PUO) is a common problem in medical practice. Patients suffer from fever for long period but initial relevant investigations remain normal. Infection is the most common cause of PUO in developing countries.
Nusrat Sultana, Rezaul Karim Chowdhury, Naseem Aktar Chowdhury, Md Fariduddin, Naved Jamal, M Abul Hasanat   +5 more
doaj   +1 more source

When idiopathic retroperitoneal fibrosis mimics Castleman disease: a challenging differential diagnosis

, 2022
Idiopathic retroperitoneal fibrosis (I-RPF) can occur either in the spectrum of IgG4-related disease or as a non-IgG4-related form. I-RPF, especially the IgG4-related forms, can sometimes mimic clinically and/or histologically Castleman disease; to ...
Paolo Graziano, Claudia Covelli, Stefano Ascani, Illuminato Carosi, Covelli, Claudia, Ascani, Stefano, Graziano, Paolo, Carosi, Illuminato   +7 more
core   +1 more source