Results 51 to 60 of about 25,001,430 (174)

Immunophenotypic characteristics of plasma cells in POEMS syndrome

Cytometry Part B: Clinical Cytometry, Volume 110, Issue 4, Page 266-273, July 2026.
Abstract To analyze the immunophenotypic characteristics of plasma cells in patients with polyneuropathy, organomegaly, endocrinopathy, myeloma protein, and skin changes (POEMS) syndrome. This retrospective study included patients with POEMS syndrome hospitalized in the Department of Hematology, Huashan Hospital, from September 2017 to August 2025 ...
Zhenhua Wang, Tianling Ding, Beiqian Wu, Qiang Niu, Leyao Gu, Yan Yuan, Ping Zhu   +6 more
wiley   +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

Update and new approaches in the treatment of Castleman disease

, 2016
Kah-Lok Chan,1 Stephen Lade,2 H Miles Prince,1,3 Simon J Harrison1,3 1Department of Haematology, 2Department of Anatomical Pathology, Peter MacCallum Cancer Centre, 3Sir Peter MacCallum Department of Oncology, The University of Melbourne, Melbourne, VIC,
Prince HM, Harrison SJ, Chan KL, Lade S
core  

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

Multisystem IgG4‐Related Disease Mimicking Malignancy With Cavitary Pulmonary Nodules, Pleural Thickening and Hepatic Mass‐Like Lesions: A Case Report

Respirology Case Reports, Volume 14, Issue 7, July 2026.
Multisystem IgG4‐RD can closely mimic metastatic malignancy and should be considered when thoracic and extrapulmonary mass‐forming lesions coexist. Timely biopsy confirmation is essential to avoid misdiagnosis and treatment delay. ABSTRACT IgG4‐related disease (IgG4‐RD) is a multisystem fibroinflammatory condition that can mimic metastatic malignancy ...
Ho Young Lee, Juyeon Kang
wiley   +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

Castleman Disease; A Rare Mass of Neck [PDF]

, 2020
Castleman hastalığı, lenfoproliferatif hastalıkların heterojen bir grubu olup tek bir hastalık olarak düşünülmemelidir. Bu hastalık çeşitli klinik şekillerde ortaya çıkmaktadır.
Güçlü, Oğuz, Göret, Ceren Canbey, Kılıç, Aytaç, Dereköy, Fevzi Sefa, Çağlar, Özge   +4 more
core   +1 more source

European S2k guidelines on management of autoimmune blistering diseases in children and adolescents

Journal of the European Academy of Dermatology and Venereology, Volume 40, Issue 7, Page 1137-1161, July 2026.
Autoimmune blistering disorders (AIBDs) in children are rare, challenging to diagnose and treat and often require immunosuppressants. Until now, no paediatric care guidelines existed. The EADV Task Force for AIBDs has developed the consensus‐based recommendations, enabling physicians to adopt a uniform, tailored treatment strategy to improve outcomes ...
A. Nanda, B. Tedbirt, C. Bodemer, M. C. Bolling, M. El Hachem, M. Nikolić, E. Benton, M. Caproni, D. De, D. Didona, K. Drenovska, M. Goebeler, M. Hertl, B. Horváth, M. Kasperkiewicz, D. Kiritsi, M. Larralde, A. V. Marzano, J. Meijer, D. F. Murrell, J. Powell, E. Sprecher, N. S. Chandran, M. M. Tomayko, S. Uzun, N. van Beek, H. Ott, A. Patsatsi, A. Torrelo, A. Welfringer‐Morin, E. Schmidt, P. Joly   +31 more
wiley   +1 more source

Castleman Disease

, 2018
HIV-negative Castleman disease has been associated with autoimmune disease, collagen vascular disorders, pulmonary arterial hypertension, and ...
Zhou, Jing, Hu, Amanda, Cohn, Jason E
core   +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