Results 41 to 50 of about 584,998 (146)

Hodgkin Lymphoma and Castleman Disease: When One Blood Disease Can Hide Another

Case Reports in Hematology, Volume 2017, Issue 1, 2017., 2017
We describe a rare case of Castleman disease associated de novo with Hodgkin lymphoma. The incidence of Castleman disease is rare; only a few studies have described it in de novo association with Hodgkin lymphoma. The patient described here complained of unique evolutionary axillary adenopathy.
L. Filliatre-Clement, H. Busby-Venner, C. Moulin, G. Roth-Guepin, A. Perrot, Yusuke Shiozawa   +5 more
wiley   +1 more source

Bronchiolitis Obliterans in a Young Female Patient with Paraneoplastic Pemphigus Associated with Unicentric Castleman’s Disease

Lymphatics
Background: Castleman’s disease (CD), also known as angiofollicular lymph node hyperplasia, describes a rare group of diseases manifesting with enlarged lymph nodes and various inflammatory symptoms.
Walid Kteiche, Vasiliki Besa, Stefanie Werther, Dirk Theegarten, Stefanie Bertram, Enno Schmidt, Anna Daniels, Silke C. Hofmann   +7 more
doaj   +1 more source

A Rare Coexistence of Retroperitoneal Pararenal Castleman's Disease with Focal Nodular Hyperplasia

Case Reports in Surgery, 2013
Castleman's disease is a distinct form of lymph node hyperplasia divided into a solitary and a multicentric type. The solitary type occurs most commonly in the mediastinum and is usually asymptomatic.
Theodosios Theodosopoulos, Andreas Karakatsanis, Anneza I. Yiallourou, Fotios Nikolakopoulos, Vassiliki Psychogiou, Eleni Karvouni, Dionysios Voros   +6 more
doaj   +1 more source

The Evolution and Recent Advances in Diagnostic Criteria for Idiopathic Multicentric Castleman Disease

American Journal of Hematology, Volume 100, Issue 11, Page 2064-2073, November 2025.
Idiopathic Multicentric Castleman Disease. ABSTRACT Idiopathic multicentric Castleman disease (iMCD) is a rare cytokine‐driven disorder characterized by systemic inflammation, organ dysfunction, and altered lymph node microscopic architecture. Over the past decade, diagnostic criteria have evolved significantly, integrating clinical, histopathological,
FNU Alnoor, Nicholas C. Spies, Jyoti Kumar, Peyman Samghabadi, Oscar Silva, Matt X. Luo, Karen M. Chisholm, Jingjing Zhang, Alexandra Rangel, David Ng, Peng Li, Robert S. Ohgami   +11 more
wiley   +1 more source

A Palpable Painless Axillary Mass as the Clinical Manifestation of Castleman’s Disease in a Patient with Hepatitis C Disease

Case Reports in Medicine, Volume 2016, Issue 1, 2016., 2016
Introduction. Castleman’s disease (CD) is a rare lymphoproliferative disorder. CD is divided into two clinical subtypes: the most common unicentric and the less usual multicentric subtype. The majority of unicentric CD affects the mediastinum, while neck, abdomen, and axilla are less common locations. Case Presentation.
Athanasia K. Papazafiropoulou, Angeliki M. Angelidi, Antonis A. Kousoulis, Georgios Christofilidis, Chariklia Sagia, Liountmila Kaftanidou, Kassiani Manoloudaki, Aikaterini Tsavari, Georgios Kranidiotis, Alexandros Kamaratos, Andreas Melidonis, Gerald S. Supinski   +11 more
wiley   +1 more source

Specific selection of antigen-reactive lymphocytes into antigenically stimulated lymph nodes in sheep [PDF]

, 1981
Sheep were primed to a variety of antigens and the efferent lymphatic from a popliteal lymph node was cannulated. The cannulated node was challenged repeatedly with PPD and all the lymph and cells removed from the animal.
Hopkins, John, P J Lachmann, McConnell, I., J Hopkins, I McConnell, Lachmann, P J   +5 more
core   +1 more source

Antitumor factors of draining lymph node cells of the mouse sensitized with ehrlich ascites tumor cells. I. Antitumor effect of subcellular factor [PDF]

, 1969
The regional lymph node cells of the mice sensitized with Ehrlich ascites tumor cells is known to possess a substance that shows antitumor activity on target cells (JTC-II cells). For the purpose to clarify the localization of this substance the regional
Nakashima, Youichi
core   +1 more source

HIV‐negative HHV8‐positive multicentric Castleman's disease coexistent with atypical Kaposi's sarcoma

JEADV Clinical Practice, Volume 3, Issue 5, Page 1606-1610, December 2024.
Abstract The co‐occurence of multicentric Castleman's disease (MCD) and Kaposi's sarcoma (KS) represents a rare clinical entity, mostly observed in individuals infected with the human immunodeficiency virus (HIV). Human herpesvirus 8 (HHV‐8) is attributed a crucial etiological role in both conditions. This study presents the case of a 75‐year‐old woman
Anna Scattone, Giacomo Loseto, Biagina Gisella Mennuni, Valentina Mastrandrea, Rosalba Buquicchio, Caterina Foti, Francesco Alfredo Zito, Raffaele Filotico   +7 more
wiley   +1 more source

Systemic Reactive Amyloidosis Associated with Castleman's Disease

Case Reports in Gastroenterology, 2013
We report this case of secondary amyloidosis associated with Castleman's disease. A 51-year-old man presented with systemic symptoms of generalized weakness, fatigue, unintended weight loss, anorexia and progressively worsening abdominal distension.
Vinaya Gaduputi, Hassan Tariq, Kanthi Badipatla, Ariyo Ihimoyan   +3 more
doaj   +1 more source

Complex Presentation of Multicentric Castleman Disease with Coexisting HIV, HHV‐8, and Other Opportunistic Infections

Case Reports in Hematology, Volume 2024, Issue 1, 2024.
Castleman disease (CD) is a rare lymphoproliferative disorder characterized by benign lymph node enlargement. We present the case of a 43‐year‐old male with a complex medical history, including Crohn’s disease treated with Adalimumab and later complicated with tuberculosis (TB) infection.
Yehya Tlaiss, Hadi Farhat, Firas Hasan, Rami Yazbek, Noura Shakaroun, Nizar Bitar, Pier Paolo Piccaluga   +6 more
wiley   +1 more source