Results 21 to 30 of about 21,386 (303)

Complications and Management of Idiopathic Multicentric Castleman Disease. [PDF]

HCA Healthc J Med
Feustel K, Keeling J, Makos O, Scherbak D.   +3 more
europepmc   +3 more sources

Concurrent HIV viral blips during two episodes of multicentric Castleman disease in an adult on antiretroviral therapy: Implication for HIV persistence

IDCases, 2021
Human herpesvirus-8 (HHV8)-associated multicentric Castleman disease (HHV8-MCD) is a rare nonmalignant lymphoproliferative disorder most commonly observed in PLWH.
Ilyse Darwish, Cecilia Costiniuk, Nadine Kronfli, David Haegert, Jean-Pierre Routy   +4 more
doaj   +1 more source

International Consensus Histopathological Criteria for Subtyping Idiopathic Multicentric Castleman Disease Based on Machine Learning Analysis. [PDF]

Am J Hematol
ABSTRACT Idiopathic multicentric Castleman disease (iMCD) is a rare lymphoproliferative disorder classified into three recognized clinical subtypes—idiopathic plasmacytic lymphadenopathy (IPL), TAFRO, and NOS. Although clinical criteria are available for subtyping, diagnostically challenging cases with overlapping histopathological features highlight ...
Nishimura MF, Haratake T, Nishimura Y, Nishikori A, Sumiyoshi R, Ujiie H, Kawahara Y, Koga T, Ueki M, Laczko D, Oksenhendler E, Fajgenbaum DC, van Rhee F, Kawakami A, Sato Y.   +14 more
europepmc   +2 more sources

A Rare Lymphoproliferative Disease: Castleman Disease

Turkish Journal of Hematology, 2021
Castleman disease is a rare lymphoproliferative disease also known as angiofollicular lymph node hyperplasia. It is classified as hyaline vascular and plasmacytic variants histologically but characteristics of both types can coexist.
Eren Gündüz, Nihal Özdemir, Şule Mine Bakanay, Sema Karakuş   +3 more
doaj   +1 more source

The Enigma of Idiopathic Multicentric Castleman Disease: An Elusive Diagnosis. [PDF]

Cureus
Ohemeng-Dapaah J, Onyechi A, Kang A, Lacasse A, Sinha J.   +4 more
europepmc   +3 more sources

Validated international definition of the thrombocytopenia, anasarca, fever, reticulin fibrosis, renal insufficiency, and organomegaly clinical subtype (TAFRO) of idiopathic multicentric Castleman disease

American journal of hematology/oncology, 2021
Thrombocytopenia, anasarca, fever, reticulin fibrosis, renal insufficiency, and organomegaly (TAFRO) syndrome is a heterogeneous entity manifesting with a constellation of symptoms described above that can occur in the context of idiopathic multicentric ...
Yoshito Nishimura, D. Fajgenbaum, S. Pierson, N. Iwaki, Asami Nishikori, M. Kawano, N. Nakamura, K. Izutsu, K. Takeuchi, M. F. Nishimura, Y. Maeda, F. Otsuka, K. Yoshizaki, É. Oksenhendler, F. Van Rhee, Y. Sato   +15 more
semanticscholar   +1 more source

Multicentric Castleman's Disease [PDF]

Medical Journal Armed Forces India, 2002
Castleman's disease is a rare, atypical lymphoproliferative disorder that is morphologically and clinically heterogeneous and is associated with a risk of developing malignant lymphoma. It represents a distinct form of lymph node hyperplasia rather than a neoplasm or a hamartoma. In Castleman's original report, this lesion was described as solitary and
M K, Gupta, S K, Magu, A, Behl
openaire   +2 more sources

Idiopathic multicentric Castleman disease and associated autoimmune and autoinflammatory conditions: practical guidance for diagnosis

Rheumatology, 2022
Idiopathic multicentric Castleman disease (iMCD) is an infrequent and life-threatening disorder characterized by systemic inflammatory symptoms, generalized lymphadenopathy, polyclonal lymphocyte proliferation and organ dysfunction caused by a ...
Andrés González García, J. Fernandez-Martin, Á. Robles Marhuenda   +2 more
semanticscholar   +1 more source

Plasma Cell-rich Nephritis with a Systemic Polyclonal Lymphoproliferative Disorder, Mimicking Idiopathic Multicentric Castleman Disease, Systemic Lupus Erythematosus, and IgG4-related Disease. [PDF]

Intern Med
Hebisawa Y, Ohta A, Sekimoto R, Sakurai N, Setoguchi K.   +4 more
europepmc   +3 more sources

Idiopathic Plasmacytic Lymphadenopathy Forms an Independent Subtype of Idiopathic Multicentric Castleman Disease

International Journal of Molecular Sciences, 2022
Idiopathic multicentric Castleman disease (iMCD) is a type of Castleman disease that is not related to KSHV/HHV8 infection. Currently, iMCD is classified into iMCD-TAFRO (thrombocytopenia, anasarca, fever, reticulin fibrosis, and organomegaly) and iMCD ...
Asami Nishikori, M. F. Nishimura, Yoshito Nishimura, F. Otsuka, Kanna Maehama, K. Ohsawa, S. Momose, N. Nakamura, Y. Sato   +8 more
semanticscholar   +1 more source