Results 21 to 30 of about 1,385 (194)

TAFRO syndrome requiring combined IL 6 and IL 1 inhibition: a case report [PDF]

open access: yesFrontiers in Immunology
IntroductionTAFRO syndrome is a rare and severe variant of idiopathic multicentric Castleman disease (iMCD). The name-giving presentation is a combination of thrombocytopenia, anasarca, fever, reticulin fibrosis/renal dysfunction, and organomegaly.
Ahmad Wael Sultan   +8 more
doaj   +2 more sources

Reversible cerebral vasoconstriction syndrome in idiopathic multicentric Castleman disease under treatment with tocilizumab. [PDF]

open access: yesBMJ Neurol Open
Background Idiopathic multicentric Castleman disease (iMCD) is a rare polyclonal lymphoproliferative disorder characterised by systemic inflammation resulting from overproduction of interleukin 6 (IL-6).
Kamimura N   +6 more
europepmc   +3 more sources

Development and implementation of the International AIDA Network Castleman's disease registry. [PDF]

open access: yesFront Med (Lausanne)
Castleman’s disease (CD) consists of a wide spectrum of rare disorders classified into unicentric CD and multicentric CD (MCD), based on the diffusion of disease distribution and the severity of clinical manifestations.
Vitale A   +35 more
europepmc   +5 more sources

PB2708: SYMPTOM BURDEN AND ITS IMPACT ON DAILY LIFE IN PATIENTS WITH IDIOPATHIC MULTICENTRIC CASTLEMAN’S DISEASE (IMCD): AN EXPLORATORY ANALYSIS OF THE SURVEY’S INTERNAL CONSTRUCT VALIDITY

open access: yesHemaSphere, 2023
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Matt Franklin   +10 more
openaire   +3 more sources

Multicentric Castleman disease presenting with orbital involvement progressing to TAFRO syndrome: a case report [PDF]

open access: yesBMC Ophthalmology
Background Castleman Disease (CD) can be unicentric or multicentric, with the ocular involvement rare; notably, the aggressive TAFRO syndrome (TS) is a subtype of idiopathic multicentric CD (iMCD). Ocular involvement in CD is rare, and to date, there are
Yuanfeng Wei   +7 more
doaj   +2 more sources

Oligocentric Castleman disease: clinical characteristics and surgical outcomes from a single-centre retrospective study. [PDF]

open access: yesFront Immunol
IntroductionOligocentric Castleman Disease (OCD), a distinct subtype of Castleman Disease (CD) intermediate between Unicentric (UCD) and idiopathic Multicentric (iMCD) forms, remains poorly characterised.MethodsThis study retrospectively analysed the ...
Duan Y   +12 more
europepmc   +3 more sources

LRG1, a novel serum biomarker for iMCD disease activity [PDF]

open access: yesBiomarker Research
Idiopathic multicentric Castleman disease (iMCD) is a rare lymphoproliferative disorder characterized by systematic inflammatory symptoms and multiorgan dysfunction caused by a cytokine storm.
Miao-yan Zhang   +7 more
doaj   +2 more sources

Idiopathic multicentric Castleman disease in children: a single-center retrospective analysis

open access: yesBMC Pediatrics
Objective To investigate the clinical features, pathological phenotype, treatment and prognosis of idiopathic multicenter Castleman disease (iMCD)in children. Methods From January 2017 to September 2023, basic information, laboratory tests, treatment and
Junye Du   +9 more
doaj   +2 more sources

No evidence for active viral infection in unicentric and idiopathic multicentric Castleman disease by Viral-Track analysis

open access: yesScientific Reports
Castleman disease (CD) is a rare hematologic disorder characterized by pathologic lymph node changes and a range of symptoms due to excessive cytokine production.
Ira Miller   +6 more
doaj   +2 more sources

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