Results 101 to 110 of about 1,018 (169)

Autoreactive Antibodies Associated with Castleman Disease Triad

Case Reports in Immunology, Volume 2024, Issue 1, 2024.
The Castleman triad has been described in a select few patients presenting with a retroperitoneal mass, mucocutaneous pemphigus vulgaris, and bronchiolitis obliterans. Here, we describe the Castleman triad in a 19‐year‐old male with unicentric hyaline vascular type Castleman disease (HV‐CD).
Jacqueline A. Turner, Ali Hakimi, Hannah Lee, Jeffrey T. Schowinsky, Jeffrey M. Sippel, Bradford J. Siegele, Raul M. Torres, William A. Robinson, Necil Kütükçüler   +8 more
wiley   +1 more source

HHV-8-negative multicentric Castleman disease presenting as a crescentic immune complexes membranoproliferative glomerulonephritis. [PDF]

, 2020
Multicentric Castleman disease is a rare polyclonal lymphoproliferative disorder mainly associated with two renal manifestations: thrombotic microangiopathy and amyloidosis.
Duss, F.R., Halfon, M., Nunes, M.B., Rotman, S.   +3 more
core   +1 more source

Anasarca, Fever, Thrombocytopenia, Organomegaly, and Multiorgan Failure in a 24-Year-Old Pregnant Woman

Case Reports in Critical Care, 2017
TAFRO syndrome is a distinct idiopathic multicentric Castleman disease characterized by the association of thrombocytopenia, anasarca, fever, reticulin fibrosis, and organomegaly. We report the first case occurring in a Caucasian pregnant woman.
Guillaume Morel, Joy Mootien, Philippe Guiot, Khaldoun Kuteifan   +3 more
doaj   +1 more source

A case of dermatomyositis complicated with pleural effusion and massive ascites [PDF]

, 2019
We report a patient with dermatomyositis (DM) complicated with progressive pleural effusion and ascites. A 40-year-old woman was hospitalized in our department because of severe myalgia and dysphagia, complicated with pleural effusion and massive ascites.
Asano, Tomoyuki, Fujita, Yuya, Kobayashi, Hiroko, Matsumoto, Haruki, Matsuoka, Naoki, Migita, Kiyoshi, Sasajima, Tomomi, Sato, Shuzo, Suzuki, Eiji, Temmoku, Jumpei, Watanabe, Hiroshi, Yashiro Furuya, Makiko, 佐藤, 秀三, 古谷, 牧子, 右田, 清志, 天目, 純平, 小林, 浩子, 松岡, 直紀, 松本, 聖生, 浅野, 智之, 渡辺, 浩志, 藤田, 雄也, 鈴木, 英二   +22 more
core   +1 more source

Concurrent idiopathic multicentric Castleman disease with TAFRO and Sjögren’s syndrome in a young patient: a challenging diagnostic overlap

European Journal of Case Reports in Internal Medicine
Background: Idiopathic multicentric Castleman disease (iMCD) with TAFRO syndrome (characterized by thrombocytopenia, anasarca, fever, reticulin fibrosis/renal failure, organomegaly) is a recently described disorder. The diagnostic criteria for iMCD-TAFRO
Maria Carolina Carvalho, Matilde Coimbra, João Fernandes Serodio, José Delgado Alves   +3 more
doaj   +1 more source

TAFRO syndrome: A case report and review of the literature

Human Pathology: Case Reports, 2017
TAFRO syndrome is a rare clinicopathologic variant of idiopathic multicentric Castleman disease characterized by Thrombocytopenia, Ascites (anasarca), myeloFibrosis, Renal dysfunction, and Organomegaly.
Tieying Hou, Jaspreet Dhillon, Wenbin Xiao, Elaine S. Jaffe, Amy M. Sands, Vishala Neppalli, George Deeb, Nan Zhang   +7 more
doaj   +1 more source

血小板減少症患者における血栓形成能を評価するための新規マイクロチップフローチャンバーシステム [PDF]

, 2021
鹿児島大学博士(医学)Doctor of Philosophy in Medical Science博士論文全文, 博士論文要旨, 最終試験結果の要旨, 論文審査の要旨Background: In the intensive care unit (ICU), patients with thrombocytopenia are at high risk for bleeding and should be assessed for their thrombogenic potential ...
139395, Atari, Bengo, アタリ, ベンゴ, 中, 弁護   +3 more
core  

Idiopathic multicentric Castleman’s disease, infrequent cause of Lupus-like. Case Report. [PDF]

, 2019
Castleman’s disease (CD) or angiofollicular lymph node hyperplasia includes a heterogeneous mix of reactive lymphoproliferative processes with well-defined histological features.
Cabezas, Antonio Fabian, Lillo, Fernando Andrés, Riquelme, Santiago Felipe Andrés, Zapata, Juan Manuel   +3 more
core   +2 more sources

Interleukin-6 in Castleman disease subtypes: look to tissues, not just blood [PDF]

Not ...
Luke Y.C. Chen, Mariam Goubran
core   +2 more sources

Renal Pathologic Findings in TAFRO Syndrome: Is There a Continuum Between Thrombotic Microangiopathy and Membranoproliferative Glomerulonephritis? A Case Report and Literature Review

Frontiers in Immunology, 2019
Background: TAFRO syndrome is a clinical subtype of idiopathic multicentric Castleman disease (iMCD) that is characterized by thrombocytopenia, anasarca, fever and/or elevated serum C-reactive protein, renal dysfunction, and organomegaly.Case ...
Amélie Leurs, Amélie Leurs, Viviane Gnemmi, Arnaud Lionet, Loïc Renaud, Loïc Renaud, Jean-Baptiste Gibier, Marie-Christine Copin, Eric Hachulla, Pierre-Yves Hatron, David Launay, David Launay, David Fajgenbaum, Louis Terriou, Louis Terriou   +14 more
doaj   +1 more source