Effectiveness of long term administration of humanized anti-interleukin-6 receptor antibody (tocilizumab) for multicentric Castleman's disease with pulmonary …

D Akahane, Y Kimura, M Sumi… - … journal of clinical …, 2006 - pubmed.ncbi.nlm.nih.gov
A 27-year-old man was admitted to our hospital with the complaint of general fatigue. He
had cervical and mediastinal lymphadenopathy. Laboratory examination revealed anemia …

Pathology of Castleman disease

D Wu, MS Lim, ES Jaffe - Hematology/Oncology Clinics, 2018 - hemonc.theclinics.com
The term Castleman disease has been applied to several different lymphoproliferatiive
disorders comprising of several distinct clinicopathologic entities. 1–4 Its prevalence has …

[引用][C] Near‐total resolution of multicentric Castleman disease by prolonged treatment with thalidomide

CR Starkey, NE Joste, FC Lee - American journal of …, 2006 - Wiley Online Library
To the Editor: Bone marrow necrosis (BMN) is a rare disease, and approximately 270 cases
with BMN have been reported in literature up to now [1]. Although malignant hematopoietic …

Isolated microcytic anemia disclosing a unicentric Castleman disease: The interleukin-6/hepcidin pathway?

S Vinzio, L Ciarloni, JL Schlienger, S Rohr… - European journal of …, 2008 - Elsevier
Castleman disease (CD) is a rare lymphoproliferative disorder of uncertain origin. Anemia is
commonly reported and is related to an inflammatory mechanism. Occasionally an …

Chronic myelomonocytic leukemia following multicentric Castleman disease

F Li, X Zhang, Y Guo, Y Zhu, Y Wu… - Case Reports in …, 2018 - Wiley Online Library
Multicentric Castleman disease (MCD) is a rare nonmalignant lymphoproliferative disorder
presenting systemic symptoms such as fever, night sweats, fatigue, anemia, effusions, and …

WHAT IS YOUR DIAGNOSIS? MULTICENTRIC PLASMA CELL TYPE CASTLEMAN'S DISEASE

DI ALAVI, SD Mansouri, S Karimi, AR NAJI, AR Moradi… - 2010 - sid.ir
A 25-year-old woman was admitted with malaise, mild fever, night sweats and intermittent
non-purulent cough since six months ago. Her symptoms gradually progressed during the …

Immune‐mediated thrombocytopenia and IL‐6‐mediated thrombocytosis observed in idiopathic multicentric Castleman disease

AI Rubenstein, SK Pierson… - British Journal of …, 2024 - Wiley Online Library
Idiopathic multicentric Castleman disease (iMCD) is a rare haematological disorder
characterized by generalized lymphadenopathy with atypical histopathological features and …

Unicentric Castleman's disease presenting as amyloid A cardiac amyloidosis: a case report

M Zhang, J Li, Y Wang, Z Tian, L Zhang - Annals of Hematology, 2024 - Springer
A 39-year-old male was admitted to our hospital with a 2-year history of fatigue and
weakness. On examination, he displayed microcytic anemia, low serum albumin …

Castleman's disease presenting as prolonged anemia and growth retardation: a case report and literature review.

M Yang, FD Wang, B Han, SJ Wang… - Acta …, 2011 - search.ebscohost.com
Departments of a Surgery, b Medicine, c Hematology, d Endocrinology, and e Pathology,
Peking Union Medical College Hospital, Beijing, China; f Department of Obstetrics and …

[HTML][HTML] Castleman disease presenting with jaundice: A case report and review of literature

B Zhai, HY Ren, WD Li, S Reddy… - World Journal of …, 2019 - ncbi.nlm.nih.gov
Castleman disease presenting with jaundice: A case report and review of literature - PMC Back
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