Results 71 to 80 of about 6,363 (176)

Diagnostic challenges in patients with Castleman disease, a single center experience from Hungary

open access: yesPathology and Oncology Research
Castleman disease is a rare and atypical lymphoproliferative disorder characterized by diverse clinical manifestations. It has both unicentric and multicentric forms, the latter with further subdivisions, i.e., human herpesvirus 8-associated and ...
Boglárka Brúgós   +6 more
doaj   +1 more source

Refractory Uveitis in Patient with Castleman Disease Successfully Treated with Tocilizumab

open access: yesCase Reports in Ophthalmological Medicine, 2012
Although multicentric Castleman disease is a rare but life-threatening disease, eye complications are extremely uncommon. We present a case of refractory uveitis accompanied with Castleman disease successfully treated with tocilizumab.
Toshiyuki Oshitari   +6 more
doaj   +1 more source

Semiautomated classification of units in volcanic terrain based on three morphometric attributes derived from a digital elevation model (DEM)

open access: yesEarth Surface Processes and Landforms, Volume 51, Issue 5, May 2026.
The proposed method better responds to the needs of detailed cartography improving the working scale (local and regional) representation; also roughness attributes facilitate the identification of geomorphological units, and the DEM generation method enhances terrain representation.
Carolina Ramírez Núñez   +3 more
wiley   +1 more source

Mesenteric Castleman's Disease

open access: yesYonsei Medical Journal, 2005
We report here a rare case of mesenteric Castleman's disease presenting as a mesenteric mass. A 13-year-old female child was admitted to our hospital complaining of intermittent vague abdominal pain. She had hypochromic anemia, thrombocytosis and an elevated erythrocyte sedimentation rate (ESR).
Kim, Sung-Hoon   +11 more
openaire   +2 more sources

Intrathoracic Castleman disease

open access: yesTURKISH JOURNAL OF MEDICAL SCIENCES, 2014
To analyze patients with Castleman disease who were diagnosed by surgery.We retrospectively investigated the postoperative pathological records of operations performed between January 1992 and December 2012 in our hospital. Files of 19 patients with the diagnosis of Castleman disease were analyzed.There were 13 male and 6 female patients with a mean ...
Karaoğlanoğlu, NURETTİN   +6 more
openaire   +3 more sources

Quantitative analysis of a rare disease network’s international contact database and E-repository provides insights into biobanking in the electronic consent era

open access: yesOrphanet Journal of Rare Diseases, 2019
Background Castleman disease (CD) describes a group of rare and poorly understood lymphoproliferative disorders that include unicentric CD (UCD), Human Herpes Virus-8 (HHV8)-associated multicentric CD (HHV8 + MCD), and HHV8-negative/idiopathic MCD (iMCD).
Alexander Suarez   +2 more
doaj   +1 more source

POEMS (polyneuropathy, organomegaly, endocrinopathy, M protein, skin lesions) syndrome: a South America's report POEMS (polineuropatia, organomegalia, endocrinopatia, proteína M, alterações de pele): relato sul-americano

open access: yesArquivos de Neuro-Psiquiatria, 2007
The POEMS syndrome, also known as Crow-Fukase syndrome, is an unusual systemic disorder described mainly in Asian individuals. It is characterized by the presence of (P)polyneuropathy, (O)organomegaly, (E)endocrinopathy, (M) M-protein, and (S) skin ...
Ana Claudia Celestino Leite   +3 more
doaj   +1 more source

The management of Castleman disease [PDF]

open access: yesBritish Journal of Haematology, 2021
Oliver C. Lomas   +6 more
openaire   +3 more sources

Immune reconstitution inflammatory syndrome, human herpesvirus 8 viremia, and HIV-associated multicentric Castleman disease

open access: yesInternational Journal of Infectious Diseases, 2016
Kaposi's sarcoma and multicentric Castleman Disease are HIV-related disease processes that are associated with human herpesvirus 8 (HHV-8) infection.
Marc O. Siegel   +3 more
doaj   +1 more source

Retroperitoneal Castleman Disease Mimicking Paraganglioma in a Patient with Klinefelter Syndrome: A Case Report

open access: yesEndocrinology Research and Practice, 2019
Castleman disease progresses with the enlargement of the affected lymph nodes and represented by a wide range of symptoms. This lymphoproliferative disease rarely affects the retroperitoneum. A patient with Klinefelter syndrome was admitted to our clinic
Sema HEPŞEN   +7 more
doaj   +1 more source

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