Results 61 to 70 of about 13,750 (216)
Idiopathic multicentric Castleman disease: A case report
Asian Journal of Medical SciencesCastleman disease is a rare disease affecting lymph nodes and is considered a non-clonal lymphoproliferative disorder. It has variable clinical presentation and is divided into clinical and histopathological subtypes.
Anna John , Sheima R Das
doaj +1 more source
Castleman Disease: An Unexpected Cause of a Solitary Pleural Mass
Case Reports in Radiology, 2013 Castleman disease (CD) is a rare benign lymphoproliferative disorder, the etiology of which is unclear. Clinically it may manifest as localized disease (unicentric) or disseminated disease (multicentric).
Fiachra Moloney +3 more
doaj +1 more source
Castleman′s disease: Hyaline vascular type
Medical Journal of Dr. D.Y. Patil University, 2014 Castleman′s disease is a rare disease of lymph node with two identified forms, the hyaline vascular type and plasma cell type. It presents as localized or systemic lymphadenopathy or even as extranodal mass and may give rise to several differential ...
Srikanth Shastry, Anandam Gadda
doaj +1 more source
, 1996 Apresentam-se dois casos clínicos de doença de Castleman, situação rara e de difícil diagnóstico, um na forma multissistémica e outro na forma localizada, um na variante plasmocitária e outro na de tipo misto.
Leitão, Sara +12 more
core +1 more source
Episodic fevers and vasodilatory shock mimicking urosepsis in a patient with HIV-associated multicentric Castleman’s Disease: a case report [PDF]
, 2016 Background: Multicentric Castleman's disease (MCD) is a pre-malignancy that presents with lymphadenopathy and features of systemic inflammation. Human immunodeficiency virus (HIV)-associated MCD is associated with human herpesvirus-8 (HHV-8) infection ...
Frederick J. Lee +5 more
core +1 more source
European S2k guidelines on management of autoimmune blistering diseases in children and adolescents
Journal of the European Academy of Dermatology and Venereology, EarlyView.Autoimmune blistering disorders (AIBDs) in children are rare, challenging to diagnose and treat and often require immunosuppressants. Until now, no paediatric care guidelines existed. The EADV Task Force for AIBDs has developed the consensus‐based recommendations, enabling physicians to adopt a uniform, tailored treatment strategy to improve outcomes ...
A. Nanda +31 more
wiley +1 more source
The “Peripheral Plaintiff”: Duty Determinations in Take-Home Asbestos Cases [PDF]
, 2012 Since the 1970s, litigation concerning the dangers of asbestos in the workplace has transformed from a few workers’ compensation claims to hundreds of thousands of lawsuits against companies in nearly every industry. While the typical plaintiff in these
Kotlarsky, Yelena
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HHV‐8/KSHV in Solid Organ Transplantation: Current Gaps of Knowledge and Future Directions
Transplant Infectious Disease, EarlyView.Risk mitigation strategies, including donors/recipients screening, DNAemia monitoring in recipients at risk, CNI‐to‐mTOR inhibitors switch, antivirals, and rituximab for KICS, may mitigate the impact of HHV‐8/KSHV infection in SOT. This review provides an update on KICS, identifies research gaps, and summarizes advances in screening and management ...
Alessandra Mularoni +9 more
wiley +1 more source
Ühekoldelise Castlemani tõve juhtum [PDF]
, 2013 Castlemani tõbi on harva esinev lümfoproliferatiivne haigus, mis esineb kas ühekoldelise või hulgikoldelisena. Haigus on tavaliselt asümptomaatiline, mistõttu diagnoosimine on sageli keeruline ja aeganõudev.
Oeselg, Airi, Semjonov, Eero
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Mesenteric Castleman's Disease
Yonsei 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