Results 91 to 100 of about 10,507 (195)

Membranous glomerulopathy associated with idiopathic hypereosinophilic syndrome

open access: yesSaudi Journal of Kidney Diseases and Transplantation, 2010
Renal involvement is rarely reported and little is known about the renal morpho-logic changes in the idiopathic hypereosinophilic syndromes. We reported a case of a 52-year-old man with idiopathic hypereosinophilic syndrome associated with membranous ...
Frigui Makram   +5 more
doaj  

Subserous Eosinophilic Gastroenteritis: A Rare Cause of Ascites [PDF]

open access: yes
Eosinophilic gastroenteritis is an inflammatory gastrointestinal disease characterized by eosinophilic infiltration of the digestive tract. The subserous type is the rarest form and diagnosis is challenging because the symptoms are heterogeneous and ...
Barbosa, Susana Manuela   +4 more
core   +1 more source

Eosinophilic pancreatitis versus pancreatitis associated with eosinophilic gastroenteritis – a systematic review regarding clinical features and diagnosis

open access: yesRomanian Journal of Internal Medicine, 2019
Background. Over the past years, eosinophil infiltration involving the gastrointestinal tract and pancreas leading to eosinophilic pancreatitis, eosinophilic gastroenteritis and hypereosinophilic syndrome has been reported in the literature.
Pinte Larisa, Băicuș Cristian
doaj   +1 more source

Biventricular thrombus in hypereosinophilic syndrome presenting with shortness of breath

open access: yesTurkish Journal of Emergency Medicine, 2016
A 48 years old male presented to clinic with 12 months of low grade fever with shortness of breath which has progressively worsened with no associated weight loss, night sweats or loss of appetite. There was no prior history of chronic illness before the
Abdul Baqi   +3 more
doaj   +1 more source

Hypereosinophilic Syndrome Simulating an Acute Coronary Syndrome

open access: yesEuropean Journal of Case Reports in Internal Medicine, 2015
Objectives: to report a case of hypereosinophilic syndrome which presented clinically acute coronary syndrome. Materials and methods: we describe a case of a 69-year-old woman with acute coronary syndrome and peripheral hypereosinophilia.
Joana Neves   +4 more
doaj   +1 more source

Clonal eosinophilia with exclusive pulmonary involvement driven by PDGFRA rearrangement treated with imatinib: A case report

open access: yesLeukemia Research Reports
Hypereosinophilic syndrome (HES) was first described in 1968 by Hardy and Anderson. It is a group of rare, multisystemic and heterogeneous pathologies, characterized by significant morbidity and mortality.
Zaineb Mlayah   +5 more
doaj   +1 more source

An Uncommon Case of Eosinophilic Myocarditis in a Patient With Autoimmune Lymphoproliferative Syndrome

open access: yesAnnals of Internal Medicine: Clinical Cases
Eosinophilic myocarditis is a rare but well-described inflammatory condition with high morbidity and mortality but is not reported as caused by underlying autoimmune lymphoproliferative disorder.
Maria T. Gamero   +6 more
doaj   +1 more source

Las alteraciones de la medula ósea en el perro y el gato [PDF]

open access: yes, 2001
El estudio de la médula ósea, como órgano hématopoyético, es necesario siempre que existan anomalías persistentes o no explicables en el hemograma. En este trabajo se realiza una revisión de las diferentes alteraciones que pueden presentarse en la médula
Aceña Fabián, M. Carmen   +1 more
core  

A case of DRESS syndrome due to Vancomycin [PDF]

open access: yes, 2013
Drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome is a severe systemic reaction that usually begins 2-6 weeks after the introduction of the inciting agent.
Steinmann, William, Zimmerman, Danielle
core  

Systemic Mastocytosis - a Diagnostic Challenge [PDF]

open access: yes, 2014
Mastocytosis refers to a group of disorders characterized by the infiltration of clonally derived mast cells to the skin or extracutaneous tissues resulting in a heterogeneous clinical picture. It is a rare hematologic disorder in all its forms.
Galzerano, A   +3 more
core  

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