Results 81 to 90 of about 1,228,094 (210)

Suspected “T-Cell-Mediated” Hypereosinophilic Syndrome Presenting with Cerebral Watershed Infarcts [PDF]

, 2011
We describe a case of suspected “T-cell-mediated” hypereosinophilic syndrome presenting with cerebral watershed infarcts. An extensive search for potential embolic sources was negative, supporting the hypothesis that cerebrovascular endothelial ...
R. Schots, S. Dujardin, S. De Raedt, S Dujardin   +3 more
core   +1 more source

Rapid Change in Mental Status in a Patient with Hypereosinophilia

Case Reports in Hematology, 2017
We present the case of a 48-year-old female with acute onset altered mental status, who was found to have eosinophilia, elevated troponin, and embolic strokes. Extensive testing for autoimmune, infectious, and coronary artery etiologies was unremarkable.
Hanyin Wang, John K. Erban
doaj   +1 more source

An Elderly Patient with Abdominal Pain: Hypereosinophilic Syndrome

, 2019
Hypereosinophilic Syndrome (HES) is diagnosed when there is peripheral hypereosinophilia with eosinophil count of more than >1500/µL. The duration of the illness usually lasts more than 6 months, with evidence of target organ damage, affecting mainly ...
Vui, Chong Sook, Hong, Kua Chin, Than, Nan Nitra   +2 more
core  

A Case of Eosinophilic Meningitis Associated with Idiopathic Hypereosinophilic Syndrome [PDF]

, 2017
Idiopathic hypereosinophilic syndrome (IHES) is a rare disease characterized by peripheral blood eosinophilia and eosinophilic infiltration of multiple organs, including the nervous system.
박수철, 정준원
core  

Serum Eosinophil‐Derived Neurotoxin (EDN) as a Biomarker for Treatment Response in Atopic Dermatitis

Clinical &Experimental Allergy, Volume 56, Issue 9, Page 1084-1086, September 2026.
J. I. Olydam, S. Sengkerij, S. Veenbergen, D. J. Hijnen   +3 more
wiley   +1 more source

Acute hemiplegia as initial presentation in FIP1L1-PDGFRA-rearranged myeloid neoplasm with eosinophilia: a case report

Frontiers in Oncology
BackgroundMyeloid neoplasms harboring the FIP1L1-PDGFRA (F/P) fusion gene infrequently manifest as acute cerebral infarction. The F/P fusion gene induces proliferation within the eosinophilic lineage, resulting in a clonal hypereosinophilic syndrome that
Min Cheng, Wenjie Shi, Jin Xu, Doudou Wei, Yue Sun, Qian Jiang, Yongjie Li   +6 more
doaj   +1 more source

Uncommon presentation of hypereosinophilic syndrome

, 2014
The hypereosinophilic syndrome is a group of diseases characterised by persistent blood eosinophilia, defined as more than 1500 cells per micro liter [1], with end-organ involvement and no recognised ...
C C Kariyawasan, J Indrakumar, S Kamaladasa, J Rajkanna   +3 more
core  

Idiopathic Hypereosinophilic Syndrome Associated with Multiple Intracardiac Thrombi

, 2005
A 17-year-old man was referred for dyspnea, fatigue, and fever. Idiopathic hypereosinophilic syndrome was diagnosed. Transthoracic echocardiography demonstrated multiple intracardiac thrombi in the left ventricular apex.
Hasan Kocaturk, Mustafa Yilmaz, Yilmaz, M, Kocaturk, H   +3 more
core   +1 more source

Clinical and immunological biomarkers in hypereosinophilic syndrome: the second step after diagnostic algorithms

Frontiers in Medicine
BackgroundIdiopathic hypereosinophilic syndrome currently represents a major unmet need for all medical specialties dealing with this disease. Markers capable of characterising the wide variability of its clinical presentation are currently lacking ...
David Longhino, Ilaria Baglivo, Maria Antonietta Zavarella, Stefania Colantuono, Chiara Laface, Gabriele Lucca, Laura Bruno, Fabio Romano Selvi, Vincenzo Patella, Aikaterini Detoraki, Rosa Buonagura, Caterina Tatarelli, Barbara Moscatelli, Serena D’Avelli, Elisabetta Abruzzese, Elisabetta Greco, Antonio Gasbarrini, Livio Pagano, Marianna Criscuolo, Sabrina Giammarco, Cristiano Caruso   +20 more
doaj   +1 more source

CD3−CD4+ lymphoid variant of hypereosinophilic syndrome: nodal and extranodal histopathological and immunophenotypic features of a peripheral indolent clonal T-cell lymphoproliferative disorder

Haematologica, 2015
The CD3−CD4+ lymphoid variant of hypereosinophilic syndrome is characterized by hypereosinophilia and clonal circulating CD3−CD4+ T cells. Peripheral T-cell lymphoma has been described during this disease course, and we observed in our cohort of 23 ...
Guillaume Lefèvre, Marie-Christine Copin, Christophe Roumier, Hélène Aubert, Martine Avenel-Audran, Nathalie Grardel, Stéphanie Poulain, Delphine Staumont-Sallé, Julien Seneschal, Gilles Salles, Kamel Ghomari, Louis Terriou, Christian Leclech, Chafika Morati-Hafsaoui, Franck Morschhauser, Olivier Lambotte, Félix Ackerman, Jacques Trauet, Sandrine Geffroy, Florent Dumezy, Monique Capron, Catherine Roche-Lestienne, Alain Taieb, Pierre-Yves Hatron, Sylvain Dubucquoi, Eric Hachulla, Lionel Prin, Myriam Labalette, David Launay, Claude Preudhomme, Jean-Emmanuel Kahn   +30 more
doaj   +1 more source