Results 1 to 10 of about 2,437,081 (240)

HYPEREOSINOPHILIC SYNDROME

Hematology, Transfusion and Cell Therapy
Case Report: A 58-year-old female patient was referred to the hematology clinic in July for examination after leukocytosis was detected in her tests. She has a known history of CKD, Type 2 DM, HT, hyperlipidemia.
Tuba Öztoprak, Harika Shundo
doaj   +5 more sources

Idiopathic hypereosinophilic syndrome: A rare diagnosis in children

Clinical Case Reports, 2020
Idiopathic hypereosinophilic syndrome (IHES) is one of numerous hypereosinophilic syndromes. The incidence of IHES among children is unknown, but it is considered a rare disease.
Kristine Appel Uldall Pallesen, Troels Herlin, Mette Holm, Christian Høst, Mette Christiansen, Mette Ramsing, Mads Kirchheiner Rasmussen, Mette Sommerlund   +7 more
doaj   +2 more sources

Idiopathic Hypereosinophilic Syndrome with Multiple Organ Involvement

Case Reports in Oncology, 2021
Idiopathic hypereosinophilic syndrome is a rare disease which is diagnosed after excluding other conditions. The syndrome is characterized by multiple organ involvement including the heart, nervous system, lungs, and gastrointestinal tract.
Reham Abo Shdid, Bahjat Azrieh, Seham Alebbi, Shafik Mansour, Muhammad Naeem   +4 more
doaj   +2 more sources

Bone marrow morphology is a strong discriminator between chronic eosinophilic leukemia, not otherwise specified and reactive idiopathic hypereosinophilic syndrome

Haematologica, 2017
Chronic eosinophilic leukemia, not otherwise specified can be difficult to distinguish from idiopathic hypereosinophilic syndrome according to the current World Health Organization guideline.
Sa A. Wang, Robert P. Hasserjian, Wayne Tam, Albert G. Tsai, Julia T. Geyer, Tracy I. George, Kathryn Foucar, Heesun J. Rogers, Eric D. Hsi, Bryan A. Rea, Adam Bagg, Carlos E. Bueso-Ramos, Daniel A. Arber, Srdan Verstovsek, Attilio Orazi   +14 more
doaj   +2 more sources

Hypereosinophilic syndrome

The Turkish Journal of Gastroenterology, 1995
The hypereosinophilic syndrome is a multisystem syndrome characterized by peripheral blood eosinophilia and eosinophil infiltration of bone marrow, heart, and other organs. The syndrome is associated with cardiac, hematological, pulmonary, neurological, and cutaneous involvement and, if untreated, has a high fatality rate. Criteria for the diagnosis of
Azmi SERİN, Senem KÜÇÜKBAŞ, Tülin ŞAHİN   +2 more
doaj   +3 more sources

Benralizumab for acute thromboembolism in hypereosinophilic syndrome: a case report [PDF]

Allergy, Asthma & Clinical Immunology
Background Hypereosinophilic syndrome is a group of disorders characterized by organ dysfunction caused by hypereosinophilia, which frequently leads to thromboembolic complications with potentially fatal outcomes.
Daiki Nagira, Satoshi Miyamoto, Taishiro Mizukoshi, Atsushi Yanagisawa, Atsushi Funauchi, Kensuke Kanaoka, Hanako Yoshimura, Tatsunori Jo, Masayoshi Higashiguchi, Yujiro Naito, Takayuki Shiroyama, Satoshi Tetsumoto, Haruhiko Hirata, Yoshito Takeda, Atsushi Kumanogoh   +14 more
doaj   +2 more sources

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

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   +2 more sources

Myocarditis with neurological and dermatological involvement in idiopathic Hypereosinophilic syndrome: Case report [PDF]

Radiology Case Reports
Eosinophilic myocarditis (EM), irrespective of its unique etiology, is marked by varying extents of eosinophil infiltration, frequently accompanied by peripheral eosinophilia.In some instances, the etiology remains undetermined, thus classified as ...
Merimi Ihssane, Mrabet Asmae, Abarkane Nisrine, Bennesser Alaoui Habiba, Noha Elouafi, Nabila Ismaili   +5 more
doaj   +2 more sources

Unmet needs and evidence gaps in hypereosinophilic syndrome and eosinophilic granulomatosis with polyangiitis.

Journal of Allergy and Clinical Immunology, 2023
Hypereosinophilic syndrome (HES) and eosinophilic granulomatosis with polyangiitis (EGPA) are rare systemic inflammatory disorders with overlapping symptoms, elevated eosinophil counts, and heterogenous clinical presentations.
M. Wechsler, B. Hellmich, M. Cid, D. Jayne, X. Tian, L. Baylis, F. Roufosse   +6 more
semanticscholar   +1 more source

JAK inhibition for CD3- CD4+ lymphocytic-variant hypereosinophilic syndrome.

Clinical Immunology, 2023
Alternatives are urgently needed in patients with CD3- CD4+ lymphocytic-variant hypereosinophilic syndrome (L-HES) requiring high-level steroids or who are unresponsive and/or intolerant to conventional alternative therapies.
S. Faguer, M. Groh, F. Vergez, M. Hunault-Berger, Nicolas Duployez, Yves Renaudineau, Carle Paul, G. Lefèvre, J. Kahn   +8 more
semanticscholar   +1 more source