Results 31 to 40 of about 1,228,094 (210)

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   +1 more source

Hypereosinophilia–An Unusual Cause of Multiple Embolic Strokes and Multi-Organ Dysfunction [PDF]

Journal of Clinical and Diagnostic Research, 2013
‘Eosinophilia’ can occur due to a large number of allergic, infectious, neoplastic, and idiopathic diseases. It can range in severity from a self-limiting condition to a life-threatening disorder. The term ‘hypereosinophilia’ refers to eosinophil levels
Geeta A. Khwaja, Ashish Duggal, Amit Kulkarni, Neera Choudhary, Meena Gupta, Debashish Chowdhury, Vikram Bohra, Dhruv Zutshi   +7 more
doaj   +1 more source

Hepatitis in Idiopathic Hypereosinophilic Syndrome: Report of an Unusual Case

Haematology Journal of Bangladesh, 2021
World Health Organization defines a rare diagnosis Idiopathic hypereosinophilic syndrome (HES) as a persistent eosinophilia for 6 months and resulting in end-organ dysfunction.
Mahbuba Sharmin, Amin Lutful Kabir, Md. Abdul Aziz , Sonia Shormin Miah , Umme Shahera, Nahida Sultana , Khaza Amirul Islam   +6 more
doaj   +1 more source

Hypereosinophilic Syndrome with Endomyocarditis: Identification by Next-Generation Sequencing of the JAK2-V617F Mutation

, 2023
Hypereosinophilic syndrome requires a peripheral absolute eosinophil count of ≥1.5 × 109 /L with clinical manifestations attributable to peripheral or tissue hypereosinophilia.
Thomas Domin Lee, Ruta Tesfamicael, Thanda Aung, Ernest Brahn, Tesfamicael, Ruta, Domin Lee, Thomas, Brahn, Ernest, Aung, Thanda   +7 more
core   +1 more source

Mepolizumab Reduces Hypereosinophilic Syndrome Flares Irrespective of Blood Eosinophil Count and Interleukin-5. [PDF]

, 2022
Mepolizumab, an anti-interleukin-5 (IL-5) antibody, reduces disease flares in patients with hypereosinophilic syndrome (HES).
Rothenberg, Marc E, HES Mepolizumab Study Group, Faguer, Stanislas, Kwon, Namhee, Gleich, Gerald J, Steinfeld, Jonathan, Roufosse, Florence, Mavropoulou, Eleni, Yancey, Steven W, Blockmans D., Wehbe L., Chupp G. L., Héctor Glenn Valdéz-López, Gleich G. J., Geoffrey L. Chupp, Martti Anton Antila, Tobias Welte, Kahn J. -E., Izabela R. Kupryś-Lipińska, Steven W. Yancey, Regina Garcia Delgado, Lefevre G., Steinfeld J., Aránzazu Alonso, Wardlaw A. J., Knut Brockow, Stanislas Faguer, Maria Laura Fox, Bastian Walz, Gabriel Ricardo García, Faguer S., Jean-Emmanuel Kahn, Mihnea Tudor Zdrenghea, Luis Wehbe, Popov V., Daniela Blanco, Maria Cinta Cid Xutgla, Reiter A. J., Namhee Kwon, Alonso A., Anahí Yañez, Jacek Musial, Mihaly E., Devi Jhaveri, Zdrenghea M. T., Alfredo Gazca-Aguilar, Guillermo Sanz Santillana, Kern P. M., Francisco Pez A. L., Marc E. Rothenberg, Fabrizio Pane, Andreia Luisa Francisco Pez, Joseph H. Butterfield, Sergio Grava, Yancey S. W., Viola Popov, Rothenberg M. E., Vladimir Ivanov, Musial J., Sergey V. Gritsaev, Hernandez Rivas J. M., Dante D. Hernández-Colín, Fox M. L., Butterfield J. H., John B. Cox, Gazca-Aguilar A., Guillaume Lefévre, Vannucchi A. M., Mavropoulou E., Ruth Cerino-Javier, Sosso A., Jonathan Steinfeld, Adriana Sosso, Peter M. Kern, Kwon N., Hernandez-Colin D. D., Jesús María Hernández Rivas, Delgado R. G., Prejzner W., Witold Prejzner, Walz B., Gerald J. Gleich, Florence Roufosse, Vannucchi, Alessandro Maria, Eleni Mavropoulou, Antila M. A., Cerino-Javier R., Valdez-Lopez H. G., Andreas J. Reiter, Jhaveri D., Brockow K., Hamidou M. A., Praveen Akuthota, Kuprys-Lipinska I. R., Cox J. B., Roufosse F., Gritsaev S. V., Cid Xutgla M. C., Akuthota P., Yanez A., Welte T., Ana Isabel González, Eniko Mihaly, Blanco D., Santillana G. S., Ivanov V., Gonzalez A. I., Mohamed A. Hamidou, Alessandro M. Vannucchi, Garcia G. R., Grava S., Andrew J. Wardlaw, Lima M. A., Nikolay Tsyba, Pane F., Marina Andrade Lima, Daniël Blockmans, Tsyba N.   +117 more
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Recalcitrant course of bullous pemphigoid indicating coexisting hypereosinophilic syndrome: A case report and literature review

Clinical Case Reports, 2023
Key Clinical Message As dermatologists, we must be aware that even limited localized lesions may signal a life‐threatening condition, for which early diagnosis and treatment can improve the prognosis. Abstract Bullous pemphigoid is an autoimmune disorder
Raziyeh Ganji, Reem Diab, Farideh Mousavi, Fahimeh Abdollahimajd   +3 more
doaj   +1 more source

Watershed Infarctions and Hypereosinophilic Syndrome Secondary to Metastatic Lung Cancer: A Case Report [PDF]

, 2021
Watershed infarcts are traditionally attributed to ischemia caused by hypoperfusion, with or without vessel stenosis. Implicated diseases usually include atherosclerosis, congestive heart failure, hypotension, angiitis, and less commonly ...
Tsui, Brian Q, Thomas, Mariam, Hathout, Gasser, Tsui, Brian Q ; Thomas, Mariam ; Hathout, Gasser, Brian Tsui   +4 more
core   +1 more source

Hypereosinophilic Syndrome Simulating an Acute Coronary Syndrome [PDF]

, 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.
Neves, Clarinda, Neves, Joana, Franco, Fátima, Clarinda Neves, José Mesquita Bastos, Joana Neves, Ferreira, Raquel, Raquel Ferreira, Fátima Franco, Bastos, José Mesquita   +9 more
core   +1 more source

Acute kidney injury secondary to thrombotic microangiopathy associated with idiopathic hypereosinophilic syndrome: a case report and review of the literature

Journal of Medical Case Reports, 2019
Background Renal involvement in idiopathic hypereosinophilic syndrome is uncommon. The mechanism of kidney damage can be explained as occurring via two distinct pathways: (1) thromboembolic ischemic changes secondary to endocardial disruption mediated by
Diana Curras-Martin, Swapnil Patel, Huzaif Qaisar, Sushil K. Mehandru, Avais Masud, Mohammad A. Hossain, Gurpreet S. Lamba, Harry Dounis, Michael Levitt, Arif Asif   +9 more
doaj   +1 more source

Eosinophilia characterized by a rare CCT6B mutation and responsive to tyrosine kinase inhibition: Case report and literature review

Leukemia Research Reports, 2021
Hypereosinophilic syndrome is a rare disorder arising from neoplastic, or idiopathic causes. The availability of NGS panels has increasingly identified rare mutations as underlying pathogenic events and have led to reclassification of cases of idiopathic
Abhay Singh, Jeffrey Baron, Namrata Singh, Gopisree Peringeth, Eunice S. Wang   +4 more
doaj   +1 more source