Idiopathic hypereosinophilic syndrome


Hypereosinophilia

A severely increased count of eosinophils in the blood defined as a blood eosinophil count of 1.5 × 10e9/L or greater (one and a half billion cells per liter).


Total: 24

                       


(per page)
PMID (PMCID)
29523179
(5845136)
 FEMALE Adult
A young female presenting with heart failure secondary to eosinophilic myocarditis: a case report and review of the literature.
Ralapanawa DMPUK, Kumarihamy KWMPP, Sundararajah M, Jayalath WATA.
BMC Res Notes. 2018;11(1):168.
Secondary causes for hypereosinophilia were excluded and the diagnosis of idiopathic hypereosinophilic syndrome and eosinophilic myocarditis was made.
28065613
 FEMALE Middle Aged
ANCA-Negative Churg-Strauss Syndrome Presenting as Acute Multiple Cerebral Infarcts: A Case Report.
Psychogios K, Evmorfiadis I, Dragomanovits S, Stavridis A, Takis K, Kaklamanis L, Stathis P.
J Stroke Cerebrovasc Dis. 2017;26(3):e47-e49.
We furthermore underscore the need for careful differential diagnosis of the "ANCA negative" cases with persistent hypereosinophilia from the idiopathic hypereosinophilic syndrome.
22999560
 MALE Adult
Idiopathic hypereosinophilic syndrome revealed by encephalopathy.
Wang L, Wei L, Wang JC, Liu YH, Deng YC.
J Clin Neurosci. 2012;19(12):1746-8.
Idiopathic hypereosinophilic syndrome (HES) is characterized by persistent hypereosinophilia ( 8805 1500/mm(3)) with evidence of end-organ damage without a definite underlying cause.
20523982
 FEMALE
Encephalitis in idiopathic hypereosinophilic syndrome in childhood.
Kim HY, Kim YM, Kim SH, Kim HJ.
Pediatr Radiol. 2010;40 Suppl 1:S130-3.
Idiopathic hypereosinophilic syndrome (IHES) is a heterogeneous spectrum of disorders characterized by hypereosinophilia and the presence of dysfunction in various end organs without an identifiable underlying cause.
20236287
 MALE Middle Aged
Lymphocytic variant of hypereosinophilic syndrome.
Zaheri S, Alam A, Marks AJ, Wakelin S.
Clin Exp Dermatol. 2010;35(6):634-6.
When thorough evaluation of a patient with chronic hypereosinophilia fails to reveal an underlying disease, the diagnosis of idiopathic hypereosinophilic syndrome (HES) should be considered.
19142161
 MALE Adult
Successful treatment of refractory idiopathic hypereosinophilic syndrome with etoposide.
Razaq W, Beautyman E.
Am J Ther. 2009;16(1):68-70.
Idiopathic hypereosinophilic syndrome represents a heterogenous group of leukoproliferative disorders with hypereosinophilia of an unknown etiology resulting in multiorgan dysfunction.
17963925
 MALE
Idiopathic hypereosinophilic syndrome with infiltration of cerebrospinal fluid by immature eosinophils: a case report and literature review.
Chou CW, Hsu SP, Chen MT, Chen MH, Shih YH, Lee LS, Lin CF.
Surg Neurol. 2007;68 Suppl 1:S52-5; discussion S55.
Idiopathic hypereosinophilic syndrome is characterized by persistent hypereosinophilia with end organ damage and no definite underlying cause.
17249259
 MALE Adult
Treatment of idiopathic hypereosinophilic syndrome with imatinib mesylate.
Garg A, Duggal L, Aggarwal S, Jain N.
J Assoc Physicians India. 2006;54:883-6.
Patients with idiopathic hypereosinophilic syndrome (HES) show persistent hypereosinophilia of unknown etiology that is associated with end-organ damage.
15863852
 MALE Adult
A case of hypereosinophilic syndrome.
Amano A, Sakai N, Higashi N, Yoshizawa Y, Kawana S.
J Dermatol. 2005;32(4):286-9.
Examination revealed hypereosinophilia, and, because he had symptoms of organ involvement by the heart, lung, and inguinal lymph nodes as well as the skin, we diagnosed him with idiopathic hypereosinophilic syndrome (HES).
15951264
 MALE Adult
[Idiopathic hypereosinophilic syndrome: toward a new molecular-targeted therapy and a new cytomorphological and molecular definition].
Moles MP, Landry J, Roche-Lestienne C, Godon A, Schmidt-Tanguy A, Gardembas M, Le Clech C, Verret JL, Zandecki M, Blanchet O.
Ann Biol Clin (Paris). 2005;63(3):317-22.
Idiopathic hypereosinophilic syndrome is characterised by chronic hypereosinophilia leading to tissue damage, and after exclusion of reactive eosinophilia.
15329768
 MIXED_SAMPLE Adult
Pulmonary hypereosinophilia.
Khoo KL, Lim TK.
Ann Acad Med Singapore. 2004;33(4):521-3.
The arbitrary label of "pulmonary hypereosinophilia" enables the differential diagnoses to be narrowed to the 4 main categories of infections with parasites or fungus, the Churg-Strauss syndrome, chronic eosinophilic pneumonia and the idiopathic hypereosinophilic syndrome.
15293573
 MALE Adult
Successful treatment of idiopathic hypereosinophilic syndrome with imatinib mesylate: a case report.
Tan D, Hwang W, Ng HJ, Goh YT, Tan P.
Int J Hematol. 2004;80(1):75-7.
Patients with idiopathic hypereosinophilic syndrome (HES) show persistent hypereosinophilia of unknown etiology that is associated with end-organ damage.
12856373
 MALE Middle Aged
[Association of hyponatremia and eosinophilia: correlated idiopathic hypereosinophilic syndrome and SIADH or adrenal insufficiency with secondary eosinophilia].
Caliandro D, Bulfoni A.
Clin Ter. 2003;154(2):131-4.
SIADH and Idiopathic Hypereosinophilic Syndrome was diagnosed because we found systemic failure signs due to hypereosinophilia (hepatitis, gastritis, pulmonary hypertension, and encefalopathy).
12514518
 MALE Middle Aged
[Idiopathic hypereosinophilic syndrome and bullous pemphigoid].
Belgnaoui F, Idrissi M, Benyoussef K, Loudiye T, Bella A, Senouci K, Aouni M, Mansouri F, Heid E, Hassam B.
Ann Dermatol Venereol. 2002;129(11):1291-4.
In parallel, the idiopathic hypereosinophilic syndrome was evoked in view of persisting hypereosinophilia without detected aetiology and associated with pulmonary infiltration.
11785010
 MALE Child
[Eosinophilic myositis in a 9 year old boy].
Pena Segura JL, Adrados I, Jimenez Bustos JM, Cabello A, Lopez Pison J.
Rev Neurol. 2001;33(10):960-3.
They may be associated with parasite infections or drugs, or be features of rare systemic disorders of hypereosinophilia, such as the myalgia eosinophilia syndrome and the idiopathic hypereosinophilic syndrome.
11930757
 FEMALE Adult
[Idiopathic eosinophilia with ascites (case report)].
Anic B, Crkvencic N, Mayer M.
Lijec Vjesn. 2001;123(11-12):308-12.
If these disorders are ruled out, consideration should also be given to the diagnosis of primary hypereosinophilia, including idiopathic hypereosinophilic syndrome.
11399591
 OTHER
Malignancy: Case Report: Hypereosinophilia Progressing to Granulocytic Sarcoma and Acute Myelocytic Leukemia with Trisomy 8: A Case Report and Review of the Literature.
Lynott A, Ravandi-Kashani F, Giles FJ.
Hematology. 2000;4(6):487-493.
Criteria for the diagnosis of idiopathic hypereosinophilic syndrome (HES) include the exclusion of other known causes of hypereosinophilia.
11484424
 MALE Child
The hypereosinophilic syndrome after residence in a tropical country: report of 4 cases.
Wynants H, Van Gompel A, Morales I, Vervoort T, Ponomarenko N, Surmont I, Bourgeois P, Van den Enden E, Van Marck E, Van den Ende J.
Acta Clin Belg. 2000;55(6):334-40.
The underlying origin of the hypereosinophilia may be infectious, allergic, toxic, malignant or systemic (the secondary or reactive hypereosinophilic syndrome), but in a number of cases no cause can be found (the idiopathic hypereosinophilic syndrome).
27420743
 OTHER
Hypereosinophilia Progressing to Granulocytic Sarcoma and Acute Myelocytic Leukemia with Trisomy 8: A Case Report and Review of the Literature.
Lynott A, Ravandi-Kashani F, Giles FJ.
Hematology. 1999;4(6):487-93.
Criteria for the diagnosis of idiopathic hypereosinophilic syndrome (HES) include the exclusion of other known causes of hypereosinophilia.
8642249
(2192315)
 MALE Adult
Expansion of cytokine-producing CD4-CD8- T cells associated with abnormal Fas expression and hypereosinophilia.
Simon HU, Yousefi S, Dommann-Scherrer CC, Zimmermann DR, Bauer S, Barandun J, Blaser K.
J Exp Med. 1996;183(3):1071-82.
We identified one patient with idiopathic hypereosinophilic syndrome and one HIV-1-infected individual with associated hypereosinophilia who demonstrated high numbers of CD4-CD8- T cells in peripheral blood.