2023, Number 4
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Rev Hematol Mex 2023; 24 (4)
Hypereosinophilia secondary to B acute lymphoblastic leukemia in an adult patient
Blanco PPM, Pérez MGC, Iglesias JO, Montes APS
Language: Spanish
References: 36
Page: 201-208
PDF size: 277.54 Kb.
ABSTRACT
Background: Hypereosinophilic syndromes are pathological conditions in which
patients present a marked increase in eosinophils in peripheral blood; this alteration
may or may not generate symptoms in affected patients. Their etiology is variable, they
can be of neoplastic and non-neoplastic origin.
Clinical cases: A 65-year-old male patient who presented hypereosinophilic syndrome
secondary to B acute lymphoblastic leukemia, which was approached and managed
with complete remission of the disease.
Conclusions: In hypereosinophilia a causal relationship, the time course and
clinical manifestations may not be easily recognized, which often leads to exhaustive
study. Therefore, the complete study has a place in most cases, since secondary reactive
eosinophilia is a diagnosis of exclusion.
REFERENCES
Klion A. Hypereosinophilic syndrome: approach totreatment in the era of precision medicine. HematologyAm Soc Hematol Educ Program 2018; 2018 (1): 326-331.Doi: https://doi.org/10.1182/asheducation-2018.1.326.
Kelemen K, Saft L, Craig FE, Orazi A, Nakashima M,Wertheim GB, George TI, Horny HP, King RL, Quintanilla-Martinez L, Wang SA, Rimsza LM, Reichard KK. Eosinophilia/hypereosinophilia in the setting of reactive andidiopathic causes, well-defined myeloid or lymphoidleukemias, or germline disorders. Am J Clin Pathol2021; 155 (2): 179-210. Doi: https://doi.org/10.1093/ajcp/aqaa244.
Terwilliger T, Abdul-Hay M. Acute lymphoblastic leukemia:a comprehensive review and 2017 update. BloodCancer J 2017; 7 (6): e577. Doi: https://doi.org/10.1038/bcj.2017.53.
Sas V, Moisoiu V, Teodorescu P, Tranca S, Pop L, Iluta S, etal. Approach to the adult acute lymphoblastic leukemiapatient. J Clin Med 2019; 8 (8):1175. Doi: https://doi.org/10.3390/jcm8081175.
Kuang FL. Approach to patients with eosinophilia. MedClin North Am 2020; 104 (1):1-14. Doi: https://doi.org/10.1016/j.mcna.2019.08.005.
Shomali W, Gotlib J. World Health Organization-definedeosinophilic disorders: 2022 update on diagnosis, riskstratification, and management. Am J Hematol 2022; 97(1): 129-148. Doi: https://doi.org/10.1002/ajh.26352.
Leru PM. Eosinophilic disorders: evaluation of currentclassification and diagnostic criteria, proposal of a practicaldiagnostic algorithm. Clin Transl Allergy 2019; 9: 36. Doi:https://doi.org/10.1186/s13601-019-0277-4.
Abo Shdid R, Azrieh B, Alebbi S, Mansour S, Naeem M.Idiopathic hypereosinophilic syndrome with multiple organinvolvement. Case Rep Oncol 2021; 14 (1): 249-255. Doi:https://doi.org/10.1159/000511396.
Shao H, Wang W, Song J, Tang G, Zhang X, Tang Z, et al.Myeloid/lymphoid neoplasms with eosinophilia and FLT3rearrangement. Leuk Res 2020; 99: 106460. Doi: https://doi.org/10.1016/j.leukres.2020.106460.
Weller PF, Bubley GJ. The idiopathic hypereosinophilicsyndrome. Blood 1994; 83 (10): 2759-79. Doi: http://dx.doi.org/10.1182/blood.V83.10.2759.2759.
Rezk S, Wheelock L, Fletcher JA, Oliveira AM, Keuker CP,Newburger PE, Xu B, Woda BA, Miron PM. Acute lymphocyticleukemia with eosinophilia and unusual karyotype.Leuk Lymphoma 2006; 47 (6): 1176-9. Doi: https://doi.org/10.1080/10428190500508710.
Shi M, Rech KL, Otteson GE, Horna P, Olteanu H, PardananiA, Chen D, Jevremovic D. Prevalence and spectrum of T-celllymphoproliferative disorders in patients with hypereosinophilia:A reference laboratory experience. Ann DiagnPathol 2020; 44: 151412. Doi: https://doi.org/10.1016/j.anndiagpath.2019.151412.
Roufosse F, Garaud S, de Leval L. Lymphoproliferativedisorders associated with hypereosinophilia. Semin Hematol2012; 49 (2): 138-48. Doi: https://doi.org/10.1053/j.seminhematol.2012.01.003.
Spitzer, Gary; Garson M. Lymphoblastic eosinophilia leukemia:A report with of two marked cases. Blood 1973; 42 (3):377-84. Doi: https://doi.org/10.1182/blood.V42.3.377.377.
Gerds AT, Gotlib J, Bose P, Deininger MW, Dunbar A,Elshoury A, et al. Myeloid/Lymphoid neoplasms witheosinophilia and TK fusion genes, version 3.2021, NCCNClinical Practice Guidelines in Oncology. J Natl ComprCanc Netw 2020; 18 (9): 1248-1269. Doi: https://doi.org/10.6004/jnccn.2020.0042.
McClure BJ, Heatley SL, Rehn J, Breen J, Sutton R, HughesTP, Et al. High-risk B-cell acute lymphoblastic leukaemiapresenting with hypereosinophilia and acquiring a novelPAX5 fusion on relapse. Br J Haematol 2020; 191 (2): 301-304. Doi: https://doi.org/10.1111/bjh.17002.
Leverone N, Tran S, Barry J, Akuthota P. Diagnoses associatedwith peripheral blood eosinophilia: A 5-year review.Ann Allergy Asthma Immunol 2021; 127 (5): 597-598. Doi:https://doi.org/10.1016/j.anai.2021.08.013.
Bejarano-Malta F, Ramírez-Pineda S, Cáceres-Paredes J,Rodríguez-Paz N y col. Leucemia linfoblástica aguda asociadacon eosinofilia en paciente escolar. Hematol Méx2017; 18 (2): 85-91.
Narayanan G, Soman LV, Kumar R. Hypereosinophilia: A rarepresentation of acute lymphoblastic leukaemia. J PostgradMed 2018; 64 (1):50-52.
Blatt J, Proujansky R, Horn M, Phebus C, Longworth D,Penchansky L. Idiopathic hypereosinophilic syndrometerminating in acute lymphoblastic leukemia. PediatrHematol Oncol 1992; 9 (2): 151-5. Doi: https://doi.org/10.3109/08880019209018330.
Ferruzzi V, Santi E, Gurdo G, Arcioni F, Caniglia M, EspositoS. Acute lymphoblastic leukemia with hypereosinophiliain a child: case report and literature review. Int J EnvironRes Public Health 2018; 15 (6): 1169. Doi: https://doi.org/10.3390/ijerph15061169.
D'Angelo G, Hotz AM, Todeschin P. Acute lymphoblastic leukemiawith hypereosinophilia and 9p21 deletion: case reportand review of the literature. Lab Hematol 2008; 14 (1): 7-9.
Moita F, Bogalho I, Alaiz H, Parreira J, Frade MJ, NunesA, Gomes da Silva M. Clonal hypereosinophilia withETV6 rearrangement evolving to T-cell lymphoblasticlymphoma: A case report and review of the literature.Case Rep Hematol 2013; 2013: 652745. Doi: https://doi.org/10.1155/2013/652745.
Song G, Liu H, Sun F, Gu L, Wang S. Acute lymphocyticleukemia with eosinophilia: a case report and review ofthe literature. Aging Clin Exp Res 2012; 24 (5): 555-8. Doi:https://doi.org/10.3275/8337.
Ayhan AC, Timur C, Ayhan Y, Cakır B, Erguven M. Doeshypereosinophilic syndrome precede common B acutelymphoblastic leukaemia in childhood? A case report.Acta Haematol 2012; 127 (2): 90-2. Doi: https://doi.org/10.1159/000333085.
Follows GA, Owen RG, Ashcroft AJ, Parapia LA. Eosinophilicmyelodysplasia transforming to acute lymphoblasticleukaemia. J Clin Pathol 1999; 52 (5): 388-9. Doi: http://dx.doi.org/10.1136/jcp.52.5.388.
Chien AJ, Argenyi ZB, Colven RM, Kirby P. Acute lymphoblasticleukemia presenting with urticarial plaques andhypereosinophilia in a child. J Am Acad Dermatol 2004;51 (5 Suppl): S151-5. Doi: https://doi.org/10.1016/j.jaad.2004.04.018.
Hill A, Metry D. Urticarial lesions in a child with acutelymphoblastic leukemia and eosinophilia. Pediatr Dermatol2003; 20 (6): 502-5. Doi: https://doi.org/10.1111/j.1525-1470.2003.20610.x.
Kaneko H, Shimura K, Yoshida M, Ohkawara Y, OhshiroM, Tsutsumi Y, et al. Acute lymphoblastic leukemia witheosinophilia lacking peripheral blood leukemic cell: a rareentity. Indian J Hematol Blood Transfus 2014; 30 (Suppl 1):80-3. Doi: https://doi.org/10.1007/s12288-013-0255-2.
Wynn TT, Heerema NA, Hammond S, Ranalli M, KahwashSB. Acute lymphoblastic leukemia with hypereosinophilia:report of a case with 5q deletion and review of the literature.Pediatr Dev Pathol 2003; 6 (6): 558-63. Doi: https://doi.org/10.1007/s10024-003-2019-8.
Donahue TP. Images in cardiology: Loeffler's endocarditisresulting from acute lymphoblastic leukemia. ClinCardiol 2002; 25 (7): 345. Doi: https://doi.org/10.1002/clc.4950250708.
Fishel RS, Farnen JP, Hanson CA, Silver SM, Emerson SG.Acute lymphoblastic leukemia with eosinophilia. Medicine(Baltimore) 1990; 69 (4): 232-43.
Kobayashi D, Kogawa K, Imai K, Tanaka T, Sada A, NonoyamaS. Hyper-eosinophilia in granular acute B-cell lymphoblasticleukemia with myeloid antigen expression. Pediatr Int2012; 54 (4): 543-6. Doi: https://doi.org/10.1111/j.1442-200X.2011.03471.x.
Rezamand A, Ghorashi Z, Ghorashi S, Nezami N. Eosinophilicpresentation of acute lymphoblastic leukemia. Am JCase Rep 2013; 14: 143-6.
Parasole R, Petruzziello F, De Matteo A, Maisto G, CastelliL, Errico ME, Menna G, Poggi V. Hypereosinophilia in childhoodacute lymphoblastic leukaemia at diagnosis: reportof 2 cases and review of the literature. Ital J Pediatr 2014;40: 36. Doi: https//doi.org/10.1186/1824-7288-40-36.
Sahu KK, Malhotra P, Khadwal A, Sachdeva MS, Sharma P,Varma N, Varma SC. Hypereosinophilia in Acute LymphoblasticLeukemia: Two Cases with Review of Literature.Indian J Hematol Blood Transfus 2015; 31 (4): 460-5. Doi:https://doi.org/10.1007/s12288-014-0436-7.