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Differenzialdiagnose der Hypereosinophilie

Differential diagnosis of hypereosinophilia

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Zusammenfassung

Als Eosinophilie bezeichnet man eine Erhöhung der absoluten Eosinophilenzahl und unterscheidet hierüber auch bezüglich der Schwere. Die häufigsten Ursachen sind allergische (auch Medikamentennebenwirkungen) und infektiöse Auslöser, aber auch maligne und autoimmune Erkrankungen können mit einer Eosinophilie einhergehen. Ausgeprägte Eosinophilien mit Eosinophilenzahlen >5000/µl finden sich meist bei myeloproliferativen Erkrankungen, der eosinophilen Granulomatose mit Polyangiitis (EGPA) und bei Gewebsmigration von Gewebeparasiten. Als hypereosinophiles Syndrom bezeichnet man eine über 6 Monate bestehende Eosinophilie mit >1500 Eosinophilen/µl bei Ausschluss einer Parasitose, Allergie oder anderer Ursache und Zeichen einer Gewebeeosinophilie mit Endorganschädigung. Zur Abklärung sollten bei persistierender Eosinophilie neben einer genauen Anamnese und körperlichen Untersuchung auch früh ein Organscreening, eine Wurmdiagnostik sowie eine hämatologische Labordiagnostik inklusive Knochenmarkuntersuchung erwogen werden.

Abstract

Eosinophilia is defined as an elevated absolute number of eosinophilic leukocytes in peripheral blood or tissue. Its absolute number also defines the grade of eosinophilia. The main causes are allergic (including drug side effects) and infectious triggers but malignant and autoimmune diseases can also result in eosinophilia. Severe eosinophilia with the number of eosinophils >5000/µl are mostly caused by myeloproliferative disorders, eosinophilic granulomatosis with polyangiitis or during tissue migration in parasitic tissue infections. Hypereosinophilic syndrome is defined as eosinophilia with >1500 eosinophils/µl and a duration of more than 6 months by exclusion of parasitic infections, allergies or other causes of tissue eosinophilia with end-organ damage. For the diagnosis of a persistent eosinophilia a detailed medical history and physical examination should be followed by early organ screening, infection diagnostics especially for helminth infections and hematological laboratory analyses including bone marrow investigations.

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Literatur

  1. Brigden M, Graydon C (1997) Eosinophilia detected by automated blood cell counting in ambulatory North American outpatients. Incidence and clinical significance. Arch Pathol Lab Med 121(9):963–967

    CAS  PubMed  Google Scholar 

  2. Rothenberg ME (1998) Eosinophilia. N Engl J Med 338(22):1592–1600

    Article  CAS  PubMed  Google Scholar 

  3. Tefferi A, Patnaik MM, Pardanani A (2006) Eosinophilia: secondary, clonal and idiopathic. Br J Haematol 133(5):468–492

    Article  CAS  PubMed  Google Scholar 

  4. Valent P, Klion AD, Horny HP, Roufosse F, Gotlib J, Weller PF et al (2012) Contemporary consensus proposal on criteria and classification of eosinophilic disorders and related syndromes. J Allergy Clin Immunol 130(3):607–612 e9

    Article  PubMed  PubMed Central  Google Scholar 

  5. Peju M, Deroux A, Pelloux H, Bouillet L, Hypereosinophilia EO (2018) Biological investigations and etiologies in a French metropolitan university hospital, and proposed approach for diagnostic evaluation. PLoS ONE 13(9):e204468

    Article  PubMed  PubMed Central  Google Scholar 

  6. Crane MM, Chang CM, Kobayashi MG, Weller PF (2010) Incidence of myeloproliferative hypereosinophilic syndrome in the United States and an estimate of all hypereosinophilic syndrome incidence. J Allergy Clin Immunol 126(1):179–181

    Article  PubMed  PubMed Central  Google Scholar 

  7. Pardanani A, Ketterling RP, Li CY, Patnaik MM, Wolanskyj AP, Elliott MA et al (2006) FIP1L1-PDGFRA in eosinophilic disorders: prevalence in routine clinical practice, long-term experience with imatinib therapy, and a critical review of the literature. Leuk Res 30(8):965–970

    Article  CAS  PubMed  Google Scholar 

  8. Wynn SR, Sachs MI, Keating MU, Ostrom NK, Kadota RP, O’Connell EJ et al (1987) Idiopathic hypereosinophilic syndrome in a 5 1/2-month-old infant. J Pediatr 111(1):94–97

    Article  CAS  PubMed  Google Scholar 

  9. Arber DA, Orazi A, Hasserjian R, Thiele J, Borowitz MJ, Le Beau MM et al (2016) The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia. Blood 127(20):2391–2405

    Article  CAS  PubMed  Google Scholar 

  10. Simon HU, Plotz SG, Dummer R, Blaser K (1999) Abnormal clones of T cells producing interleukin-5 in idiopathic eosinophilia. N Engl J Med 341(15):1112–1120

    Article  CAS  PubMed  Google Scholar 

  11. Lefevre G, Copin MC, Staumont-Salle D, Avenel-Audran M, Aubert H, Taieb A et al (2014) The lymphoid variant of hypereosinophilic syndrome: study of 21 patients with CD3-CD4+ aberrant T‑cell phenotype. Medicine (Baltimore) 93(17):255–266

    Article  CAS  Google Scholar 

  12. Hellmich B, Holl-Ulrich K, Gross WL (2007) Hypereosinophilic syndrome—recent developments in diagnosis and treatment. Dtsch Med Wochenschr 132(37):1892–1896

    Article  CAS  PubMed  Google Scholar 

  13. Khoury P, Bochner BS (2018) Consultation for Elevated Blood Eosinophils: Clinical Presentations, High Value Diagnostic Tests, and Treatment Options. J Allergy Clin Immunol Pract 6(5):1446–1453

    Article  PubMed  PubMed Central  Google Scholar 

  14. Di Stefano F, Amoroso A (2005) Clinical approach to the patient with blood eosinophilia. Eur Ann Allergy Clin Immunol 37(10):380–386

    PubMed  Google Scholar 

  15. Roufosse F, Weller PF (2010) Practical approach to the patient with hypereosinophilia. J Allergy Clin Immunol 126(1):39–44

    Article  PubMed  PubMed Central  Google Scholar 

  16. Criado PR, Avancini J, Santi CG, Medrado AT, Rodrigues CE, de Carvalho JF (2012) Drug reaction with eosinophilia and systemic symptoms (DRESS): a complex interaction of drugs, viruses and the immune system. Isr Med Assoc J 14(9):577–582

    PubMed  Google Scholar 

  17. Rossert J (2001) Drug-induced acute interstitial nephritis. Kidney Int 60(2):804–817

    Article  CAS  PubMed  Google Scholar 

  18. Curtis C, Hypereosinophilic Syndrome OP (2016) Clin Rev Allergy Immunol 50(2):240–251

    Article  CAS  PubMed  Google Scholar 

  19. Klion A (2009) Hypereosinophilic syndrome: current approach to diagnosis and treatment. Annu Rev Med 60:293–306

    Article  CAS  PubMed  Google Scholar 

  20. Behera SK, Das S, Xavier AS, Selvarajan S (2018) DRESS syndrome: a detailed insight. Hosp Pract 46(3):152–162

    Article  Google Scholar 

  21. Menendez C, Fernandez-Suarez J, Boga Ribeiro JA, Rodriguez-Perez M, Vazquez F, Gonzalez-Sotorrios N et al (2018) Epidemiological and clinical characteristics of Dientamoeba fragilis infection. Enferm Infecc Microbiol Clin. https://doi.org/10.1016/j.eimc.2018.07.008

    Article  Google Scholar 

  22. Kling K, Kuenzli E, Blum J, Neumayr A (2016) Acute strongyloidiasis in a traveller returning from South East Asia. Travel Med Infect Dis 14(5):535–536

    Article  PubMed  Google Scholar 

  23. Kaplan MH, Hall WW, Susin M, Pahwa S, Salahuddin SZ, Heilman C et al (1991) Syndrome of severe skin disease, eosinophilia, and dermatopathic lymphadenopathy in patients with HTLV-II complicating human immunodeficiency virus infection. Am J Med 91(3):300–309

    Article  CAS  PubMed  Google Scholar 

  24. Schulte C, Krebs B, Jelinek T, Nothdurft HD, von Sonnenburg F, Loscher T (2002) Diagnostic significance of blood eosinophilia in returning travelers. Clin Infect Dis 34(3):407–411

    Article  CAS  PubMed  Google Scholar 

  25. Hellmich B, Holl-Ulrich K, Merz H, Gross WL (2008) Hypereosinophilic syndrome and Churg-Strauss syndrome: is it clinically relevant to differentiate these syndromes? Internist (Berl) 49(3):286–296

    Article  CAS  Google Scholar 

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Correspondence to J. C. Henes.

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J.C. Henes, S. Wirths und B. Hellmich geben an, dass kein Interessenkonflikt besteht.

Dieser Beitrag beinhaltet keine von den Autoren durchgeführten Studien an Menschen oder Tieren.

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B. Hellmich, Kirchheim-Teck

F. Moosig, Neumünster

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Henes, J.C., Wirths, S. & Hellmich, B. Differenzialdiagnose der Hypereosinophilie. Z Rheumatol 78, 313–321 (2019). https://doi.org/10.1007/s00393-018-0587-2

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