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Fehlreguliertes angeborenes Immunsystem

Neutrophile Dermatosen

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hautnah dermatologie Aims and scope

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© Luise Erpenbeck

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© Luise Erpenbeck

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© Luise Erpenbeck

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© Luise Erpenbeck

Literatur

  1. Villarreal-Villarreal C et al. Sweet syndrome: a review and update. Actas dermo-sifiliograficas. 2016; 107: 369-78

  2. Agarwal A et al. Refractory Subcutaneous Sweet Syndrome Treated With Adalimumab. JAMA Dermatol. 2016; 152: 842-4

  3. Reuss-Borst MA et al. The possible role of G-CSF in the pathogenesis of Sweet's syndrome. Leuk Lymphoma. 1994; 15: 261-4

  4. Kawakami T et al. Elevated serum granulocyte colony-stimulating factor levels in patients with active phase of sweet syndrome and patients with active behcet disease: implication in neutrophil apoptosis dysfunction. Arch Dermatol. 2004; 140: 570-4

  5. Patterson J et al. The vasculopathic reaction pattern. Weedon's Skin Pathology 4th ed Philadelphia, PA: Elsevier Churchill Livingstone. 2016.

  6. Croia C et al. Evaluation of neutrophil extracellular trap deregulated formation in pyoderma gangrenosum. Exp Dermatol. 2021; 30: 1340-4

  7. Bonnekoh H et al. Skin and Systemic Inflammation in Schnitzler's Syndrome Are Associated With Neutrophil Extracellular Trap Formation. Front Immunol. 2019; 10: 546

  8. Heath MS et al. Insights Into the Pathogenesis of Sweet's Syndrome. Front Immunol. 2019; 10: 414

  9. Takahama H et al. Neutrophilic dermatosis of the dorsal hands: a case showing HLA B54, the marker of Sweet's syndrome. Int J Dermatol. 2010; 49: 1079-80

  10. von den Driesch P. Sweet's syndrome (acute febrile neutrophilic dermatosis). J Am Acad Dermatol. 1994; 31: 535-56; quiz 557-60

  11. Su WP et al. Diagnostic criteria for Sweet's syndrome. Cutis. 1986; 37: 167-74

  12. Cohen PR et al. Sweet's syndrome and cancer. Clin Dermatol. 1993; 11: 149-57

  13. Raza S et al. Insight into Sweet's syndrome and associated-malignancy: a review of the current literature. Int J Oncol. 2013; 42: 1516-22

  14. Sujobert P et al. Evidence of differentiation in myeloid malignancies associated neutrophilic dermatosis: a fluorescent in situ hybridization study of 14 patients. J Invest Dermatol. 2013; 133: 1111-4

  15. Aliper AM et al. A role for G-CSF and GM-CSF in nonmyeloid cancers. Cancer Med. 2014; 3: 737-46

  16. Stucki A et al. Endothelial cell activation by myeloblasts: molecular mechanisms of leukostasis and leukemic cell dissemination. Blood. 2001; 97: 2121-9

  17. Cohen PR et al. Sweet's syndrome: a review of current treatment options. Am J Clin Dermatol. 2002; 3: 117-31

  18. Garcovich S et al. Drug management of neutrophilic dermatoses. Expert Rev Clin Pharmacol 2017; 10: 1119-28

  19. Kluger N et al. Efficacy of anti-interleukin-1 receptor antagonist anakinra (Kineret®) in a case of refractory Sweet's syndrome. Dermatology. 2011; 222: 123-7

  20. Marzano AV et al. A Comprehensive Review of Neutrophilic Diseases. Clin Rev Allergy Immunol. 2018; 54: 114-30

  21. Su WP et al. Pyoderma gangrenosum: clinicopathologic correlation and proposed diagnostic criteria. Int J Dermatol. 2004; 43: 790-800

  22. Maverakis E et al. Diagnostic Criteria of Ulcerative Pyoderma Gangrenosum: A Delphi Consensus of International Experts. JAMA Dermatol. 2018; 154: 461-6

  23. Marzano AV et al. Pyoderma gangrenosum and its syndromic forms: evidence for a link with autoinflammation. Br J Dermatol. 2016; 175: 882-91

  24. Kontos AP et al. An open-label study of topical tacrolimus ointment 0.1% under occlusion for the treatment of pyoderma gangrenosum. Int J Dermatol. 2006; 45: 1383-5

  25. Ben Abdallah H et al. Pyoderma gangrenosum and tumour necrosis factor alpha inhibitors: A semi-systematic review. Int Wound J. 2019; 16: 511-21

  26. Herberger K et al. Biologics and immunoglobulins in the treatment of pyoderma gangrenosum - analysis of 52 patients. J Dtsch Dermatol Ges. 2019; 17: 32-41

  27. Kolios AG et al. Canakinumab in adults with steroid-refractory pyoderma gangrenosum. Br J Dermatol. 2015; 173: 1216-23

  28. Szatkowski J et al. Acute generalized exanthematous pustulosis (AGEP): A review and update. J Am Acad Dermatol. 2015; 73: 843-8

  29. Sneddon IB et al. Subcorneal pustular dermatosis. Br J Dermatol 1956; 68: 385-94

  30. Watts PJ et al. Subcorneal Pustular Dermatosis: A Review of 30 Years of Progress. Am J Clin Dermatol 2016; 17: 653-71

  31. Sanchez N et al. Subcorneal pustular dermatosis: a variant of pustular psoriasis. Acta Derm Venereol Suppl (Stockh) 1979; 59: 147-51

  32. Ratnarathorn M et al. Subcorneal pustular dermatosis (Sneddon-Wilkinson disease) occurring in association with nodal marginal zone lymphoma: a case report. Dermatol Online J 2008; 14: 6

  33. Kretschmer L et al. Interruption of Sneddon-Wilkinson Subcorneal Pustulation with Infliximab. Case Rep Dermatol 2017; 9: 140-44

  34. Gooderham MJ et al. An update on generalized pustular psoriasis.Expert Rev Clin Immunol. 2019; 15: 907-19

  35. Booij MT et al. Acitretin revisited in the era of biologics. J Dermatolog Treat. 2011; 22: 86-9

  36. Onoufriadis A et al. Mutations in IL36RN/IL1F5 are associated with the severe episodic inflammatory skin disease known as generalized pustular psoriasis. Am J Hum Genet. 2011; 89: 432-7

  37. Sugiura K et al. The majority of generalized pustular psoriasis without psoriasis vulgaris is caused by deficiency of interleukin-36 receptor antagonist. J Invest Dermatol. 2013; 133: 2514-21

  38. Zhou J et al. An update on genetic basis of generalized pustular psoriasis (Review). Int J Mol Med. 2021; 47

  39. Mossner R et al. The genetic basis for most patients with pustular skin disease remains elusive. Br J Dermatol. 2018; 178: 740-8

  40. Bachelez H et al. Inhibition of the Interleukin-36 Pathway for the Treatment of Generalized Pustular Psoriasis. N Engl J Med. 2019; 380: 981-3

  41. Benjegerdes KE et al. Pustular psoriasis: pathophysiology and current treatment perspectives. Psoriasis (Auckl). 2016; 6: 131-44

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Schrenker, S., Erpenbeck, L. Neutrophile Dermatosen. hautnah dermatologie 38, 44–50 (2022). https://doi.org/10.1007/s15012-021-6823-5

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