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The 2021 European Alliance of Associations for Rheumatology/American College of Rheumatology points to consider for diagnosis and management of autoinflammatory type I interferonopathies: CANDLE/PRAAS, SAVI and AGS.
Cetin Gedik K, Lamot L, Romano M, Demirkaya E, Piskin D, Torreggiani S, Adang LA, Armangue T, Barchus K, Cordova DR, Crow YJ, Dale RC, Durrant KL, Eleftheriou D, Fazzi EM, Gattorno M, Gavazzi F, Hanson EP, Lee-Kirsch MA, Montealegre Sanchez GA, Neven B, Orcesi S, Ozen S, Poli MC, Schumacher E, Tonduti D, Uss K, Aletaha D, Feldman BM, Vanderver A, Brogan PA, Goldbach-Mansky R. Cetin Gedik K, et al. Ann Rheum Dis. 2022 May;81(5):601-613. doi: 10.1136/annrheumdis-2021-221814. Epub 2022 Jan 27. Ann Rheum Dis. 2022. PMID: 35086813 Free PMC article.
OBJECTIVE: Autoinflammatory type I interferonopathies, chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature/proteasome-associated autoinflammatory syndrome (CANDLE/PRAAS), stimulator of interferon genes (STING)-associated vasculopathy …
OBJECTIVE: Autoinflammatory type I interferonopathies, chronic atypical neutrophilic dermatosis with lipodystrophy and elevate …
Pyoderma gangrenosum: A systematic review of the molecular characteristics of disease.
Flora A, Kozera E, Frew JW. Flora A, et al. Exp Dermatol. 2022 Apr;31(4):498-515. doi: 10.1111/exd.14534. Epub 2022 Feb 15. Exp Dermatol. 2022. PMID: 35114021 Review.
Pyoderma gangrenosum is a painful recurrent ulcerative neutrophilic dermatosis in which the pathogenesis is incompletely defined. ...
Pyoderma gangrenosum is a painful recurrent ulcerative neutrophilic dermatosis in which the pathogenesis is incompletely defin …
Chronic Atypical Neutrophilic Dermatosis With Lipodystrophy and Elevated Temperature Syndrome: A Systemic Review.
Altom A, Khader SAE, Gad AG, Anadani R, Dang DP, Ansar F, Chaudhari J, Crespo-Quezada J, Huy NT. Altom A, et al. Am J Dermatopathol. 2023 Jun 1;45(6):355-370. doi: 10.1097/DAD.0000000000002345. Epub 2023 Feb 17. Am J Dermatopathol. 2023. PMID: 37191371
BACKGROUND: Chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature syndrome is a rare, hereditary, autoinflammatory disease. ...CONCLUSIONS: Fever, skin lesions, and systemic inflammatory response were the prominent features of chronic …
BACKGROUND: Chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature syndrome is a rare, hereditar …
The 2021 European Alliance of Associations for Rheumatology/American College of Rheumatology Points to Consider for Diagnosis and Management of Autoinflammatory Type I Interferonopathies: CANDLE/PRAAS, SAVI, and AGS.
Cetin Gedik K, Lamot L, Romano M, Demirkaya E, Piskin D, Torreggiani S, Adang LA, Armangue T, Barchus K, Cordova DR, Crow YJ, Dale RC, Durrant KL, Eleftheriou D, Fazzi EM, Gattorno M, Gavazzi F, Hanson EP, Lee-Kirsch MA, Montealegre Sanchez GA, Neven B, Orcesi S, Ozen S, Poli MC, Schumacher E, Tonduti D, Uss K, Aletaha D, Feldman BM, Vanderver A, Brogan PA, Goldbach-Mansky R. Cetin Gedik K, et al. Arthritis Rheumatol. 2022 May;74(5):735-751. doi: 10.1002/art.42087. Epub 2022 Mar 21. Arthritis Rheumatol. 2022. PMID: 35315249
OBJECTIVE: Autoinflammatory type I interferonopathies, chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature/proteasome-associated autoinflammatory syndrome (CANDLE/PRAAS), stimulator of interferon genes (STING)-associated vasculopathy …
OBJECTIVE: Autoinflammatory type I interferonopathies, chronic atypical neutrophilic dermatosis with lipodystrophy and elevate …
Is neutrophilic dermatosis a manifestation of familial Mediterranean fever?
Delplanque M, Ducharme-Bénard S, Moguelet P, Chasset F, Grateau G, Georgin-Lavialle S, Bachmeyer C. Delplanque M, et al. Scand J Rheumatol. 2022 Jan;51(1):42-49. doi: 10.1080/03009742.2021.1904588. Epub 2021 Jun 23. Scand J Rheumatol. 2022. PMID: 34159892
Patients can display dermatological manifestations such as erysipelas-like erythema, generally considered as a neutrophilic dermatosis (ND). It has been suggested that FMF can be associated with other types of ND. ...Three independent investigators identified report …
Patients can display dermatological manifestations such as erysipelas-like erythema, generally considered as a neutrophilic dermat …
Pyoderma gangrenosum: a systematic review.
Cozzani E, Gasparini G, Parodi A. Cozzani E, et al. G Ital Dermatol Venereol. 2014 Oct;149(5):587-600. G Ital Dermatol Venereol. 2014. PMID: 25213386 Review.
Pyoderma gangrenosum (PG) is a rare, chronic neutrophilic dermatosis of unknown etiology. The world wide incidence is estimated to be around 3-10 cases per million population per year. ...
Pyoderma gangrenosum (PG) is a rare, chronic neutrophilic dermatosis of unknown etiology. The world wide incidence is estimate …
The genetics of pyoderma gangrenosum and implications for treatment: a systematic review.
DeFilippis EM, Feldman SR, Huang WW. DeFilippis EM, et al. Br J Dermatol. 2015 Jun;172(6):1487-1497. doi: 10.1111/bjd.13493. Epub 2015 Feb 27. Br J Dermatol. 2015. PMID: 25350484 Review.
Pyoderma gangrenosum (PG) is a rare neutrophilic dermatosis characterized by painful skin ulcerations for which treatment can be challenging. ...
Pyoderma gangrenosum (PG) is a rare neutrophilic dermatosis characterized by painful skin ulcerations for which treatment can …
Inflammatory arthritis-associated pyoderma gangrenosum: a systematic review.
Sawka E, Zhou A, Latour E, Friedman M, Ortega-Loayza AG. Sawka E, et al. Clin Rheumatol. 2021 Oct;40(10):3963-3969. doi: 10.1007/s10067-021-05768-7. Epub 2021 May 18. Clin Rheumatol. 2021. PMID: 34002351
INTRODUCTION/OBJECTIVES: Pyoderma gangrenosum (PG) is a rare, rapidly progressive neutrophilic dermatosis commonly associated with systemic inflammatory diseases. ...
INTRODUCTION/OBJECTIVES: Pyoderma gangrenosum (PG) is a rare, rapidly progressive neutrophilic dermatosis commonly associated …
Pyoderma gangrenosum in hematologic malignancies: A systematic review.
Montagnon CM, Fracica EA, Patel AA, Camilleri MJ, Murad MH, Dingli D, Wetter DA, Tolkachjov SN. Montagnon CM, et al. J Am Acad Dermatol. 2020 Jun;82(6):1346-1359. doi: 10.1016/j.jaad.2019.09.032. Epub 2019 Sep 24. J Am Acad Dermatol. 2020. PMID: 31560977
BACKGROUND: Pyoderma gangrenosum (PG) is a devastating neutrophilic dermatosis that may be associated with trauma or systemic diseases. ...
BACKGROUND: Pyoderma gangrenosum (PG) is a devastating neutrophilic dermatosis that may be associated with trauma or systemic …
Pyoderma gangrenosum: a review with special emphasis on Latin America literature.
Rodríguez-Zúñiga MJM, Heath MS, Gontijo JRV, Ortega-Loayza AG. Rodríguez-Zúñiga MJM, et al. An Bras Dermatol. 2019 Nov-Dec;94(6):729-743. doi: 10.1016/j.abd.2019.06.001. Epub 2019 Nov 1. An Bras Dermatol. 2019. PMID: 31789268 Free PMC article.
Pyoderma gangrenosum is a neutrophilic dermatosis characterized by chronic ulcers due to an abnormal immune response. ...
Pyoderma gangrenosum is a neutrophilic dermatosis characterized by chronic ulcers due to an abnormal immune response. ...
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