Journals / International Journal of Computational and Experimental Science and Engineering / 2023 / Cilt: 9 Sayı: 3

Pyoderma Gangrenosum: Retrospective Evaluation of Clinical Features and Treatment Responses in 23 Cases

Pages
307–312
Publication Date
2023-09-30
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Although systemic steroids are most commonly used in the treatment of pyoderma gangrenosum, it should be kept in mind that there are various treatment options ranging from systemic and topical anti-inflammatory therapies to biologic agents according to close follow-up of the patients and additional systemic diseases.

📌 3 Key Takeaways

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Objective & Hypothesis:Pyoderma gangrenosum (PG) is a rare inflammatory disease in the spectrum of neutrophilic diseases characterized by rapidly progressive, painful and large ulcers.
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Key Findings & Data:Between 2018 and 2023, 23 patients diagnosed with PG in our clinic were included in the study.
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Conclusion & Impact:Although systemic steroids are most commonly used in the treatment of pyoderma gangrenosum, it should be kept in mind that there are various treatment options ranging from systemic and topical anti-inflammatory therapies to biologic agents according to close follow-up of the patients and additional systemic diseases.
🔬Design:Research Article
📍Scope:2018 Verileri
⚙️Variables:pyoderma gangrenosum · concomitant systemic diseases · treatment

Abstract

Pyoderma gangrenosum (PG) is a rare inflammatory disease in the spectrum of neutrophilic diseases characterized by rapidly progressive, painful and large ulcers. In this study, we aimed to investigate the relationship between the clinical characteristics and treatment responses of patients diagnosed with PG, treated and followed up in our clinic. Between 2018 and 2023, 23 patients diagnosed with PG in our clinic were included in the study. Medical file records were retrospectively analyzed and various demographic and clinical characteristics, comorbid systemic diseases, treatment protocols and treatment responses of the patients were recorded. Twelve (52.2%) of the patients were female and 11 (47.8%) were male, with a mean age of 42.4±12.9 years. The median disease duration was 52 months (range: 10-540 months). Systemic diseases accompanying PG were present in 14 patients (60.9%). Systemic steroids were the most common treatment (43.5%). Other treatment approaches included adalimumab, infliximab, cyclosporine, oral doxycycline, topical tacrolimus, topical corticosteroids and intralesional steroids. Remission was achieved in 14 patients (60.9%), relapse was observed in 5 patients (21.74%), and no remission/relapse information was available for 4 patients (17.4%) who lost follow-up. The median duration of remission was 23 months (range: 3-96 months). Although systemic steroids are most commonly used in the treatment of pyoderma gangrenosum, it should be kept in mind that there are various treatment options ranging from systemic and topical anti-inflammatory therapies to biologic agents according to close follow-up of the patients and additional systemic diseases.

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Cite This Article

BALIK, Z. B., AKOĞLU, G. (2023). Pyoderma Gangrenosum: Retrospective Evaluation of Clinical Features and Treatment Responses in 23 Cases. International Journal of Computational and Experimental Science and Engineering, Cilt: 9 Sayı: 3, 307–312. https://ajindex.com/articles/964284

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References (1)

  1. Langan, S.M., Groves, R.W., Card, T.R., Gulliford, M.C. (2012). Incidence, mortality, and disease associations of pyoderma gangrenosum in the United Kingdom: a retrospective cohort study. J Invest Dermatol. 132(9):2166-2170. DOI: 10.1038/jid.2012.130. [2] Braun–Falco, M., Kovnerystyy, O., Lohse, P., Ruzicka, T. (2012). Pyoderma gangrenosum, acne, and suppurative hidradenitis (PASH) – a new autoinflammatory syndrome distinct from PAPA syndrome. J Am Acad Dermatol. 66(3):409-415. DOI: 10.1016/j.jaad.2010.12.025. [3]Ortega-Loayza, A.G., Nugent, W.H., Lucero, O.M., Washington, S.L., Nunley, J.R., Walsh, S.W. (2018). Dysregulation of inflammatory gene expression in lesional and nonlesional skin of patients with pyoderma gangrenosum. Br J Dermatol. 178(1):e35–e36. DOI: 10.1111/bjd.15837. [4]Ortega-Loayza, A.G., Friedman, M.A., Reese, A.M., Liu, Y., Greiling, T.M., Cassidy, P.B., … rosenbaum, J.T. (2022). Molecular and cellular characterization of pyoderma gangrenosum: implications for the use of gene expression. J Investig Dermatol. 142(4):1217-1220. DOI: 10.1016/j.jid.2021.08.431. [5]Weenig, R.H., Davis, M.D., Dahl, P.R., Su, W.P.D. (2002). Skin ulcers misdiagnosed as pyoderma gangrenosum. N Engl J Med. 347:1412–1418. DOI: 10.1056/NEJMoa013383. [6]Chevrant-Breton, J., Logeais, B., Pibouin, M. (1989). Pyoderma gangrenosum. Ann Dermatol Venereol. 116: 577–589. [7]Ormerod, A.D., Thomas, K.S., Craig, F.E., Mitchell, E., Greenlaw, M., Norrie, J….Willams, H.C. (2015). Comparison of the two most commonly used treatments for pyoderma gangrenosum: results of the STOP GAP randomised controlled trial. BMJ. 350:h2958. DOI: 10.1136/bmj.h2958. [8]Ben Abdallah, H., Fogh, K., Bech, R. (2019). Pyoderma gangrenosum and tumour necrosis factor alpha inhibitors: a semi-systematic review. Int Wound J. 16(2):511–521. DOI: 10.1111/iwj.13067. [9]Mlika, R.B., Riahi, I., Fenniche, S., Mokni, M., Dhaoui, M.R., Dess, N., …Mokhtar, I. (2022). Pyoderma gangrenosum: a report of 21 cases. Int J Dermatol. 41:65-8. DOI: 10.1046/j.1365-4362.2002.01329.x. [10]Ehling, A., Karrer, S., Klebl, F., Schäffler, A., Müller-Ladner, U. (2004). Therapeutic management of pyoderma gangrenosum. Arthritis Rheum. 50:3076-3084. DOI: 10.1002/art.20559. [11]von den Driesch, P. (1997). Pyoderma gangrenosum: a report of 44 cases with follow-up. Br J Dermatol. 137:1000-1005. [12]Güngör, E., Karakayali, G., Alli, N., Artüz, F., Lenk, N. (1999). Penile pyoderma gangrenosum. J Eur Acad Dermatol Venereol. 12:59-62. [13]