Abstract
Piyodermagangrenozum PG , nedeni tam olarak aydınlatılamamış, nötrofilikdermatozlar grubundan bir hastalıktır. Primer olarak anormal nötrofilkemotaksisininpatogenezde sorumlu olduğu düşünülmektedir. Lezyonlar ağrılı, deriden kabarık, hassas ve ülsere nodüller şeklindedir. PG, birçok hastalıkla birlikte görülebilir. Ancak, PG idiyopatik olarak da görülebilir.Burada atipik yerleşimli olarak sol lateralgluteal bölgede ortaya çıkan büyük, ülsere, etrafı endüre ve eritemli olan, lezyonun yara kenarından alınan biyopside piyodermagangrenosum olarak değerlendirilen vakamızı sunuyoruz
References
- Abdelrazeq AS, Lund JN, Leveson SH. Pouchitis-associated pyoderma gangrenosum following restorative proctoco- lectomy for ulcerative colitis. Eur J Gastroenterol Hepatol 2004; 16: 1057-8.
- Callen JP. Pyoderma gangrenosum. Lancet 1998; 351: 581- 5.
- Powell FC, Schroeter AL, Su WP, Perry HO. Pyoderma gangrenosum: a review of 86 patients. Q J Med 1985; 55: 173-13.
- Powell FC, Su WP, Perry HO. Pyoderma gangrenosum: classification and management. J Am Acad Dermatol 1996; 34: 395-14.
- Mir-Madjlessi SH, Taylor JS, Farmer RG. Clinical course and evolution of erythema nodosum and pyoderma gang- renosum in chronic ulcerative colitis: a study of 42 patients. Am J Gastroenterol 1985; 80: 615-5.
- Sampson JA, Harris OD, Van Deth AG. Pyoderma gangre- nosum and chronic active hepatitis: a casereport. Australas J Dermatol 1982; 23: 93-5.
- Ahmadi S, Powell FC. Pyoderma gangrenosum: uncom- mon presentations.Clin Dermatol 2005; 23: 612-8.
- Abela CB, Soldin M, Gateley D. Pyoderma gangreno- sum-Case report. Br J Oral Maxillo fac Surg (in press).
Abstract
Pyoderma gangrenosum PG is a chronic inflammatory skin disease that is present in a group of rare, compromised, neutrophilic dermatoses. It is seen in adult ages, especially ages 25-50. From the lesions that start as painful nodules or pustules, ulcers develop on the edges, which tend to be puffy, tender, and gradually expanding. Lesions may be seen as idiopathic, single or multiple lesions with or without systemic diseases such as malignancy, ulcerative colitis, Crohn's disease, polyarthritis, monoclonal gammopathy. Here we present our case, which is a large, ulcerated, circumscribed, and erythematous lesion located at the left lateral gluteal region as atypically localized, biopside pyoderma gangrenosum taken from the wound side of the lesion
References
- Abdelrazeq AS, Lund JN, Leveson SH. Pouchitis-associated pyoderma gangrenosum following restorative proctoco- lectomy for ulcerative colitis. Eur J Gastroenterol Hepatol 2004; 16: 1057-8.
- Callen JP. Pyoderma gangrenosum. Lancet 1998; 351: 581- 5.
- Powell FC, Schroeter AL, Su WP, Perry HO. Pyoderma gangrenosum: a review of 86 patients. Q J Med 1985; 55: 173-13.
- Powell FC, Su WP, Perry HO. Pyoderma gangrenosum: classification and management. J Am Acad Dermatol 1996; 34: 395-14.
- Mir-Madjlessi SH, Taylor JS, Farmer RG. Clinical course and evolution of erythema nodosum and pyoderma gang- renosum in chronic ulcerative colitis: a study of 42 patients. Am J Gastroenterol 1985; 80: 615-5.
- Sampson JA, Harris OD, Van Deth AG. Pyoderma gangre- nosum and chronic active hepatitis: a casereport. Australas J Dermatol 1982; 23: 93-5.
- Ahmadi S, Powell FC. Pyoderma gangrenosum: uncom- mon presentations.Clin Dermatol 2005; 23: 612-8.
- Abela CB, Soldin M, Gateley D. Pyoderma gangreno- sum-Case report. Br J Oral Maxillo fac Surg (in press).
Details
| Primary Language | Turkish |
|---|---|
| Journal Section | Original Article |
| Authors | |
| Publication Date | September 1, 2018 |
| Published in Issue | Year 2018 Volume: 28 Issue: 3 |
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