This is the first case in the literature showing the association of this Syndrome and tuberculosis.
📌 3 Key Takeaways
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Objective & Hypothesis:Disseminated subcorneal pustular skin lesions that developed after a week of combined 4-drug therapy for cervical lymph node tuberculosis in a 41 years old female patient who had chronic renal failure and was receiving haemodialysis for 4 years were investigated and Sneddon-Wilkinson Syndrome was diagnosed by clinical and histopathological findings.
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Key Findings & Data:Disseminated subcorneal pustular skin lesions that developed after a week of combined 4-drug therapy for cervical lymph node tuberculosis in a 41 years old female patient who had chronic renal failure and was receiving haemodialysis for 4 years were investigated and Sneddon-Wilkinson Syndrome was diagnosed by clinical and histopathological findings.
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Conclusion & Impact:This is the first case in the literature showing the association of this Syndrome and tuberculosis.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Böbrek yetmezliği · kronik · Deri hastalıkları
Abstract
Disseminated subcorneal pustular skin lesions that developed after a week of combined 4-drug therapy for cervical lymph node tuberculosis in a 41 years old female patient who had chronic renal failure and was receiving haemodialysis for 4 years were investigated and Sneddon-Wilkinson Syndrome was diagnosed by clinical and histopathological findings. This is the first case in the literature showing the association of this Syndrome and tuberculosis.
Özet
Kronik böbrek yetmezliği olan, 4 yıldır hemodiyalize giren 41 yaşındaki bayan hastada, servikal tüberküloz lenfadenit tanısıyla 4'lü anti-tüberküloz tedavi almaya başladıktan bir hafta sonra gelişen yaygın püstüler subkorneal yerleşimli dermatoz araştırılmış ve klinik-histopatolojik olarak Sneddon-Wilkinson Sendromu ile uyumlu bulunmuştur. Bu, tüberküloz zemininde geliştiği bildirilen literatürdeki ilk olgudur
OLUT, A. I., ÖZÜNLÜ, H., ÖZSAKARYA, F., UÇMAK, M., ÇUKUROVA, İ. (2005). Sneddon-Wilkinson syndrome that developed in a patient with lymph node tuberculosis. ANKEM Dergisi, Cilt: 19 - Sayı: 1, 52–54. https://ajindex.com/articles/207598
Khachemoune A, Blyumin ML: Sneddon-Wilkinson disease resistant to dapsone and colchicine succesfully controled with PUVA, Dermatol Online J 2003;9(5):24
Reichert-Penetrat S, Barbaud A, Antunes A, Borsa-Dorion A, Vidailhet M, Schmutz JL: An unusual form of Stevens-Johnson syndrome with subcorneal pustules associated with Mycoplasma pneumoniae infection, Pediatr Dermatol 2000;17(3):202-4
Roujeau JC: Neutrophilic drug eruptions, Clin Dermatol 2000;18(3):331-7
Scheinfeld NS, Worth R, Mallea J, Shookster L, Weinberg JM: Subcorneal pustular dermatosis developing in a patient with rheumatoid arthritis; rheumatoid, anti-microsomal and anti-mitochondrial autoantibodies; and a goiter, Skinmed 2003;2(4):258-9