Chemotherapy-induced Sweet's syndrome in a patient with recurrent laryngeal carcinoma
Correspondence to Dr Mahmoud Abdelnabi; mahmoud.hassan.abdelnabi@outlook.com Description A man in his 60s, who used to smoke at least one pack a day for more than 50 years, with a previous history of intravenous drug use, multiple tattoos and a medical history of hypertension, hypothyroidism, chroni...
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Published in | BMJ case reports Vol. 15; no. 6; p. e250412 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
England
BMJ Publishing Group LTD
20.06.2022
BMJ Publishing Group |
Subjects | |
Online Access | Get full text |
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Summary: | Correspondence to Dr Mahmoud Abdelnabi; mahmoud.hassan.abdelnabi@outlook.com Description A man in his 60s, who used to smoke at least one pack a day for more than 50 years, with a previous history of intravenous drug use, multiple tattoos and a medical history of hypertension, hypothyroidism, chronic latent hepatitis C virus (HCV) infection (no previous treatment was received), recurrent laryngeal squamous cell carcinoma (SCC) status post total laryngectomy and neck irradiation. Drug-induced Sweet’s syndrome is a hypertensive reaction characterised by abrupt onset of painful erythematous nodules, papules and plaques or pustular dermatosis usually affecting the face, neck and upper extremities, histopathological evidence of dense neutrophilic dermal infiltrates without evident leucocytoclastic vasculitis, a temporal relation between drug ingestion and clinical presentation and resolution of symptoms after drug withdrawal or treatment with systemic corticosteroids. Rarely, in cases of corticosteroids failure, other alternative therapies such as dapsone, potassium iodide, colchicine, indomethacin, clofazimine, α-interferon, naproxen and ciclosporin can be used.1 We present a case of drug-induced Sweet’s syndrome in a man with a known solid tumour diagnosis. |
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Bibliography: | ObjectType-Case Study-2 SourceType-Scholarly Journals-1 ObjectType-Feature-4 content type line 23 ObjectType-Report-1 ObjectType-Article-3 |
ISSN: | 1757-790X 1757-790X |
DOI: | 10.1136/bcr-2022-250412 |