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Three Cases of Allergic Contact Dermatitis to 2-(Thiocyanomethylthio)benzothiazole in Leather Items.
Contact Dermatitis
December 2024
Department of Dermatology, Montpellier University Hospital and Montpellier University, Montpellier, France.
Background: 2-(Thiocyanomethylthio)benzothiazole (TCMTB) is a fungicide product widely used in the leather industry, particularly since the 1990s. However, reports of allergic contact dermatitis triggered by this chemical are scarce.
Objectives: To investigate three cases of dermatitis following contact with leather products, possibly related to TCMTB.
Sofa dermatitis: Value of patch test with 2-(thiocyanomethylthio)benzothiazole.
Contact Dermatitis
July 2023
Department of Dermatology, Cliniques Universitaires Saint-Luc, Université Catholique de Louvain (UCLouvain), Brussels, Belgium.
Background: In 2008, numerous cases of allergic contact dermatitis caused by leather chairs (sofa dermatitis) were reported, with dimethylfumarate being the culprit allergen. However, octylisothiazolinone, methylisothiazolinone and cobalt have also been associated with cases of sofa dermatitis. An antifungal agent, 2-(thiocyanomethylthio)benzothiazole (TCMTB), has also previously been described as a contact allergen in leather.
View Article and Find Full Text PDFUnrecognized leather sofa dermatitis complicating chronic plaque psoriasis.
Contact Dermatitis
July 2021
Dermatology Consultant, Circle Bath Hospital, Bath, UK.
Sofa dermatitis again? A case report of allergic contact dermatitis to octylisothiazolinone from a leather reclining chair.
Contact Dermatitis
March 2020
Bristol Dermatology Centre, University Hospitals Bristol NHS Foundation Trust, Bristol, UK.
The influence of acute kidney injury on the outcome of Stevens-Johnson syndrome and toxic epidermal necrolysis: The prognostic value of KDIGO staging.
PLoS One
February 2019
Kidney Research Center, Department of Nephrology, Change Gung Memorial Hospital, Linkou branch, Taoyuan, Taiwan.
Background: Stevens-Johnson syndrome (SJS), toxic epidermal necrolysis (TEN), and SJS/TEN overlap syndrome are severe drug-induced cutaneous adverse reactions with high mortality. Acute kidney injury (AKI) was a common complication in an SJS/TEN group and noted as an independent risk factor for mortality in patients with SJS/TEN. To determine whether AKI staging can predict the outcome of patients with SJS/TEN, we compared the discriminative power of an AKI KDIGO staging system with that of SCROTEN, APACHE II, APACHE III, and SOFA.
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