An unusual case of tinzaparin-induced haemorrhagic bullous dermatosis: diagnostic and therapeutic challenges

Delayed onset (8-10 days post-initiation of low molecular weight heparin), dose independent.Haemorrhagic bullous dermatosis is not a hypersensitivity reaction.High-risk profile: age >70 years-old, estimated glomerular filtration rate <30 ml/min, concomitant steroids, or vascular fragility.

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Publication Details

Journal
European Journal of Case Reports in Internal Medicine
Published
2025-09-04
DOI
https://doi.org/10.12890/2025_005636
Citations
1
Primary Topic
Autoimmune Bullous Skin Diseases
Type
article
Field-Weighted Citation Impact
1.47
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article

An unusual case of tinzaparin-induced haemorrhagic bullous dermatosis: diagnostic and therapeutic challenges

V. Salle, G. Chaby, K. Abdel-Hamid, J. Schmidt et al.
1 citations
European Journal of Case Reports in Internal Medicine
Autoimmune Bullous Skin Diseases
1.47
article

An unusual case of tinzaparin-induced haemorrhagic bullous dermatosis: diagnostic and therapeutic challenges

V. Salle, G. Chaby, K. Abdel-Hamid, J. Schmidt, Marine Serpier-Vangheluwe
article en
1 citations

Abstract

Delayed onset (8-10 days post-initiation of low molecular weight heparin), dose independent.Haemorrhagic bullous dermatosis is not a hypersensitivity reaction.High-risk profile: age >70 years-old, estimated glomerular filtration rate <30 ml/min, concomitant steroids, or vascular fragility.

European Journal of Case Reports in Internal MedicineVol. 12(10)
Centre Hospitalier Universitaire Amiens-Picardie (FR)
Openalex Percentile: Top 15%
Autoimmune Bullous Skin Diseases
1.47
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