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Research Article Open access CC BY 4.0

Bullous Hemorrhagic Dermatosis Induced By Heparin: An Indonesian Case Report

Syahfori Widiyani, Irsalina Rahmawati, W. Yohannes Widodo, Dian Zamroni, Fajar L. Gultom, Forman Erwin Siagian, Hardi Hutabarat

International Journal of Medical and Pharmaceutical Case Reports · pp. 8–12 · Published 26 Nov 2021

10.9734/ijmpcr/2021/v14i430139

Abstract

Introduction: Bullous haemorrhagic dermatosis is a rare clinical disorder which is usually related to a treatment with unfractionated heparin (UFH) or low molecular weight heparin (LMWH), characterized by multiple intra-epidermal haemorrhages distant from the site of injection. Presentation of Case: A 62-year-old male patient with coronary heart disease who received heparin treatment experienced several tense, haemorrhagic bullae located on the right arm area, close to the injection site, and followed by the formation of several hematomas on his back trunk 2 days after he had received UFH. The lesions regressed after discontinuation of heparin and supportive topical treatments. Discussion: The lesions in this patient have similar characteristic with heparin-induced skin necrosis and demonstrate thrombocytopenia probably related to heparin. There are some proposed hypotheses of pathophysiology which include hypersensitivity reaction and idiosyncratic dose-related reaction. Given the clinically course, the discontinuation of heparin treatment was essential for lesion regression in addition other supportive measures. Conclusion: Heparin-induced skin lesions may indicate the presence of life-threatening heparin-induced thrombocytopenia. An early diagnosis is crucial to enable discontinuation of heparin if required.

Low molecular weight heparin UFH bullous haemorrhagic dermatosis hypersensitivity idiosyncracy dose-related reaction

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