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Coagulation disorders and their cutaneous presentations: Diagnostic work-up and treatment
Journal article   Peer reviewed

Coagulation disorders and their cutaneous presentations: Diagnostic work-up and treatment

Ganary Dabiri, Elizabeth Damstetter, Yunyoung Chang, Emily Baiyee Ebot, Jennifer Gloeckner Powers and Tania Phillips
Journal of the American Academy of Dermatology, Vol.74(5), pp.795-804
05/2016
DOI: 10.1016/j.jaad.2015.08.071
PMID: 27085226

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Abstract

Both inherited and acquired hypercoagulable states can present with nonspecific clinical manifestations, such as petechiae, purpura, livedo reticularis, and ulcerations. A good history and physical examination are crucial to diagnoses of these conditions. Inherited conditions tend to present either in neonatal period or later in life, while acquired conditions typically occur later in life. Diagnostic studies are performed to identify the coagulation cascade deficiency or defect. Treatment primarily hinges on anticoagulation and wound care. In this article, we provide an in-depth analysis of the clinical manifestations, diagnostic considerations, and management options of patients in hypercoagulable states.
Thrombosis hyperhomocysteinemia thrombophilia livedoid vasculopathy protein C deficiency protein S deficiency hypercoagulable state warfarin necrosis factor V Leiden mutation ulcers

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