Literature DB >> 27085226

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

Ganary Dabiri1, Elizabeth Damstetter2, Yunyoung Chang2, Emily Baiyee Ebot3, Jennifer Gloeckner Powers4, Tania Phillips5.   

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.
Copyright © 2015 American Academy of Dermatology, Inc. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  factor V Leiden mutation; hypercoagulable state; hyperhomocysteinemia; livedoid vasculopathy; protein C deficiency; protein S deficiency; thrombophilia; thrombosis; ulcers; warfarin necrosis

Mesh:

Year:  2016        PMID: 27085226     DOI: 10.1016/j.jaad.2015.08.071

Source DB:  PubMed          Journal:  J Am Acad Dermatol        ISSN: 0190-9622            Impact factor:   11.527


  2 in total

Review 1.  Bar code reader - an algorithmic approach to cutaneous occluding vasculopathies? Part I: small vessel vasculopathies.

Authors:  Gudrun Ratzinger; Bettina G Zelger; Bernhard W Zelger
Journal:  J Dtsch Dermatol Ges       Date:  2019-09-05       Impact factor: 5.584

2.  Recurrent painful ecchymosis in an adolescent female.

Authors:  Payvand Kamrani; Rachel Giesey; Gregory R Delost; Brian Moore
Journal:  JAAD Case Rep       Date:  2019-12-24
  2 in total

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