Document Detail


Klippel-Trenaunay syndrome with a life-threatening thromboembolic event.
MedLine Citation:
PMID:  12692362     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Klippel-Trenaunay syndrome is a congenital disorder characterised by the triad of cutaneous vascular nevi, soft tissue or bony hypertrophy, and varicose veins or venous malformations involving one or more extremities. An incidence of venous thromboembolism of up to 22% has been reported in this disorder. Also reported but rare is the development of trophic changes. Herein, we report the case of a male with Klippel-Trenaunay syndrome, deep vein thrombosis, venous ulceration, and death due to recurrent pulmonary embolism.
Authors:
Kamal Aggarwal; Vijay K Jain; Sanjeev Gupta; Hari K Aggarwal; Jyotsna Sen; Vishal Goyal
Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  The Journal of dermatology     Volume:  30     ISSN:  0385-2407     ISO Abbreviation:  J. Dermatol.     Publication Date:  2003 Mar 
Date Detail:
Created Date:  2003-04-14     Completed Date:  2003-05-23     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  7600545     Medline TA:  J Dermatol     Country:  Japan    
Other Details:
Languages:  eng     Pagination:  236-40     Citation Subset:  IM    
Affiliation:
Department of Skin, V.D. & Leprosy, Pt. B.D. Sharma Post Graduate Institute of Medical Sciences, Rohtak, India.
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MeSH Terms
Descriptor/Qualifier:
Anticoagulants / administration & dosage
Critical Illness
Follow-Up Studies
Humans
Klippel-Trenaunay-Weber Syndrome / complications,  diagnosis*
Male
Middle Aged
Pulmonary Embolism / complications,  drug therapy,  ultrasonography*
Recurrence
Respiratory Function Tests
Risk Assessment
Treatment Outcome
Ultrasonography, Doppler, Color
Varicose Veins / physiopathology,  ultrasonography
Venous Thrombosis / complications,  drug therapy,  ultrasonography*
Chemical
Reg. No./Substance:
0/Anticoagulants

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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