Literature DB >> 19537283

Limb hyperplasia: case report of an unusual variant of Klippel-Trenaunay syndrome and review of the literature.

Julie K Gober-Wilcox1, David L Gardner, Nancy E Joste, Carol L Clericuzio, Barrett Zlotoff.   

Abstract

Klippel-Trenaunay syndrome (KTS) is a rare disorder involving a triad of cutaneous capillary malformations (port-wine stain), varicose veins or venous malformations, and bony or soft tissue hyperplasia of an extremity. It is one of many heterogeneous disorders known as overgrowth syndromes that are characterized by either generalized or localized somatic overgrowth. Overgrowth syndromes each have unique clinical, behavioral, and genetic features, but some of these features overlap, causing diagnostic difficulty. Cutaneous manifestations, however, can be key to distinguishing the various syndromes. We present a patient with an unusual variant of KTS consisting of right upper extremity hyperplasia, lymphedema, and cutaneous and visceral lymphangiomas. We review several closely related syndromes and discuss the differential diagnosis of limb hyperplasia.

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Year:  2009        PMID: 19537283

Source DB:  PubMed          Journal:  Cutis        ISSN: 0011-4162


  2 in total

1.  Klippel Trenaunay syndrome and the anaesthesiologist.

Authors:  Smitha Elizabeth George; A Sreevidya; Anil Asokan; V Mahadevan
Journal:  Indian J Anaesth       Date:  2014 Nov-Dec

2.  Klippel-Trenaunay syndrome presenting with acanthocytosis and splenic and retroperitoneal lymphangioma: a case report.

Authors:  Milinda Withana; Chaturaka Rodrigo; Mitrakrishnan Chrishan Shivanthan; Sachini Warnakulasooriya; Manu Wimalachandra; Lallindra Gooneratne; Senaka Rajapakse
Journal:  J Med Case Rep       Date:  2014-11-27
  2 in total

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