Gober-Wilcox Julie K, Gardner David L, Joste Nancy E, Clericuzio Carol L, Zlotoff Barrett
Department of Pathology, University of New Mexico Health Sciences Center, Albuquerque, NM 87131-0001, USA.
Cutis. 2009 May;83(5):255-62.
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.
克-特综合征(KTS)是一种罕见的疾病,包括皮肤毛细血管畸形(葡萄酒色斑)、静脉曲张或静脉畸形以及肢体的骨或软组织增生三联征。它是众多被称为过度生长综合征的异质性疾病之一,其特征为全身性或局部性躯体过度生长。每种过度生长综合征都有独特的临床、行为和遗传特征,但其中一些特征相互重叠,导致诊断困难。然而,皮肤表现可能是区分各种综合征的关键。我们报告一例克-特综合征的不寻常变异型,其表现为右上肢增生、淋巴水肿以及皮肤和内脏淋巴管瘤。我们回顾几种密切相关的综合征,并讨论肢体增生的鉴别诊断。