EURORAD ESR

Case 869

Klippel-Trenaunay-Weber Syndrome

Author(s)
D. Henroteaux
 
Patient
male, 30 year(s)

Clinical History

Right lower limb venous insufficiency, hemosiderin pigmentation and a varicose ulcer at the malleolar region. At clinical examination, his right thigh was swollen and painful with numerous and tortuous varicosities, particularly in the region of the saphenous vein. There was a thrill on palpation and a murmur on auscultation of the right thigh. A phlebography of the right lower limb was performed and showed no opacification of the deep venous system. Subsequently an arteriography was carried out. A scanogram, not shown, revealed a lengthening of the right lower limb

Imaging Findings

A 30-year-old man was admitted to the hospital with right lower limb venous insufficiency, hemosiderin pigmentation and a varicose ulcer at the malleolar region. At clinical examination, his right thigh was swollen and painful with numerous and tortuous varicosities, particularly in the region of the saphenous vein. There was a thrill on palpation and a murmur on auscultation of the right thigh. A phlebography of the right lower limb was performed and showed no opacification of the deep venous system. Subsequently an arteriography was carried out. A scanogram, not shown, revealed a lengthening of the right lower limb

Discussion

Klippel-Trenaunay Syndrome (KTS) is an uncommon disease (300 cases published). KTS is an association of soft tisssue and bone hypertrophy, cutaneous hemangiomas and superficial varicosities. Klippel-Trenaunay-Wever Syndrome (KTWS) is the association of KTS with arterio-venous fistulae. KTS and KTWS are due to a congenital malformation of the deep venous system with agenesis, hypoplasia or segmental atresia. The etiology is not clear but the syndrome is most likely the result of a diffuse mesodermal abnormality. KTS and KTWS are not hereditary but show some female predominance. Usually KTS and KTWS affect only lower SWOP-Coated extremities, are sometimes bilateral of may also involve the upper extremities. Soft tissue and bone hypertrophy associated with portwine hemangiomas suggest the diagnosis at birth. Varicosities appear later in the disease course. Phlebography and arteriography are necessary to define the extension of the abnormalities and to demonstrate the presence or absence of arterio-venous fistulae. Arterio-venous fistulae worsen the prognosis of the disease.

Final Diagnosis

Klippel-Trenaunay Syndrome
 

MeSH

  1. Klippel-Trenaunay-Weber Syndrome [C14.907.077.410]
    A rare condition usually affecting one extremity, characterized by hypertrophy of the bone and related soft tissues, large cutaneous hemangiomas, persistent nevus flammeus, and skin varices. (Dorland, 27th ed)

References

Citation

D. Henroteaux (2001, Feb 23).
Klippel-Trenaunay-Weber Syndrome, {Online}.
URL: http://www.eurorad.org/case.php?id=869
 
  • Published 23.02.2001
  • DOI 10.1594/EURORAD/CASE.869
  • Section Cardiovascular
  • Case-Type Clinical Case
  • Difficulty Resident
  • Views 854
  • Language(s)
  • Figure 1
    Right common femoral artery examination
    a b  

    Arteriography of the right common femoral artery, proximal segment, shows cirsoid aneurysm of the deep femoral artery, arterio-venous malformation with fistulae and hypoplasia of the distal deep femoral vein.

    Arteriography of the right common femoral artery, distal segment, demonstrates an arterio-venous malformation in the distal third of the right thigh. Absence of hemangiomas or vascular nevi.

     
Figure 1

Right common femoral artery examination

Figure 1a
Arteriography of the right common femoral artery, proximal segment, shows cirsoid aneurysm of the deep femoral artery, arterio-venous malformation with fistulae and hypoplasia of the distal deep femoral vein.
 
Figure 1b
Arteriography of the right common femoral artery, distal segment, demonstrates an arterio-venous malformation in the distal third of the right thigh. Absence of hemangiomas or vascular nevi.
 
 
Home Search History FAQ Contact Disclaimer Imprint