We report the case of a 62-year old woman hospitalized for acute ischa
emia of the right lower limb, caused by stenosis of the superficial fe
moral artery associated with thrombosis of the deep femoral artery. Th
rombo-endarteriectomy was performed, and histology of the operative sp
ecimen showed thickening of the media with clusters of giant cells and
fragmentation of the internal elastic lamina, without atheroma. The d
iagnostic of giant cell arteritis was then considered and confirmed by
the presence of headaches, 38-degrees-C fever and inflammatory syndro
me with ESR at 75 mm in the first hour. On the other hand, biopsy of a
temporal artery was negative. Corticosteroid therapy was prescribed a
nd gave excellent clinical, laboratory and arteriographic results. It
has now been demonstrated that the arteries of the lower limbs may be
involved in Horton's giant cell arteritis, which is often overlooked.
This involvement is rare and exceptionally proven at histology. Clinic
ally, the most frequently described form is one of pseudo-arteritis wi
th claudication, but a few cases of gangrene have been reported. Withd
rawal of corticosteroid might be a facilitating factor. As in our pati
ent, the arteriographic lesions are often segmental, multifocal and sy
mmetrical, predominant in the superficial femoral artery and the arter
ies of the legs. The lesions regress under corticosteroid therapy, and
surgery can usually be avoided. Anticoagulants are commonly prescribe
d when the large vessels are involved. When surgery is not indicated t
he diagnosis can be confirmed by biopsy of the temporal artery, which
is positive in the majority of cases.