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À̹«Çü Annal of Dermatol 2002³â 14±Ç 3È£ 158
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A
21-year-old Korean male was referred to our department
in June, 1999 for the evaluation of extensive reddish
patches and gray-bluish pigmentation since birth.
Physical examination revealed two kinds of patches
over the various parts of the body. Reddish patches
suggesting nevus flammeus were located on the left
side of face, chest, and both upper and lower extremities.
Gray-bluish pigmented patches suggesting nevus of
Ota were found on both the periorbital areas. A
0.5 0.6§¯ erythematous papule was found on the right
anterior chest. The results of its histopathologic
examination were compatible with pyogenic granuloma.
We made the diagnosis of phakomatosis pigmentovascularis
associated with pyogenic granuloma as well as Sturge-Weber
syndrome and Klippel-Trenanunay syndrome. |