1.
Pediatr Dermatol
; 12(2): 159-63, 1995 Jun.
Article
En
| MEDLINE
| ID: mdl-7659644
We report a 1-year-old boy with an extensive cutaneous vascular malformation, oculocutaneous pigmentation, and severe neurologic abnormalities from birth, as well as a selective IgA deficiency. Ultrastructural study demonstrated prominent endothelial cells in the luminal of the blood vessels. The diagnosis of phacomatosis pigmentovascularis type IIb seemed appropriate for this patient.
Blood Vessels/abnormalities , IgA Deficiency/pathology , Pigmentation Disorders/pathology , Skin/blood supply , Angiomatosis/pathology , Brain Diseases/pathology , Endothelium, Vascular/pathology , Eye Diseases/pathology , Humans , Infant , Intellectual Disability/pathology , Male , Nevus, Pigmented/pathology , Skin Neoplasms/pathology