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Article
July 1966

Generalized Congenital Phlebectasia: Report of a Case

Author Affiliations

ELMHURST, NY
From the departments of pediatrics and dermatology, Mount Sinai Hospital, New York, and the Mount Sinai Hospital Services at Elmhurst.

Am J Dis Child. 1966;112(1):72-75. doi:10.1001/archpedi.1966.02090100108016
Abstract

FOUR INSTANCES of generalized congenital phlebectasia have been described previously. In 1922, Von Lohuizen1 reported on a vascular abnormality in a newborn infant. He called the condition "cutis marmorata telangiectica congenita." The same year Von Giles2 reported a similar case. The first report in the English literature was by Humphries3 in 1952. He utilized the term "generalized congenital phlebectasia." The fourth case was described by Bedell and Allison4 in 1964.

Generalized congenital phlebectasia should be differentiated from the so-called diffuse genuine phlebectasia, first described by Bockenheimer in 1907, as quoted by Schmidt.5 The former is present at birth and appears to have a benign course. The latter is a slowly progressing lesion of the venous system of an extremity. The enlarged veins form large strands and tumorlike prominences, over which the skin frequently becomes atrophic. If the condition is left untreated, serious complications ensue. Thus

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