Partial unilateral lentiginosis.

Abstract:

BACKGROUND:We review our experience with nine patients with partial unilateral lentiginosis (PUL), a rare pigmentary disorder. OBJECTIVE:Our purpose was to define the characteristics of PUL and to discuss the differential diagnosis. METHODS:The records of nine patients with PUL were reviewed. A literature review on diagnosis, association with other disorders, and differential diagnosis is presented. RESULTS:PUL is a rare benign disorder that has no known inheritance pattern and has no commonly associated abnormalities. CONCLUSION:Careful history and physical examination may enable the distinction between PUL, nevus spilus, and other more serious genetic disorders associated with lentiginosis.

journal_name

J Am Acad Dermatol

authors

Trattner A,Metzker A

doi

10.1016/0190-9622(93)70232-i

subject

Has Abstract

pub_date

1993-11-01 00:00:00

pages

693-5

issue

5 Pt 1

eissn

0190-9622

issn

1097-6787

pii

0190-9622(93)70232-I

journal_volume

29

pub_type

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