Schneiderman Prelims Vol-I. qxd

HYPERPIGMENTATION IN
BLASCHKO’S LINES
JAAD 31:157–190, 1994; J Pediatr 116:581–586, 1990
Acquired dermal melanocytosis (acquired nevus of Ota-like
macules) 
JAAD 43:934–936, 2000
Cutaneous amyloidosis, Partington type (X-linked reticulate
pigmentary disorder) 
Basaloid follicular hamartoma
Blaschkitis
Chondrodysplasia punctata (X-linked variant) 
Ped Derm 13:1–4,
1996
Chromosome X-autosome translocation
Epidermal nevus – early stage
Goltz’s syndrome
Incontinentia pigmenti – third stage 
Ped Derm 15:108–111,
1998; Curr Prob Derm VII:143–198, 1995; AD 112:535–542,
1976
Linear and whorled nevoid hypermelanosis 
Ped Derm
10:156–158, 1993; JAAD 19:1037–1044, 1988
Linear atrophoderma of Moulin – acquired atrophic pigmented
band-like lesions following Blaschko’s lines 
Eur J Dermatol
10:611–613, 2000; Int J Dermatol 39:850–852, 2000;
JAAD 38:366–368, 1998; BJD 135:277–279, 1996; Ann
DV 119:729–736, 1992
McCune–Albright syndrome – melanotic macules
BJD 130:215–220, 1994
Melanocytic nevi, café-au-lait macules, and nevi spili 
Acta
DV 78:378–380, 1998
Mosaic 13q11 deletion
Mosaic tetrasomy 12p
Mosaic 15;22
Mosaic trisomy 18
Mosaicism/chimerism
Nevus comedonicus – areas of hyperpigmentation
AD 116:1048–1050, 1980
Linear porokeratosis 
AD 135:1544–1555,1547–1548, 1999;
Ped Derm 4:209, 1987; AD 109:526–528, 1974
Ring 10;45
Ring X/46
Ring X
+
ring
Scleroderma – linear scleroderma (en coup de sabre)
JAAD 38:366–368, 1998
Trisomy 14
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A CLINICIAN’S GUIDE TO DERMATOLOGIC DIFFERENTIAL DIAGNOSIS, VOLUME 1
Schneiderman page 200-300.qxd 5/16/2006 6:49 PM Page 254

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