Schneiderman Prelims Vol-I. qxd

PHOTODERMATOSES
Hydroa vacciniforme – red macules progress to tender papules,
hemorrhagic vesicles or bullae, umbilication and crusting; pock-
like scars 
JAAD 42:208–213, 2000; Dermatology 189:428–429,
1994; JAAD 25:892–895, 1991; JAAD 25:401–403, 1991; BJD
118:101–108, 1988; AD 118:588–591, 1982; familial BJD
140:124–126, 1999; AD 114:1193–1196, 1978; AD
103:223–224, 1971; late onset BJD 144:874–877, 2001
PRIMARY CUTANEOUS DISEASES
Acne necrotica miliaris 
Rook p.1122, 1998, Sixth Edition
Acne necrotica varioliformis 
AD 132:1365–1370, 1996; JAAD
16:1007–1014, 1987
Acrokeratoelastoidosis of Costa – umbilicated hyperkeratotic
papules of palms and soles 
AD 140:479–484, 2004; Ped Derm
19:320–322, 2002; JAAD 22:468–476, 1990; Acta DV
60:149–153, 1980; Dermatologica 107:164–168, 1953
Darier’s disease – umbilicated white papules on oral mucosa
Clin Dermatol 19:193–205, 1994; JAAD 27:40–50, 1992
Degenerative collagenous plaques of the hands – linear
crateriform papules; may coalesce to form a band 
JAAD
47:448–451, 2002; AD 82:362–366, 1960
Elastosis perforans serpiginosa 
J Dermatol 20:329–340, 1993;
Hautarzt 43:640–644, 1992; JAAD 10:561–581, 1984; AD
97:381–393, 1968
Erythema of Jacquet – erosive diaper dermatitis with
umbilicated papules 
Ped Derm 15:46–47, 1998
Focal acral hyperkeratosis (acrokeratoelastoidosis without
elastorrhexis) – autosomal dominant; crateriform papules of the
sides of the hands and feet 
JAAD 47:448–451, 2002; AD
120:263–264, 1984; BJD 109:97–103, 1983
Fox–Fordyce disease 
JAAD 48:453–455, 2003
Granuloma annulare – in HIV disease 
JAAD:S184–186, 2003;
umbilicated papular granuloma annulare 
AD 140:877–882,
2004; Int J Dermatol 36:207–209, 1997; AD 128:1375–1378,
UMBILICATED LESIONS
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1992; perforating granuloma annulare Int J Dermatol
36:340–348, 1997; AD 103:65–67, 1971
Kyrle’s disease (hyperkeratosis follicularis et parafollicularis in
cutem penetrans) 
Int J Dermatol 36:340–348, 1997; J Derm
20:329–340, 1993; JAAD 16:117–123, 1987; AD 103:65–67,
1971
Lichen sclerosus et atrophicus – personal observation
Muir–Torre syndrome – autosomal dominant; sebaceous
adenomas, sebaceous carcinomas, keratoacanthomas
Cutis 75:149–155, 2005; Curr Prob Derm 14:41–70, 2002;
BJD 136:913–917, 1997; JAAD 33:90–104, 1995;
JAAD 10:803–817, 1984; AD 98:549–551, 1968;
Br J Surg 54:191–195, 1967
Papular elastorrhexis 
Dermatology 205:198–200, 2002;
Clin Exp Dermatol 27:454–457, 2002; JAAD 19:409–414, 1988;
AD 123:433–434, 1987
Perforating folliculitis 
JAAD 40:300–302, 1999; Am J
Dermatopathol 20:147–154, 1998; AD 97:394–399, 1968
Periumbilical pseudoxanthoma elasticum 
AD 132:223–228, 1996
Pityriasis rosea, vesicular
Prurigo nodularis
Reactive perforating collagenosis – early childhood, precipitated
by trauma; skin-colored umbilicated papules; heal with
hypopigmentation or scar 
BJD 140:521–524, 1999; Int J
Dermatol 36:340–348, 1997; AD 121:1554–1555, 1557–1558,
1985; AD 103:65–67, 1971