Schneiderman Prelims Vol-I. qxd

PARANEOPLASTIC
Bullous pyoderma gangrenosum 
Int J Dermatol 40:327–329, 2001
Glucagonoma syndrome – necrolytic migratory erythema
Necrobiotic xanthogranuloma with paraproteinemia
AD 133:97–102, 1997; JAAD 29:466–469, 1993; Medicine
(
Baltimore) 65:376–388, 1986; BJD 113:339–343, 1985;
JAAD 3:257–270, 1980
Paraneoplastic vasculitis – ulcers of the buttocks 
J Rheumatol
18:721–727, 1991; Medicine (Baltimore) 67:220–230, 1988
PRIMARY CUTANEOUS DISEASES
Acne fulminans 
JAAD 52:S118–120, 2005; AD 124:414–417,
1988
Aplasia cutis congenita (ACC)
Type 1 – ACC without associated anomalies 
JAAD
13:429–433, 1985; AD 108:252–253, 1973
Type 2 – ACC with distal limb reduction abnormalities
(Adams–Oliver syndrome) – autosomal dominant; persistent
cutis marmorata; congenital heart disease in 8%; differentiate
from ACC with split hand deformities 
Birth Defects
18:123–128, 1982; differentiate from ACC with postaxial
polydactyly 
Hum Genet 71:86–88, 1985; J Med Genet
24:493–496, 1987
Type 3 – ACC of scalp with epidermal nevi 
Clin Res 33:130,
1985; including bullous ACC J Med Genet 30:962–963, 1993
Type 4 – ACC overlying developmental malformations – hair
collar sign; surface is translucent or membranous 
AD
125:1253–1256, 1989; may overlie defects of the vertebrae
and spinal cork 
J Pediatr 96:687–689, 1980
Type 5 – ACC associated with fetus papyraceus – delivery
of dead twin or triplet (death during second trimester)
AD 141:554–556, 2005; ACC on trunk and extremities with
linear or stellate configuration 
JAAD 25:1983–1985, 1991;
fibrous constriction bands of extremities 
Aust Paediatr J
18:294–296, 1982
Type 6 – ACC as presentation of junctional and dystrophic
epidermolysis bullosa; ulcerations of feet and lower legs
AD 93:296–303, 1966
Type 7 – ACC caused by teratogens – methimazole or
carbimazole 
Ped Derm 3:327–330, 1986; Can Med Assoc
130:1264, 1984
Type 8 – ACC as sign of intrauterine infection – herpes
simplex 
JAAD 15:1148–1155, 1986; varicella-zoster – linear
ulcers or scars; zosteriform 
NEJM 314:1542–1546, 1986