Schneiderman Prelims Vol-I. qxd

PARANEOPLASTIC DISEASES
Acanthosis nigricans 
BJD 153:667–668, 2005
Bazex syndrome
Florid cutaneous papillomatosis – palmar 
Rook p.1555, 1998
Sixth Edition
Keratoacanthoma visceral carcinoma syndrome – cancers of
the genitourinary tract 
AD 139:1363–1368, 2003; AD
120:123–124, 1984
Necrobiotic xanthogranuloma with paraproteinemia
– periorbital
site most common, but multiple lesions always present;
ulceration common; central clearing and atrophy; IgG-kappa
most common, then IgG-lambda; mucous membrane, lung,
myocardial lesions, and associated lymphoreticular malignancy
AD 128:94–100, 1992
Paraneoplastic pemphigus 
JAAD 39:876–871, 1998
PRIMARY CUTANEOUS DISEASE
Acanthosis nigricans
Acral mucinous syringometaplasia – associated with verrucous
hyperplasia 
Arch Pathol Lab Med 110:248–249, 1986
Adolescent onset ichthyosiform erythroderma – verrucous
rippling 
BJD 144:1063–1066, 2001
Atopic dermatitis
Confluent and reticulated papillomatosis
Darier’s disease (keratosis follicularis) 
Clin Dermatol 19:193–205,
1994; JAAD 27:40–50, 1992; of foot Caputo p.124, 2000
Epidermolysis bullosa pruriginosa – mild acral blistering at
birth or early childhood; violaceous papular and nodular lesions
in linear array on shins, forearms, trunk; lichenified hypertrophic
and verrucous plaques in adults 
BJD 130:617–625, 1994
Epidermolytic hyperkeratosis – overlying bony prominences,
scalp, nipples 
Rook p.1506, 1998, Sixth Edition
Erythema elevatum diutinum 
JAAD 50:652–653, 2004
Granular parakeratosis (axillary (or submammary) granular
hyperkeratosis) (axillary granular parakeratosis) 
AD
137:1241–1246, 2001; JAAD 40:813–814, 1999; JAAD
39:495–496, 1998; JAAD 33:373–375, 1995; JAAD 37:789–790,
1997; JAAD 24:541–544, 1991
Hailey–Hailey disease – genital papules
JAAD 26:951–955, 1992
Hyperkeratosis of the nipple (hyperkeratosis areolae mammae)
JAAD 41:274–276, 1999; AD 113:1691–1692, 1977
Kyrle’s disease – chronic scattered generalized papules with
hyperkeratotic cone shaped plugs; chronic genetically
determined disorder 
JAAD 16:117–123, 1987
Keratosis lichenoides chronica 
JAAD 49:511–513, 2003;
BJD 144:422–424, 2001; AD 129:914–915, 1993;
AD 105:739–743, 1972
Lichen myxedematosus
Lichen planus – hypertrophic lichen planus 
AD 139:933–938,
2003; Rook p.1904–1912, 1998, Sixth Edition
Lichen sclerosus et atrophicus 
JAAD 38:831–833, 1998
Lichen simplex chronicus, including giant lichenification of
Pautrier – genitocrural lichenification with solid tumorous
plaques with verrucous cribriform surface 
AD Syphilol
39:1012–1020, 1939
Lichen striatus
Malignant pyoderma – rare potentially lethal disease
characterized by necrotizing pyodermatous ulcers
predominantly involving the face, neck, and upper trunk with a
predilection for the preauricular areas; malignant pyoderma is
distinct from pyoderma gangrenosum with an unrelenting
destructive progression if untreated, a different clinical
distribution, an earlier age of onset, a lack of deeply
undermined necrotic borders, and the lack of association with
any underlying diseases 
Int J Derm 26:42, 1987
Necrolytic acral erythema – serpiginous, verrucous plaques of
dorsal aspects of hands, legs; associated with hepatitis C
infection 
JAAD 50:S121–124, 2004
Palmoplantar keratodermas
Perianal pseudoverrucous papules and nodules in children –
perianal hypertrophic plaques 
Cutis 67:335–338, 2001; AD
128:240–242, 1992
Periumbilical pseudoxanthoma elasticum – verrucous plaque
JAAD 39:338–344, 1998; South Med J 84:788–789, 1991
Prurigo nodularis
Pseudo-acanthosis nigricans
Pseudoepitheliomatous keratotic and micaceous balanitis 
Cutis
35:77–79, 1985; Bull Soc Fr Dermatolog Syphiligr 68:164–167,
1961
Psoriasis, elephantine, rupioid 
Rook p.1598–1599, 1998,
Sixth Edition
Superficial vegetating pyoderma