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Dermatologic Differential Diagnosis.pdf. - Famona Site

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PRIMARY CUTANEOUS DISEASE<br />

Acanthosis nigricans<br />

Acrodermatitis continua of Hallopeau<br />

Acrokeratoelastoidosis BJD 106:337–344, 1982<br />

Acrokeratosis verruciformis of Hopf<br />

Aquagenic syringeal acrokeratoderma JAAD 45:124–126, 2001<br />

Atopic hand–foot dermatitis Ped Derm 18:102–106, 2001<br />

Darier’s disease, including hemorrhagic acral Darier’s disease<br />

Hautarzt 51:857–861, 2000; onychauxis (hypertrophy of nail)<br />

Ghatan p.82, 2002, Second Edition<br />

Dyshidrosis (resolving)<br />

Ectopic nail – cutaneous horn JAAD 10:114–116, 1984; usually<br />

of palmar aspect of fifth finger Textbook of Neonatal<br />

Dermatology, p.509, 2001<br />

Epidermolysis bullosa; non-Herlitz junctional epidermolysis<br />

bullosa with collagen XVII mutation – palmoplantar callosities<br />

JAAD 52:371–373, 2005; AD 122:704–710, 1986;<br />

<strong>Dermatologic</strong>a 152:72–86, 1976<br />

Epidermolysis bullosa, epidermolytic type – palmoplantar<br />

callosities JAAD 42:1051–1066, 2000<br />

Epidermolysis bullosa simplex – palmoplantar callosities<br />

JAAD 42:1051–1066, 2000<br />

Focal acral hyperkeratosis Dermatol Online J 1:10, 2001;<br />

AD 123:1225, 1228, 1987<br />

Hereditary papulotranslucent acrokeratoderma Z Hautkr<br />

60:211–214, 1985<br />

Hyperkeratotic dermatitis of the palms BJD 107:195–201, 1982<br />

Ichthyosis bullosa of Siemens<br />

Ichthyosis vulgaris palmaris et plantaris dominans<br />

<strong>Dermatologic</strong>a 165:627–635, 1982<br />

Id reaction<br />

Keratolysis exfoliativa (acquired peeling of the palms) –<br />

recurrent Rook p.652, 1998, Sixth Edition; Trans St John’s<br />

Hosp Dermatol Soc 53:165–167, 1967<br />

Keratosis punctata of the palmar creases Cutis 32:75–76, 1983<br />

Knuckle pads Ped Derm 17:450–452, 2000<br />

Lichen planus BJD 142:310–314, 2000<br />

Lichen sclerosus et atrophicus<br />

Lichen simplex chronicus<br />

Lichen striatus<br />

Music box spicules – spiny keratoderma, porokeratosis punctata<br />

palmaris et plantaris, multiple minute digitate hyperkeratoses<br />

Cutis 54:389–394, 1994; AD 125:816–819, 1989; JAAD<br />

18:431–436, 1988<br />

Necrolytic acral erythema – serpiginous, verrucous plaques of<br />

dorsal aspects of hands, legs; associated with hepatitis C<br />

infection JAAD 50:S121–124, 2004; Int J Derm 35:252–256,<br />

1996<br />

Onychogryphosis – acquired; inherited forms – autosomal<br />

dominant, congenital forms Neonatal Dermatology, p.510, 2001<br />

Palmoplantar keratodermas<br />

Pincer nail deformity<br />

Pityriasis rubra pilaris<br />

Porokeratotic palmoplantar keratoderma discreta Clin Exp<br />

Dermatol 21:451–453, 1996<br />

Progressive symmetric erythrokeratoderma AD 122:434–440,<br />

1986<br />

Prurigo nodularis – idiopathic or associated with lymphoma,<br />

peripheral T-cell lymphoma (Lennert’s lymphoma) Cutis<br />

51:355–358, 1993; Hodgkin’s disease <strong>Dermatologic</strong>a<br />

HYPERKERATOTIC LESIONS OF THE HANDS 253<br />

182:243–246, 1991; Ped Derm 7:136–139, 1990; gluten<br />

sensitive enteropathy BJD 95:89–92, 1976; AIDS JAAD<br />

33:837–838, 1995; uremia South Med J 68:138–141, 1975;<br />

depression, liver disease, alpha-1 antitrypsin deficiency<br />

Sustralas J Dermatol 32:151–157, 1991; malabsorption<br />

<strong>Dermatologic</strong>a 169:211–214, 1984; The Clinical Management<br />

of Itching; Parthenon; p.xvi, 2000<br />

Psoriasis<br />

Pustular eruptions of the palms and soles, chronic recalcitrant –<br />

including pustular bacterid, acrodermatitis of Hallopeau,<br />

pustular psoriasis<br />

Symmetrical interdigital hyperkeratosis of the hands Acta DV<br />

73:459–460, 1993<br />

Terra firme (Diogenes syndrome) Lancet i:366–368, 1975<br />

Transient reactive papulotranslucent acrokeratoderma Australas<br />

J Dermatol 41:172–174, 2000<br />

Tylosis<br />

Xerotic dermatitis (winter hand dermatitis)<br />

PSYCHOCUTANEOUS DISEASES<br />

Bulemia – callosities of the hands Am J Psychiatr 5:655, 1985<br />

SYNDROMES<br />

Apert’s syndrome – circumferential nail at tip of fused digits<br />

Textbook of Neonatal Dermatology, p.509, 2001<br />

Bannayan–Riley–Ruvulcaba syndrome – acral keratoses<br />

AD 132:1214–1218, 1996<br />

Costello syndrome – warty papules around nose and mouth,<br />

legs, perianal skin; loose skin of neck, hands, and feet, thick<br />

palmoplantar surfaces, hypoplastic nails, short stature,<br />

craniofacial abnormalities Eur J Dermatol 9:533–536, 1999;<br />

Aust Paediat J 13:114–118, 1977<br />

Deletion of long arm of chromosome 6 – circumferential nail<br />

Textbook of Neonatal Dermatology, p.509, 2001<br />

Epidermodysplasia verruciformis – spiny hyperkeratosis of<br />

palms and soles Ped Derm 20:176–178, 2003<br />

Familial multiple acral mucinous fibrokeratomas – verrucous<br />

papules of the fingers JAAD 38:999–1001, 1998<br />

Greither’s syndrome – poikiloderma of face and extremities;<br />

warty keratoses over hands, feet, and legs; plantar<br />

keratoderma; normal nails and hair Hautarzt 9:364–369, 1958<br />

Haim–Munk syndrome – autosomal recessive; mutation in<br />

cathepsin C gene (like Papillon–Lefevre syndrome);<br />

palmoplantar keratoderma, scaly red patches on elbows, knees,<br />

forearms, shins, atrophic nails, gingivitis with destruction of<br />

periodontium, onychogryphosis, arachnodactyly, recurrent<br />

pyogenic infections BJD 152:353–356, 2005<br />

Hereditary (bullous) acrokeratotic poikiloderma of Weary<br />

(acrokeratotic poikiloderma) (Kindler’s syndrome?) – autosomal<br />

dominant – vesiculopustular eruption of hands and feet in<br />

infancy and childhood; extensive dermatitis in childhood,<br />

persistent poikiloderma sparing face, scalp and ears, keratotic<br />

verrucous papules of hands, feet, elbows, and knees AD<br />

103:409–422, 1971; pseudoainhum and sclerotic bands<br />

Int J Dermatol 36:529–533, 1997; AD 103:409–422, 1971<br />

Hidrotic ectodermal dysplasia – thick nails<br />

Lipoid proteinosis BJD 151:413–423, 2004; JID 120:345–350,<br />

2003; BJD 148:180–182, 2003; Hum Molec Genet 11:833–840,<br />

2002; Int J Derm 39:203–204, 2000; Ped Derm 14:22–25, 1997;<br />

AD 132:1239–1244, 1996<br />

Mal de Meleda<br />

Pachyonychia congenita – subungual hyperkeratosis

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