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Dermatologic Differential Diagnosis.pdf. - Famona Site

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296 A CLINICIAN’S GUIDE TO DERMATOLOGIC DIFFERENTIAL DIAGNOSIS, VOLUME 1<br />

Haber’s syndrome – intertriginous pigmentation<br />

Hereditary mucoepithelial dysplasia – psoriasiform intertrigo<br />

Hyper-IgE syndrome (Job’s syndrome) (Buckley’s syndrome) –<br />

papular, pustular, excoriated dermatitis of scalp, buttocks, neck,<br />

axillae, groin; furunculosis; growth failure; dermatitis of face,<br />

behind ears, scalp, axillae, and groin; recurrent bacterial<br />

infections of skin with cold abscesses, contact urticaria,<br />

infections of nasal sinuses and respiratory tract J Pediatr<br />

141:572–575, 2002; NEJM 340:692–702, 1999; Curr Prob<br />

Derm 10:41–92, 1998; Clin Exp Dermatol 11:403–408, 1986;<br />

Medicine 62:195–208, 1983; Lancet 1:1013–1015, 1966<br />

Hyper-IgM syndrome – diaper area ulcers Ped Derm 18:48–50,<br />

2001<br />

Incontinentia pigmenti – hyperpigmentation of axillae and groin<br />

JAAD 47:169–187, 2002<br />

Kawasaki’s disease<br />

Keratosis–ichthyosis–deafness syndrome – exaggerated diaper<br />

dermatitis Ped Derm 13:105–113, 1996; BJD 122:689–697,<br />

1990<br />

Lipoid proteinosis Ghatan p.52, 2002, Second Edition<br />

Netherton’s syndrome – intertrigenous and perigenital<br />

dermatitis, edema, papillomatosis resembling cellulitis<br />

BJD 131:615–621, 1994; JAAD 13:329–337, 1985<br />

Neurofibromatosis type I – Crowe’s sign – intertriginous<br />

pigmentation<br />

Olmsted syndrome – follicular hyperkeratosis of buttocks and<br />

knees; follicular papules; intertrigo, mutilating palmoplantar<br />

keratoderma, linear streaky hyperkeratosis, leukokeratosis of<br />

the tongue, sparse hair anteriorly JAAD 53:S266–272, 2005;<br />

Ped Derm 21:603–605, 2004; Ped Derm 20:323–326, 2003; Eur<br />

J Derm 13:524–528, 2003; BJD 136:935–938, 1997; AD<br />

132:797–800, 1996; AD 131:738–739, 1995; Semin Derm<br />

14:145–151, 1995; JAAD 10:600–610, 1984; Am J Dis Child<br />

33:757–764, 1927<br />

Pseudoxanthoma elasticum – linear and reticulated yellow<br />

papules and plaques JAAD 42:324–328, 2000; Dermatology<br />

199:3–7, 1999; AD 124:1559, 1988<br />

Sjögren–Larsson syndrome – ichthyosis, mental retardation,<br />

spastic diplegia, short stature, kyphoscoliosis, retinal changes,<br />

yellow pigmentation, intertrigo (flexural accentuation), deficiency<br />

of fatty aldehyde dehydrogenase Ped Derm 20:179–180, 2003;<br />

JAAD 35:678–684, 1996<br />

Sweet’s syndrome<br />

Xeroderma pigmentosum – intertriginous pigmentation<br />

TOXIC<br />

Arsenic poisoning – acute; baboon syndrome (anogenital<br />

intertrigo) with intertriginous exanthem BJD 149:757–762, 2003<br />

Methylbromide fumigation – bullae and urticaria<br />

AD 127:917–921, 1991<br />

TRAUMATIC<br />

Child abuse<br />

Friction and bacterial infection<br />

Runner’s rump (intertriginous hyperpigmentation)<br />

JAAD 21:1257–1262, 1989<br />

IRIS LESIONS, PIGMENTED<br />

AUTOIMMUNE DISORDERS, AND DISEASES<br />

OF IMMUNE DYSFUNCTION<br />

Scleroderma – periorbital linear scleroderma associated with<br />

heterochromic iridis Am J Ophthalmol 90:858–861, 1980<br />

INFECTIONS AND INFESTATIONS<br />

Leprosy – leproma<br />

Syphilis – papulat of secondary or tertiary lues<br />

INFILTRATIVE DISEASES<br />

Juvenile xanthogranuloma – iris heterochromia Eye and Skin<br />

Disease, pp.56–57, Lippincott, 1996<br />

INFLAMMATORY DISEASES<br />

Sarcoidal iris granuloma Clin Dermatol 4:129–135, 1986<br />

NEOPLASTIC DISEASES<br />

Aniridia with associated Wilms’ tumor<br />

Benign epithelial melanosis<br />

Conjunctival nevus<br />

Iris freckles<br />

Leiomyoma Rook p.3007, 1998, Sixth Edition<br />

Melanocytic nevus<br />

Melanoma AD 139:1067–1073, 2003<br />

Melanosis oculi<br />

Metastatic melanoma<br />

Iris nevus<br />

Nevus of Ota Dermatol Clin 10:609–622, 1992<br />

Pigmented episcleral spot (Axenfeld’s nerve loop)<br />

Primary acquired melanosis<br />

SYNDROMES<br />

Aniridia with chromosome 18 defects<br />

Cat eye syndrome – iris coloboma with trisomy 22<br />

Down’s syndrome – hypoplastic iris with lighter areas in the<br />

outer third (Brushfield spots) Rook p.373, 1998, Sixth Edition<br />

Incontinentia pigmenti – conjunctival pigmentation<br />

JAAD 47:169–187, 2002<br />

Iris coloboma<br />

4p deletion syndromes<br />

Cat eye syndrome<br />

Chromosome 18 defects (including trisomy 18)<br />

Focal dermal hypoplasia<br />

Linear nevus sebaceus syndrome<br />

Trisomy 22<br />

Iris nevus syndrome (Cogan–Reese syndrome)<br />

Nail–patella syndrome – cloverleaf iris (Lester iris) Rook<br />

p.421, 1998, Sixth Edition<br />

Neurofibromatosis – Lisch nodule NEJM 343:1573, 2000; Rook<br />

p.379, 1998, Sixth Edition; NEJM 324:1264–1266, 1991; J Med<br />

Genet 26:712–721, 1989; Am J Ophthalmol 96:740–742, 1983

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