PSYCHOCUTANEOUS DISEASES
Self-inflicted
Ghatan p.92, 2002, Second Edition
SYNDROMES
Clouston’s syndrome (hidrotic ectodermal dysplasi) –
autosomal dominant; palmoplantar hyperkeratosis, hair
defects, nail dysplasia, leukoplakic lesions
Oral Surg
57:258–262, 1984
Cole–Engman syndrome – leukoplakia of the tongue
J Oral
Maxillofac Surg 57:1138–1141, 1999
Dyskeratosis benigna intraepithelialis mucosae et cutis
hereditaria – conjunctivitis, umbilicated keratotic nodules of
scrotum, buttocks, trunk; palmoplantar verruca-like lesions,
leukoplakia of buccal mucosa, hypertrophic gingivitis, tooth loss
J Cutan Pathol 5:105–115, 1978
Dyskeratosis congenita (Zinsser–Engman–Cole syndrome) –
Xq28; oral bullae and erosions
Rook p.415, 1998, Sixth Edition;
J Med Genet 33:993–995, 1996; Dermatol Clin 13:33–39, 1995;
BJD 105:321–325, 1981
Focal palmoplantar and oral mucosa (gingival) hyperkeratosis
syndrome (MIM:148730) (hereditary painful callosities) –
palmoplantar keratoderma, leukoplakia (gingival keratosis), and
cutaneous horn of the lips
JAAD 52:403–409, 2005;
BJD 146:680–683, 2002; Oral Surg 50:250, 1980;
Birth Defects 12:239–242, 1976; Arch Int Med
113:866–871, 1964
Grinspan’s syndrome – oral lichen planus, diabetes mellitus,
hypertension
Ghatan p.202, 2002, Second Edition
Hereditary benign intra-epithelial dyskeratoses (Witkop–von
Sallmann syndrome) – conjunctivitis; leukoplakia of buccal
mucosa, lips, tongue in Haliwa–Saponi Native Americans of
North Carolina
JAAD 45:634–636, 2001; Arch Pathol
70:696–711, 1960
Hereditary mucoepithelial dysplasia
Ghatan p.93, 2002,
Second Edition
Howell–Evans syndrome – autosomal dominant; focal PPK; oral
leukokeratosis, carcinoma of the esophagus
Curr Prob Derm
14:71–116, 2002; Q J Med 155:317–333, 1970; QJMed
27:413–429, 1958
Keratosis–ichthyosis–deafness (KID) syndrome – oral
leukoplakia, reticulated severe diffuse hyperkeratosis of
palms and soles, well marginated, serpiginous erythematous
verrucous plaques, perioral furrows, leukoplakia, sensory
deafness, photophobia with vascularizing keratitis, blindness
Ped Derm 13:105–113, 1996; BJD 122:689–697, 1990;
JAAD 23:385–388, 1990; AD 123:777–782, 1987;
AD 117:285–289, 1981
Olmsted syndrome – oral leukokeratosis, periorificial keratotic
plaques; congenital diffuse sharply marginated transgradient
keratoderma of palms and soles, onychodystrophy, constriction
of digits, diffuse alopecia, thin nails, chronic paronychia, linear
keratotic streaks, follicular keratosis, constriction of digits
(ainhum), anhidrosis, small stature; differential diagnostic
considerations include Clouston hidrotic ectodermal dysplasia,
pachyonychia congenita, acrodermatitis enteropathica,
Vohwinkel’s keratoderma, mal de Meleda, and other
palmoplantar keratodermas
JAAD 53:S266–272, 2005;
Ped Derm 21:603–605, 2004; Ped Derm 20:323–326, 2003;
BJD 136:935–938, 1997; AD 132:797–800, 1996; JAAD
10:600–610, 1984
Oral florid papillomatosis
Pachyonychia congenita – white sponge nevus (oral
leukokeratosis)
BJD 152:800–802, 2005; JAAD 19:705–711,
1988
Plummer–Vinson syndrome
Pseudoxanthoma elasticum
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