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PUNCTATE AND RETICULATE
HYPERPIGMENTATION
JAAD 10:1–16, 1984
Acropigmentation symmetrica of Dohi – autosomal dominant,
sporadic; Asians with onset under 20 years of age; acral
hyperpigmentation (reticulate pattern becoming patches
with hypopigmented macules of face, trunk, distal extremities
JAAD 43:113, 2000
Atopic dermatitis – ‘dirty neck’; reticulate pigmentation of the
neck
Clin Exp Derm 12:1–4, 1987
Benzoyl peroxide
Acta DV 78:301–302, 1998
Bleomycin
Dermatologica 180:255–257, 1990
Cantu’s syndrome
Contact dermatitis – prurigo pigmentosa
Contact Dermatitis
44:289–292, 2001
Da Costa’s syndrome
Ped Derm 6:91–101, 1989
Dermatopathia pigmentosa reticularis – autosomal dominant;
reticulate pigmentation, alopecia, nail changes, palmoplantar
hyperkeratosis, loss of dermatoglyphics
JAAD 26:298–301,
1992; AD 126:935–939, 1990
Diffuse pigmentation with macular depigmentation of trunk with
reticulate pigmentation of neck
Hautarzt 6:458–460, 1955
Dowling–Degos syndrome (reticulated pigmented anomaly of
the flexures) – reticulated pigmentation of axillae, groin, and
other intertrigenous areas, freckles of vulva, comedo-like
lesions, pitted scars around mouth
JAAD 40:462–467, 1999;
Clin Exp Dermatol 9:439–350, 1984
Down’s syndrome – short stature, cutis marmorata,
acrocyanosis, low-set, small ears
JAAD 46:161–183, 2002;
Rook p.3015–3016, 1998, Sixth Edition
Dyskeratosis congenita – Dyskeratosis congenita – X-linked
recessive; reticulate hyperpigmentation (poikiloderma) of neck,
chest, thighs; nail dystrophy, oral, ocular, and anal leukoplakia
J Med Genet 25:843–846, 1988
Ectodermal dysplasia
Epidermolysis bullosa simplex with mottled pigmentation
Dermatology 189:173–178, 1994
Familial pigmentary anomaly
Familial pigmentation – Becker
Familial progressive hyperpigmentation (Moon–Adams)
Fanconi’s anemia
Br J Hematol 85:9–14, 1993
5-fluorouracil – reticulate pigmentation
Int J Derm 34:219–220,
1995
Franceschett–Jadassohn–Naegeli syndrome
JAAD 28:942–950,
1993
Galli–Galli syndrome – Dowling–Degos disease with
acantholysis – hyperkeratotic follicular papules
JAAD
45:760–763, 2001
Goltz’s syndrome
Gougerot–Carteau syndrome
Haber’s syndrome
JAAD 40:462–467, 1999
Heavy metal poisoning
Hereditary acrokeratotic poikiloderma of Weary –
vesiculopustules of hands and feet at age 1–3 months which
resolve; widespread atopic dermatitis-like dermatitis; diffuse
poikiloderma with striate and reticulate atrophy; keratotic
papules of hands and feet, elbows and knees; autosomal
dominant
AD 103:409–422, 1971
Hereditary hemorrhagic telangiectasia – arteriovenous
malformation – red patch, reticulated, mottled, spider-like,
speckled, plaque-like with faded margin or white halo
BJD 145:641–645, 2001
Hoyeraal–Hreidarsson syndrome – reticulate hyperpigmentation
(resembles dyskeratosis congenita), growth retardation,
microcephaly, mental retardation, cerebellar malformation,
progressive bone marrow failure, and muctocutaneous lesions
J Pediatr 136:390–393, 2000
Hidrotic ectodermal dysplasia – reticulate acropigmentation
JAAD 6:476–480, 1982
Hypotrichosis, striate, reticulated pitted palmoplantar keratoderma,
acro-osteolysis, psoriasiform plaques, lingua plicata, ventricular
arrhythmias, periodontitis
BJD 147:575–581, 2002
Incontinentia pigmenti (hypopigmentation)
AD 139:1163–1170,
2003; Ped Derm 7:174–178, 1990
Keratosis–ichthyosis–deafness (KID) syndrome – reticulated
severe diffuse hyperkeratosis of palms and soles, well
marginated, serpiginous erythematous verrucous plaques,
perioral furrows, leukoplakia, sensory deafness, photophobia
with vascularizing keratitis, blindness
BJD 148:649–653, 2003;
AD 117:285–289, 1981
Kindler’s syndrome – reticulated erythema precedes
poikiloderma
JAAD 46:447–450, 2001
Lymphoma (CTCL)
Int J Derm 30:658–659, 1991
Macrocephaly – cutis marmorata telangiectatica congenita
syndrome (macrocephaly, cutis marmorata, hemangioma, and
syndactyly syndrome) – macrocephaly, hypotonia,
hemihypertrophy, hemangioma, cutis marmorata telangiectatica
congenita, internal arteriovenous malformations, syndactyly,
joint laxity, hyperelastic skin, thickened subcutaneous tissue,
developmental delay, short stature, hydroocephalus
Ped Derm
16:235–237, 1999; Genet Couns 9:245–253, 1998; Am J Med
Genet 70:67–73, 1997
Macular amyloid
Microphthalmia with linear skin defects syndrome (MLS
syndrome)
Am J Med Genet 49:229–234, 1994
Phakomatosis pigmentovascularis type 5 – cutis marmorata
telangiectatica congenital and Mongolian spot
BJD
148:148:342–345, 2003
Pigmented reticularis faciei and colli with epithelial cystomatosis
Dermatoligae Tokyo:University of Tokyo Press 89–90, 1982
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