Schneiderman Prelims Vol-I. qxd

RETICULATED
HYPERPIGMENTATION
Clin Exp Dermatol 9:439–450, 1984
Acquired dermal melanocytosis 
BJD 124:96, 1991
Amyloidosis, macular
Arsenic intoxication
Atopic ‘dirty neck’
Bolognia p.997, 2003
Bleomycin 
Dermatologica 180:255–257, 1990
Calcinosis cutis – hyperpigmented reticulated plaques 
BJD
142:820–822, 2000
Cantu’s syndrome – reticulated hyperpigmentation of face,
forearms, feet with palmoplantar keratoderma 
Bolognia p.997,
2003; Clin Genet 14:165, 1978
Confluent and reticulated papillomatosis of Gougerot and
Carteaud 
Bolognia p.997, 2003
Cutaneous arteritis – round, linear, reticulated
hyperpigmentation 
JAAD 49:519–522, 2003
Dermatitis 
Clin Exp Derm 15:380–381, 1990
Dermatopathia pigmentosa retularis – autosomal dominant,
reticulate hyperpigmentation of trunk, onychodystrophy,
alopecia, oral hyperpigmentation, punctate hyperkeratosis of
palms and soles, hypohidrosis; atrophic macules over joints
with hypertrophic scarring 
Semin Cut Med Surg 16:72–80,
1997; AD 126:935–939, 1990; Hautarzt 6:262, 1960
Dowling–Degos disease 
Semin Cut Med Surg 16:72–80, 1997;
AD 114:1150, 1978
Dyschromatosis symmetrica hereditaria (reticulate
acropigmentation of Dohi) (acropigmentation symmetrica of
Dohi) 
BJD 153:342–345, 2005; BJD 150:633–639, 2004; BJD
144:162–168, 2001; JAAD 45:760–763, 2001; JAAD
43:113–117, 2000; sun-exposed areas only JAAD 10:1–16,
1984
Dyschromatosis universalis hereditaria 
Semin Cut Med Surg
16:72–80, 1997; Clin Exp Derm 2:45, 1977
Dyskeratosis congenita 
Semin Cut Med Surg 16:72–80, 1997
Ectodermal dysplasia 
JAAD 6:476–480, 1982
Epidermolysis bullosa herpetiformis 
Bolognia p.997, 2003
Epidermolysis bullosa with mottled pigmentation – wart-like
hyperkeratotic papules of axillae, wrists, dorsae of hands, palms
and soles; P25L mutation of keratin 5 
JAAD 52:172–173, 2005
Erythema ab igne 
Rook p.1688, 1998, Sixth Edition
Exudative retinopathy with bone marrow failure (Revesz
syndrome) – intrauterine growth retardation, reticulate
hyperpigmentation of trunk, palms, and soles; fine sparse hair,
ataxia with cerebellar hypoplasia, hypertonia, progressive
psychomotor retardation 
J Med Genet 29:673–675, 1992
Fanconi’s syndrome 
AD 103:581, 1971
Familial pigmentation with dystrophy of the nails 
AD 71:591–598,
1955
Familial progressive hyperpigmentation 
AD 103:581, 1971
Franceschetti–Jadassohn–Naegeli syndrome – autosomal
dominant; brown–gray reticulated hyperpigmentation,
hypohidrosis; palmoplantar hyperkeratosis 
Textbook of Neonatal
Dermatology, p.379, 2001; JAAD 10:1–16, 1984; Dematologica
108:1–28, 1954; Schweiz Med Wschr 8:48, 1927
Galli–Galli disease – acantholytic variation of Dowling–Degos
disease 
Bolognia p.997, 2003
Graft vs. host disease, chronic 
Rook p.2517, 1998, Sixth Edition
Haber’s syndrome – autosomal dominant; photo-aggravated
rosacea-like rash of face; papules, pustules, scarring and
telangiectasia; reticulate keratotic plaques on trunk and extremities
Australas J Dermatol 38:82–84, 1997; AD 117:321, 1981