Schneiderman Prelims Vol-I. qxd

INFILTRATIVE DISEASES
Amyloidosis cutis dyschromica
AD 128:966–970, 1992
Urticaria pigmentosa
INFLAMMATORY DISORDERS
Post-inflammatory dyspigmentation
METABOLIC DISEASES
Congenital erythropoietic porphyria – mottled pigmentation
Ped Derm 20:498–501, 2003
Iron deficiency anemia – heterochromic scalp hair 
JAAD
49:1148–1150, 2003
Kwashiorkor – protein and caloric deprivation 
JAAD 21:1–30, 1989
Malnutrition – dyschromatosis 
Ped Derm 19:523–526, 2002
Pernicious anemia – diffuse or mottled of face, hands, and feet
J Dermatol 28:282–285, 2001
Porphyria – porphyria cutanea tarda – dyschromatosis
Rook
p.2589–2590, 1998, Sixth Edition; congenital erythropoietic
porphyria
Semin Liver Dis 2:154–63, 1982
NEOPLASTIC DISEASES
Generalized nevoid hyperpigmentation
Melanocytic nevus- congenital nevi
Nevus depigmentosus – repigmenting
Nevus spilus
PHOTODERMATOSES
Acquired brachioradial cutaneous dyschromatosis
(dermatoheliosis) 
JAAD 42:680–684, 2000
PRIMARY CUTANEOUS DISEASES
Atopic dermatitis – in the adult
Epidermolysis bullosa simplex with stippled and mottled
pigmentation – autosomal dominant; bullae heal without
scarring, atrophy, or milia; improves with age; mottled macular
pigmentation of the trunk, proximal extremities; diffuse or
punctate keratoderma with nail dystrophy 
BJD 128:679–685,
1993; Clin Genet 15:228–238, 1979
Idiopathic eruptive macular hyperpigmentation 
Ped Derm
13:274, 1996
Mottled hyperpigmentation, epidermolysis bullosa, and punctate
keratoses 
JAAD 15:1289–1291, 1986
Mottled pigmentation of neck and elbows 
Z Haut-u Geschl
Krankh 32:33–44, 1962
Piebaldism 
BJD 132:929–935, 1995
Universal acquired melanosis (carbon baby)
Vitiligo
SYNDROMES
Acrogeria (Gottron’s syndrome) – micrognathia, atrophy of tip of
nose, atrophic skin of distal extremities with telangiectasia, easy
bruising, mottled pigmentation or poikiloderma of extremities,
dystrophic nails 
BJD 151:497–501, 2004; BJD 103:213–223,
1980; Arch Dermatol Syphiligr 181:571–583, 1941
Acromelanosis albo-punctata (Siemens’) 
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
Anonychia with bizarre flexural pigmentation – autosomal
dominant, absent nails, dry peeling palmoplantar skin, coarse
and sparse frontal hair; mottled hyper- and hypopigmentation
of the axillae, groin, and natal cleft 
BJD 92:469–474, 1975
Ataxia telangiectasia – telangiectasias of bulbar conjunctivae,
tip of nose, ears, antecubital and popliteal fossae, dorsal hands