Schneiderman Prelims Vol-I. qxd

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A CLINICIAN’S GUIDE TO DERMATOLOGIC DIFFERENTIAL DIAGNOSIS, VOLUME 1
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Progressive cribriform and zosteriform hyperpigmentation
Prurigo pigmentosa 
Dermatology 188:219–221, 1994
Pseudoxanthoma elasticum – linear and reticulated yellow
papules and plaques 
AD 124:1559, 1988; JAAD 42:324–328,
2000; Dermatology 199:3–7, 1999; pseudoxanthoma elasticum
resembling reticulated pigmented disorders 
BJD
134:1157–1159, 1996; penicillamine-induced pseudoxanthoma
elasticum 
JAAD 30:103–107, 1994; Dermatology 184:12–18,
1992; saltpetre-induced pseudoxanthoma elasticum Acta DV
58:323–327, 1978
Reflex sympathetic dystrophy – reticulated hyperpigmentation
Cutis 68:179–182, 2001
Reticular pigmented genodermatosis with milia
(Naegeli–Franceschetti–Jadassohn syndrome?) 
Clin Exp
Dermatol 20:331–335, 1995
Reticulate acropigmentation of Dohi (dyschromatosis
symmetrica hereditaria) – autosomal dominant; mottled
pigmentation with depigmentation of dorsa of hands, feet, arms,
and legs 
JAAD 43:113–117, 2000; BJD 140:491–496, 1999;
JAAD 37:884–886, 1997
Reticulate acropigmentation of Kitamura – autosomal
dominant; freckle-like pigmentation of dorsae of hands, palmar
pits
AD 139:657–662, 2003; J Dermatol 27:745–747, 2000;
JAAD 40:462–467, 1999; BJD 109:105–110, 1983
Reticulate hyperpigmentation of Iijima, Naito, and Uyeno
Acta DV 71:248–250, 1991
Reticulate hyperpigmentation in zosteriform fashion
BJD 117:503–510, 1987
Reticulate, patchy, and mottled pigmentation of the neck
Dermatology 197:291–296, 1998
Reticulolinear aplasia cutis congenita of the face and neck –
Xp deletion syndrome, MIDAS (microphthalmia, dermal aplasia,
sclerocornea), MLS (microphthalmia and linear skin defects),
and Gazali–Temple syndrome; lethal in males; residual facial
scarring in females, short stature, organ malformations 
BJD
138:1046–1052, 1998
Rothmund–Thompson syndrome
Speckled pigmentation, palmoplantar punctate keratoses,
childhood blistering 
BJD 105:579–585, 1981
Terra firme
Trisomy 14 mosaicism syndrome – patchy reticulated
hyperpigmentation resembling that of incontinentia pigmenti
Syndromes of the Head and Neck, p.89, 1990
Trisomy 18 – reticulate vascular nevus or port wine stain
J Pediatr 72:862–863, 1968
Tumor necrosis factor (TNF) receptor 1-associated periodic
fever syndromes (TRAPS) (same as familial Hibernian fever,
autosomal dominant periodic fever with amyloidosis, and benign
autosomal dominant familial periodic fever) – erythematous
patches, tender red plaques, fever, annular, serpiginous,
polycyclic, reticulated, and migratory patches and plaques
(migrating from proximal to distal), urticaria-like lesions, lesions
resolving with ecchymoses, conjunctivitis, periorbital edema,
myalgia, arthralgia, abdominal pain, headache; Irish and
Scottish predominance; mutation in TNFRSF1A – gene
encoding 55 kDa TNF receptor 
AD 136:1487–1494, 2000
X-linked reticulate pigmentary disorder (formerly familial or
X-linked cutaneous amyloidosis) 
Am J Med Genet 52:75–78,
1994; Am J Med Genet 10:67–75, 1981
Xp microdeletion syndrome – linear skin defects of head and
neck (congenital smooth muscle hamartomas) (MIDAS
syndrome – microphthalmia, dermal aplasia, sclerocornea) 
Ped
Derm 14:26–30, 1997
Zosteriform reticulate hyperpigmentation 
BJD 121:280, 1989;
in children 
BJD 117:503–17, 1987; AD 114:98–99, 1978