Schneiderman Prelims Vol-I. qxd


Partington syndrome – X-linked reticulate pigmentary disorder



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[Encyclopedia of Differential Diagnosis in Dermatology] Paul Schneiderman, Marc E. Grossman - A Clinician\'s Guide to Dermatologic Differential Diagnosis, Volume 1 The Text (Encyclopedia of Differential Diagnosis in D


Partington syndrome – X-linked reticulate pigmentary disorder
(amyloid) (amyloidosis carrier) 
Bolognia p.873, 2003
Phakomatosis pigmentokeratotica – hemiatrophy 
AD
134:333–337, 1998
Phakomatosis pigmentovascularis – port wine stain,
oculocutaneous (dermal and scleral) melanosis, CNS
manifestations; type I – PWS and linear epidermal nevus; type II –
PWS and dermal melanocytosis; type III – PWS and nevus
spilus; type IV – PWS, dermal melanocytosis, and nevus spilus;
types II,III, and IV may also have nevus anemicus 
Ped Derm
21:642–645, 2004; J Dermatol 26:834–836, 1999; Ped Derm
15:321–323, 1998; Ped Derm 13:33–35, 1996; AD
121:651–653, 1985; Jpn J Dermatol 52:1–3, 1947
Proteus syndrome – Blaschko epidermal nevi 
JAAD
52:834–838, 2005; port wine stains, subcutaneous
hemangiomas and lymphangiomas, lymphangioma
circumscriptum, hemihypertrophy of the face, limbs, trunk;
macrodactyly, cerebriform hypertrophy of palmar and/or plantar
surfaces, macrocephaly; verrucous epidermal nevi, sebaceous
nevi with hyper- or hypopigmentation 
AD 140:947–953, 2004;
Am J Med Genet 27:99–117, 1987; vascular nevi, soft
subcutaneous masses; lipodystrophy, café au lait macules,
78
A CLINICIAN

S GUIDE TO DERMATOLOGIC DIFFERENTIAL DIAGNOSIS, VOLUME 1
Schneiderman page 1-100.qxd 5/16/2006 6:49 PM Page 78


linear and whorled macular pigmentation 
Am J Med Genet
27:87–97, 1987; Pediatrics 76:984–989, 1985;
Eur J Pediatr 140:5–12, 1983
Soto’s syndrome 
AD 132:1167–1170, 1996
Trisomy 13 – phylloid pigmentary pattern 
Ped Derm
14:278–280, 1998
Tuberous sclerosis – segmental ash leaf spot; leukodermic
macules
Well’s syndrome (eosinophilic cellulitis) 
Clin Exp Dermatol
24:449–451, 1999
X-linked hypohidrotic ectodermal dysplasia – female carriers
X-linked reticulate pigmentary disorder with systemic
manifestations (familial cutaneous amyloidosis) (Partington
syndrome II) – X-linked; rare; Xp21–22; boys with generalized
reticulated muddy brown pigmentation (dyschromatosis) with
hypopigmented corneal dystrophy (dyskeratosis), coarse unruly
hair, unswept eyebrows, silvery hair, hypohidrosis, recurrent
pneumonia with chronic obstructive disease, clubbing; failure
to thrive, female carriers with linear macular nevoid
Blascko-esque hyperpigmentation 
Ped Derm 22:122–126,
2005; Textbook of Neonatal Dermatology, p.376, 2001; Semin
Cut Med Surg 16:72–80, 1997; Am J Med Gen 10:65, 1981
VASCULAR
Angiofibromas 
Bolognia p.873, 2003
Angiokeratoma circumscriptum/verrucous hemangioma
Angioma serpiginosum 
Ped Derm 20:167–168, 2003
Glomus tumors
Lymphangioma circumscriptum
Pigmented purpuric eruptions – lichen aureus
Unilateral nevoid telangiectasia
Venous malformations
Verrucous hemangioma 
JAAD 42:516–518, 2000;
AD 132:703–708, 1996

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