Schneiderman Prelims Vol-I. qxd

PSYCHOCUTANEOUS DISEASE
Factitial dermatitis 
Ped Derm 21:205–211, 2004; NEJM
347:1412–1418, 2002; Klin Wochenschr 64:149–164, 1986;
JAAD 11:1065–1069, 1984; factitial panniculitis – ulcers of the
thigh and buttocks 
JAAD 2:47–55, 1980
Neurotic excoriations
Self-mutilation
SYNDROMES
Acro-osteolysis associated with spinal dysraphism – blister,
ulcers of the foot, hyperhidrosis of the affected limb 
Ped Derm
18:97–101, 2001
Adams–Oliver syndrome – aplasia cutis congenita of scalp and
transverse limb defects 
Ped Derm 15:48–50, 1998
Antiphospholipid antibody syndrome 
NEJM 347:1412–1418,
2002; Semin Arthritis Rheum 31:127–132, 2001; JAAD
36:149–168, 1997; JAAD 36:970–982, 1997; Semin Thromb
Hemost 20:71–78, 1994; JAAD 15:211–219, 1986; eschar and
ulceration 
JAAD 47:766–769, 2002 ; IgA antiphospholipid
antibodies 
J Rheumatol 25:1730–1736, 1998; ulcer resembling
pyoderma gangrenosum 
J La State Med Soc 147:357–361,
1995; lupus anticoagulant – pyoderma gangrenosum-like
Dermatology 189:182–184, 1994
Ataxia telangiectasia – ulcerated plaque of cutaneous
granuloma of ataxia telangiectasia 
AD 134:1145–1150, 1998
Behçet’s syndrome – extragenital ulcers 
JAAD 36:689–696, 1997
Carpal tunnel syndrome 
Dermatology 201:165–167, 2000
Charcot–Marie–Tooth syndrome – neurotrophic ulcer
Chediak–Higashi syndrome 
Rook p.2742, 1998, Sixth Edition
Congenital insensitivity to pain 
Cutis 51:373–374, 1993
Congenital sensory neuropathy with anhidrosis (self-multilation)
AD 124:564–566, 1988
Ectodermal dysplasias
Ehlers–Danlos syndrome
Familial dysautonomia (Riley–Day syndrome) 
Flynn–Aird syndrome – skin atrophy, ulceration, alopecia, and
dental caries 
J Neurol Sci 2:161–182, 1965
Goltz’s syndrome 
Ghatan p.199, 2002, Second Edition
Hereditary sensory and autonomic neuropathy type I-V
(congenital insensitivity to pain) – ulcers with self-mutilation
Ped Derm 19:333–335, 2002
Hereditary sensory radicular neuropathy
Hyper-IgM syndrome – diaper area ulcers 
Ped Derm 18:48–50,
2001
Hypereosinophilic syndrome, idiopathic 
Blood 83:2759–2779,
1994; digital ulcers Semin Dermatol 14:122–128, 1995
Johanson–Blizzard syndrome – aplasia cutis congenita of the
scalp, sparse hair, deafness, absence of permanent tooth buds,
hypoplastic ala nasi, dwarfism, microcephaly, mental
retardation, hypotonia, pancreatic insufficiency with
malabsorption, hypothyroidism, genital and rectal anomalies
Clin Genet 14:247–250, 1978; J Pediatr 79:982–987, 1971
Lesch–Nyhan syndrome – X-linked recessive;
hypoxanthineguanine phosphoribosyltransferase deficiency;
self-mutilation; biting of lower lip 
AD 94:194–195, 1966
Lumpy scalp syndrome – autosomal dominant; scalp ulcers at
birth heal as irregular scalp nodules; deformed pinnae,
rudimentary nipples 
Clin Exp Dermatol 15:240, 1989
Marfan-like phenotype – deep skin ulcers 
JAAD 35:814–818, 1996
Neutrophilic dermatosis (pustular vasculitis of the dorsal hands)
(variant of Sweet’s syndrome) – ulcers 
AD 138:361–365, 2002