Schneiderman Prelims Vol-I. qxd

ERYTHRODERMAS
173
Schneiderman page 100-200.qxd 5/16/2006 6:49 PM Page 173

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49:189–192, 1992 telangiectasia macularis eruptiva perstans
Cutis 71:357–359, 2003
INFLAMMATORY DISEASES
Erythema multiforme, Stevens–Johnson syndrome – acute
erythroderma
Sarcoid 
Hautarzt 61:675, 1986; BJD 95:93–97, 1976; may
mimic pityriasis rubra pilaris 
BJD 95:93–97, 1976
Pseudolymphoma – CD8
+
pseudolymphoma in HIV disease
JAAD 49:139–141, 2003
Rosai–Dorfman disease (sinus histiocytosis with massive
lymphadenopathy) – psoriasiform exfoliative dermatitis 
JAAD
50:159–161, 2004; JAAD 41:335–337, 1999; J Dermatol
20:49–55, 1993; AD 114:191–197, 1978
Toxic epidermal necrolysis 
BJD 68:355–361, 2005
METABOLIC
Biotinidase deficiency (biotin-responsive multiple carboxylase
deficiency) – neonatal and infantile; autosomal recessive;
neonatal – holocarboxylase synthetase deficient; first 6 weeks
of life; erythrodermic with fiery red intertriginous dermatitis 
AD
123:1696–1698, 1987; Pediatrics 68:113–118, 1981; infantile –
biotinidase deficient; after 3 months of life, intertriginous rash
with keratoconjunctivitis, xerosis, generalized pallor, periorificial
dermatitis, alopecia, branny desquamation, and atrophic
glossitis 
Semin Dermatol 10:296–302, 1991; JAAD 9:97–103,
1983
Citrullinemia 
Ghatan p.108, 2002, Second Edition
Essential fatty acid deficiency 
Ghatan p.108, 2002, Second
Edition,
Gaucher’s disease – collodion babies 
Arch Dis Child 66:667,
1991
Hyper-IgE syndrome 
JAAD 36:106–107, 1997
Idiopathic hypoparathyroidism 
AD 109:242–244, 1974
Kwashiorkor 
Ped Derm 16:95–102, 1999
Maple syrup urine disease 
AD 129:384–385, 1993
Thyrotoxicosis – pruritic exfoliative dermatitis 
Dermatology
184:157, 1992