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PRIMARY CUTANEOUS DISEASE
Acropustulosis of infancy – palmoplantar bullae of infancy
Ped Derm 15:108–111, 1998
Acute parapsoriasis (pityriasis lichenoides et varioliformis acuta)
(Mucha-Habermann disease) – vesiculo-papule
AD
123:1335–1339, 1987; AD 118:478, 1982; bullous form JAAD
23:473–478, 1990
Anetoderma – bullous appearance of anetoderma overlying a
pilomatrixoma
JAAD 25:1072–1076, 1991
Angina bullosa hemorrhagica
Rook p.3085, 1998, Sixth Edition
Balanitis xerotica obliterans
AD Syphilol 56:613, 1928
Bullous congenital ichthyosiform erythroderma
Darier’s disease
AD 118:278–279, 1982
Dyshidrotic eczema, including dyshidrotic id reaction
Eosinophilic cellulitis
BJD 146:160–161, 2002
Epidermolysis bullosa simplex (EBS)
Epidermolysis Bullosa:
Basic and Clinical Aspects. New York: Springer, 1992:89–117;
oral bullae with epidermolysis bullosa – simplex – generalized,
herpetiform, superficialis
AD 125:633–638, 1989; junctional –
Herlitz, generalized mild, localized, inverse, progressive;
dominant dystrophic – hyperplastic, albopapuloid, and
polydysplastic dystrophic type; recessive dystrophic – localized,
generalized, mutilating, inverse
Rook p.3065, 1998, Sixth
Edition; Oral Surg 43:859–872, 1977; variants Oral Surg
67:555–563, 1989; Oral Surg Oral Med Oral Pathol 71:440–446,
1991; late onset junctional epidermolysis bullosa (epidermolysis
junctionalis progressiva) – bullae of hands and feet, nail
dystrophy, loss of dermatolyphic pattern, tooth enamel
abnormalities, hyperhidrosis
BJD 144:1054–1057, 2001;
autosomal recessive epidermolysis bullosa with muscular
dystrophy or congenital myasthenia gravis
AD 125:931–938,
1989; dominant dystrophic epidermolysis bullosa; dystrophic
epidermolyosis bullosa inversa – flexural bullae, oral ulcers,
dental caries, milia
Ped Derm 20:243–248, 2003; epidermolysis
bullosa simplex with mutation of collagen 17A1 gene; ITGB4
coding for integrin beta-4
BJD 151:669–674, 2004; JID
118:185–192, 2002
EBS of hands and feet – Weber Cockayne
EBS with anodontia/hypodontia (Kallin syndrome) – thickened
or curved nails, alopecia with brittle hair
Ghatan p.216, 2002,
Second Edition
EBS, generalized – Koebner variant
EBS herpetiformis – Dowling–Meara
JAAD 28:859–861, 1993
EBS with mottled pigmentation of neck, upper trunk, arms
and leg with or without keratoderma (punctate keratoses);
cutaneous atrophy, nail dystrophy
BJD 128:679–685, 1993;
Clin Genet 15:228–238, 1979; acral blistering, hemorrhagic
bullae, focal punctate keratoderma, dystrophic thick nails
BJD
144:40–45, 2001
EBS Mendes da Costa variant – X-linked recessive
Ghatan p.216, 2002, Second Edition
EBS with muscular dystrophy – plectin mutation (premature
termination codon)
JAAD 41:950–956, 1999
EBS superficialis – atrophic scarring, oral, conjunctival
blisters
AD 125:633–638, 1989
EBS, Ogna variant – autosomal dominant; plectin
abnormality; seasonal blistering of hands and feet,
bruising, hemorrhagic bullae, onychogryphotic first
toenails
Hum Hered 23:189–196, 1973
EBS with or without neuromuscular diseases – autosomal
recessive; muscular dystrophy, myasthenia gravis, spinal
muscular atrophy; possible mental retardation; early death
reported
AD 125:931–938, 1989
EBS Mendes de Coosta variant (dystrophia bullosa, typus
maculatus)
EBS with superficial erosions resembling peeling skin
syndrome
AD 125:633–638, 1989
Kallin’s syndrome – bullae of hands and feet, nail dystrophy,
anodontia, alopecia, deafness
Acta DV (Stockh) 65:526–530,
1985
Lethal autosomal recessive EBS
BJD 113:135–143, 1985
Junctional EB
Epidermolysis Bullosa: Basic and Clinical
Aspects. New York: Springer, 1992:118–134
Localized forms
JEB inversa (non-lethal inverse junctional EB) – groin,
perineum, axillae; heals with atrophic white streaks;
late onset
Proc R Soc Med 70:576–577, 1977
Non-lethal localized junctional EB – legs and feet only;
hyperkeratosis with erosions of soles
J R Soc Med 78
(Suppl 11); 32–33, 1985
JEB localized, other
Ghatan p.216, 2002, Second Edition
JEB progressiva (neurotrophic) variant – autosomal
recessive
Ghatan p.216, 2002, Second Edition
Progressive junctional EB (neurotropic) – partial deafness,
bullae of hands and feet, elbows, and knees, atrophy, oral
erosions
JAAD 16:195–200, 1987
Cicatricial junctional EB – scarring, alopecia, syndactyly,
contractures
JAAD 12:836–844, 1985
Generalized forms
EB atrophicans generalisata gravis, Herlitz type –
extensive blistering and erosions at birth; perioral and
nasal exuberant granulation tissue; bulbous finger tips
with crusting and erosions
Rook p.1828–1829, 1998,
Sixth Edition
Generalized atrophic benign EB (GABEB) (mitis) –
non-lethal junctional – generalized blistering
beginning in infancy; atrophic scarring; alopecia of
scalp, eyebrows, eyelashes
Dermatologica 152:72–86,
1976; nevi or acquired macular pigmented lesions
with irregular borders
AD 122:704–710, 1986;
GABEB – giant nevi at sites of blistering
AD 132:145–150, 1996
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