Schneiderman Prelims Vol-I. qxd


PAPULOVESICULAR DERMATITIS IN INFANTS



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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

PAPULOVESICULAR DERMATITIS IN INFANTS
Absent dermatoglyphics and transient facial milia (vesicles)
JAAD 32:315–318, 1995
Behcet’s disease, neonatal
Congenital candidiasis
Congenital self-healing Langerhans cell histiocytosis 
JAAD
31:910–6, 1994
Eosinophilic pustular folliculitis
Erythema toxicum neonatorum
Herpes simplex infection
Infantile acropustulosis
Incontinentia pigmenti
Listeria monocytogenes infection, perinatal
Miliaria
Transient neonatal pustular melanosis
BULLAE, HEMORRHAGIC
AUTOIMMUNE DISEASES, AND DISEASES
OF IMMUNE DYSFUNCTION
Allergic contact dermatitis to poison ivy
Bullous pemphigoid 
Clin Exp Dermatol 13:242–243, 1988
Cicatricial pemphigoid – including hemorrhagic bullae of buccal
mucosae; adult or childhood form of cicatricial pemphigoid
Dermatitis herpetiformis 
JAAD 16:1274–1276, 1987
Epidermolysis bullosa acquisita, including buccal mucosa 
JAAD
11:820–832, 1984
Graft vs. host disease
Linear IgA disease (chronic bullous disease of childhood) –
perioral, eyelids, ears, scalp, perineum, vulva; annular polycyclic
bullae; hemorrhagic bullae 
Ped Derm 15:108–111, 1998;
neonatal linear IgA disease 
Ped Derm 10:171–176, 1993
Lupus erythematosus – systemic lupus – bullous sunburn
reaction 
Rook p.2472–2473, 1998, Sixth Edition; BJD
82:125–128, 1970; AD 83:910–914, 1961
Mixed connective tissue disease – with vasculitis
Morphea 
Cutis 44:118–119, 1989
Pemphigus vulgaris
Rheumatoid vasculitis 
JAAD 53:191–209, 2005; BJD
147:905–913, 2002; AD 125:1101–1104, 1989
CONGENITAL LESIONS
Aplasia cutis congenital 
Ped Derm 21:150–153, 2004
DRUG-INDUCED
Bullous pemphigoid – penicillin, sulfasalazine, topical
5-fluorouracil, PUVA, electron beam radiotherapy 
Clinics
in Derm 11:515–520, 1993
Chemotherapy extravasation
Coumarin necrosis – associated with protein C deficiency
(autosomal dominant); begins 3–5 days after commencing
coumarin therapy
Fixed drug reaction
Gemcytabine extravasation
Heparin necrosis

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