PSYCHOCUTANEOUS DISORDERS
Factitial dermatitis
SYNDROMES
Behçet’s disease
Yonsei Med J 38:380–389, 1997
Erythrokeratoderma variabilis
Kawasaki’s disease – erythema multiforme-like
Cutis 72:354–356, 2003; JAAD 39:383–398, 1998;
Jpn J Allergol 16:178–222, 1967
Marshall’s syndrome
AD 131:1175–1177, 1995
Rowell’s syndrome – lupus erythematosus and erythema
multiforme-like syndrome – papules, annular targetoid lesions,
vesicles, bullae, necrosis, ulceration, oral ulcers; perniotic
lesions
JAAD 21:374–377, 1989
Sweet’s syndrome
AD 141:881–884, 2005; Textbook of Neonatal
Dermatology, p.305, 2001; in chronic granulomatous disease Ped
Derm 11:237–240, 1994
Turner’s syndrome – halo nevi
JAAD 51:354–358, 2004
Vogt–Koyanagi–Harada syndrome – halo nevi; occurs
primarily in Asians, blacks, and darkly pigmented Caucasians;
stage 1 – aseptic meningitis; stage 2 – uveitis (iritis, iridocyclitis)
and dysacusis (tinnitus, hearing loss); stage 3 – depigmentation of
skin (60% of patients), depigmentation of hair (poliosis –
eyelashes, eyebrows, scalp, and body hair – 90% of patients),
alopecia areata
Ann DV 127:282–284, 2000; AD 88:146–149,
1980
TRAUMA
Radiation therapy
Australas Radiol 40:334–337, 1996
Ricocheted action safety bullet marks
Am J Forensic Med
Pathol 18:15–20, 1997
S/P treatment with liquid nitrogen
VASCULAR DISORDERS
Acute hemorrhagic edema of infancy (Finkelstein’s
disease) (Seidlmayer’s purpura)
Ped Int 45:697–700,
2003; Cutis 68:127–129, 2001; J Dermatol 28:279–281,
2001; Cutis 61:283–284, 1998; AD 130:1055–1060, 1994
Angiolymphoid hyperplasia with eosinophilia
Ped Derm
15:91–96, 1998
Bossed hemangioma with telangiectasia and peripheral pallor
AD 134:1145–1150, 1998
Cherry angioma
BJD 112:209–211, 1985
Churg–Strauss disease – erythema multiforme-like lesions
Rook p.2221, 1998, Sixth Edition
Degos’ disease (malignant atrophic papulosis)
BJD 100:21–36,
1979; Ann DV 79:410–417, 1954
Hemangioma of pregnancy
JAAD 32:282–284, 1995
Hemangioma, traumatized
Henoch–Schönlein purpura mimicking erythema multiforme
Leukocytoclastic vasculitis; Henoch-Schönlein purpura;
urticarial vasculitis
AD 134:231–236, 1998; erythema
multiforme-like lesions
Rook p.2178, 1998, Sixth Edition
Non-involuting congenital hemangioma – round to ovoid pink to
purple papule or plaque with central or peripheral pallor, coarse
telangiectasias
JAAD 50:875–882, 2004
Pustular vasculitis – annular pustular plaques with central
necrosis
Rook p.2167, 1998, Sixth Edition
Targetoid hemosiderotic hemangioma – brown to violaceous
nodule with ecchymotic halo
Cutis 72:51–52, 2003; AD
138:117–122, 2002; AD 136:1571–1572, 2000; J Cutan
Pathol 26:279–286, 1999; JAAD 32:282–284, 1995;
JAAD 41:215–224, 1999
Wegener’s granulomatosis – erythema multiforme-like lesions
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