Glucagonoma syndrome (necrolytic migratory erythema)
JAAD 24:473–477, 1991
Lymphoma – annular red and reticulated plaques due to
cutaneous granulomas associated with systemic lymphoma
JAAD 51:600–605, 2004
Necrobiotic xanthogranuloma with paraproteinemia
Paraneoplastic autoimmune multiorgan syndrome
(paraneoplastic pemphigus) – arciform and polycyclic lesions
AD 137:193–206, 2001
Pityriasis rotunda
Cutis 58:406–408, 1996; AD
119:607–6098, 1983
PHOTODERMATOSES
Actinic lichen planus
AD 135:1543–1548, 1999
Annular elastolytic granuloma (actinic granuloma)
Disseminated superficial actinic porokeratosis
JAAD
40:479–480, 1999; Int J Derm 38:204–206, 1999
Phototoxic dermatitis
Polymorphic light eruption
PRIMARY CUTANEOUS DISEASES
Alopecia mucinosa (follicular mucinosis)
Derm 197:178–180,
1998; JAAD 10:760–768, 1984; AD 76:419–426, 1957
Annular atrophic plaques of the face
AD 100:703–716, 1969
Annular epidermolytic ichthyosis
BJD 141:642–646, 1999;
JAAD 27:348–355, 1992
Annular erythema of infancy
Atrophia maculosa varioliformis cutis – linear, varioliform scars
Ped Derm 18:230–233, 2001; JAAD 21:309, 1989; BJD
115:105–109, 1986
Atrophoderma of Pasini and Pierini
JAAD 30:441–446, 1994
Circumscribed palmar or plantar hypokeratosis – red depressed
or atrophic patch with ridged border
JAAD 51:319–321, 2004;
JAAD 49:1197–1198, 2003; JAAD 47:21–27, 2002
Confluent and reticulated papillomatosis
Dyshidrosis
Cutis 23:819–821, 1979
Elastosis perforans serpiginosa
AD 141:1457–1462, 2005;
JAAD 51:1–21, 2004; AD 129:205–207, 1993; seen in Down’s
syndrome, osteogenesis imperfecta, pseudoxanthoma
elasticum, Rothmund-Thomson syndrome, penicillamine
JAAD 46:161–183, 2002; elastosis perforans serpiginosa with
pseudoxanthoma elasticum-like changes in Moya-Moya disease
(bilateral stenosis and occlusion of basa intracranial vessels
and carotid arteries)
BJD 153:431–434, 2005
Eosinophilic pustular folliculitis of Ofuji – circinate and
serpiginous plaques with overlying papules and pustules in
seborrheic areas; pustules are follicular
J Dermatol 16:388–391,
1989; Hautarzt 39:527–530, 1988; Acta DV 50:195–203, 1970;
red plaque with pustules
JAAD 46:827–833, 2002
Epidermolysis bullosa simplex, dystrophica; epidermolysis
bullosa herpetiformis (Dowling-Meara)
Textbook of Neonatal
Dermatology, p.160, 2001; JAAD 28:859–861, 1993;
epidermolysis bullosa S/P ECG
Epidermolytic hyperkeratosis – annular and polycyclic plaques
JAAD 27:348–355, 1992
Erythema annulare centrifugum
Erythema dyschromicum perstans
JAAD 21:438–442, 1989
Erythema elevatum diutinum
Rook p.2194, 1998, Sixth Edition;
BJD 67:121–145, 1955
Erythrokeratoderma hiemalis (erythrokeratolysis hiemalis
(Oudtshoorn disease)) – palmoplantar erythema, cyclical
and centrifugal peeling of affected sites, targetoid lesions of
the hands and feet; annular serpiginous lesions of lower
legs, knees, thighs, upper arms, shoulders – seen in South
African whites; precipitated by cold weather or fever
BJD
98:491–495, 1978
Erythrokeratoderma variabilis (Mendes da Costa syndrome) –
autosomal dominant – dark red fixed plaques with transient
polycyclic red macules with fine scale
JID 113:1119–1122,
1999; Ped Derm 12:351–354, 1995
Familial annular erythema – autosomal dominant; early
infancy to puberty; vesiculation or scaling
Textbook of
Neonatal Dermatology, p.295, 2001
Figurate erythemas
Erythema annulare centrifugum
Am J Dermatopathol
25:4510462, 2003; Rook p.2088, 1998, Sixth Edition; in
infancy
JAAD 14:339–343, 1986
Associations with erythema annulare centrifugum:
Acute myeloblastic leukemia
Ann Dermatol Venereol
116:6–7,1989
AIDS Tyring p.369, 2002
Alendronate
JAAD 48:945–946, 2003
Ampicillin
J Indian Med Assoc 65:307–308, 1975
Ascariasis
AD 117:582–585, 1981
Blood dyscrasia
Arch Klin Exp Dermatol
195:434–446, 1953
Breast cancer
Cutis 26:282–284, 1980
Bullous pemphigoid
Br J Dermatol 110:378–379, 1984
Candida Hautarzt 236:466–470, 1975
Carcinoid tumor
Nt J Frtmsyol 94:452–456, 2976
Cat scratch disease
Int J Derm 17:656–658, 1988
Chloroquine
AD 95:37–39, 1967
Chronic polyarthritis
J Rheumatol 38:59–66, 1979
Cimetidine
Br Med J [Clin Res Ed] 283:698, 1981
Dysproteinemia
Br J Dermatol 85:546–560, 1971
Epstein–Barr virus
Acta Paediatr Scand 63:788–792, 1974
Familial
Cutis 44:139–170, 1989
Gold thiomalate therapy
JAAD 25:557–560, 1991; JAAD
27:284–287, 1992
Graves’ disease
AD 118:623, 1982
Hodgkin’s disease
Int J Dermatol 32:59–61, 1993
Hydrochlorothiazide
Int J Dermatol 27:129–130, 1988
Hydroxychloroquine sulfate
Cutis 36:129–30, 1985
Hypereosinophilic syndrome
Med Cutan Ibero Lat Am
16:299–304, 1988; Cutis 35:53–55, 1985
Congenital ichthyosis
Dermatologica 140:75, 1970
Infectious mononucleosis
Tyring p.149, 2002
Ingested fungus (cheese)
AD 90:54–58, 1964
Inflammatory carcinoma (carcinoma erysipelatoides)
ActaDerm Venereol (Stockh) 73:138–140, 1993
Internal malignancy
AD 87:246–251, 1963
Liver disease
AD 122:1239–1270, 1986
Lyme disease
Dermatol Clin 3:129–139, 1985
Malignant histiocytosis
Clin Exp Dermatol
9:608–613, 1984
Molluscum contagiosum
AD 114:1853, 1978
Phenothiazine
Hautarzt 41:161–163, 1990
Phthirus pubis infestation
BJD 149:1291, 2003
Piroxicam
JAAD 13:840–841, 1985
Polycythemia vera
Ann Dermatol Venereol
111:767–768, 1984
Prostate adenocarcinoma
Ann Dermatol Venereol
106:789–92,1979
Psoriasis
Hautarzt 38:509–520, 1987
Sarcoidosis
Br J Dermatol 1060:713–716, 1982
Sjögren’s syndrome and systemic lupus erythematosus
JAAD 25:557–560, 1991
Spironolactone
Ann DV 114:375–376, 1987
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