PRIMARY CUTANEOUS DISEASES
Acne rosacea (lupus miliaris disseminata facei)
Rook
p.2104–2110, 1998, Sixth Edition; AD 134:679–683, 1998; Clin
Exp Dermatol 16:295–296, 1991; Int J Derm 23:542–544, 1984;
acne agminata (granulomatous rosacea) – monomorphic brown
papules of chin, cheeks, eyelids
BJD 134:1098–1100, 1996
Acne vulgaris – inflammatory papules; multiple miliary osteoma
cutis
AD 110:113–114, 1974
Alopecia mucinosa
Angiolymphoid hyperplasia with eosinophilia – angiofibroma-like
JAAD 12:781–796, 1985
Chronic acquired dyskeratotic papulosis
Cutis 69:469–471, 2002
Facial Afro-Caribbean childhood eruption – resembles perioral
dermatitis
Clin Exp Dermatol 15:163–166, 1990; BJD
91:435–438, 1976
Granuloma annulare
Pediatr Rev 11 (9):262–267, 1990; photo-
induced granuloma annulare of AIDS
Granuloma faciale
JAAD 51:269–273, 2004
Granulomatous periorificial dermatitis – extrafacial and
generalized periorificial dermatitis
AD 138:1354–1358, 2002;
facial granulomatous perioral dermatitis in children
AD 125:369–373, 1989
Granulosis rubra nasi
G Ital Dermatol Venereol 125:275–276,
1990
Infantile nodulocystic acne
AD 123:432–433, 1987
Keratosis lichenoides chronica
Clin Exp Dermatol 27:283–285,
2002; BJD 144:422–424, 2001
Keratosis pilaris, including scarring keratosis pilaris
Lichen nitidus
Lichen striatus
Pityriasis rosea
Cutis 32:352–360, 1983
Pseudofolliculitis barbae
Dermatol Clin 6:387–395, 1988
Steatocystoma multiplex
AD 122:205–207, 1986;
Cutis 51:449–452, 1993; AD 129:35–37, 1993
Trichostasis spinulosa
AD 133:1579,1582, 1997
SYNDROMES
Anhidrotic ectodermal dysplasia – carrier state for X-linked
anhidrotic ectodermal dysplasia
Atrichia with keratin cysts – face, neck, scalp; then trunk and
extremities
Ann DV 121:802–804, 1994
Atrichia with papular lesions – autosomal recessive; follicular
cysts
AD 139:1591–1596, 2003; JAAD 47:519–523, 2002
Bannayan–Riley–Ruvalcaba syndrome (macrocephaly and
subcutaneous hamartomas) (lipomas and hemangiomas) –
autosomal dominant
; multiple verrucous facial papules
(trichilemmomas and warts)
JAAD 53:639–643, 2005; AD
132:1214–1218, 1996; AD 128:1378–1386, 1992; Eur J Ped
148:122–125, 1988; lipoangiomas (perigenital pigmented
macules, macrocephaly)
AD 128:1378–1386, 1992; lipomas in
Ruvalcaba–Myhre–Smith syndrome
Ped Derm 5:28–32, 1988
Basaloid follicular hamartoma syndrome (generalized basaloid
follicular hamartoma syndrome) – multiple skin-colored, red,
and hyperpigmented papules of the face, neck chest, back,
proximal extremities, and eyelids; syndrome includes milia-like
cysts, comedones, sparse scalp hair, palmar pits, and parallel
bands of papules of the neck (zebra stripes)
JAAD 49:698–705,
2003; BJD 146:1068–1070, 2002; JAAD 43:189–206, 2000
Behçet’s syndrome – erythema nodosum; nodule
AD
138:467–471, 2002
Birt–Hogg–Dube syndrome – fibrofolliculomas – autosomal
dominant; white or yellow facial and nose papules
JAAD
50:810–812, 2004; JAAD 49:698–705, 2003; Australas J
Dermatol 44:52–56, 2003; JAAD 48:111–114, 2003; AD
135:1195–1202, 1999; JAAD 16:452–457, 1987; AD
133:1161–1166, 1997; AD 113:1674–1677, 1977; renal and
colonic neoplasms
Cancer Epidemiol Biomarkers Prev
11:393–400, 2002; AD 135:1195–1202, 1999; facial
angiofibromas
JAAD 53:S108–111, 2005
Blue rubber bleb nevus syndrome
Brooke–Spiegler syndrome – trichoepitheliomas and
cylindromas
JAAD 49:698–705, 2003; Dermatol Surg
26:877–882, 2000; also eccrine spiradenomas of forehead Am J
Dermatopathol 20:56–60, 1998; Cutis 46:46–50, 1990
Carney complex – myxoma
Costello syndrome – warty papules around nose and mouth,
legs, perianal skin; loose skin of neck, hands, and feet;
acanthosis nigricans; low set protuberant ears, thick
palmoplantar surfaces with single palmar crease, gingival
hyperplasia, hypoplastic nails, moderately short stature,
craniofacial abnormalities, hyperextensible fingers, sparse curly
hair, perianal and vulvar papules, diffuse hyperpigmentation,
generalized hypertrichosis, multiple nevi
Ped Derm 20:447–450,
2003; JAAD 32:904–907, 1995; Aust Paediat J 13:114–118,
1977
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