Dermatologic Differential Diagnosis.pdf. - Famona Site

592 A CLINICIAN’S GUIDE TO DERMATOLOGIC DIFFERENTIAL DIAGNOSIS, VOLUME 1
Confluent and reticulated papillomatosis of Gougerot and
Carteaud JAAD 49:1182–1184, 2003; BJD 142:1252–1253,
2000; AD 132:1400–1401, 1996; BJD 129:351–353, 1993; Bull
Soc Fr Dermatol Syphilol 34:719–721, 1927
Congenital erosions and vesicles healing with reticulate scarring
Dermatology 194:278–280, 1997; JAAD 17:369–376, 1987
Dowling–Degos syndrome (reticulated pigmented anomaly of the
flexures) JAAD 40:462–467, 1999; AD 114:1150–1157, 1978
Epidermolysis bullosa, Dowling–Meara epidermolysis bullosa
with mottled, reticulate dyspigmentation AD 122:900–908, 1986
Epidermolysis bullosa pruriginosa – reticulate scarring,
dermatitis with lichenified plaques, violaceous linear scars,
albopapuloid lesions of the trunk, prurigo nodularis-like lesions,
milia BJD 152:1332–1334, 2005
Epidermolysis bullosa simplex, Mendes de Costa variant –
reticulate hyperpigmentation and atrophy JAAD 21:425–432,
1989; Ped Derm 6:91–101, 1989
Erythema craquele
Erythrokeratoderma variabilis
Folliculitis ulerythematosa reticulata – scarring and honeycomb
atrophy; associated with Noonan’s syndrome AD
124:1101–1106, 1988
Granular parakeratosis JAAD 52:863–867, 2005; Ped Derm
20:215–220, 2003
Granuloma annulare, generalized Curr Prob Derm 8:137–188,
1996
Infantile febrile psoriasiform dermatitis Ped Derm 12:28–34, 1995
Lichen planus of tongue/buccal mucosa Rook p.1904–1912,
Sixth Edition; J Oral Pathol 14:431–458, 1985
Lichen sclerosus et atrophicus, oral – bluish–white plaques;
may mimic lichen planus Rook p.2549–2551, 1998, Sixth
Edition; BJD 131:118–123, 1994; Br J Oral Maxillofac Surg
89:64–65, 1991
Mid-dermal elastophagocytosis – reticulate erythema Australas
J Dermatol 42:50–54, 2001
Parakeratosis variegata – reticulated and atrophic Dermatology
201:54–57, 2000; BJD 137:983–987, 1997; Dermatology
190:124–127, 1995
Periumbilical perforating pseudoxanthoma elasticum – plaque AD
126:1639–1644, 1990; Arch Pathol Lab Med 100:544–546, 1976
Pigmentatio reticularis faciei and colli with epithelial
cystomatosis JAAD 37:884–886, 1997; Dermatoligae Tokyo:
University of Tokyo Press 89–90, 1982
Poikiloderma vasculare atrophicans AD 125:1265–70, 1989
Prurigo pigmentosa – red papules or reticulate plaques Cutis
63:99–102, 1999; JAAD 34:509–11, 1996; AD 130:507–12,
1994; BJD 120:705–708, 1989; AD 125:1551–1554, 1989;
JAAD 12:165–169, 1985
Psoriasis
Ulceronecrotic Mucha–Habermann disease – generalized
reticulate necrotic lesions
Unilateral laterothoracic exanthem JAAD 34:979–984, 1996
Vermiculate atrophoderma – honeycomb atrophy Rook p.2011,
1998, Sixth Edition
Zosteriform reticulate hyperpigmentation BJD 121:280, 1989;
BJD 117:503–510, 1987
SYNDROMES
Acropigmentation symmetrica of Dohi – autosomal dominant,
sporadic; Asians with onset under 20 years of age; acral
hyperpigmentation (reticulate pattern becoming patches with
hypopigmented macules of face, trunk, distal extremities
JAAD 43:113, 2000
Adams–Oliver syndrome – 10% cutis marmorata telangiectatica
congenita Dermatology 187:205–208, 1993
Ataxia telangiectasia
Bockenheimer’s syndrome – diffuse genuine phlebectasia
Cantu’s syndrome – autosomal dominant, onset in early
adolescence with 1mm brown macules which become confluent
over face, feet, forearms; hyperkeratotic papules of palms and
soles Clin Genet 14:165, 1978
Cobb’s syndrome
Coffin–Lowry syndrome – X-linked inheritance; straight coarse
hair, prominent forehead, prominent supraorbital ridges,
hypertelorism, large nose with broad base, thick lips with mouth
held open, large hands, tapering fingers, severe mental
retardation; loose skin easily stretched, cutis marmorata,
dependent acrocyanosis, varicose veins Clin Genet
34:230–245, 1988; Am J Dis Child 112:205–213, 1966
Congenital reticular ichthyosiform erythroderma (ichthyosis
variegata) BJD 139:893–896, 1998; ichthyosis ‘en confettis
Dermatology 188:40–45, 1994
Cornelia de Lange syndrome – cutis marmorata, short stature,
specific facies, hypertrichosis of forehead, face, back,
shoulders, and extremities, synophrys; long delicate eyelashes,
skin around eyes and nose with bluish tinge Rook p.428, 1998,
Sixth Edition; JAAD 37:295–297, 1997
CRIE syndrome – congenital reticulated ichthyosiform
erythroderma (ichthyosis variegata) BJD 139:893–896, 1998;
Dermatology 188:40–45, 1994
Dermatopathia pigmentosa reticularis (dermatopathia
pigmentosa reticularis hyperkeratosis et mutilans) – autosomal
dominant; reticulate pigmentation, alopecia, nail changes,
palmoplantar hyperkeratosis (punctate palmoplantar
keratoderma), loss of dermatoglyphics; infantile bullae, reticular
hyperpigmentation of flexures, ainhum-like contraction,
periodontopathy JAAD 26:298–301, 1992;AD 126:935–939,
1990
Divry–Van Bogaert syndrome – autosomal recessive; congenital
livedo reticularis; diffuse leptomeningeal angiomatosis Rook
p.584, 1998, Sixth Edition; J Neurol Sci 14:301–314, 1971
Dyschromatosis universalis hereditaria Ped Derm 17:70–72,
2000
Dyskeratosis congenita (Zinsser–Engman–Cole syndrome) –
Xq28 J Med Genet 33:993–995, 1996; Dermatol Clin 13:33–39,
1995; BJD 105:321–325, 1981
Extensive reticular hyperpigmentation and milia Ped Derm
16:108–110, 1999
Familial multiple follicular hamartoma JAAD 37:884–886, 1997;
Dermatologica 159:316–324, 1979
Familial pigmentary anomaly
Goltz’s syndrome (focal dermal hypoplasia) – asymmetric linear
and reticulated streaks of atrophy and telangiectasia; yellow–red
nodules; raspberry-like papillomas of lips, perineum, acrally, at
perineum, buccal mucosa; xerosis; scalp and pubic hair sparse
and brittle; short stature; asymmetric face; syndactyly,
polydactyly; ocular, dental, and skeletal abnormalities with
osteopathia striata of long bones JAAD 25:879–881, 1991
Haber’s syndrome – reticulate keratotic plaques on trunk and
limbs; rosacea-like eruption of face BJD 77:1–8, 1965
Hereditary angioneurotic edema – reticulate erythema in
prodromal stage Rook p.2135–2136, 1998, Sixth Edition; BJD
101:549–552, 1979
Hereditary sclerosing poikiloderma AD 100:413–422, 1969