Dermatologic Differential Diagnosis.pdf. - Famona Site

Immunocytoma, multiple cutaneous BJD 143:165–170, 2000
Juvenile xanthogranuloma Ann DV 128:291, 2001; BJD
140:541–542, 1999
Langerhans cell histiocytosis, vesicular (Hashimoto-Pritzker
disease) Clin Exp Dermatol 19:350–352, 1994
Leeches Int J Derm 35 (3):226–227, 1996
Leprosy – lepromatous Dermatologica 135:329, 1967
Lichen planus Bolognia p.1542, 2003
Lupus erythematosus – systemic or DLE Rook p.2012,
1998, Sixth Edition
Lyme disease JAAD 48:S86–88, 2003
Lymphocytoma cutis Bolognia p.1542, 2003
Lymphoma – B-cell lymphoma, CTCL
Mastocytosis Bolognia p.1542, 2003
Melanocytic nevi Bolognia p.1542, 2003
Overlying inflammatory processes
Penicillamine Bolognia p.1542, 2003
Perifolliculitis
Pilomatrixoma JAAD 25:1072–1076, 1991
Plasmacytoma or benign cutaneous lymphoid hyperplasia
AD131:365–6, 1995
Porphyria (congenital poikiloderma and anetoderma) Arch
Argent Dermatol 16:190–194, 1966
Post-inflammatory elastolysis and cutis laxa (PECL) BJD
92:183–190, 1975
Anetoderma of prematurity Eichenfeld, p.105, 2001; AD
133:789, 1997; AD 132:671–674, 1996; anetoderma of
prematurity in association with ECG electrodes JAAD
40:479–481, 1999
Prurigo nodularis Bolognia p.1542, 2003
Sarcoid Bolognia p.1542, 2003
Staphylococcus epidermidis – perifollicular macular atrophy
Syphilis – congenital, secondary, tertiary, latent Rook
p.2012, 1998, Sixth Edition
Takayasu’s arteritis
Tinea versicolor Textbook of Pediatr Derm; Ed. Harper
p.1295
Tuberculosis Bolognia p.1542, 2003
Upper respiratory infection AD 79:516–518, 1959
Urticaria pigmentosa (mastocytosis) Ann DV 108:269–275,
1981
Varicella Bolognia p.1542, 2003
Xanthomas Bolognia p.1542, 2003
Annular and semicircular lipoatrophies JAAD 20:433–436, 1989
Annular atrophic plaques of the face AD 100:703–716, 1969
Aplasia cutis congenita (ACC) Ped Derm 19:326–329, 2002;
Textbook of Neonatal Dermatology, p.126, 2001; giant variant
Ped Derm 21:150–153, 2004
I – ACC without multiple anomalies
II – Scalp ACC with associated limb anomalies; hypoplastic
or absent distal phalanges, syndactyly, club foot, others
(most cases are Adams–Oliver syndrome)
III – Scalp ACC with associated epidermal and organoid nevi
IV – ACC overlying embryologic malformations, such as
gastroschisis, omphalocele, meningomyelocele, and others
V – ACC with associated fetus papyraceus or placental
infarcts
VI – ACC with epidermolysis bullosa
Junctional EB with pyloric atresia; ACC with gastrointestinal
atresia
VII – ACC localized to extremities without blistering
VIII – ACC caused by specific teratogens
IX – ACC asociated with malformation syndromes, such as
Goltz syndrome, trisomy 13, ectodermal dysplasia, others
Cranial stenosis (Spear–Mickle syndrome) Plast Reconstr
Surg 71:413–417, 1983
4p deletion syndrome (chromosome 4 short arm deletion
syndrome)
ATROPHIC LESIONS 67
Delleman–Orthuys syndrome
Focal facial dermal dysplasia
Johanson–Blizzard syndrome
Goltz syndrome
Amniotic band syndrome
XY gonadal dysgenesis
Adams–Oliver syndrome
Atrophia maculosa varioliformis cutis – linear, varioliform scars
BJD 153:821–824, 2005; Ped Derm 18:230–233, 2001; JAAD
30:837–840, 1994; JAAD 21:309, 1989; BJD 115:105–109,
1986; AD 64:59–61, 1951; J Cutan Dis 36:285–288, 1918
Atrophoderma elastolytica discreta Am J Dermatopathol
18:212–217, 1996
Atrophoderma of Moulin (linear atrophoderma of Moulin) –
acquired atrophic pigmented band-like lesions following
Blaschko’s lines JAAD 49:492–498, 2003; Eur J Dermatol
10:611–613, 2000; Int J Dermatol 39:846–852, 2000; JAAD
38:366–368, 1998; BJD 135:277–279, 1996; Ann DV
119:729–736, 1992
Atrophoderma of Pasini and Pierini Dermatol 190:203–206,
1995; JAAD 30:441–446, 1994; Int J Derm 10:643–645, 1984
Atrophoderma vermiculatum (folliculitis ulerythematosa
reticulata) – scarring with cribriform depressions
JAAD 43:310–312, 2000; JAAD 18:538–542, 1988;
AD 124:1101–1106, 1988
Balanitis xerotica obliterans
Barraquer–Simons (partial cephalothoracic) lipodystrophy –
involves face and trunk JAAD 49:768–769, 2003; JAAD
32:130–133, 1995
Blepharochalasis Br J Ophthalmol 72:863–867, 1988; AD
115:479–481, 1979
Brauer lines – associated with aplasia cutis congenita Bolognia
p.924, 2003
Centrifugal lipodystrophy – of abdomen in Japanese children
AD 126:206–209, 1990; of face BJD 127:407–410, 1992; of
neck Dermatology 188:142–144, 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
Congenital total lipodystrophy (Seip–Berardinelli) JAAD
32:130–133, 1995
Congenital vertex alopecia
Cutis laxa – congenital; acquired – with amyloidosis, myeloma
AD 112:853–855, 1976; lupus erythematosus, hypersensitivity
reaction to penicillin Hautarzt 26:191–198, 1975; complement
deficiency, penicillamine, inflammatory skin disease;
sarcoidosis, syphilis, Klippel–Trenaunay syndrome JID
75:399–403, 1980; after urticaria and angioedema
AD 103:661–669, 1971; generalized cutis laxa – autosomal
dominant or autosomal recessive Rook p.2019–2020, 1998,
Sixth Edition; post-inflammatory elastosis and cutis laxa in
African children BJD 92:183–190, 1975
Dimples – acromial, facial, sacral
Dunnigan–Cobberling lipodystrophy – involves trunk, spares
face JAAD 49:768–769, 2003
Elastoderma – cutis laxa-like changes JAAD 33:389–392, 1995
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
Epidermolysis bullosa, recessive dystrophic – symblepharon
Epidermolysis Bullosa: Basic and Clinical Aspects. New York:
Springer, 1992:135–151; dominant dystrophic – atrophic scars