Dermatologic Differential Diagnosis.pdf. - Famona Site

122 A CLINICIAN’S GUIDE TO DERMATOLOGIC DIFFERENTIAL DIAGNOSIS, VOLUME 1
diffuse multiple osteomas of the extremities, Albright’s
hereditary osteodystrophy (short stature, round face, absence
of several knuckles with or without mental retardation),
fibrodysplasia ossificans progressiva (ossification of fascia,
aponeurosis, and muscular structures, microdactyly)
JAAD 20:973–978, 1989
Papillomatosis cutis carcinoides Cutis 62:77–80, 1998
Penile carcinoma with HPV 18 – either HPV 16 or 18 may be
implicated in penile carcinoma JAAD 20:887–889, 1989
Sebaceous gland hypertrophy of labia minora Genital Skin
Disorders, Fischer and Margesson, CV Mosby, p.104, 1998;
Rook p.3205, 1998, Sixth Edition
Seborrheic keratosis
Smooth muscle hamartoma
Spitz nevus Great Cases from the South; AAD Meeting;
March 2000
Squamous cell carcinoma
Syringocystadenoma papilliferum
Trichoblastoma AD 137:219–224, 2001
Trichodiscomas – multiple agminated trichodiscomas of earlobe
JAAD 49:729–730, 2003
Trichoepitheliomas, multiple Bolognia p.1736, 2003; Am J
Dermatopathol 24:402–405, 2002; of nose AD 87:102–114, 1963
Xanthogranulomas – generalized lichenoid juvenile
xanthogranulomas Br J Derm 126:66–70,1992
PARANEOPLASTIC
Acanthosis nigricans, malignant
Bazex syndrome BJD 103:301–306, 1980
Necrobiotic xanthogranuloma Cutis 59:333–336, 1997
Tripe palms J Clin Oncol 7:669–678, 1989; JAAD 16:217–219,
1987
PHOTODERMATOSES
Actinic reticuloid (chronic actinic dermatitis) – chronic
photosensitivity disorder associated with CTCL; sensitive to
UVB JAAD 21:1134–1137, 1989; JAAD 38:877–905, 1998;
Sem Derm 161, Sept 1982; AD 115:1078–1083, 1979
PRIMARY CUTANEOUS DISEASE
Acantholytic dermatosis of the vulvocrural area – vulvar
papules, cobblestoning of the vulva and thighs Cutis
67:217–219, 2001
Acanthosis nigricans, pseudo-acanthosis nigricans, benign
Acquired plantar hyperkeratosis
Acrokeratoelastoidosis of Costa
Darier’s disease JAAD 27:40–50, 1992
Epidermolytic hyperkeratosis AD 130:1026–1033, 1994
Excess skin folds with cobblestone appearance in:
Dermatosparaxis AD 129:1310–1315, 1993
Cutis laxa – autosomal dominant (good prognosis),
autosomal recessive (one form with severe cardiorespiratory
symptoms), X-linked recessive (X-linked Ehlers–Danlos
syndrome-joint laxity, bladder diverticula, hernia, cranial
occipital exostoses), or acquired (may follow febrile illnesses,
seen in offspring of mothers with cystinuria taking
penicillamine; also DeBarsy syndrome, Patterson syndrome,
wrinkly skin syndrome, geroderma osteoplastica,
pseudoxanthoma elasticum, SCARF syndrome (skeletal
abnormalities, ambiguous genitalia, craniostenosis,
retardation, and facial abnormalities), amyloidosis and
plasma cell dyscrasia) AD 129:757–762, 1993
Fox–Fordyce disease
Granular parakeratosis Ped Derm 20:215–220, 2003
Hailey–Hailey disease JAAD 26:951–955, 1992
Hyperkeratosis of the nipple and areola (hyperkeratosis
areolae mammae) JAAD 41:274–276, 1999; Eur J Dermatol
8:131–132, 1998 JAAD 13:596–598, 1985; AD 126:687, 1990;
estrogen-induced Cutis 26:95–96, 1980
Ichthyosis hystrix (Lambert type) JAAD 36:646–647, 1997
Lichen planus
Lichen simplex chronicus; of the vulva Genital Skin
Disorders, Fischer and Margesson, CV Mosby, 1998, p.158;
nodular lichen simplex chronicus of the scrotum
BJD 144:915–916, 2001
Mal de Meleda (recessive transgressive palmoplantar
keratoderma) – lichenoid cobblestoned plaques on the knees
Ped Derm 14:186–191, 1997
Ofuji’s disease (eosinophilic pustular folliculitis) – crops of
follicular papules and pustules on face, trunk and extremities;
leukocytosis with eosinophilia and elevated IgG, IgA and IgE
JAAD 12:268–273, 1985
Perforating granuloma annulare AD 137:1647–1652, 2001
Perianal pseudoverrucous papules and nodules AD
128:24–242, 1992
Pityriasis rubra pilaris in AIDS JAAD 27:260–262, 1992
Pseudoepitheliomatous keratotic and micaceous balanitis
Genital Skin Disorders, Fischer and Margesson, CV Mosby
p.84, 1998; Cutis 35:77–79, 1985
Psoriasis with tripe palms Clin Exp Dermatol 5:181–189, 1980
Pseudoxanthoma elasticum-like papillary dermal elastolysis
JAAD 51:165–185, 2004
Rhinophyma
Scleredema
Scrotal glans penis Int J Derm 36:762–763, 1997
Striae atrophicae
Terra firme
Vohwinkel’s palmoplantar keratoderma
White fibrous papulosis of the neck (fibroelastolytic
papulosis) – cobblestoning with 2–4-mm skin-colored
papules JAAD 51:958–964, 2004; Int J Derm 35:720–722,
1996; JAAD 20:1073–1077, 1989
SYNDROMES
Birt–Hogg–Dube syndrome – fibrofolliculomas; autosomal
dominant; fibrofolliculomas (of mesodermal and epithelial
origin), trichodiscomas (of mesodermal origin) and
acrochordons on face, neck, scalp and upper trunk; differential
diagnosis includes multiple trichoepitheliomas (autosomal
dominant), Cowden’s syndrome (autosomal dominant),
fibrofolliculomas (autosomal dominant), trichodiscomas
(autosomal dominant), perifollicular fibromas and adenoma
sebaceum (autosomal dominant); association with renal cell
carcinoma JAAD 16:452–457, 1987
Buschke–Ollendorff syndrome – skin-colored to yellow papules
Ped Derm 22:133–137, 2005; JAAD 49:1163–1166, 2003;
BJD 144:890–893, 2001
Congenital erosive and vesicular dermatitis with reticulate
scarring – cobblestoned scars AD 121:361–367, 1985