Dermatologic Differential Diagnosis.pdf. - Famona Site

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Progressive cribriform and zosteriform hyperpigmentation Prurigo pigmentosa Dermatology 188:219–221, 1994 Pseudoxanthoma elasticum – linear and reticulated yellow papules and plaques AD 124:1559, 1988; JAAD 42:324–328, 2000; Dermatology 199:3–7, 1999; pseudoxanthoma elasticum resembling reticulated pigmented disorders BJD 134:1157–1159, 1996; penicillamine-induced pseudoxanthoma elasticum JAAD 30:103–107, 1994; Dermatology 184:12–18, 1992; saltpetre-induced pseudoxanthoma elasticum Acta DV 58:323–327, 1978 Reflex sympathetic dystrophy – reticulated hyperpigmentation Cutis 68:179–182, 2001 Reticular pigmented genodermatosis with milia (Naegeli–Franceschetti–Jadassohn syndrome?) Clin Exp Dermatol 20:331–335, 1995 Reticulate acropigmentation of Dohi (dyschromatosis symmetrica hereditaria) – autosomal dominant; mottled pigmentation with depigmentation of dorsa of hands, feet, arms, and legs JAAD 43:113–117, 2000; BJD 140:491–496, 1999; JAAD 37:884–886, 1997 Reticulate acropigmentation of Kitamura – autosomal dominant; freckle-like pigmentation of dorsae of hands, palmar pits AD 139:657–662, 2003; J Dermatol 27:745–747, 2000; JAAD 40:462–467, 1999; BJD 109:105–110, 1983 Reticulate hyperpigmentation of Iijima, Naito, and Uyeno Acta DV 71:248–250, 1991 Reticulate hyperpigmentation in zosteriform fashion BJD 117:503–510, 1987 Reticulate, patchy, and mottled pigmentation of the neck Dermatology 197:291–296, 1998 Reticulolinear aplasia cutis congenita of the face and neck – Xp deletion syndrome, MIDAS (microphthalmia, dermal aplasia, sclerocornea), MLS (microphthalmia and linear skin defects), and Gazali–Temple syndrome; lethal in males; residual facial scarring in females, short stature, organ malformations BJD 138:1046–1052, 1998 Rothmund–Thompson syndrome Speckled pigmentation, palmoplantar punctate keratoses, childhood blistering BJD 105:579–585, 1981 Terra firme Trisomy 14 mosaicism syndrome – patchy reticulated hyperpigmentation resembling that of incontinentia pigmenti Syndromes of the Head and Neck, p.89, 1990 Trisomy 18 – reticulate vascular nevus or port wine stain J Pediatr 72:862–863, 1968 Tumor necrosis factor (TNF) receptor 1-associated periodic fever syndromes (TRAPS) (same as familial Hibernian fever, autosomal dominant periodic fever with amyloidosis, and benign autosomal dominant familial periodic fever) – erythematous patches, tender red plaques, fever, annular, serpiginous, polycyclic, reticulated, and migratory patches and plaques (migrating from proximal to distal), urticaria-like lesions, lesions resolving with ecchymoses, conjunctivitis, periorbital edema, myalgia, arthralgia, abdominal pain, headache; Irish and Scottish predominance; mutation in TNFRSF1A – gene encoding 55 kDa TNF receptor AD 136:1487–1494, 2000 X-linked reticulate pigmentary disorder (formerly familial or X-linked cutaneous amyloidosis) Am J Med Genet 52:75–78, 1994; Am J Med Genet 10:67–75, 1981 Xp microdeletion syndrome – linear skin defects of head and neck (congenital smooth muscle hamartomas) (MIDAS syndrome – microphthalmia, dermal aplasia, sclerocornea) Ped Derm 14:26–30, 1997 Zosteriform reticulate hyperpigmentation BJD 121:280, 1989; in children BJD 117:503–17, 1987; AD 114:98–99, 1978 RETICULATED HYPERPIGMENTATION 595 RETICULATED HYPERPIGMENTATION Clin Exp Dermatol 9:439–450, 1984 Acquired dermal melanocytosis BJD 124:96, 1991 Amyloidosis, macular Arsenic intoxication Atopic ‘dirty neck’ Bolognia p.997, 2003 Bleomycin <strong>Dermatologic</strong>a 180:255–257, 1990 Calcinosis cutis – hyperpigmented reticulated plaques BJD 142:820–822, 2000 Cantu’s syndrome – reticulated hyperpigmentation of face, forearms, feet with palmoplantar keratoderma Bolognia p.997, 2003; Clin Genet 14:165, 1978 Confluent and reticulated papillomatosis of Gougerot and Carteaud Bolognia p.997, 2003 Cutaneous arteritis – round, linear, reticulated hyperpigmentation JAAD 49:519–522, 2003 Dermatitis Clin Exp Derm 15:380–381, 1990 Dermatopathia pigmentosa retularis – autosomal dominant, reticulate hyperpigmentation of trunk, onychodystrophy, alopecia, oral hyperpigmentation, punctate hyperkeratosis of palms and soles, hypohidrosis; atrophic macules over joints with hypertrophic scarring Semin Cut Med Surg 16:72–80, 1997; AD 126:935–939, 1990; Hautarzt 6:262, 1960 Dowling–Degos disease Semin Cut Med Surg 16:72–80, 1997; AD 114:1150, 1978 Dyschromatosis symmetrica hereditaria (reticulate acropigmentation of Dohi) (acropigmentation symmetrica of Dohi) BJD 153:342–345, 2005; BJD 150:633–639, 2004; BJD 144:162–168, 2001; JAAD 45:760–763, 2001; JAAD 43:113–117, 2000; sun-exposed areas only JAAD 10:1–16, 1984 Dyschromatosis universalis hereditaria Semin Cut Med Surg 16:72–80, 1997; Clin Exp Derm 2:45, 1977 Dyskeratosis congenita Semin Cut Med Surg 16:72–80, 1997 Ectodermal dysplasia JAAD 6:476–480, 1982 Epidermolysis bullosa herpetiformis Bolognia p.997, 2003 Epidermolysis bullosa with mottled pigmentation – wart-like hyperkeratotic papules of axillae, wrists, dorsae of hands, palms and soles; P25L mutation of keratin 5 JAAD 52:172–173, 2005 Erythema ab igne Rook p.1688, 1998, Sixth Edition Exudative retinopathy with bone marrow failure (Revesz syndrome) – intrauterine growth retardation, reticulate hyperpigmentation of trunk, palms, and soles; fine sparse hair, ataxia with cerebellar hypoplasia, hypertonia, progressive psychomotor retardation J Med Genet 29:673–675, 1992 Fanconi’s syndrome AD 103:581, 1971 Familial pigmentation with dystrophy of the nails AD 71:591–598, 1955 Familial progressive hyperpigmentation AD 103:581, 1971 Franceschetti–Jadassohn–Naegeli syndrome – autosomal dominant; brown–gray reticulated hyperpigmentation, hypohidrosis; palmoplantar hyperkeratosis Textbook of Neonatal Dermatology, p.379, 2001; JAAD 10:1–16, 1984; Dematologica 108:1–28, 1954; Schweiz Med Wschr 8:48, 1927 Galli–Galli disease – acantholytic variation of Dowling–Degos disease Bolognia p.997, 2003 Graft vs. host disease, chronic Rook p.2517, 1998, Sixth Edition Haber’s syndrome – autosomal dominant; photo-aggravated rosacea-like rash of face; papules, pustules, scarring and telangiectasia; reticulate keratotic plaques on trunk and extremities Australas J Dermatol 38:82–84, 1997; AD 117:321, 1981
596 A CLINICIAN’S GUIDE TO DERMATOLOGIC DIFFERENTIAL DIAGNOSIS, VOLUME 1 Hereditary focal transgressive palmoplantar keratoderma – autosomal recessive; hyperkeratotic lichenoid papules of elbows and knees, psoriasiform lesions of scalp and groin, spotty and reticulate hyperpigmentation of face, trunk, and extremities, alopecia of eyebrows and eyelashes BJD 146:490–494, 2002 Lymphoma – cutaneous T-cell lymphoma Int J Derm 30:658, 1991 Macular amyloidosis Melanosis universalis hereditaria AD 125:1442, 1989 Mendes da Costa syndrome (dystrophia bullosa, typus maculatus) – X-linked recessive; tense bullae, alopecia, coarse reticulated hyperpigmentation of face and extremities with atrophy, mental retardation Acta DV (Stockh) 18:265, 1937 Naegeli–Franceschetti–Jadassohn syndrome Bolognia p.997, 2003 Pigmentatio reticularis faciei et colli with multiple epithelial cysts AD 121:109, 1985 Poikiloderma of Civatte Ann Dermatol Syphilol 9:381–420, 1938 Post-inflammatory hyperpigmentation – secondary to allergic contact dermatitis to benzoyl peroxides Bolognia p.997, 2003 Prurigo pigmentosa AD 125:1551–1554, 1989 Reticulate acropigmentation of Kitamura – differs from acropigmentation symmetrica of Dohi by the absence of hypopigmented macules BJD 144:162–168, 2001; Semin Cut Med Surg 16:72–80, 1997; AD 115:760, 1979 Reticulate hyperpigmentation of Iijima, Naito, Vyeno Arch Derm Vener 71:248–250, 1991 Reticulate hyperpigmentation with alopecia, nail changes, and growth retardation with or without blisters Schweiz Med Wochenschr 100:228–233, 1970; Monatsschr Kinderheilkd 78:773–781, 1939 Reticulate non-melanocytic hyperpigmented anomaly Int J Derm 30:39–42, 1991 Revesz syndrome Bolognia p.997, 2003 Tar melanosis Contact Derm 3:249, 1977 Unilateral dermatomal pigmentary dermatosis Semin Cut Med Surg 16:72–80, 1997 X-linked reticulate pigmentary disorder (familial cutaneous amyloidosis) (Partington syndrome II) – X-linked; rare; Xp21–22; boys with generalized reticulated muddy brown pigmentation with hypopigmented corneal dystrophy, unruly hair, recurrent pneumonia; female carriers with macular nevoid Blascko-esque hyperpigmentation Semin Cut Med Surg 16:72–80, 1997; Am J Med Gen 10:65:1981 Zosteriform reticulate hyperpigmentation BJD 121:280, 1989; BJD 117:503–510, 1987 ROSETTE LESIONS Acute hemorrhagic edema of infancy Epidermolysis bullosa – Dowling–Meara type Fire ant stings Cutis 75:85–89, 2005 Henoch–Schönlein purpura – children or adults AD 125:53–56, 1989 Intraepidermal neutrophilic IgA dermatosis JAAD 22:917–919, 1990 Linear IgA disease Pemphigoid en cocarde JAAD 20:1125, 1989 Pemphigus vulgaris – anti-desmoglein 1 antibody dominant JAAD 52:839–845, 2005 Smallpox vaccination – inadvertent inoculation Clin Inf Dis 37:251–271, 2003 Staphylococcal sepsis with widespread pustular exanthema Verrucae vulgaris – rosettes after cryotherapy or cantharadin Tyring p.286, 2002 SCALP CYSTS AD 125:1253–1256, 1989 CONGENITAL ANOMALIES Aplasia cutis congenita Cephalocoele – includes meningocoele (rudimentary meningocoele), meningoencephalocele, meningomyelocele; blue nodule with overlying hypertrichosis JAAD 46:934–941, 2002; AD 137:45–50, 2001; sequestrated meningocoele Ped Derm 11:315–318, 1994 Congenital inclusion cysts of the subgaleal space Surg Neurol 21:61–66, 1984; J Neurosurg 56:540–544, 1982 Dermoid cyst and sinus JAAD 46:934–941, 2002; Curr Prob Dermatol 13:249–300, 2002; Neurosurg Clin N Am 6:359–366, 1995; Acta Neurochir (Wien) 128:115–121, 1994; AD 107:237–239, 1973 Encephalocele Heterotopic brain tissue (heterotopic meningeal nodules) – blue–red cystic mass with overlying alopecia JAAD 46:934–941, 2002; bald cyst of scalp with surrounding hypertrichosis AD 131:731, 1995; JAAD 28:1015, 1993; BJD 129:183–185, 1993; AD 125:1253–1256, 1989 INFECTIONS AND INFESTATIONS Molluscum contagiosum – occurring in an epidermoid cyst Cutis 26:180, 184, 1980 Myiasis – Dermatobia hominis – scalp cyst in a child Ped Derm 15:116–118, 1998 INFILTRATIVE DISEASES Eosinophilic granuloma, transcranial – subcutaneous scalp mass J Derm Surg Oncol 19:631–634, 1993 NEOPLASTIC DISEASES Cutaneous ciliated cyst of the scalp Am J Dermatopathol 16:76–79, 1994 Cutaneous ectopic meningioma (psammoma) Epidermoid cyst Hybrid cyst – combined epidermoid and pilar cyst JAAD 9:872–875, 1983 Lymphoma – cutaneous T-cell lymphoma with underlying epidermoid cysts AD 115:622, 1979 Malignant proliferating trichelemmal tumor Am J Clin Oncol 24:351–353, 2001; JAAD 32:870–873, 1995 Metaplastic synovial cyst Am J Dermatopathol 10:531–535, 1988 Metastasis – mimicking epidermoid cyst AD 104;301–303, 1971; salivary gland adenocarcinoma mimicking kerion Ghatan p.254, 2002, Second Edition Microcystic adnexal carcinoma J Derm Surg Oncol 15:768–771, 1989
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A Clinician’s Guide to Dermatolog
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A Clinician’s Guide to Dermatolog
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Contents Dedication ii Foreword vii
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Pore 524 Port wine stain 524 Preaur
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Introduction Dermatologic different
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ABSCESS AUTOIMMUNE DISEASES, AND DI
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Leishmaniasis (Leishmania major) -
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Kaposi’s sarcoma Lipoma - inflame
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philtrum, thin upper lip, broad mou
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Bacterial cellulitis Candida - Cand
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Comedo-like acantholytic dyskeratos
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Sepsis Streptococcus pneumoniae - w
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Subacute bacterial endocarditis Gha
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PRIMARY CUTANEOUS DISEASES Alopecia
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Necrolytic migratory erythema witho
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Self-healing juvenile cutaneous muc
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Perineurioma - soft tissue perineur
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Lipomatosis of the hands - Madelung
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Osteoarthritis Osteomalacia Polymyo
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DEGENERATIVE DISEASES Follicular de
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Multiple carboxylase deficiency - t
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Porokeratosis of Mibelli of the sca
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Dwarfism-alopecia-pseudoanodontia-c
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Multiple follicular hamartomas with
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XXYY syndrome - features of Klinefe
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Kabuki makeup syndrome - short stat
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ANGIOKERATOMA CORPORIS DIFFUSUM BJD
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Pinta Scabies Skin & Allergy News 2
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Terbinafine AD 131:960-961, 1995 Th
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somatostatin, sulfa, vigabatrin, pi
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Erythema gyratum perstans BJD 58:11
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Trisomy 13 (trisomy D (13-15) - mem
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Serum sickness NEJM 311:1407-1413,
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Rocky Mountain spotted fever Ghatan
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PRIMARY CUTANEOUS DISEASES Acne con
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Pachydermoperiostosis JAAD 38:359-3
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Familial dysautonomia (Riley-Day sy
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Onchocerciasis - atrophic changes e
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Immunocytoma, multiple cutaneous BJ
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type); hypertrophy of lower part of
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Follicular atrophoderma Bazex-Dupre
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Tricho-odonto-onycho-ectodermal dys
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Onychomycosis - black nail Ghatan p
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DRUG ERUPTIONS Linear fixed drug er
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linear and whorled macular pigmenta
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Carcinoid syndrome - flushing, patc
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PHOTODERMATOSES Lichen planus actin
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Pigmented purpuric eruption Purpura
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PRIMARY CUTANEOUS DISEASES Atopic d
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severe intrauterine growth retardat
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Cinnarizine - lichen planus pemphig
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Coxsackie A (5,9,10,16) - maculopap
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INFILTRATIVE DISEASES Amyloidosis,
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JEB cicatricial - autosomal recessi
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Superficial mucocoele - oral bulla
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INFLAMMATORY DISORDERS Erythema mul
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BULLAE IN NEWBORN Textbook of Neona
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with or without neuromuscular disea
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Orf AD 126:356-358, 1990 Papular ur
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INFECTIONS AND INFESTATIONS AIDS -
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CALM and pulmonary stenosis Ann DV
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Staphylococcus epidermidis AD 120:1
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CHALKY MATERIAL EXTRUDED FROM LESIO
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PHOTODERMATITIS Acute sunburn Rook
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INFILTRATIVE DISEASES Amyloidosis I
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Localized lichen myxedematosus (pap
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Cowden’s syndrome (multiple hamar
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CUTIS LAXA-LIKE APPEARANCE AUTOIMMU
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Kabuki makeup syndrome - short stat
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CTCL JAAD 29:331-334, 1993 Eruptive
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IPEX syndrome - X-linked; immune dy
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p.219, 2001; Rook p.636,1006 1998,
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Ichthyosis Interstitial granulomato
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Hypogammaglobulinemia Ghatan p.107,
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Leprosy Lyme disease - including de
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INFILTRATIVE DISEASES Langerhans ce
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Famotidine (Pepcid) JAAD 31:671-678
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and feet; atrophy with mottled hypo
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EAR, HARD (PETRIFIED AURICLES) Cond
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Protothecosis - verrucous plaque Sc
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Granuloma faciale, extrafacial BJD
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Greig cephalopolysyndactyly - malfo
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Hemangiomas J Pediatr Surg 35:420-4
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and face with perioral rugae; aged
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Pyomyositis - with purpura JAAD 10:
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Distichiasis-lymphedema syndrome -
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Itraconazole AD 130:260-261, 1994 V
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UNILATERAL FOOT EDEMA Freiberg’s
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of the buttocks and thighs with ele
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Lymphatic malformation Lymphedema -
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Melanocytic nevi - erosions overlyi
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Intravenous immunoglobulin (IVIG) B
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Keratosis-ichthyosis-deafness (KID)
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Psoriasis AD 136:875-880, 2000; Ped
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seborrheic dermatitis AD 138:117-12
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Psittacosis - morbilliform eruption
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urticarial, and rubella-like exanth
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CONGENITAL LESIONS Collodion baby R
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Dermatomyositis - eyelid edema JAAD
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METABOLIC DISEASES Acrodermatitis e
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vesiculopustules, red papules, crus
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dermatitis, cribriform scrotal atro
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urticaria, rhinoconjunctivitis Am J
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Parinaud’s oculoglandular fever -
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31:145-158, 1986; Am J Ophtalmol 88
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TOXINS Alkali burn Arsenic poisonin
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PSYCHOCUTANEOUS Anorexia nervosa -
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Ascher’s syndrome Carcinoid syndr
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Histoplasmosis in HIV disease Cutis
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Inverted follicular keratosis J Cli
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Cowden’s syndrome - trichilemmoma
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INFECTIONS AND INFESTATIONS Alterna
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Morphea, linear (en coup de sabre)
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PARANEOPLASTIC Bazex syndrome Necro
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Reactive perforating collagenosis U
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SELF-MUTILATION Hereditary sensory
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Calcium oxalate Am J Kid Dis 25:492
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Connective tissue disease - eosinop
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Herpes simplex infection, chronic i
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Thyroid releasing hormone Thyrotrop
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Diabetes mellitus Epidermolysis bul
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Dentist 24:65-69, 2004; Burkitt cel
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aldehyde Br Dent J 168:115-118, 199
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Job’s syndrome Kindler’s syndro
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Mukamel syndrome - autosomal recess
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Hypertension, post-traumatic Olfact
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Horner’s syndrome - medullary inf
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140:689-695, 1999; JID 103:277-281,
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Melanoma - verrucous and keratotic
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hyperkeratosis, sensorineural deafn
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Juvenile plantar dermatosis Acta DV
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PRIMARY CUTANEOUS DISEASE Acanthosi
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HYPERPIGMENTATION, DIFFUSE AUTOIMMU
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PHOTODERMATOSES Bronze baby syndrom
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Cyclophosphamide - black longitudin
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Liver disease, chronic - diffuse mu
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Pigmentary mosaicism - phylloid hyp
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Pigmented purpuric eruptions includ
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Kaposi’s sarcoma in AIDS JAAD 22:
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Penicillamine Rook p.3395, 1998, Si
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Schinzel-Giedion syndrome - autosom
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Hairy cutaneous malformation of the
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METABOLIC Acromegaly - hirsutism in
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Cornelia de Lange syndrome - specif
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plugged pit; may be verrucous; fili
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Corticosteroids - injected; topical
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Progressive macular hypomelanosis A
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Laser Traumatic scars Clin Inf Dis
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NEOPLASTIC Kaposi’s sarcoma JAAD
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mutation in gene encoding 3β-hydro
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Bruton’s hypogammaglobulinemia -
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Epidermolysis bullosa acquisita IgA
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Atopic dermatitis Confluent and ret
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Romberg’s syndrome - heterochromi
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PSYCHOCUTANEOUS DISEASES Bulimia ne
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spot lentigo (reticulated black sol
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BJD 144:594-596, 2001; JAAD 44:273-
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TRAUMA Minor trauma Dermatol Clin 6
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Trichothiodystrophy syndromes - BID
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Leeches Leishmaniasis - post-kala-a
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AD 109:526-528, 1974; unilateral pu
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SYNDROMES Aarskog syndrome - single
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TOXINS Arsenical keratoses Eosinoph
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Ehlers-Danlos syndrome, type IV - p
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METABOLIC DISEASES Milia-like calci
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Pemphigus vulgaris Scleroderma Sjö
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Down’s syndrome Familial cold urt
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enal failure; associated with hepat
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2003; JAAD 31:561-566, 1994; Ann Rh
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Lipomas BJD 146:125-128, 2002; J Fo
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Familial mitral valve prolapse synd
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Ganglioneuroma of cervical sympathe
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Nailbed or nailplate hemorrhage Rup
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METABOLIC DISEASES Homocystinuria -
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Epstein’s pearls (milia) in oral
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Reticular erythematous mucinosis Se
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Darier’s disease Granuloma facial
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PSYCHOCUTANEOUS DISEASES Factitial
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Phaeoacremonium inflatipes - fungem
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Lichen spinulosus JAAD 22:261-264,
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facial asymmetry, macrostomia, epib
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Juvenile hyaline fibromatosis (syst
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INFECTIONS AND INFESTATIONS Acantha
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Phaeohyphomycosis, subcutaneous Ped
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PHOTODERMATITIS Hydroa vacciniforme
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Congestive heart failure Overwhelmi
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CONGENITAL AND/OR ACQUIRED NEVI Bar
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lipoatrophic streaks extend down le
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Congenital self-healing Langerhans
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Epidermoid cysts, plantar - HPV-60-
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INFLAMMATORY DISEASES Bunion Extrav
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IgM storage papule - pink or skin-c
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Nevus lipomatosis superficialis - m
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1990; Nephron 53:73-75, 1989; dialy
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JAAD 47:251-257, 2002; JAAD 45:596-
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Syphilis Sex Transm Dis 14:52-53, 1
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Vascular calcification - cutaneous
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Arteriovenous fistulae - congenital
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papules JAAD 44:324-329, 2001; prim
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Squamous cell carcinoma Sweat gland
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Leprosy - lepromatous leprosy Rook
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Desmoid tumor - subcutaneous mass i
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PRIMARY CUTANEOUS DISEASES Axillary
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Hemangiopericytoma JAAD 37:887-920,
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Langerhans cell histiocytosis - ulc
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Noonan’s syndrome - keloids Regre
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Malignant fibrous histiocytoma Mela
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JAAD 12:207-212, 1985 Phialophora r
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Merkel cell tumor AD 140:609-614, 2
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esponse element binding protein Ped
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Basan’s syndrome Dermatopathia pi
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PRIMARY CUTANEOUS DISEASES Alopecia
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INFECTIONS Abscess of buccal mucosa
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PRIMARY CUTANEOUS DISEASES Acanthos
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Calcium channel blockers J Am Dent
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Desquamative gingivitis Eosinophili
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Muckle-Wells syndrome Am J Med Gene
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Plaquenil Quinacrine Quinidine - bl
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Malignant schwannoma (neurofibrosar
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METABOLIC DISEASES Acrodermatitis e
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heel Ped Derm 21:655-656, 2004; Med
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AD 124:1678-1682, 1988; JAAD 13:908
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Porokeratosis of Mantoux - craterif
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Epidermolytic hyperkeratosis (bullo
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Sclerodactyly, non-epidermolytic pa
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Incontinentia pigmenti - plantar hy
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Type IX - PPK with sclerodactyly, H
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Eccrine nevus - brown papule JAAD 5
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J Trop Med Hyg 89:43-45, 1986; Bol
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Relapsing linear acantholytic derma
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Keratoacanthoma - digital papule AD
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PHOTODERMATOSES Disseminated superf
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Mixed tumor of the face J Dermatol
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Fibroepithelioma of Pinkus - flat-t
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Bacterial folliculitis, usually sta
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Atrophoderma vermiculatum Ped Derm
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widespread dermatitis, palmoplantar
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Juvenile xanthogranuloma Dis Chest
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SYNDROMES Alagille syndrome (arteri
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Papular urticaria Roseola infantum
Page 482 and 483:
Irritant contact dermatitis Sea urc
Page 484 and 485:
Tanapox - pruritic papule, initiall
Page 486 and 487:
Neurofibroma Neuroma, including sol
Page 488 and 489:
Angiomas, eruptive - treatment with
Page 490 and 491:
Poroma - papilloma, especially of s
Page 492 and 493:
Toxoplasmosis - pityriasis lichenoi
Page 494 and 495:
Keratoacanthoma visceral carcinoma
Page 496 and 497:
Bowen’s disease AD 130:204-209, 1
Page 498 and 499:
Primary lymphoma Leuk Lymphoma 26:4
Page 500 and 501:
Granular cell tumor (granular cell
Page 502 and 503:
paraffinoma resulting in penile enl
Page 504 and 505:
Basal cell carcinoma Genital Skin D
Page 506 and 507:
myopathy JAAD 53:639-643, 2005; AD
Page 508 and 509:
Amebiasis - Entameba histolytica De
Page 510 and 511:
Candidiasis Int J Derm 38:618-622,
Page 512 and 513:
PERIANAL ULCERS, SINGLE OR MULTIPLE
Page 514 and 515:
testis, nasopharyngeal carcinoma; l
Page 516 and 517:
Syphilis - primary (chancre), secon
Page 518 and 519:
Psoriasis Seborrheic dermatitis Vit
Page 520 and 521:
Alprazolam (Xanax) - phototoxic JAA
Page 522 and 523:
Oxyphenbutazone - UVA Paraquat - du
Page 524 and 525:
Occlusive dressings - photosensitiv
Page 526 and 527:
Variegate porphyria - weatherbeaten
Page 528 and 529:
Pityriasis rubra pilaris - seborrhe
Page 530 and 531:
Salvarson Thiazides Tripelennamine
Page 532 and 533:
Juvenile plantar dermatosis Lamella
Page 534 and 535:
Poikiloderma vasculare atrophicans
Page 536 and 537:
Parkes-Weber syndrome - port wine s
Page 538 and 539:
contractures; taut shiny skin; feta
Page 540 and 541:
Red sea coral contact dermatitis In
Page 542 and 543:
BJD 152:1085-1086, 2005; BJD 152:3-
Page 544 and 545:
PSYCHOCUTANEOUS DISEASES Anorexia n
Page 546 and 547:
Terbinifine JAAD 36:858-862, 1997 T
Page 548 and 549:
SYNDROMES Arthropathy, rash, chroni
Page 550 and 551:
Lipoid proteinosis BJD 151:413-423,
Page 552 and 553:
Myotonic dystrophy Syndromes of the
Page 554 and 555:
Mutation in 3β-hydroxysteroid dehy
Page 556 and 557: virus (Southeast Brazil), Whitewate
Page 558 and 559: Leptospirosis Meningococcemia Pneum
Page 560 and 561: Calciphylaxis Chronic renal failure
Page 562 and 563: Dermatosparaxis - easy bruisability
Page 564 and 565: Acroangiodermatitis (gravitational
Page 566 and 567: DRUG-INDUCED Dilantin hypersensitiv
Page 568 and 569: Streptococcus viridans Strongyloide
Page 570 and 571: Fogo selvagem JAAD 20:657, 1989 Her
Page 572 and 573: Coccidioidomycosis - papulopustules
Page 574 and 575: Tularemia - Franciscella tularensis
Page 576 and 577: SYNDROMES Behçet’s disease - pap
Page 578 and 579: Corticosteroid (topical) atrophy; s
Page 580 and 581: Robert’s syndrome (hypomelia-hypo
Page 582 and 583: hyperkeratoses extending over Achil
Page 584 and 585: PRIMARY CUTANEOUS DISEASES Acne vul
Page 586 and 587: Helicobacter cinaedi - cellulitis A
Page 588 and 589: Squamous cell carcinoma - intraoral
Page 590 and 591: Radiation mucositis - intraoral red
Page 592 and 593: Post-vaccination Semin Pediatr Infe
Page 594 and 595: Parvovirus B19 infection - red/viol
Page 596 and 597: Eccrine angiomatous hamartoma Eccri
Page 598 and 599: Muckle-Wells syndrome Multicentric
Page 600 and 601: PARANEOPLASTIC DISEASES Cutis verti
Page 602 and 603: INFECTIONS Coxsackie B4 hemorrhagic
Page 604 and 605: Hunter’s syndrome - decreased sul
Page 608 and 609: Pilar cyst (trichilemmal cyst) JAAD
Page 610 and 611: Ectodermal dysplasias with clefting
Page 612 and 613: Melanocytic nevus Rook p.1722-1723,
Page 614 and 615: Microcystic adnexal carcinoma - ski
Page 616 and 617: Burns Carcinoma Dental sinus Eczema
Page 618 and 619: INFECTIONS OR INFESTATIONS Brucello
Page 620 and 621: GEMSS syndrome - autosomal dominant
Page 622 and 623: Verruciform xanthoma BJD 150:161-16
Page 624 and 625: EXOGENOUS AGENTS Mustard gas exposu
Page 626 and 627: INFLAMMATORY DISORDERS Erythema mul
Page 628 and 629: Abruzzo-Erickson syndrome (cleft pa
Page 630 and 631: Kenny syndrome (tubular stenosis) C
Page 632 and 633: Tay syndrome - autosomal recessive,
Page 634 and 635: Russell-Silver syndrome - large hea
Page 636 and 637: Dissecting cellulitis of the scalp
Page 638 and 639: Squamous cell carcinoma Staphylococ
Page 640 and 641: Nasal alar colobomas, mirror hands
Page 642 and 643: Mycobacterium avium-intracellulare
Page 644 and 645: TATTOO, PALPABLE: LESIONS IN A TATT
Page 646 and 647: hypodontia, short upper lip bound d
Page 648 and 649: Coats’ disease - cutaneous telang
Page 650 and 651: NEOPLASTIC DISEASES Actinic keratos
Page 652 and 653: Neurofibromatosis - usually unilate
Page 654 and 655: Candidiasis Ghatan p.93, 2002, Seco
Page 656 and 657:
Plummer-Vinson syndrome AD 105:720,
Page 658 and 659:
INFLAMMATORY DISORDERS Crohn’s di
Page 660 and 661:
exanthem with islands of sparing (
Page 662 and 663:
74:278-281, 2000; Br J Plast Surg 5
Page 664 and 665:
central scaling, scarring, atrophy,
Page 666 and 667:
Cryptococcosis - punched out ulcers
Page 668 and 669:
Ulcers with regional adenopathy - a
Page 670 and 671:
Type 9 - ACC as feature of malforma
Page 672 and 673:
Sclerosing lymphangitis of the peni
Page 674 and 675:
Rat bite fever Rhizopus azygosporus
Page 676 and 677:
Felty’s syndrome - arthritis, leu
Page 678 and 679:
Sixth Edition; Int J Dermatol 27:49
Page 680 and 681:
Omphalitis - periumbilical erythema
Page 682 and 683:
DeBarsey syndrome - umbilical herni
Page 684 and 685:
Pyoderma gangrenosum-like lesions,
Page 686 and 687:
DRUG-INDUCED ACE inhibitors - lisin
Page 688 and 689:
Eosinophilic pustular folliculitis
Page 690 and 691:
cold-induced cholinergic urticaria
Page 692 and 693:
Phenylbutazone Phenytoin Piperazine
Page 694 and 695:
LYMPHOCYTIC Peripheral vascular dis
Page 696 and 697:
Cryptococcosis Leishmaniasis - leis
Page 698 and 699:
Leishmaniasis - verrucous form of l
Page 700 and 701:
Pagetoid reticulosis AD 125:402-406
Page 702 and 703:
VASCULAR Angiokeratomas Angiokerato
Page 704 and 705:
Thermal burn - child abuse; vulvar
Page 706 and 707:
DRUGS Corticosteroid-induced fat ne
Page 708 and 709:
PSYCHOCUTANEOUS DISEASES Factitial
Page 710 and 711:
Kaposi’s sarcoma Tyring p.224, 20
Page 712 and 713:
Phenylthiourea - hypopigmentation o
Page 714 and 715:
Griscelli’s syndrome Hallerman-St
Page 716 and 717:
Vogt-Koyanagi-Harada syndrome - occ
Page 718 and 719:
Connective tissue nevus Ped Derm 22
Page 720 and 721:
Retinoid dermatitis - isotretinoin,
Page 722 and 723:
YELLOW NAIL SYNDROME JAAD 28:792-79
Page 724 and 725:
lesions BJ Clin Pract 27:271-273, 1
Page 726 and 727:
PRIMARY CUTANEOUS DISEASE Atopic de
Page 728 and 729:
Plane xanthomas - normolipemic plan
Page 730 and 731:
Dermatomyositis - centripetal flage
Page 732 and 733:
ZOSTERIFORM LESIONS/SEGMENTAL DISOR
Page 734 and 735:
PHOTODERMATOSES Favre-Racouchot syn
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