Hugh Morris Gloster, Jr.,
Lauren E. Gebauer,
Rachel L. Mistur
Springer International Publishing
2015e druk, 2015
9783319032177
Absolute Dermatology Review
Mastering Clinical Conditions on the Dermatology Recertification Exam
Specificaties
Paperback, 967 blz.
|
Engels
Springer International Publishing |
2015e druk, 2015
ISBN13: 9783319032177
Rubricering
Levertijd ongeveer 8 werkdagen
Samenvatting
Each dermatologist that was board certified after 1992 is required by the American Board of Dermatology to take a recertification exam every ten years. One of the major components of the exam is to be able to identify clinical photographs of approximately 200 skin diseases, and while there are other components to the test, they vary according to subspecialty. However, everyone is required to identify the images, so several months before the exam, the American Board of Dermatology releases a list of the skin diseases that will be tested, but does not provide the images or reveal which ones will appear.
Review of Clinical Conditions for the Dermatology Recertification Examination provides a thorough, concise review of clinical images of the specific conditions that the reader will be required to recognize during the American Board of Dermatology recertification test. In addition, concise key clinical features for each image will be provided that will assist the reader in recognizing the clinical images on the examination, enabling them a more efficient way to study for the test without having to look up images online or in a large text book. Written by a board certified dermatologic surgeon who recently took the recertification exam, this book proves indispensable to dermatologists taking the exam or residents who want a quick reference of the clinical appearances of the main conditions generally encountered by a dermatologist.
Specificaties
ISBN13:9783319032177
Taal:Engels
Bindwijze:paperback
Aantal pagina's:967
Uitgever:Springer International Publishing
Druk:2015
Inhoudsopgave
<p>Table of Contents</p><p> </p><p> </p><p>Absolute Dermatology Review</p><p>Mastering Clinical Conditions on the Dermatology Recertification Exam</p><p> </p><p>Author: Hugh Gloster, Jr., MD</p><p> </p><p>Section One: Papulosquamous and Eczematous Dermatoses</p><p>1. Psoriasis</p><p>a. Chronic plaque</p><p>b. Erythrodermic </p><p>c. Pustular</p><p>d. Palmoplantar</p><p>e. Guttate</p>f. Nail disease</p><p>2. Lichen planus</p><p>a. Hypertrophic</p><p>b. Oral</p><p>c. Nails</p><p>d. Vulvovaginal</p><p>e. Annular</p><p>f. Drug induced</p><p>3. Dermatitis</p><p>a. Contact</p><p>b. Seborrheic</p><p>c. Atopic</p><p>d. Perioral</p><p>e. Stasis</p><p>f. Asteatotic</p><p>g. Dishydrotic</p><p>4. Keratosis pilaris</p><p>5. Lichen simplex chronicus</p><p>6. Lichen striatus</p><p>7. Pityriasis lichenoides</p><p>a. Pityriasis lichenoides et varioliformis acuta</p><p>b. Pityriasis lichenoides chronica</p><p>8. Pityriasis rosea</p><p>9. Pityriasis alba</p><p>10. Pityriasis rubra pilaris</p><p>11. Axillary granular parakeratosis</p><p>Section Two: Cutaneous vasculitis, vasculopathy, and microvascular occlusion syndromes</p><p>12. Small vessel (leukocytoclastic) vasculitis</p><p>a. Henoch-Schonlein purpura</p><p>b. Acute hemorrhagic edema of infancy</p><p>c. Urticarial vasculitis</p><p>d. Erythema elevatum diutinum</p><p>13. Mixed small and medium vessel vasculitis</p><p>a. Cryoglobulnemic vasculitis</p><p>b. ANCA- associated vasculitis</p><p> i. Microscopic polyangitis</p><p> ii. Wegener’s granulomatosis</p><p> iii. Churg-Strauss syndrome</p><p>14. Medium size vasculitis</p><p>a. Polyarteritis nodosa</p><p>15. Livedo vasculopathy and livedo reticularis</p><p>16. Coumadin necrosis</p><p>Section Three: Vesiculobullous diseases</p><p>17. Bullous pemphigoid</p><p>18. Cicatricial pemphigoid</p><p>19. Pemphigoid gestationis</p><p>20. Pemphigus vulgaris</p><p>21. Pemphigus foliaceous</p><p>22. Pemphigus vegetans</p><p>23. Benign familial pemphigus (Hailey-Hailey disease)</p><p>24. Dermatitis herpetiformis</p><p>25. Linear IgA bullous dermatosis</p><p>26. Epidermolysis bullosa</p><p>a. Simplex</p><p>b. Dystrophic</p><p>c. Acquired</p><p>d. Junctional</p><p>27. Newborn</p><p>a. Erythema toxicum neonatorum</p><p>28. Paraneoplastic pemphigus</p><p>Section Four: Adnexal diseases</p><p>29. Acne vulgaris</p><p>30. Rosacea</p><p>31. Fox Fordyce disease</p><p>32. Hidradenitis suppurativa</p><p>Section Five: Autoimmune disorders</p><p>33. Lupus erythematous</p><p>a. Discoid</p><p>b. Subacute cutaneous</p><p>c. Neonatal</p><p>d. Systemic</p><p>e. Acute cutaneous</p><p>f. Tumid</p><p>g. Panniculitis</p><p>h. Pernio</p>i. Bullous</p><p>34. Dermatomyositis</p><p>35. Scleroderma and sclerodermoid skin conditions</p><p>a. Systemic sclerosis</p><p>b. Morphea</p><p> i. Plaque</p><p> ii. Linear</p><p> iii. Generalized</p><p>c. Eosinophilic fasciitits</p><p>d. Lichen sclerosus</p><p>e. Nephrogenic systemic fibrosis</p><p>f. Lipodermatosclerosis</p><p>36. Graft versus host disease</p><p>Section Six: Metabolic and deposition diseases</p><p>37. Mucinoses</p><p>a. Scleromyedema</p><p>b. Scleredema</p><p>c. Pretibial myxedema</p><p>d. Follicular mucinosis</p><p>38. Amyloidosis</p><p>39. Porphyria cutanea tarda and pseudoporphyrias</p><p>40. Calcifying disorders</p><p>a. Calcinosis cutis</p><p>b. Calciphylaxis</p><p>41. Nutritional diseases</p><p>a. Scurvy</p><p>b. Pellagra</p><p>c. Zinc deficiency (acrodermatitis enteropathica)</p><p>42. Ochronosis</p><p>Section Seven: Cutaneous manifestations of systemic diseases</p><p>43. Rheumatoid arthritis</p><p>44. Diabetes</p><p>a. Necrobiosis lipoidica</p><p>b. Acanthosis nigricans</p><p>c. Bullous diabeticorum</p><p>d. Diabetic dermopathy</p><p>e. Neuropathic ulcers</p><p>f. Scleredema diabeticorum</p><p>g. Eruptive xanthomas</p><p>45. Thyroid disease</p><p>a. Pretibial myxedema</p><p>b. Generalized myxedema</p><p>c. Acquired ichthyosis</p><p>d. Alopecia</p><p>46. Cushing’s syndrome</p><p>47. Addison’s disease</p><p>48. Gastrointestinal</p><p>a. Ulcerative colitis and Crohn’s</p><p> i. Erythema nodosum</p><p> ii. Leukocytoclastic vasculitis</p> iii. Sweet’s syndrome</p><p> iv. Pyoderma gangrenosum</p><p> v. Acrodermatitis enteropathica</p><p>b. Gastrointestinal bleeding</p><p> i. Hereditary hemorrhagic telangiectasia</p><p> ii. Blue rubber bleb nevus syndrome</p> iii. Pseudoxanthoma elasticum</p><p> iv. Peutz-Jeuger</p><p> v. Muir-Torre</p><p>c. Liver disease</p><p> i. Telangiectasias</p><p> ii. Spider angiomas</p> iii. Palmar erythema</p><p> iv. Terry’s nails</p><p> v. Primary biliary cirrhosis</p><p>1. Tuberous xanthomas</p><p> vi. Hemochromatosis</p><p> vii. Wilson’s disease</p><p>49. Renal disease</p><p>a. Nephrogenic systemic sclerosis</p><p>50. Internal malignancy</p><p>a. Acanthosis nigricans</p><p>b. Acrokeratosis neoplastica (Bazek’s syndrome)</p><p>c. Erythema gyratum repens </p><p>d. Necrolytic migratory erythema </p><p>e. Acquired hypertrichosis lagunosa</p><p>f. Cutaneous metastases</p><p>g. Paraneoplastic pemphigus</p><p>Section Eight: Genodermatoses and developmental anomalies</p><p>51. Genodermatoses</p><p>a. Darier’s disease</p><p>b. Ichthyoses</p><p> i. vulgaris</p><p> ii. lamellar</p><p> iii. x-linked</p><p> iv. bullous congenital ichthyosiform erythroderma</p><p> v. Netherton’s syndrome</p><p>c. neurofibromatosis</p><p>d. tuberous sclerosus</p><p>e. Incontinentia pigmenti</p><p>f. Cowden’s syndrome</p><p>g. Cutis laxa</p><p>h. Ehlers-Danlos syndrome</p><p>i. Pachonychia congenita</p><p>j. Pseudo xanthoma elasticum</p><p>52. Developmental anomalies</p><p>a. Aplasia cutis congenita</p><p>b. Hair collar sign</p><p>Section Nine: Infections</p><p>53. Viral</p><p>a. Condyloma acuminata</p><p>b. Fifth disease</p><p>c. Hand-foot-mouth</p><p>d. Herpes simplex</p><p> i. Eczema herpeticum</p><p> ii. Herpetic Whitlow</p><p> iii. Neonatal</p><p>e. Herpes zoster</p><p>f. Varicella</p><p>g. Molluscum contagiosum</p><p>h. Verruca</p><p>54. Fungal</p><p>a. Deep fungal infections</p><p> i. Blastomycosis</p><p> ii. Sporotrichosis</p><p> iii. Coccidiodomycosis</p><p> iv. Cryptococcosis</p><p>b. Folliculitis</p><p> i. Dermatophyte</p><p>1. Tinea barbae</p><p>2. Majocchi’s</p><p> ii. Pityrosporum</p><p>c. Onychomycosis</p><p>d. Tinea</p> i. Pedis and manuum</p><p> ii. Corporis</p><p> iii. Faceii</p><p>1. Tinea incognito</p><p>2. Tinea barbae</p><p> iv. Versicolor</p><p> v. Capitis</p> vi. Cruris</p><p>55. Bacterial</p><p>a. Cellulitis</p><p> i. Perianal streptococcal cellulitis</p><p>b. Erythrasma</p><p>c. Folliculitis</p><p>d. Gonococcemia</p><p>e. meningococcemia</p><p>f. Impetigo</p> i. Non bullous</p><p> ii. Bullous</p><p>g. Leishmaniasis</p><p>h. Leprosy</p><p>i. Mycobacterial infections</p><p> i. Tuberculosis</p><p> ii. Non tuberculous</p><p>j. Pitted keratolysis</p><p>k. Rocky mountain spotted fever</p><p>l. Syphilis</p><p>Section Ten: Infestations and bites</p><p>56. Cutaneous larva migrans</p><p>57. Bed bugs</p><p>58. Spider bites</p><p>59. Scabies</p><p>60. Fleas</p><p>61. Pediculosis (lice)</p><p>62. Tungiasis</p><p>Section Eleven: Hair, nails, and mucous membranes</p><p>63. Alopecias</p><p>a. Alopecia areata</p><p>b. Telogen effluvium</p><p>c. Anagen effluvium</p><p>d. Androgenetic alopecia</p><p>e. Trichotillomania</p><p>f. Scarring alopecias</p><p> i. Central centrifugal cicatricial alopecia</p><p> ii. Lichen planopilaris</p> iii. Discoid lupus</p><p> iv. Dissecting cellulitis</p><p> v. Folliculitis decalvans</p><p> vi. Acne keloidalis nuchae</p><p> vii. Frontal fibrosing alopecia</p><p> viii. Traction alopecia</p>64. Nail disease</p><p>a. Trachonychia</p><p>b. Beau’s lines</p><p>c. Mee’s lines</p><p>d. Half and half nails</p><p>e. Yellow nail syndrome</p><p>f. Onychorrhexis</p><p>g. Punctate leukonychia</p><p>h. Striate leukonychia</p><p>i. Onychomadesis</p><p>j. Koilonychia</p>k. Terry’s nails</p><p>l. Clubbing</p><p>65. Mucous membrane disease</p><p>a. Geographic tongue</p><p>b. Oral hairy leukoplakia</p><p>c. Aphthous stomatitis</p><p>Section Twelve: Benign neoplasms</p><p>66. Accessory tragus</p><p>67. Accessory digit</p><p>68. Acquired digital fibrokeratoma</p><p>69. Adnexal tumors</p><p>a. Trichoepithelioma</p><p>b. Cylindroma</p><p>c. Syringoma</p><p>d. Nevus sebaceous</p><p>e. Trichofolliculoma</p><p>f. Poroma</p><p>70. Becker’s nevus</p><p>71. Cysts</p><p>a. Epidermal</p><p>b. Steatocystoma multiplex</p><p>c. Eruptive vellus hair cyst</p><p>72. Dermatofibroma</p><p>73. Melanocytic</p><p>a. Halo nevi</p><p>b. Congenital nevi</p><p>c. Junctional nevi</p><p>d. Compound nevi</p><p>e. Intradermal nevi</p><p>f. Nevus spilus</p><p>g. Spitz nevi</p><p>h. Blue nevi</p><p>i. Nevus of Ito</p><p>j. Nevus of Ota</p><p>k. Nevus comedonicus</p><p>74. Mucocele</p><p>75. Pyogenic granuloma</p><p>76. Seborrheic keratosis</p><p>77. Skin tags</p><p>78. Supernumerary nipples</p><p>79. Confluent and reticulated papillomatosis</p><p>80. Linear epidermal nevus</p><p>Section Thirteen: Malignant and premalignant neoplasms</p><p>81. Actinic keratosis</p><p>82. Actinic cheilitis</p><p>83. Angiosarcoma</p><p>84. Cutaneous metastases</p><p>85. Dermatofibrosarcoma protuberans</p><p>86. Kaposi’s sarcoma</p><p>87. Keratoacanthoma</p><p>88. Melanoma </p><p>89. Basal cell carcinoma</p><p>90. Squamous cell carcinoma</p><p>a. Erythroplasia of Querat</p><p>b. Verrucous carcinoma</p>c. Bowen’s disease</p><p>d. Invasive SCC</p><p>91. Paget’s disease</p><p>92. Extramammary Paget’s disease</p><p>93. Cutaneous lymphomas</p><p>a. T-cell</p><p> i. Mycosis fungoides</p><p> ii. Folliculotrophic mycosis fungoides</p><p> iii. Pagetoid reticulosis</p><p> iv. Granulomatous slack skin</p><p> v. Sezary syndrome</p><p> vi. Primary cutaneous CD 30+ anaplastic large cell lymphoma</p><p> vii. Lymphomatoid papulosis</p><p> viii. Subacute panniculitis like T-cell lymphoma</p><p>b. B-cell</p><p> i. Follicular center lymphoma</p><p> ii. Marginal zone B-cell lymphoma</p><p>Section Fourteen: Disorders due to physical agents</p><p>94. Chondrodermatitis nodularis helicis</p><p>95. Factitial disease</p><p>96. Prurigo nodularis</p><p>97. Trauma induced skin disease</p><p>a. Talon noir</p><p>b. Erythema ab igne</p>c. Corns and calluses</p><p>d. Subungual hematoma</p><p>e. Surgical ecchymoses</p><p>f. Piezogenic papules</p><p>g. Traumatic tattoo</p><p>98. Photodermatoses</p><p>a. Phototoxicity </p><p>b. Photoallergy</p><p>c. Actinic damage</p><p> i. Actinic purpura</p> ii. Poikiloderma of Civatte</p><p>d. Polymorphous light eruption</p><p>e. Chronic actinic dermatitis</p><p>99. Foreign body granulomas</p><p>100. Radiation dermatitis</p><p>Section Fifteen: Drug reactions, erythemas, and urticarias</p><p>101. Drug reactions</p><p>a. Acute generalized exanthematous pustulosis (AGEP)</p><p>b. Drug induced hyperpigmentation</p><p>c. Drug reaction with eosinophilia and systemic symptoms (DRESS)</p>d. Fixed drug eruptions</p><p>e. Stevens Johnson Syndrome and Toxic epidermal necrolysis (TEN)</p><p>f. Steroid induced atrophy</p><p>g. Morbilliform</p><p>102. Erythemas</p><p>a. Erythema multiforme</p><p>b. Figurate erythemas</p><p> i. Erythema annulare centrifugum</p><p> ii. Erythema gyratum repens</p> iii. Erythema chronicum migrans</p><p>c. Necrolyitic acral erythema</p><p>d. Necrolyitic migratory erythema</p><p>103. Urticarias</p><p>a. Urticaria</p><p>b. Angioedema</p><p>104. Polymorphic eruption of pregnancy (PUPPP)</p><p>Section Sixteen: Vascular and lymphatic disorders</p><p>105. Telangiectasia</p><p>106. Hemangioma</p><p>107. Vascular malformations</p><p>108. lymphangiomas</p><p>Section Seventeen: Pigmentary disorders</p><p>109. Vitiligo</p><p>110. Postinflammatory pigment alteration</p><p>Section Eighteen: Neutrophilic dermatoses</p><p>111. Pyoderma gangrenosum</p><p>112. Sweet’s syndrome</p><p>113. Erosive pustular dermatosis of the scalp</p><p>Section Nineteen: Disorders of Langerhans cells, macrophages, and mast cells</p><p>114. Langerhans cell histiocytosis</p><p>a. Letterer-Siwe</p><p>b. Multicentric reticulohistiocytosis</p><p>115. Xanthogranuloma</p><p>a. Juvenile xanthogranuloma</p><p>b. Necrobiotic xanthogranuloma</p><p>116. Xanthomas</p><p>a. Plane</p><p>b. Eruptive</p><p>c. tuberous</p><p>117. Sarcoidosis</p><p>118. Granuloma annulare</p><p>a. Localized</p><p>b. Disseminated</p>119. Necrobiosis lipoidica </p><p>120. Foreign body reactions </p><p>121. Mastocytosis</p><p>a. Urticaria pigmentosa</p><p>b. Solitary mastocytoma</p><p>Section Twenty: Dermal connective tissue disorders</p><p>122. Keloids</p><p>123. Hypertrophic scars</p><p>124. Perforating diseases</p><p>a. Kyrle’s disease</p><p>b. Elastosis perforans serpiginosa </p><p>c. Reactive perforating collagenosis</p><p>Section Twenty One: Panniculitis</p><p>125. Erythema nodosum</p><p>126. Lipodermatosclerosis (sclerosing panniculitis)</p><p> </p><p>