Absolute Dermatology Review (eBook)
XVII, 534 Seiten
Springer International Publishing (Verlag)
978-3-319-03218-4 (ISBN)
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.
Dr. Hugh Gloster is Professor of Dermatology and Director of Mohs Micrographic Surgery & Cutaneous Oncology at the University of Cincinnati Department of Dermatology.
Dr. Hugh Gloster is Professor of Dermatology and Director of Mohs Micrographic Surgery & Cutaneous Oncology at the University of Cincinnati Department of Dermatology.
Table of Contents Absolute Dermatology ReviewMastering Clinical Conditions on the Dermatology Recertification Exam Author: Hugh Gloster, Jr., MD Section One: Papulosquamous and Eczematous Dermatoses1. Psoriasisa. Chronic plaqueb. Erythrodermic c. Pustulard. Palmoplantare. Guttatef. Nail disease2. Lichen planusa. Hypertrophicb. Oralc. Nailsd. Vulvovaginale. Annularf. Drug induced3. Dermatitisa. Contactb. Seborrheicc. Atopicd. Periorale. Stasisf. Asteatoticg. Dishydrotic4. Keratosis pilaris5. Lichen simplex chronicus6. Lichen striatus7. Pityriasis lichenoidesa. Pityriasis lichenoides et varioliformis acutab. Pityriasis lichenoides chronica8. Pityriasis rosea9. Pityriasis alba10. Pityriasis rubra pilaris11. Axillary granular parakeratosisSection Two: Cutaneous vasculitis, vasculopathy, and microvascular occlusion syndromes12. Small vessel (leukocytoclastic) vasculitisa. Henoch-Schonlein purpurab. Acute hemorrhagic edema of infancyc. Urticarial vasculitisd. Erythema elevatum diutinum13. Mixed small and medium vessel vasculitisa. Cryoglobulnemic vasculitisb. ANCA- associated vasculitis i. Microscopic polyangitis ii. Wegener’s granulomatosis iii. Churg-Strauss syndrome14. Medium size vasculitisa. Polyarteritis nodosa15. Livedo vasculopathy and livedo reticularis16. Coumadin necrosisSection Three: Vesiculobullous diseases17. Bullous pemphigoid18. Cicatricial pemphigoid19. Pemphigoid gestationis20. Pemphigus vulgaris21. Pemphigus foliaceous22. Pemphigus vegetans23. Benign familial pemphigus (Hailey-Hailey disease)24. Dermatitis herpetiformis25. Linear IgA bullous dermatosis26. Epidermolysis bullosaa. Simplexb. Dystrophicc. Acquiredd. Junctional27. Newborna. Erythema toxicum neonatorum28. Paraneoplastic pemphigusSection Four: Adnexal diseases29. Acne vulgaris30. Rosacea31. Fox Fordyce disease32. Hidradenitis suppurativaSection Five: Autoimmune disorders33. Lupus erythematousa. Discoidb. Subacute cutaneousc. Neonatald. Systemice. Acute cutaneousf. Tumidg. Panniculitish. Pernioi. Bullous34. Dermatomyositis35. Scleroderma and sclerodermoid skin conditionsa. Systemic sclerosisb. Morphea i. Plaque ii. Linear iii. Generalizedc. Eosinophilic fasciititsd. Lichen sclerosuse. Nephrogenic systemic fibrosisf. Lipodermatosclerosis36. Graft versus host diseaseSection Six: Metabolic and deposition diseases37. Mucinosesa. Scleromyedemab. Scleredemac. Pretibial myxedemad. Follicular mucinosis38. Amyloidosis39. Porphyria cutanea tarda and pseudoporphyrias40. Calcifying disordersa. Calcinosis cutisb. Calciphylaxis41. Nutritional diseasesa. Scurvyb. Pellagrac. Zinc deficiency (acrodermatitis enteropathica)42. OchronosisSection Seven: Cutaneous manifestations of systemic diseases43. Rheumatoid arthritis44. Diabetesa. Necrobiosis lipoidicab. Acanthosis nigricansc. Bullous diabeticorumd. Diabetic dermopathye. Neuropathic ulcersf. Scleredema diabeticorumg. Eruptive xanthomas45. Thyroid diseasea. Pretibial myxedemab. Generalized myxedemac. Acquired ichthyosisd. Alopecia46. Cushing’s syndrome47. Addison’s disease48. Gastrointestinala. Ulcerative colitis and Crohn’s i. Erythema nodosum ii. Leukocytoclastic vasculitis iii. Sweet’s syndrome iv. Pyoderma gangrenosum v. Acrodermatitis enteropathicab. Gastrointestinal bleeding i. Hereditary hemorrhagic telangiectasia ii. Blue rubber bleb nevus syndrome iii. Pseudoxanthoma elasticum iv. Peutz-Jeuger v. Muir-Torrec. Liver disease i. Telangiectasias ii. Spider angiomas iii. Palmar erythema iv. Terry’s nails v. Primary biliary cirrhosis1. Tuberous xanthomas vi. Hemochromatosis vii. Wilson’s disease49. Renal diseasea. Nephrogenic systemic sclerosis50. Internal malignancya. Acanthosis nigricansb. Acrokeratosis neoplastica (Bazek’s syndrome)c. Erythema gyratum repens d. Necrolytic migratory erythema e. Acquired hypertrichosis lagunosaf. Cutaneous metastasesg. Paraneoplastic pemphigusSection Eight: Genodermatoses and developmental anomalies51. Genodermatosesa. Darier’s diseaseb. Ichthyoses i. vulgaris ii. lamellar iii. x-linked iv. bullous congenital ichthyosiform erythroderma v. Netherton’s syndromec. neurofibromatosisd. tuberous sclerosuse. Incontinentia pigmentif. Cowden’s syndromeg. Cutis laxah. Ehlers-Danlos syndromei. Pachonychia congenitaj. Pseudo xanthoma elasticum52. Developmental anomaliesa. Aplasia cutis congenitab. Hair collar signSection Nine: Infections53. Virala. Condyloma acuminatab. Fifth diseasec. Hand-foot-mouthd. Herpes simplex i. Eczema herpeticum ii. Herpetic Whitlow iii. Neonatale. Herpes zosterf. Varicellag. Molluscum contagiosumh. Verruca54. Fungala. Deep fungal infections i. Blastomycosis ii. Sporotrichosis iii. Coccidiodomycosis iv. Cryptococcosisb. Folliculitis i. Dermatophyte1. Tinea barbae2. Majocchi’s ii. Pityrosporumc. Onychomycosisd. Tinea i. Pedis and manuum ii. Corporis iii. Faceii1. Tinea incognito2. Tinea barbae iv. Versicolor v. Capitis vi. Cruris55. Bacteriala. Cellulitis i. Perianal streptococcal cellulitisb. Erythrasmac. Folliculitisd. Gonococcemiae. meningococcemiaf. Impetigo i. Non bullous ii. Bullousg. Leishmaniasish. Leprosyi. Mycobacterial infections i. Tuberculosis ii. Non tuberculousj. Pitted keratolysisk. Rocky mountain spotted feverl. SyphilisSection Ten: Infestations and bites56. Cutaneous larva migrans57. Bed bugs58. Spider bites59. Scabies60. Fleas61. Pediculosis (lice)62. TungiasisSection Eleven: Hair, nails, and mucous membranes63. Alopeciasa. Alopecia areatab. Telogen effluviumc. Anagen effluviumd. Androgenetic alopeciae. Trichotillomaniaf. Scarring alopecias i. Central centrifugal cicatricial alopecia ii. Lichen planopilaris iii. Discoid lupus iv. Dissecting cellulitis v. Folliculitis decalvans vi. Acne keloidalis nuchae vii. Frontal fibrosing alopecia viii. Traction alopecia64. Nail diseasea. Trachonychiab. Beau’s linesc. Mee’s linesd. Half and half nailse. Yellow nail syndromef. Onychorrhexisg. Punctate leukonychiah. Striate leukonychiai. Onychomadesisj. Koilonychiak. Terry’s nailsl. Clubbing65. Mucous membrane diseasea. Geographic tongueb. Oral hairy leukoplakiac. Aphthous stomatitisSection Twelve: Benign neoplasms66. Accessory tragus67. Accessory digit68. Acquired digital fibrokeratoma69. Adnexal tumorsa. Trichoepitheliomab. Cylindromac. Syringomad. Nevus sebaceouse. Trichofolliculomaf. Poroma70. Becker’s nevus71. Cystsa. Epidermalb. Steatocystoma multiplexc. Eruptive vellus hair cyst72. Dermatofibroma73. Melanocytica. Halo nevib. Congenital nevic. Junctional nevid. Compound nevie. Intradermal nevif. Nevus spilusg. Spitz nevih. Blue nevii. Nevus of Itoj. Nevus of Otak. Nevus comedonicus74. Mucocele75. Pyogenic granuloma76. Seborrheic keratosis77. Skin tags78. Supernumerary nipples79. Confluent and reticulated papillomatosis80. Linear epidermal nevusSection Thirteen: Malignant and premalignant neoplasms81. Actinic keratosis82. Actinic cheilitis83. Angiosarcoma84. Cutaneous metastases85. Dermatofibrosarcoma protuberans86. Kaposi’s sarcoma87. Keratoacanthoma88. Melanoma 89. Basal cell carcinoma90. Squamous cell carcinomaa. Erythroplasia of Queratb. Verrucous carcinomac. Bowen’s diseased. Invasive SCC91. Paget’s disease92. Extramammary Paget’s disease93. Cutaneous lymphomasa. T-cell i. Mycosis fungoides ii. Folliculotrophic mycosis fungoides iii. Pagetoid reticulosis iv. Granulomatous slack skin v. Sezary syndrome vi. Primary cutaneous CD 30+ anaplastic large cell lymphoma vii. Lymphomatoid papulosis viii. Subacute panniculitis like T-cell lymphomab. B-cell i. Follicular center lymphoma ii. Marginal zone B-cell lymphomaSection Fourteen: Disorders due to physical agents94. Chondrodermatitis nodularis helicis95. Factitial disease96. Prurigo nodularis97. Trauma induced skin diseasea. Talon noirb. Erythema ab ignec. Corns and callusesd. Subungual hematomae. Surgical ecchymosesf. Piezogenic papulesg. Traumatic tattoo98. Photodermatosesa. Phototoxicity b. Photoallergyc. Actinic damage i. Actinic purpura ii. Poikiloderma of Civatted. Polymorphous light eruptione. Chronic actinic dermatitis99. Foreign body granulomas100. Radiation dermatitisSection Fifteen: Drug reactions, erythemas, and urticarias101. Drug reactionsa. Acute generalized exanthematous pustulosis (AGEP)b. Drug induced hyperpigmentationc. Drug reaction with eosinophilia and systemic symptoms (DRESS)d. Fixed drug eruptionse. Stevens Johnson Syndrome and Toxic epidermal necrolysis (TEN)f. Steroid induced atrophyg. Morbilliform102. Erythemasa. Erythema multiformeb. Figurate erythemas i. Erythema annulare centrifugum ii. Erythema gyratum repens iii. Erythema chronicum migransc. Necrolyitic acral erythemad. Necrolyitic migratory erythema103. Urticariasa. Urticariab. Angioedema104. Polymorphic eruption of pregnancy (PUPPP)Section Sixteen: Vascular and lymphatic disorders105. Telangiectasia106. Hemangioma107. Vascular malformations108. lymphangiomasSection Seventeen: Pigmentary disorders109. Vitiligo110. Postinflammatory pigment alterationSection Eighteen: Neutrophilic dermatoses111. Pyoderma gangrenosum112. Sweet’s syndrome113. Erosive pustular dermatosis of the scalpSection Nineteen: Disorders of Langerhans cells, macrophages, and mast cells114. Langerhans cell histiocytosisa. Letterer-Siweb. Multicentric reticulohistiocytosis115. Xanthogranulomaa. Juvenile xanthogranulomab. Necrobiotic xanthogranuloma116. Xanthomasa. Planeb. Eruptivec. tuberous117. Sarcoidosis118. Granuloma annularea. Localizedb. Disseminated119. Necrobiosis lipoidica 120. Foreign body reactions 121. Mastocytosisa. Urticaria pigmentosab. Solitary mastocytomaSection Twenty: Dermal connective tissue disorders122. Keloids123. Hypertrophic scars124. Perforating diseasesa. Kyrle’s diseaseb. Elastosis perforans serpiginosa c. Reactive perforating collagenosisSection Twenty One: Panniculitis125. Erythema nodosum126. Lipodermatosclerosis (sclerosing panniculitis)
| Erscheint lt. Verlag | 28.5.2015 |
|---|---|
| Zusatzinfo | XVII, 534 p. 769 illus. in color. |
| Verlagsort | Cham |
| Sprache | englisch |
| Themenwelt | Medizin / Pharmazie ► Medizinische Fachgebiete ► Dermatologie |
| Schlagworte | clinical conditions in dermatology • Dermatology • dermatology board exam • maintenance of certification • recertification examination • Skin Disease |
| ISBN-10 | 3-319-03218-6 / 3319032186 |
| ISBN-13 | 978-3-319-03218-4 / 9783319032184 |
| Haben Sie eine Frage zum Produkt? |
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