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奈特图解医学全集 第4卷 皮肤系统(第2版) 英文影印版
字数: 825000
装帧: 平装
出版社: 北京大学医学出版社
出版日期: 2020-01-01
商品条码: 9787565920233
版次: 1
开本: 16开
页数: 255
出版年份: 2020
定价:
¥135
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内容简介
奈特图解医学全集是世界有名的奈特品牌的主打书,整套书分为9大系统疾病,运用传统的图解形式,从基础到临床,进行了详细的精解。全书绘图精美,语言简洁地道,可读性强,无论是对临床医学生还是年轻医生,都是系统学习,掌握知识的重要参考书。
作者简介
目录
SECTION 1 ANATOMY, PHYSIOLOGY, AND EMBRYOLOGY
1-1 Embryology of the Skin
1-2 Normal Skin Anatomy
1-3 Normal Skin Histology
1-4 Skin Physiology--The Process of Keratinization
1-5 Normal Skin Flora
1-6 Vitamin D Metabolism
1-7 Photobiology
1-8 Wound Healing
1-9 Morphology: Lichenification, Plaques, and Fissures
1-10 Morphology: Macules, Patches, and Vesiculo-Pustules
SECTION 2 BENIGN GROWTHS
2-1 Acrochordon
2-2 Becker's Nevus (Smooth Muscle Hamartoma)
2-3 Dermatofibroma (Sclerosing Hemangioma)
2-4 Eccrine Poroma
2-5 Eccrine Spiradenoma
2-6 Eccrine Syringoma
2-7 Ephelides and Lentigines
2-8 Ephelides and Lentigines (Continued)
2-9 Epidermal Inclusion Cyst
2-10 Epidermal Nevus
2-11 Fibrofolliculoma
2-12 Fibrous Papule
2-13 Ganglion Cyst,
2-14 Glomus Tumor and Glomangioma
2-15 Hidradenoma Papilliferum
2-16 Hidrocystoma
2-17 Keloid and Hypertrophic Scar
2-18 Leiomyoma
2-19 Lichenoid Keratosis
2-20 Lipoma
2-21 Median Raphe Cyst
2-22 Melanocytic Nevi: Blue Nevi
2-23 Melanocytic Nevi: Common Acquired Nevi and Giant Congenital Melanocytic Nevi
2-24 Melanocytic Nevi: Congenital Nevi
2-25 Milia
2-26 Neurofibroma
2-27 Nevus Lipomatosus Superficialis
2-28 Nevus of Ota and Nevus of Ito
2-29 Nevus Sebaceus
2-30 Osteoma Cutis
2-31 Palisaded Encapsulated Neuroma
2-32 Pilar Cyst (Trichilemmal Cyst)
2-33 Porokeratosis
2-34 Pyogenic Granuloma
2-35 Reticulohistiocytoma
2-36 Seborrheic Keratosis
2-37 Spitz Nevus
SECTION 3 MALIGNANT GROWTHS
3-1 Adnexal Carcinoma
3-2 Angiosarcoma
3-3 Basal Cell Carcinoma: Basic Facial Anatomy
3-4 Basal Cell Carcinoma: Clinical and Histological Evaluation
3-5 Bowen's Disease
3-6 Bowenoid Papulosis
3-7 Cutaneous Metastases
3-8 Dermatofibrosarcoma Protuberans
3-9 Mammary and Extramammary Paget's Disease
3-10 Kaposi's Sarcoma
3-11 Keratoacanthoma
3-12 Melanoma: Mucocutaneous Malignant Melanoma
3-13 Melanoma: Metastatic Melanoma
3-14 Merkel Cell Carcinoma
3-15 Mycosis Fungoides: Clinical Subtypes of Cutaneous T-Cell Lymphoma
3-16 Mycosis Fungoides: Histological Analysis of Cutaenous T-Cell Lymphoma
3-17 Sebaceous Carcinoma
3-18 Squamous Cell Carcinoma: Genital Squamous Cell Carcinoma
3-19 Squamous CellCarcinoma:Clinical and Histological Evaluation
SECTION 4 RASHES
4-1 Acanthosis Nigricans
4-2 Acne Vulgaris
4-3 Acne Variants
4-4 Acne Keloidalis Nuchae
4-5 Acute Febrile Neutrophilic Dermatosis (Sweet's Syndrome)
4-6 Allergic Contact Dermatitis: Morphology
4-7 Allergic Contact Dermatitis: Patch Testing and Type IV Hypersensitivity
4-8 Atopic Dermatitis: Infants and Children
4-9 Atopic Dermatitis: Adolescents and Adults
4-10 Autoinflammatory Syndromes: Pathophysiology
4-11 Autoinflammatory Syndromes: Clinical Manifestations
4-12 Bug Bites: Brown Recluse Spiders and Scabies Mites
4-13 Bug Bites: Arthropods and Diseases They Carry
4-14 Calciphylaxis
4-15 Cutaneous Lupus: Band Test
4-16 Cutaneous Lupus: Systemic Manifestations of Systemic Lupus Erythematosus
4-17 Cutaneous Lupus: Manifestations
4-18 Cutis Laxa
4-19 Dermatomyositis: Manifestations
4-20 Dermatomyositis: Cutaneous and Laboratory Findings
4-21 Disseminated Intravascular Coagulation,
4-22 Elastosis Perforans Serpiginosa
4-23 Eruptive Xanthomas: Congenital Hyperlipoproteinemia
4-24 Eruptive Xanthomas: Acquired Hyperlipoproteinemia
4-25 Erythema Ab lgne
4-26 Erythema Annulare Centrifugum,
4-27 Erythema Multiforme, Stevens-Johnson Syndrome, and Toxic Epidermal Necrolysis
4-28 Erythema Multiforme, Stevens-Johnson Syndrome, and Toxic Epidermal Necrolysis (Continued)
4-29 ErythemaNodosum
4-30 Fabry Disease
4-31 Fixed Drug Eruption
4-32 Gout: Gouty Arthritis
4-33 Gout: Tophaceous Gout
4-34 Craft-versus-Host Disease
4-35 Granuloma Annulare,
4-36 Graves Disease and Pretibial Myxedema
4-37 Hidradenitis Suppurativa (Acne Inversa)
4-38 Irritant Contact Dermatitis, 109
4-39 Keratosis Pilaris
4-40 Langerhans Cell Histiocytosis: Presentation in Childhood
4-41 Langerhans Cell Histiocytosis: Eosinophilic Granuloma
4-42 Leukocytoclastic Vasculitis
4-43 Lichen Planus
4-44 Lichen Simplex Chronicus
4-45 Lower Extremity Vascular Insufficiency
4-46 Mast Cell Diesase
4-47 Mast Cell Disease: Degranulation Blockers
4-48 Morphea
4-49 Mvxedema
4-50 Necrobiosis Lipoidica
4-51 Necrobiotic Xanthogranuloma
4-52 Neutrophilic Eccrine Hidradenitis
4-53 Ochronosis: Metabolic Pathway and Cutaneous Findings
4-54 Ochronosis:Systemic Findings
4-55 Oral Manifestations in Blood Dyscrasias
4-56 Phytophotodermatitis
4-57 PigmentedPurpura
4-58 Pityriasis Rosea
4-59 Pityriasis Rubra Pilaris
4-60 Polyarteritis Nodosa
4-61 Pruritic Urticarial Papules and Plaques Of Pregnancy
4-62 Pseudoxanthoma Elasticum
4-63 Psoriasis: Histopathological Features and Typical Distribution
4-64 Psoriasis: Inverse Psoriasis and Psoriasis in the Genital Area
4-65 Psoriasis: Psoriatic Arthritis
4-66 Radiation Dermatitis
4-67 Reactive Arthritis (Reiter's Syndrome)
4-68 Rosacea
4-69 Sacroid: Cutaneous Manifestations
4-70 Sarcoid: Systemic Manifestations
4-71 Scleroderma (Progressive Systemic Sclerosis)
4-72 Seborrheic Dermatitis
4-73 Skin Manifestations of Inflammatory Bowel Disease: Mucocutaneous Manifestations
4-74 Skin Manifestations of Inflammatory Bowel Disease: Cutaneous Manifestations
4-75 Stasis Dermatitis
4-76 Urticaria
4-77 Vitiligo
SECTION 5 AUTOIMMUNE BLISTERING DISEASES
5-1 Basement Membrane Zone and Hemidesmosome
5-2 Desmosome
5-3 Bullous Pemphigoid
5-4 Mucous Membrane Pemphigoid
5-5 Dermatitis Herpetiformis
5-6 Epidermolysis Bullosa Acquisita
5-7 Linear IgA Bullous Dermatosis
5-8 Paraneoplastic Pemphigus
5-9 Pemphigus Foliaceus
5-10 Pemphigus Vulgaris
SECTION 6 INFECTIOUS DISEASES
6-1 Actinomycosis
6-2 Blastomycosis
6-3 Chancroid
6-4 Coccidioidomycosis
6-5 Cryptococcosis
6-6 Cutaneous Larva Migrans
6-7 Dermatophytoses: Tinea Faciei and Tinea Corporis
6-8 Dermatophytoses: Tinea Cruris and Tinea Capitis
6-9 Dermatophvtoses: Tinea Pedis and Tinea Unguium
6-10 Herpes Simplex Virus: Lesions
6-11 Herpes Simplex Virus: Lesions (Continued)
6-12 Herpes Simplex Virus: Encephalitis
6-13 Histoplasmosis
6-14 Leprosy (Hansen's Disease)
6-15 Lice: Clinical Manifestations
6-16 Lice: Clinical Findings and Management
6-17 Lyme Disease
6-18 Lymphogranuloma Venereum
6-19 Meningococcemia: Acute Adrenal Insufficiency (Waterhouse-Friderichsen Syndrome)
6-20 Meningococcemia: Bacterial Meningitis
6-21 Molluscum Contagiosum,
6-22 Paracoccidioidomycosis
6-23 Scabies
6-24 Sporotrichosis,
6-25 Staphylococcus aureus Skin Infections: Types of Skin Infections
6-26 Staphylococcus aureus Skin Infections: Toxic Shock Syndrome
6-27 Syphilis: Genitalia
6-28 Syphilis: Oral Cavity
6-29 Syphilis: Pregnancy
6-30 Varicella
6-31 Herpes Zoster: Clinical Presentation
6-32 Varicella Zoster with Keratitis
6-33 Verrucae: Human Papillomavirus (HPV) Infection
6-34 Verrucae: Condylomata Acuminata (Genital Warts)
SECTION 7 HAIR AND NAIL DISEASES
7-1 Alopecia Areata,
7-2 Androgenic Alopecia
7-3 Common Nail Disorders: Fingernail Disorders
7-4 Common Nail Disorders: Toenail Disorders
7-5 Common Nail Disorders
7-6 Hair Shaft Abnormalities
7-7 Normal Structure and Function of the Hair Follicle Apparatus
7-8 Normal Structure and Function of the Nail Unit
7-9 Telogen Effluvium and Anagen Effluvium
7-10 Trichotillomania
SECTION 8 NUTRITIONAL AND METABOLIC DISEASES
8-1 Beriberi: Sources and Metabolism ot Thiamine (Vitamin B1)
8-2 Beriberi: Clinical Manifestations of Dry and Wet Beriberi
8-3 Hemochromatosis
8-4 Metabolic Diseases: Niemann-Pick Disease, von Gierke Disease, and Galactosemia
8-5 Pellagra: Main Sources, Causes, and Skin Findings
8-6 Pellagra: Mucosal and Central Nervous System Manifestations
8-7 Phenylketonuria: Normal and Abnormal Metabolism
8-8 Phenylketonuria: Clinical Manifestations and Hereditary Patterns
8-9 Scurvy: Dietary Sources and Classic Cutaneous Manifestations
8-10 Scurvy: Bony and Skin Abnormalities
8-11 Vitamin A Deficiency
8-12 Vitamin K Deficiency and Vitamin K Antagonists: Potential Clinical Consequences of Warfarin Use
8-13 Vitamin K Deficiency and Vitamin K Antagonists: Anticoagulation Effects on the Clotting Cascade
8-14 Wilson's Disease
SECTION 9 GENODERMATOSES AND SYNDROMES
9-1 Addison's Disease
9-2 Amyloidosis
9-3 Basal Cell Nevus Syndrome
9-4 Carney Complex
9-5 Cushing's Syndrome and Cushing's Disease
9-6 Cushing's Syndrome: Pathophysiology
9-7 Down Syndrome
9-8 Ehlers-Danlos Syndrome
9-9 Marfan Syndrome
9-10 Neurofibromatosis: Cutaneous Manifestations
9-11 Neurofibromatosis: Cutaneous and Skeletal Manifestations
9-12 Tuberous Sclerosis
REFERENCES
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