奈特图解医学全集 第4卷 皮肤系统(第2版) 英文影印版 皮肤、性病及精神病学 (美)弗兰克·奈特(frank h.ter),(美)布莱恩·安德森(bryan e.anderson) 编 新华正版
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作者(美)弗兰克·奈特(frank h.ter),(美)布莱恩·安德森(bryan e.anderson) 编
出版社北京大学医学出版社
ISBN9787565920233
出版时间2020-01
版次1
装帧平装
开本16
页数255页
字数825千字
定价135元
货号xhwx_1201990019
上书时间2024-09-29
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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, ques, and fissures
1-10 morphology: macules, patches, and vesiculo-pustules
section 2 benign growths
2-1 acrochordon
2-2 beckers 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: mon acquired nevi and giant congenital melanocytic nevi
2-24 melanocytic nevi: congenital nevi
2-25 milia
2-26 neurofibroma
2-27 nevus lipomatosus superfiis
2-28 nevus of ota and nevus of ito
2-29 nevus sebaceus
2-30 osteoma cutis
2-31 palisaded encaulated 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 angiosara
3-3 basal cell carcinoma: basic fa anatomy
3-4 basal cell carcinoma: clinical and histological evaluation
3-5 bowens disease
3-6 bowenoid papulosis
3-7 cutaneous metastases
3-8 dermatofibrosara protuberans
3-9 mammary and extramammary pagets disease
3-10 kais sara
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 ae vulgaris
4-3 ae variants
4-4 ae keloidalis nuchae
4-5 acute febrile neutrophilic dermatosis (sweets syndrome)
4-6 allergic contact dermatitis: morphology
4-7 allergic contact dermatitis: patch testing and type iv hypersensitivity
4-8 atopic dermatitis: infants and ren
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 calciphylas
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 fins
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 toc epidermal necrolysis
4-28 erythema multiforme, stevens-johnson syndrome, and toc 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 (ae inversa)
4-38 irritant contact dermatitis, 109
4-39 keratosis pilaris
4-40 langerhans cell histiocytosis: presentation in hood
4-41 langerhans cell histiocytosis: eosinophilic granuloma
4-42 leukocytoclastic vasculitis
4-43 lichen nus
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 medema
4-50 necrobiosis lipoidica
4-51 necrobiotic xanthogranuloma
4-52 neutrophilic eccrine hidradenitis
4-53 ochronosis: metabolic pathway and cutaneous fins
4-54 ochronosis:systemic fins
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 ques of pregnancy
4-62 eudoxanthoma elasticum
4-63 oriasis: histopathological features and typical distribution
4-64 oriasis: inverse oriasis and oriasis in the genital area
4-65 oriasis: oriatic arthritis
4-66 radiation dermatitis
4-67 reactive arthritis (reiters 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 paraneostic 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 histosmosis
6-14 leprosy (hansens disease)
6-15 lice: clinical manifestations
6-16 lice: clinical fins 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: toc 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 mon nail disorders: fingernail disorders
7-4 mon nail disorders: toenail disorders
7-5 mon 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 fins
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 wilsons disease
section 9 genodermatoses and syndromes
9-1 addisons disease
9-2 amyloidosis
9-3 basal cell nevus syndrome
9-4 carney plex
9-5 cushings syndrome and cushings disease
9-6 cushings 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
referenc
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