SKIBO-diseases : disorders affecting the skin and bones : a clinical, dermatologic, and radiologic synopsis
著者
書誌事項
SKIBO-diseases : disorders affecting the skin and bones : a clinical, dermatologic, and radiologic synopsis
Springer, c1999
- タイトル別名
-
Haut-, Schleimhaut- und Skeletterkrankungen
Disorders affecting the skin, mucous membranes, and bones
大学図書館所蔵 全3件
  青森
  岩手
  宮城
  秋田
  山形
  福島
  茨城
  栃木
  群馬
  埼玉
  千葉
  東京
  神奈川
  新潟
  富山
  石川
  福井
  山梨
  長野
  岐阜
  静岡
  愛知
  三重
  滋賀
  京都
  大阪
  兵庫
  奈良
  和歌山
  鳥取
  島根
  岡山
  広島
  山口
  徳島
  香川
  愛媛
  高知
  福岡
  佐賀
  長崎
  熊本
  大分
  宮崎
  鹿児島
  沖縄
  韓国
  中国
  タイ
  イギリス
  ドイツ
  スイス
  フランス
  ベルギー
  オランダ
  スウェーデン
  ノルウェー
  アメリカ
注記
Includes bibliographical references and index
内容説明・目次
内容説明
Numerous diseases in the areas of orthopaedics, rheumatology, and radiology can only be completely diagnosed if the corresponding conditions of the skin and mucous membranes are included in the diagnostic work-up (skin-bone). Conversely, dermatologic assessment of skin symptoms in isolation may lead to serious delays and errors in the diagnosis and treatment of associated changes in the musculoskeletal system. This monograph gives an interdisciplinary synopsis, from a dermatologic and clinical radiologic perspective, of 85 disease entities which in practice are likley to present. For orientation purposes the main dermatologic and radiologic symptoms are presented in table form at the beginning of the book.
目次
Tables of Differential Diagnoses.- 1 Congenital Disorders1 and Developmental Anomalies.- 1.1 Nail-Patella Syndrome.- 1.2 Enchondromatosis with Cavernous Hemangiomas (e.g., Maffucci's Syndrome).- 1.3 Fibroosseous Lesions with Cafe-au-lait Spots.- 1.3.1 Fibrous Metaphyseal Defects with Cafe-au-lait Spots (Jaffe-Campanacci Syndrome).- 1.3.2 Fibrous Dysplasia.- 1.4 Neurofibromatosis Type 1.- 1.5 Tuberous Sclerosis.- 1.6 Osteopoikilosis with Dermatofibrosis Lenticularis Disseminata and Other Cutaneous Lesions.- 1.7 Osteopathia Striata and Other Skeletal Malformations with Focal Cutaneous Hypoplasia or Cutaneous Atrophy (e.g., Goltz-Gorlin Syndrome).- 1.8 Melorheostosis with Circumscribed Scleroderma.- 1.9 Gardner's Syndrome.- 1.10 Cronkhite-Canada Syndrome.- 1.11 Proteus Syndrome.- 1.12 Basal Cell Nevus Syndrome (Gorlin-Goltz Syndrome).- 1.13 Ichthyosis with Chondrodysplasia Punctata (Conradi-Hunermann Syndrome, Happle's Syndrome).- 1.14 Congenital Ichthyosiform Erythroderma with Acro-osteolysis.- 1.15 Refsum's Syndrome.- 1.16 Hereditary Palmoplantar Keratosis with Drumstick Fingers and Bony Hypertrophy.- 1.17 Mutilating Palmoplantar Keratoderma.- 1.18 Epidermolysis Bullosa Dystrophica with Acro-osteolysis.- 1.19 Rothmund-Thomson Syndrome.- 1.20 Werner's Syndrome.- 1.21 Ehlers-Danlos Syndrome.- 1.22 Metaphyseal Chondrodysplasia with Complete Alopecia.- 1.23 Satoyoshi's Syndrome.- 1.24 Gaucher's Disease.- 1.25 Fabry's Disease.- 1.26 Congenital Copper Deficiency.- 2 Collagen Diseases.- 2.1 Progressive Systemic Sclerosis (PSS).- 2.2 Systemic Lupus Erythematosus (SLE).- 2.3 Polymyositis and Dermatomyositis.- 2.4 Sjogren's Syndrome.- 2.5 Jo-1 (Antisynthetase) Syndrome.- 2.6 Sharp's Syndrome.- 2.7 Undifferentiated Inflammatory Systemic Connective Tissue Disease.- 3 Rheumatic Disorders.- 3.1 Rheumatoid Arthritis.- 3.2 Fibroblastic Rheumatism.- 3.3 Gouty Arthritis.- 3.4 Hemochromatosis.- 3.5 Relapsing Polychondritis (RP).- 3.6 Seronegative Spondyloarthropathies.- 3.6.1 Ankylosing Spondylitis (AS).- 3.6.2 Psoriatic Spondylarthritis and Psoriatic Arthritis.- 3.6.3 Pustulotic Arthro-osteitis (PAO).- 3.6.4 Reiter's Syndrome and Other Forms of Reactive Arthritis.- 3.6.5 Oligoarticular Juvenile Rheumatoid Arthritis (Type II).- 3.6.6 Enterospondylarthritis (Crohn's Disease, Ulcerative Colitis, etc.).- 3.6.7 Undifferentiated Spondyloarthropathy.- 3.7 Other Forms of Reactive Arthritis.- 3.7.1 Lyme Arthritis.- 3.7.2 Rheumatic Fever.- 3.8 Behcet's Syndrome.- 3.9 Acne-Associated Skeletal Changes.- 4. Infectious Diseases.- 4.1 Leprosy.- 4.2 Syphilis.- 4.3 Actinomycosis.- 4.4 Mycetoma.- 4.5 Bacillary (Epitheloid) Angiomatosis in AIDS.- 5 Neoplastic and Granulomatous Diseases.- 5.1 Lymphoma.- 5.2 Mycosis Fungoides.- 5.3 POEMS Plasmacytoma.- 5.4 Langerhans Cell Histiocytosis.- 5.4.1 Abt-Letterer-Siwe Syndrome.- 5.4.2 Eosinophilic Granuloma.- 5.4.3 Hand-Schuller-Christian Syndrome.- 5.5 Multicentric Reticulohistiocytosis (MR).- 5.6 Sarcoidosis.- 5.7 Mastocytosis.- 6 Angiodysplastic Skin Lesions and Skeletal Changes.- 6.1 Congenital Angiodysplasias.- 6.1.1 Weber Type.- 6.1.2 Klippel-Trenaunay Type.- 6.1.3 Servelle-Martorell Type.- 6.1.4 Stewart-Bluefarb Syndrome.- 6.2 Acquired Angiodysplasias.- 6.2.1 Hemangioma with Osteomalacia.- 6.2.2 Glomus Tumors.- 7 Periostoses.- 7.1 Pachydermoperiostosis.- 7.2 EMO Syndrome.- 7.3 Hypertrophic Osteoarthropathy.- 7.4 Periosteal Ossification in Varicose Symptom Complex.- 7.5 Scurvy.- 8 Other Diseases.- 8.1 Nonsystemic Trophic Disorders of the Hands and Feet with Acro-osteolysis.- 8.2 Sudeck's Syndrome.- 8.3 Lipoatrophic Diabetes Mellitus.- 8.4 Pancreatitic Bone Lesions.- 8.5 Interstitial Calcinosis.- 8.6 Chromium and Nickel Allergy Due to Internal Fixation Material.
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