The Cambridge Encyclopedia of Human Paleopathology
The Cambridge Encyclopedia of Human Paleopathology
Editor/Author
Aufderheide, Arthur C. and Rodriguez-Martin, Conrado
Publication Year: 2011
Publisher: Cambridge University Press
Price: Core Collection Only

ISBN: 978-1-10-740377-2
Category: Science - Biology
Image Count:
310
Book Status: Available
Table of Contents
The Cambridge Encyclopedia of Human Paleopathology is a major reference work for all those interested in the identification of disease in human remains.
This book is found in the following Credo Collections:
Table of Contents
- Preface
- Acknowledgements
- Part One: History of paleopathology
- Introduction
- Antecedent phase
- Genesis of paleopathology
- Interbellum consolidation phase
- The new paleopathology
- Part Two: Pseudopathology
- Pseudopathology: Introduction
- Soft tissue pseudopathology
- Skeletal tissue pseudopaleopathology
- Part Three: Traumatic conditions
- Traumatic conditions
- Skeletal evidence of trauma
- Fracture
- Skull fractures and crushing injuries
- Vertebral and thoracic fractures
- Dislocations
- Traumatic myositis ossificans
- Localized subperiosteal thickenings
- Skeletal injuries by weapons
- Decapitation
- Strangulation
- Amputation: the skeletal evidence
- Amputation: the soft tissue (finger) evidence
- Trephination
- Cranial deformation
- Cauterization
- Bloodletting
- Scalping
- Crucifixion
- Soft tissue injuries: inflicted by others
- Lacerations and stab wounds
- Sacrifice victims
- Accidental injuries
- Soft tissue injuries: mutilation
- Introduction
- Labrets
- Nasal and earrings
- Hair and nails
- Circumcision
- Tattoos and scarification
- Purpose(s)
- Part Four: Congenital anomalies
- Congenital skeletal anomolies
- Skull malformations
- Craniosynostoses
- Complex craniofacial deformities
- Anencephaly
- Microcephaly
- Macrocephaly
- Hydrocephalus
- Congenital herniation of meninges and brain
- Cleft palate (palatoschisis)
- Enlarged parietal foramina (foramina parietalia permagna; Catlin Mark)
- Congenital malformations of the spine
- Atlas occipitalization (atlanto-occipital fusion; atlanto-occipital assimilation)
- Basilar impression
- Klippel-Feil syndrome
- Jarcho-Levin syndrome of vertebral anomalies
- Congenital absence of the odontoid process
- Spina bifida
- Butterfly vertebra
- Anterior spina bifida
- Incomplete segmentation of vertebral segments
- Spondylolysis and spondylolisthesis
- Hemivertebrae
- Sacrococcygeal agenesis
- Sacral agenesis
- Congenital absence of the pedicles
- Transitional vertebrae
- Scoliosis
- Congenital kyphosis
- Congenital malformations of the thorax
- Cervical ribs
- Costal fusion
- Other rib anomalies
- Congenital malformations of the pelvis
- Congenital dislocation of the hip
- Extrophy of bladder and cleft pelvis
- Aplasia and hypoplasia of the extremities
- Failures in the development of a limb
- Failures in the development of bones
- Upper extremity malformations
- Dysostosis cleidocranialis
- Sprengel's deformity
- Madelung's deformity
- Congenital radio-ulnar synostosis
- Congenital dislocation of the radius
- Congenital pseudoarthrosis of the clavicle
- Carpal blocks
- Lower extremity malformations
- Developmental coxa vara
- Genu recurvatum congenitum
- Bipartite patella
- Congenital angulation of the tibia
- Congenital pseudoarthrosis of the tibia
- Tibial-fibular synostosis
- Tarsal blocks
- Talipes equinovarus
- Metatarsus varus congenitus
- Talus verticalis congenitus
- Malformations of fingers and toes
- Adactyly
- Syndactyly
- Polydactyly
- Symphalangism
- Hyperphalangism
- Part Five: Circulatory disorders
- Aneurysms
- Congenital aortic disease
- Osteochondritis dissecans
- Osteochondroses
- Necrosis of the femoral head
- Primary necrosis of the medial femoral condyle
- Slipped femoral capital epiphysis
- Hypertrophic osteoarthropathy
- Part Six: Joint diseases
- Degenerative joint disease
- Degenerative disease of the spine
- Diffuse idiopathic skeletal hyperostosis (DISH)
- Rheumatoid arthritis
- Juvenile chronic arthritis
- Ankylosing spondylitis (AS)
- Psoriatic arthritis
- Reiter's syndrome (reactive arthritis)
- Enteropathic arthropathies
- Traumatic arthritis
- Nonspecific septic arthritis
- Neurotrophic arthropathy
- Gout
- Definition and etiology
- Ochronosis
- Hemochromatosis
- Definition
- Genetic (primary, hereditary, idiopathic) hemochromatosis
- Acquired hemochromatosis
- Paleopathology
- Part Seven: Infectious diseases
- Infectious Diseases: Introduction
- Bacterial Infections
- Tuberculosis
- Leprosy
- Treponematosis
- Osteomyelitis
- Pneumonia
- Salmonellosis
- Brucellosis
- Actinomycosis
- Nocardiosis
- Plague
- Cholera
- Gas gangrene
- Lyme disease
- Glanders
- Tropical ulcer
- Tropical ulcer
- Ainhum
- Virus Infections
- Introduction
- Smallpox
- Measles
- Rubella
- Influenza
- Poliomyelitis
- Miscellaneous virus infections
- Fungal Infections
- Introduction
- History of the fungal infections
- Systemic mycoses
- Subcutaneous Mycoses
- Parasitic Infections
- Introduction
- Protozoan infections
- Helminth infections
- Part Eight: Diseases of the viscera
- Diseases of the viscera: Introduction
- Soft tissue lesions of the head and neck
- Heart and pericardial diseases
- Pulmonary diseases
- Liver and biliary tract diseases
- Gastrointestinal tract diseases
- Urinary diseases
- Genital diseases
- Breast diseases
- Dermatological diseases
- Part Nine: Metabolic diseases
- Vitamin D-related syndromes: rickets and osteomalacia
- Scurvy
- Osteoporosis
- Intoxications
- Fluorosis
- Lead poisoning
- Mercury poisoning
- Arsenic poisoning
- Mycotoxicosis
- Part Ten: Endocrine disorders
- Endocrine disorders: Introduction
- The pituitary gland
- The parathyroid glands
- Disorders affecting gender expression
- The thyroid
- The adrenals
- Diabetes mellitus
- Part Eleven: Hematological disorders
- Hematological disorders: Introduction
- Disorders of red blood cells (anemias)
- Disorders of white blood cells
- Bleeding disorders
- Part Twelve: Skeletal dysplasias
- Skeletal dysplasias: Introduction
- Growth defects of long bones and spine
- Introduction
- Achondroplasia
- Chondrodysplasia punctata
- Camptomelic Dysplasia
- Multiple epiphyseal dysplasia
- Short-limbed dwarfism with prominent spine alterations
- Congenital spondyloepiphyseal dysplasia
- Kniest dysplasia
- Larsen's syndrome
- Metaphyseal and diaphyseal disorders
- Diaphyseal aclasis
- Metaphyseal chondrodysplasia
- Metatrophic dysplasia
- Dystrophic dysplasia
- Dyschondrosteosis
- Chondroectodermal dysplasia
- Developmental anomalies of cartilaginous and fibrous components of the skeleton
- Dyschondroplasia
- Disorders of diaphyseal density or metaphyseal remodeling
- Osteopetrosis
- Dysosteosclerosis
- Pyknodysostosis
- Infantile cortical hyperostosis
- Diaphyseal dysplasia
- Frontometaphyseal dysplasia
- Craniometaphyseal dysplasia
- Metaphyseal dysplasia
- Craniodiaphyseal dysplasia
- Melorheostosis
- Hyperphosphatasia
- Hypophosphatasia
- Collagen disorders leading to inappropriate mineralization
- Introduction
- Osteogenesis imperfecta
- Fibrogenesis imperfecta ossium
- Fibrodysplasia ossificans progressiva
- Osteopoikilosis
- Osteopathia striata
- Nail–Patella syndrome
- Marfan's syndrome
- Homocystinuria
- Skeletal dysplasias due to chromosomal aberrations
- Introduction
- Trisomy 21
- Trisomy 8
- Deletion 5p
- Turner's syndrome
- Klinefelter's syndrome
- Skeletal dysplasias due to congenital metabolic disorders
- Mucopolysaccharidoses
- Mucolipidoses
- Lipid storage diseases
- Part Thirteen: Neoplastic conditions
- General principles of neoplasia
- Definition
- Characteristics of benign and malignant tumors
- Function of neoplastic cells
- Epidemiology
- Causes of neoplasia
- Cancer in antiquity
- Paleopathological study of neoplasms
- Tumors of osseous origin or differentiation
- Osteoma
- Solitary enostosis
- Osteoid osteoma
- Osteoblastoma
- Ossifying fibroma
- Osteogenic sarcoma
- Tumors of cartilage origin or differentiation
- Chondroma
- Chondroblastoma
- Chondromyxoid fibroma
- Osteochondroma
- Chondrosarcoma
- Tumors of fibrous connective tissue origin or differentiation
- Introduction
- Desmoplastic fibroma
- Nonossifying fibroma
- Fibrosarcoma
- Fibrous histiocytoma and malignant fibrous histiocytoma
- Lipoma, liposarcoma, and leiomyosarcoma
- Tumors of vascular differentiation
- Hemangioma of bone
- Glomus tumor, hemangiopericytoma, and hemangioendothelioma
- Angiosarcoma
- Tumors of neural tissue
- Neurilemmoma (Schwannoma), neurofibroma, and neurofibrosarcoma
- Notochord tumors
- Chordoma
- Miscellaneous tumors of unknown origin
- Giant cell reparative granuloma
- Meningioma
- Giant cell tumor
- Ewing's sarcoma
- Primary malignant lymphoma of bone
- Metastatic skeletal lesions
- Bone cysts
- Part Fourteen: Diseases of the dentition
- Oral biology
- Attrition
- Temporomandibular joint disease
- Periodontal disorders
- Dental caries
- Enamel hypoplasia
- Miscellaneous dentition-related conditions
- Part Fifteen: Miscellaneous conditions
- Paget's disease of bone
- Leontiasis ossea
- Hyperostosis frontalis interna
- Generalized hyperostosis with pachydermia (pachydermo-hyperostosis)
- Fibrous dysplasia of bone (fibro-osseous dysplasia)
- Skeletal neurofibromatosis (von Recklinghausen's disease)
- Harris lines
- References