This document discusses various bone and joint diseases and their radiological features. It covers rickets and osteomalacia, noting their effects on bone mineralization and growth plates. Hyperparathyroidism is discussed as causing decreased bone density and subperiosteal bone resorption. Paget's disease causes thickening of bone trabeculae and cortex, leading to bone enlargement. Hemolytic anemias like thalassemia can cause bone marrow hyperplasia seen as thinning cortices and prominent trabeculae. Radiation exposure may lead to osteonecrosis, osteoporosis or sarcomatous changes. Osteoarthritis is characterized by joint space narrowing and subchondral
This document summarizes bone and joint diseases as seen on radiographs. It describes generalized decreased and increased bone density caused by conditions like osteoporosis, osteomalacia, hyperparathyroidism and Paget's disease. Specific findings of osteoporosis, rickets, osteomalacia and hyperparathyroidism are outlined. Joint diseases discussed include osteoarthritis and its features of joint space narrowing and soft tissue swelling. Diagnosis of arthritis depends on the number and location of involved joints and presence of underlying diseases.
This document summarizes various joint conditions and their radiological features. It discusses gout, joint infection including pyogenic and TB infections, Charcot joints, avascular necrosis, osteochondritis, Perthes disease, slipped femoral epiphysis, and developmental dysplasia of the hips. For each condition, it provides details on causes, affected areas, and characteristic radiological findings such as bone changes, cartilage erosion, and effusion.
Presentation1.pptx, lecture for md oral examination.Abdellah Nazeer
This document discusses hemolytic anemia, which is a disorder where red blood cells are destroyed faster than they can be replaced. There are two types: intrinsic, where defects in red blood cells cause their premature destruction, and extrinsic, where red blood cells are destroyed by outside factors like infections, medications, or autoimmune disorders. Symptoms include paleness, jaundice, dark urine, fatigue, and enlarged organs. Specific conditions that can cause hemolytic anemia like sickle cell anemia and thalassemia are also examined radiographically.
Presentation1.pptx, radiological imaging of skeletal dysplasiaAbdellah Nazeer
This document provides radiological images and descriptions of several skeletal dysplasias. It discusses conditions such as cleidocranial dysplasia, which can cause respiratory distress in newborns. Other conditions summarized include osteopoikilosis, mucopolysaccharidoses, multiple epiphyseal dysplasia, metaphyseal dysplasia, spondyloepiphyseal dysplasia, chondroectodermal dysplasia, achondroplasia, fibrous dysplasia, and dysplasia epiphysealis hemimelica. For each condition, the document highlights features visible in imaging and clinical symptoms.
Orthopedic Aspects Of Metabolic Bone Disease By XiuXiu Srithammasit
This document summarizes various metabolic bone diseases and their orthopedic manifestations and radiographic findings. It covers osteoporosis, rickets and osteomalacia, hyperparathyroidism, hypoparathyroidism, hyperthyroidism, and renal osteodystrophy. For each condition, it describes clinical presentation, pathogenesis, characteristic radiographic findings including areas of bone involvement and patterns of bone changes, and differential diagnoses.
This document discusses seronegative spondyloarthropathies, which are musculoskeletal syndromes linked by common features including being negative for rheumatoid factor and often involving the axial skeleton. There are five main subgroups, including ankylosing spondylitis, psoriatic arthritis, reactive arthritis, enteropathic arthritis, and undifferentiated spondyloarthritis. The document then provides details on the clinical presentation and radiographic findings for each of these three conditions in three sample patient cases.
This document discusses scurvy, its causes, symptoms, diagnosis, and radiographic findings. Scurvy results from a long-term vitamin C deficiency and can affect infants and the elderly. It causes vascular fragility, inhibited bone and cartilage growth, and hemorrhages. Radiographs show osteopenia, provisional calcification lines, epiphyseal abnormalities, and metaphyseal changes that allow accurate diagnosis.
This document discusses various bone and joint diseases and their radiological features. It covers rickets and osteomalacia, noting their effects on bone mineralization and growth plates. Hyperparathyroidism is discussed as causing decreased bone density and subperiosteal bone resorption. Paget's disease causes thickening of bone trabeculae and cortex, leading to bone enlargement. Hemolytic anemias like thalassemia can cause bone marrow hyperplasia seen as thinning cortices and prominent trabeculae. Radiation exposure may lead to osteonecrosis, osteoporosis or sarcomatous changes. Osteoarthritis is characterized by joint space narrowing and subchondral
This document summarizes bone and joint diseases as seen on radiographs. It describes generalized decreased and increased bone density caused by conditions like osteoporosis, osteomalacia, hyperparathyroidism and Paget's disease. Specific findings of osteoporosis, rickets, osteomalacia and hyperparathyroidism are outlined. Joint diseases discussed include osteoarthritis and its features of joint space narrowing and soft tissue swelling. Diagnosis of arthritis depends on the number and location of involved joints and presence of underlying diseases.
This document summarizes various joint conditions and their radiological features. It discusses gout, joint infection including pyogenic and TB infections, Charcot joints, avascular necrosis, osteochondritis, Perthes disease, slipped femoral epiphysis, and developmental dysplasia of the hips. For each condition, it provides details on causes, affected areas, and characteristic radiological findings such as bone changes, cartilage erosion, and effusion.
Presentation1.pptx, lecture for md oral examination.Abdellah Nazeer
This document discusses hemolytic anemia, which is a disorder where red blood cells are destroyed faster than they can be replaced. There are two types: intrinsic, where defects in red blood cells cause their premature destruction, and extrinsic, where red blood cells are destroyed by outside factors like infections, medications, or autoimmune disorders. Symptoms include paleness, jaundice, dark urine, fatigue, and enlarged organs. Specific conditions that can cause hemolytic anemia like sickle cell anemia and thalassemia are also examined radiographically.
Presentation1.pptx, radiological imaging of skeletal dysplasiaAbdellah Nazeer
This document provides radiological images and descriptions of several skeletal dysplasias. It discusses conditions such as cleidocranial dysplasia, which can cause respiratory distress in newborns. Other conditions summarized include osteopoikilosis, mucopolysaccharidoses, multiple epiphyseal dysplasia, metaphyseal dysplasia, spondyloepiphyseal dysplasia, chondroectodermal dysplasia, achondroplasia, fibrous dysplasia, and dysplasia epiphysealis hemimelica. For each condition, the document highlights features visible in imaging and clinical symptoms.
Orthopedic Aspects Of Metabolic Bone Disease By XiuXiu Srithammasit
This document summarizes various metabolic bone diseases and their orthopedic manifestations and radiographic findings. It covers osteoporosis, rickets and osteomalacia, hyperparathyroidism, hypoparathyroidism, hyperthyroidism, and renal osteodystrophy. For each condition, it describes clinical presentation, pathogenesis, characteristic radiographic findings including areas of bone involvement and patterns of bone changes, and differential diagnoses.
This document discusses seronegative spondyloarthropathies, which are musculoskeletal syndromes linked by common features including being negative for rheumatoid factor and often involving the axial skeleton. There are five main subgroups, including ankylosing spondylitis, psoriatic arthritis, reactive arthritis, enteropathic arthritis, and undifferentiated spondyloarthritis. The document then provides details on the clinical presentation and radiographic findings for each of these three conditions in three sample patient cases.
This document discusses scurvy, its causes, symptoms, diagnosis, and radiographic findings. Scurvy results from a long-term vitamin C deficiency and can affect infants and the elderly. It causes vascular fragility, inhibited bone and cartilage growth, and hemorrhages. Radiographs show osteopenia, provisional calcification lines, epiphyseal abnormalities, and metaphyseal changes that allow accurate diagnosis.
SKELETAL DYSPLASIA Radiodiagnosis BY ABHIJIT R SINGHDrABHIJITRSINGH
This document discusses skeletal dysplasias, which are a group of genetic disorders that affect bone development. There are over 400 known skeletal dysplasias caused by mutations in over 200 genes. The four most common dysplasias are achondroplasia, osteogenesis imperfecta, achondrogenesis, and thanatophoric dysplasia. These four conditions along with several other lethal skeletal dysplasias are described in detail with their characteristic clinical and radiographic findings. Both lethal and non-lethal conditions affecting the long bones, spine, skull and other bones are outlined.
This document summarizes various metabolic bone diseases and their imaging manifestations. It discusses osteoporosis, rickets, osteomalacia, hypophosphatasia, hyperparathyroidism, renal osteodystrophy, hypoparathyroidism, hypothyroidism, hyperthyroidism, acromegaly, and scurvy. For each condition, it describes the pathophysiology, typical skeletal findings on imaging, and examples of radiographic manifestations. Common findings include generalized osteopenia, vertebral fractures, Looser zones, subperiosteal bone resorption, brown tumors, and osteosclerosis in varying patterns depending on the specific disease process.
radiological features of Mucopolysaccharidosesvik28
This document summarizes the imaging findings in mucopolysaccharidoses (MPS). It describes abnormalities seen in the skeletal system including dysostosis multiplex, thickened skull bones, abnormal sella turcica shape, and abnormalities in the spine, ribs, pelvis and long bones. It also describes brain abnormalities such as white matter lesions, perivascular space enlargement and brain atrophy. Other findings discussed include otitis media, airway obstruction, corneal clouding and joint abnormalities. The purpose is to evaluate the common radiological manifestations of MPS to aid in diagnosis.
Arthritis and arthroplasty- dr. Mahmoud Abdel KareemAhmed-shedeed
This document provides information about osteoarthritis (OA), including its definition, prevalence, risk factors, pathology, diagnosis, natural history, differential diagnosis, and treatment. It notes that OA is the most common form of arthritis, affecting over 20 million people in the US. Risk factors include age, obesity, family history, and previous joint injury or disorder. Diagnosis is typically based on symptoms like pain and stiffness, physical exam findings, and x-ray evidence of cartilage loss, bone spurs, and bone changes. Treatment includes conservative options like medications, exercise, and weight loss, as well as intra-articular injections or surgery for advanced cases.
This document discusses osteopetrosis, also known as marble bone disease, which is a rare hereditary disorder characterized by defective osteoclast function that results in abnormally dense and brittle bones. There are two subtypes: infantile autosomal recessive osteopetrosis, which is more severe and often fatal in childhood, and autosomal dominant osteopetrosis, which is less severe and allows survival into adulthood. The document describes the clinical features, radiographic findings, differential diagnoses, and key features that distinguish osteopetrosis from similar conditions like pyknodysostosis and melorheostosis.
This document discusses osteopetrosis, also known as marble bone disease, which is a rare hereditary disorder characterized by defective osteoclast function that results in abnormally dense and brittle bones. There are two subtypes: infantile autosomal recessive osteopetrosis, which is more severe and often fatal in childhood, and autosomal dominant osteopetrosis, which is less severe and allows survival into adulthood. The document describes the clinical features, radiographic findings, differential diagnoses, and key features that distinguish osteopetrosis from similar conditions like pyknodysostosis and melorheostosis.
This document discusses the classification and types of benign bone tumors. It begins by classifying bone tumors based on their site of origin, such as osteogenic, cartilage, fibrogenic, and others. It then provides details on specific benign bone tumor types including osteochondroma, enchondroma, chondroblastoma, chondromyxoid fibroma, and osteoma. For each tumor type, it discusses etiology, clinical features, radiographic findings, pathology, treatment and recurrence rates.
This document summarizes three conditions - Achondroplasia, Pseudoachondroplasia, and Hypochondroplasia. Achondroplasia is characterized by failure of normal cartilage growth, resulting in short stature and limb abnormalities. Pseudoachondroplasia involves irregular, fragmented epiphyses and flared metaphyses. Hypochondroplasia causes short stature through mild metaphyseal flare and narrowing of the lumbar spine.
A 5-year-old male patient presented with fever, cough and expectoration. Chest x-rays showed consolidation in the left middle and lower lung zones initially. Follow up x-rays 4 days later revealed no lung abnormalities but detected an expansile bony lesion of the right 3rd rib. Differential diagnoses for expansile rib lesions in pediatric patients were provided, including both benign conditions like fibrous dysplasia, aneurysmal bone cyst, and neurofibromatosis, as well as malignant conditions such as Ewing sarcoma. Proper diagnosis and timely treatment of rib lesions are important given the risk of malignancy.
This document discusses fibro-osseous lesions, which replace normal bone with fibrous tissue containing newly formed mineralized structures. It describes several types of fibro-osseous lesions including fibrous dysplasia, cemento-osseous dysplasias like periapical cemental dysplasia, and fibro-osseous neoplasms like ossifying fibroma. For each type, it covers definitions, clinical features, radiographic appearances, differential diagnosis, and treatment approaches.
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This document discusses several benign non-odontogenic tumors of the jaws including fibro-osseous diseases like fibrous dysplasia and cemento-osseous dysplasia, osteoblastoma, osteoma, Langerhans cell histiocytosis, schwannoma, neurofibroma, and Paget's disease. These lesions are described in terms of their etiology, clinical and radiographic features, treatment options, and other relevant characteristics to aid in diagnosis and management.
Inflammatory arthritis can be evaluated through various imaging modalities. Radiography is often the initial study and can demonstrate features like bone erosions, osteopenia, joint space narrowing, and soft tissue swelling that suggest inflammatory arthritis over degenerative changes. Conditions like rheumatoid arthritis are characterized by symmetrical involvement of multiple small and large joints, while ankylosing spondylitis typically affects the sacroiliac joints and spine. Imaging plays an important role in diagnosis and monitoring disease progression and response to treatment.
This document summarizes several congenital bone defects. It describes Ellis VanCreveld syndrome, which causes dwarfism, polydactyly, and dental/nail defects. It also discusses several types of metaphyseal dysplasias that result in abnormal growth plate formation and short stature. Osteopetrosis is described as causing excessive bone density due to osteoclast dysfunction. Craniometaphyseal dysplasia causes thinning of long bones. Other conditions mentioned include osteopathia striata, osteopoikilosis, and melorheostosis. Case studies with images are provided to illustrate the radiographic findings of several of these bone diseases.
D. Firas lecture minimum muhadharaty requirehussainAltaher
This document summarizes various bone imaging techniques and bone pathologies that can be identified on imaging. It discusses radiological techniques for bone imaging including their advantages and disadvantages. It also provides details on identifying characteristics of primary bone tumors like osteosarcoma and chondrosarcoma, metastatic bone lesions, and benign bone conditions including osteoid osteoma, fibrous dysplasia, and aneurysmal bone cyst on imaging studies. Common causes of generalized bone abnormalities such as osteoporosis, rickets/osteomalacia, hyperparathyroidism, and renal osteodystrophy are also summarized.
The document discusses several non-neoplastic bone lesions that can mimic bone tumors including malignant lesions on imaging. These include brown tumors caused by hyperparathyroidism, bone islands, bone infarcts, stress fractures, and post-traumatic osteolysis. Correct diagnosis is important to avoid unnecessary biopsies, as many of these lesions can be diagnosed based on clinical history, lab tests, and characteristic imaging features without biopsy.
This document discusses skeletal changes seen in various blood disorders including thalassemia, sickle cell anemia, and hemophilia. Thalassemia causes bone marrow expansion leading to osteoporosis, cortical thinning, and bone deformities. Sickle cell anemia results in bone infarcts, osteonecrosis, and vertebral endplate abnormalities. Hemophilia produces joint hemorrhages, pseudo-tumors, osteoporosis, and eventual joint destruction. Radiographs are useful for identifying characteristic findings in these inherited bleeding and hemolytic disorders.
The document summarizes diagnostic radiology findings of musculoskeletal infectious diseases and joint disorders. It describes imaging features of acute and chronic osteomyelitis caused by bacteria and tuberculosis including bone destruction, periosteal reaction, and abscess formation. It also compares findings of pyogenic and tuberculous arthritis, noting tuberculosis involves bone margins and causes osteoporosis while pyogenic arthritis affects weight-bearing areas and leads to more bone destruction and sclerosis. Common joint disorders like osteoarthritis, ankylosis, and dislocations are outlined.
The document discusses osteomyelitis, which is an inflammatory condition of bone that begins as an infection of the medullary cavity and spreads to involve the periosteum. It can be acute or chronic, and is caused by bacteria or fungi entering via trauma or a blood-borne route. Symptoms include pain, swelling, and pus drainage. Diagnosis involves medical imaging and biopsy. Treatment involves antibiotics, drainage of pus, debridement of infected tissue, and sometimes surgery. Chronic osteomyelitis can be difficult to treat and may require repeated surgeries. Risk factors include reduced blood supply to bone from conditions like diabetes.
The Indian Dental Academy is the Leader in continuing dental education , training dentists in all aspects of dentistry and
offering a wide range of dental certified courses in different formats.
How to Control Your Asthma Tips by gokuldas hospital.Gokuldas Hospital
Respiratory issues like asthma are the most sensitive issue that is affecting millions worldwide. It hampers the daily activities leaving the body tired and breathless.
The key to a good grip on asthma is proper knowledge and management strategies. Understanding the patient-specific symptoms and carving out an effective treatment likewise is the best way to keep asthma under control.
“Psychiatry and the Humanities”: An Innovative Course at the University of Mo...Université de Montréal
“Psychiatry and the Humanities”: An Innovative Course at the University of Montreal Expanding the medical model to embrace the humanities. Link: https://www.psychiatrictimes.com/view/-psychiatry-and-the-humanities-an-innovative-course-at-the-university-of-montreal
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SKELETAL DYSPLASIA Radiodiagnosis BY ABHIJIT R SINGHDrABHIJITRSINGH
This document discusses skeletal dysplasias, which are a group of genetic disorders that affect bone development. There are over 400 known skeletal dysplasias caused by mutations in over 200 genes. The four most common dysplasias are achondroplasia, osteogenesis imperfecta, achondrogenesis, and thanatophoric dysplasia. These four conditions along with several other lethal skeletal dysplasias are described in detail with their characteristic clinical and radiographic findings. Both lethal and non-lethal conditions affecting the long bones, spine, skull and other bones are outlined.
This document summarizes various metabolic bone diseases and their imaging manifestations. It discusses osteoporosis, rickets, osteomalacia, hypophosphatasia, hyperparathyroidism, renal osteodystrophy, hypoparathyroidism, hypothyroidism, hyperthyroidism, acromegaly, and scurvy. For each condition, it describes the pathophysiology, typical skeletal findings on imaging, and examples of radiographic manifestations. Common findings include generalized osteopenia, vertebral fractures, Looser zones, subperiosteal bone resorption, brown tumors, and osteosclerosis in varying patterns depending on the specific disease process.
radiological features of Mucopolysaccharidosesvik28
This document summarizes the imaging findings in mucopolysaccharidoses (MPS). It describes abnormalities seen in the skeletal system including dysostosis multiplex, thickened skull bones, abnormal sella turcica shape, and abnormalities in the spine, ribs, pelvis and long bones. It also describes brain abnormalities such as white matter lesions, perivascular space enlargement and brain atrophy. Other findings discussed include otitis media, airway obstruction, corneal clouding and joint abnormalities. The purpose is to evaluate the common radiological manifestations of MPS to aid in diagnosis.
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This document provides information about osteoarthritis (OA), including its definition, prevalence, risk factors, pathology, diagnosis, natural history, differential diagnosis, and treatment. It notes that OA is the most common form of arthritis, affecting over 20 million people in the US. Risk factors include age, obesity, family history, and previous joint injury or disorder. Diagnosis is typically based on symptoms like pain and stiffness, physical exam findings, and x-ray evidence of cartilage loss, bone spurs, and bone changes. Treatment includes conservative options like medications, exercise, and weight loss, as well as intra-articular injections or surgery for advanced cases.
This document discusses osteopetrosis, also known as marble bone disease, which is a rare hereditary disorder characterized by defective osteoclast function that results in abnormally dense and brittle bones. There are two subtypes: infantile autosomal recessive osteopetrosis, which is more severe and often fatal in childhood, and autosomal dominant osteopetrosis, which is less severe and allows survival into adulthood. The document describes the clinical features, radiographic findings, differential diagnoses, and key features that distinguish osteopetrosis from similar conditions like pyknodysostosis and melorheostosis.
This document discusses osteopetrosis, also known as marble bone disease, which is a rare hereditary disorder characterized by defective osteoclast function that results in abnormally dense and brittle bones. There are two subtypes: infantile autosomal recessive osteopetrosis, which is more severe and often fatal in childhood, and autosomal dominant osteopetrosis, which is less severe and allows survival into adulthood. The document describes the clinical features, radiographic findings, differential diagnoses, and key features that distinguish osteopetrosis from similar conditions like pyknodysostosis and melorheostosis.
This document discusses the classification and types of benign bone tumors. It begins by classifying bone tumors based on their site of origin, such as osteogenic, cartilage, fibrogenic, and others. It then provides details on specific benign bone tumor types including osteochondroma, enchondroma, chondroblastoma, chondromyxoid fibroma, and osteoma. For each tumor type, it discusses etiology, clinical features, radiographic findings, pathology, treatment and recurrence rates.
This document summarizes three conditions - Achondroplasia, Pseudoachondroplasia, and Hypochondroplasia. Achondroplasia is characterized by failure of normal cartilage growth, resulting in short stature and limb abnormalities. Pseudoachondroplasia involves irregular, fragmented epiphyses and flared metaphyses. Hypochondroplasia causes short stature through mild metaphyseal flare and narrowing of the lumbar spine.
A 5-year-old male patient presented with fever, cough and expectoration. Chest x-rays showed consolidation in the left middle and lower lung zones initially. Follow up x-rays 4 days later revealed no lung abnormalities but detected an expansile bony lesion of the right 3rd rib. Differential diagnoses for expansile rib lesions in pediatric patients were provided, including both benign conditions like fibrous dysplasia, aneurysmal bone cyst, and neurofibromatosis, as well as malignant conditions such as Ewing sarcoma. Proper diagnosis and timely treatment of rib lesions are important given the risk of malignancy.
This document discusses fibro-osseous lesions, which replace normal bone with fibrous tissue containing newly formed mineralized structures. It describes several types of fibro-osseous lesions including fibrous dysplasia, cemento-osseous dysplasias like periapical cemental dysplasia, and fibro-osseous neoplasms like ossifying fibroma. For each type, it covers definitions, clinical features, radiographic appearances, differential diagnosis, and treatment approaches.
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Inflammatory arthritis can be evaluated through various imaging modalities. Radiography is often the initial study and can demonstrate features like bone erosions, osteopenia, joint space narrowing, and soft tissue swelling that suggest inflammatory arthritis over degenerative changes. Conditions like rheumatoid arthritis are characterized by symmetrical involvement of multiple small and large joints, while ankylosing spondylitis typically affects the sacroiliac joints and spine. Imaging plays an important role in diagnosis and monitoring disease progression and response to treatment.
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This document summarizes various bone imaging techniques and bone pathologies that can be identified on imaging. It discusses radiological techniques for bone imaging including their advantages and disadvantages. It also provides details on identifying characteristics of primary bone tumors like osteosarcoma and chondrosarcoma, metastatic bone lesions, and benign bone conditions including osteoid osteoma, fibrous dysplasia, and aneurysmal bone cyst on imaging studies. Common causes of generalized bone abnormalities such as osteoporosis, rickets/osteomalacia, hyperparathyroidism, and renal osteodystrophy are also summarized.
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This guideline is directed principally toward new Molecular Entities that are
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GASTROINTESTINAL INFECTIONS AND GASTRITIS
Osvaldo Bernardo Muchanga
Gastrointestinal Infections
GASTROINTESTINAL INFECTIONS result from the ingestion of pathogens that cause infections at the level of this tract, generally being transmitted by food, water and hands contaminated by microorganisms such as E. coli, Salmonella, Shigella, Vibrio cholerae, Campylobacter, Staphylococcus, Rotavirus among others that are generally contained in feces, thus configuring a FECAL-ORAL type of transmission.
Among the factors that lead to the occurrence of gastrointestinal infections are the hygienic and sanitary deficiencies that characterize our markets and other places where raw or cooked food is sold, poor environmental sanitation in communities, deficiencies in water treatment (or in the process of its plumbing), risky hygienic-sanitary habits (not washing hands after major and/or minor needs), among others.
These are generally consequences (signs and symptoms) resulting from gastrointestinal infections: diarrhea, vomiting, fever and malaise, among others.
The treatment consists of replacing lost liquids and electrolytes (drinking drinking water and other recommended liquids, including consumption of juicy fruits such as papayas, apples, pears, among others that contain water in their composition).
To prevent this, it is necessary to promote health education, improve the hygienic-sanitary conditions of markets and communities in general as a way of promoting, preserving and prolonging PUBLIC HEALTH.
Gastritis and Gastric Health
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2. Several systemic diseases manifest on the
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The diagnosis can be clinched on a single
hand radiograph if characteristic findings are
present.
3. Common indications
Evaluation of the bone age and
Trauma
Systemic hematologic and
Metabolic conditions.
Radiologists interpreting the hand radiograph
can make the diagnosis or direct appropriate
investigations for diagnosis.
6. Congenital/Developmental
Osteopetrosis
rare hereditary and familial bone abnormality
characterized by defective osteoclast function.
Bone remodelling is impaired -thick but
structurally weak and brittle.
generalized increase in bone density with
obliteration of normal trabecular pattern
Marrow is encroached upon and extra-
medullary hematopoiesis occurs.
7.
8.
9. Pyknodysostosis
a rare autosomal recessive disorder
increased bone density with preservation of
medullary canal –no anemia
dwarfism and skeletal fragility.
13. Marfan’s Syndrome
an autosomal dominant entity , affect the body’s
connective tissue.
three systems: skeletal, ocular and cardiovascular.(aortic
aneurysm)
The elongation of tubular bones ,most marked in distal
portion of the extremities-the phalanges, metacarpals
and metatarsals without an increase in width
long, slender and gracile-arachnodactyly or spider-like
fingers.
Radiographically, the metacarpal index is abnormal(8.8 for
males or 8.4 for females)
the skull reveals dolichocephaly. individuals are taller
14. Arachnodactyly in a 16-year-old
girl. Radiograph shows a
metacarpal index of approximately
9.5.
The tubular bones of the hands
(Metacarpals and phalanges) are long,
slender and gracile – Arachnodactyly or
spider-like fingers
15. METAPHYSEAL DYSPLASIAS
ACHONDROPLASIA
Rhizomelic dwarfism with normal trunk, large head, and
midface hypoplasia
Mc nonlethal skeletal dysplasia
○ Findings are evident at birth
PATHOLOGY
Form of chondrodysplasia – Failure of conversion of
cartilage to bone
16. Hands
Trident hand with short, broad,
splayed and cone-shaped
phalanges and shortened
metacarpals
17. Hand radiograph shows approximation of second and
third digits and also the fourth and fifth digits forming the
trident hand appearance.
Tubular bones are short and show coned phalanges.
18. Pseudoachondroplasia
autosomal dominant manner.
It is a form of short-limb dwarfism.
diagnosis is made 2-3 years of age.
the trunk appears long with lumbar lordosis and
rhizomelic shortening of the limbs.
Pseudoachondroplasia have normal head size
and facial features.
Radiographic changes include shortening of
tubular bones, flaring of metaphyses, variable
epiphyseal maldevelopment and some degree of
vertebral end-plate malformation
19. four yr old boy
Short metacarpals with metaphyseal cupping
short and stubby phalangeal bones
delayed ossification of the small and irregular carpal bones
20. Chondrodysplasia punctata,
brachytelephalangic
subtype (CDP-BT)
rare congenital disorders caused by peroxisomal
dysfunction.
-erratic cartilage calcification within apophyses and
epiphyses,
carpal and tarsal bones, vertebrae and cartilages of the
trachea and bronchi.
types of chondrodysplasia punctata include autosomal-
dominant (non-rhizomelic, non-lethal)
autosomal-recessive (rhizomelic, lethal type) and rare x-
linked dominant and recessive forms.
21. short triangular-shaped distal phalanges suggestive of
brachytelephalangy.
The fifth middle phalanx is small with clinodactyly.
The metacarpals are relatively small.
22. Sickle cell disease
autosomal-recessive hemoglobinopathy
caused by formation of a defective hemoglobin
called hemoglobin S (Hb S).
Pathology -Bone infarcts in the diaphyses of
small tubular bones in the hands and feet
Age (from 6 months to 3 years) are called
sickle cell dactylitis or hand-foot syndrome
caused by the presence of red marrow in
these regions
23. Hand radiograph shows
cortical thickening, and metaphyseal
cupping involving the proximal phalanx of
the third digit.
Findings are in keeping with prior
infarction
24. Thalassemia
hereditary disorders caused by genetic
deficiency in the synthesis of beta-globin
chains of hemoglobin.
Excess unpaired alpha-chains aggregate to
form precipitates that cause hemolysis.
Erythroid hyperplasia causes medullary
expansion within the bones. Extramedullary
hematopoiesis
25. Hand radiograph shows expansion,
groundglass appearance,
lace-like thin trabeculae and
thin cortex involving
predominantly metacarpals, in keeping with
medullary expansion
26. Inflammatory joint disease
This is characterized by bone erosions,
osteopenia, soft-tissue swelling and uniform,
symmetric joint space loss.
Inflammation of a single joint should raise
concern for infection.
27. Infective/Inflammatory
Disorders.
Tubercular Dactylitis/Spina Ventosa
Dactylytis is an inflammatory disorder of the
digit (hand or foot)
seronegative arthropathies-psoriatic
arthropathy and ankylosing spondylitis,
sickle cell disease
infectious conditions -tuberculosis and leprosy.
Tuberculous dactylytis -as a painless swelling
in the hand or foot.
28. Plain radiograph-
diaphyseal lytic lesion, either round and cystic
with a variable amount of sclerosis and minimal
periostitis
Sickle cell dactylytis may present silently or with a
painful bone crisis,
radiographs in young children similarly show
diaphyseal lytic lesions within the tubular bones of
the hands or feet. Periostitis is uncommon.
29. Radiograph of the little finger of the right
hand -a rounded lucency in the proximal
phalanx of a child. There is minimal
periostitis.
30. Gout
crystal deposition arthropathy caused by the
deposition of monosodium urate crystals
(tophi)
Presentation -the acute phase with soft tissue
swelling and joint effusion.
chronic tophaceous phase (6-12 years after
the initial attack) with eccentric asymmetrical
nodular tophi within the synovium and
subchondral bone.
31. Plain radiograph
Bony erosions may be intra-articular, peri-
articular or distinct from the joint with a
rounded or ‘punched out’ appearance.
The erosion margins are typically thin and
sclerotic with a raised, overhanging, cortical
lip, giving a ‘rat bite’ appearance.
This characteristic late finding is caused by
peri-articular tophaceous nodules and erosion.
osteopaenia is seen until late in the disease.
32. Radiograph of the index and middle finger
of the right hand showing
periarticular soft tissue swellings (arrows
A) and
eccentric ‘punched out’ lytic bone erosions
with thin sclerotic margins and overhanging
edges (arrows B).
There is preservation of the
interphalangeal joint spaces and absence
of periarticular demineralisation (features
that respectively help to differentiate gout
from psoriatic or rheumatoid arthropathy
35. Rheumatoid arthritis
chronic systemic connective tissue disease
principally involving synovial joints
hands and wrists are a focal target area.
Typical features -symmetrical,
deforming polyarthropathy, -proximal joints:
the distal radio-ulnar joint (especially the ulnar
styloid),
radio-carpal, mid-carpal and the
metacarpophalangeal joints.
Most patients have radiological evidence of
erosions by three years .
36. Right hand radiograph -proximal
osteoarthropathy and
ulnar subluxation of the 5th
metacarpophalangeal joint.
Peri-articular osteoporosis, marginal bone
erosions and subluxations.
37. Progressive narrowing of a joint in
rheumatoid arthritis.
(A) Y ear 1. The
metacarpophalangeal joint
looks normal.
(B) Y ear 3. There is
narrowing of the
metacarpophalangeal joint of the
index finger with associated
local soft-tissue swelling. Erosive
change is demonstrated at the
metacarpal head.
(C) Y ear 4. Little change over the
year.
(D) Y ear 13. On
this late film the soft tissues
remain thickened. The joint space
is obliterated.
Erosive change is demonstrated,
especially at the metacarpal head
38. Obliteration of the medullary cavity of the
distal phalanges .
The new bone is very dense and well
defined. The change is especially marked
at little and ring fingers.
39. Left wrist radiograph –
concentric joint space narrowing and
fusion of the carpal bones of the left
wrist (late signs).
changes in the ulna styloid and distal
radioulnar joint (early signs).
40.
41. Gross rheumatoid arthritis at the carpus
with ulnar deviation,
subluxation and joint narrowing at the
metacarpophalangeal joints.
42.
43. Psoriatic arthritis
common seronegative spondyloarthropathy which affects
20% of patients with psoriasis.
characterised by -inflammatory arthritis, a predilection for the
distal joints of the hands and feet.
Erosions tend to occur at the margins of the distal
interphalangeal -such that the terminal phalanx may sit at an
angle resembling a pencil resting in a cup.
Bone proliferation is also a feature;
periostitis -phalanges, bilateral and asymmetrical, associated
with soft tissue swelling giving rise to the typical ‘sausage
digit’ appearance.
Occasionally acroosteolysis of the distal phalanx is also
seen. Bone mineral density is preserved.
44. Right index finger radiograph shows
distal interphalangeal joint erosion with
characteristic ‘pencil in cup’ deformity, (ill-
defined erosion with adjacent periosteal
new bone formation).
45. Left middle finger radiograph of the same
patient shows
distal interphalangeal joint erosion
new bone formation at the distal phalanx
(arrows).
Soft tissue swelling of the digit ‘sausage
digit’ is also noted.
46. Erosive osteoarthritis
Key findings
Arthropathy with the age of onset and
distribution of osteoarthritis, with an
inflammatory and erosive component.
Clinical
Inflammatory form of osteoarthritis of the hand
Affects the DIP and PIP joints and the first
carpometacarpal joint of the hand most
frequently, just like osteoarthritis.
47. Radiological findings
Articular: joint space narrowing
Bone: sclerosis, productive bony changes with
osteophyte formation, ankylosis
Cartilage: subchondral central erosions
Distribution: see illustration. Same distribution as with
osteoarthritis, with a preference for the IP joints (DIP
more than PIP)
Extra findings: occurs primarily in postmenopausal
women
Soft tissue: rheumatoid arthritis-like proliferative intra
articular synovitis, soft tissue swelling around the joint
48. Erosive changes of PIP 2-5 and DIP 3-
5.
Typical gullwing deformity in DIP 3
(white arrow).
49. Ball catcher view of the hands in a patient
with erosive osteoarthritis.
There is bilateral extensive damage to the
IP joints.
.
50. Dermatomyositis
autoimmune inflammatory myopathy, with
diffuse nonsuppurative inflammation of striated
muscle and skin.
female m/c
c/f -gradual onset muscle weakness, elevated
muscle enzymes and elevated myositis-
specific antibodies, (anti-Jo-1).
swelling of the distal joints of the hands
51. Radiographic features include
cutaneous calcific deposits (40%), and
rarely, acro-osteolysis (more common in
scleroderma).
The calcific deposits are usually more ‘linear,
reticular and lacy’, and more widespread than
those seen in scleroderma (5).
found in the soft tissues of extremities as well as
overlying large joints, chest and abdominal wall
(especially in younger patients).
Unlike scleroderma, osteopaenia is not a feature.
52. Radiograph of the index finger of the right
hand showing confluent digital soft tissue
calcifications. No peri-articular erosions.
53. Endocrinal and nutritional/metabolic
disorders.
Acromegaly
adulthood, excessive growth hormone secretion
from a pituitary eosinophilic adenoma -growth of
intramembranous bone tissue and subcutaneous
hypertrophy.
prominent in hands and feet (Acral parts) from
which the term acromegaly is derived.
Heel pad thickness is greater than 20mm.
A reliable indicator is the generalized increase in
joint space width owing to cartilage overgrowth.
54. Radiographs may reveal osseous enlargement,
presenting with ‘spade-like’ hands and
widening of the terminal phalangeal tufts, giving
an ‘arrow-head’ appearance
Other features in the hand may include prominent
muscle attachments and widened joint spaces
(due to cartilage hypertrophy).
Generalised osteoporosis and cystic changes in
the carpal bones are also described.
55. Radiograph of the left hand showing
widening of the terminal phalangeal tufts
with a ‘arrow-head’ appearance.
The hand is enlarged and soft tissue
swelling is noted
56. Hyperparathyroidism
uncontrolled production of parathyroid hormone which usually leads
to an increase in serum alkaline phosphatase and calcium and a
decrease in serum phosphate.
Bone pain and tenderness may be the presenting features.
Hand radiographs often show osteopaenia and bone
demineralisation.
The most pathognomic finding however is subperiosteal bone
resorption. -radial aspect of the middle phalanges of the index and
middle fingers.
Early findings are of proximal metaphyseal cortical irregularity.
Chronic features include spiculated cortical scalloping (may involve
the entire digit),
acro-osteolysis
in rare cases, lytic lesions caused by accumulations of osteoclastic
giant cells known as ‘brown tumours.’
57. Radiograph of the index finger of the right
hand showing
subperiosteal bone resorption of the radial
aspect of the entire digit but particularly
affecting the middle phalanx.
58. Radiograph of the middle finger showing
more developed features of
hyperparathyroidism including acro-
osteolysis
coarse spiculated cortical reaction (B). This
involves the entire digit but is more marked
on the radial aspect.
59. Radiograph showing
subperiosteal
resorption of the radial margins
of the proximal
and middle phalanges of the
second and third digits.
Central, slightly expansile,
septated,
lytic lesion is seen in proximal
end of the fifth metacarpal
(Brown tumour)
60. Thyroid acropachy
Acropachy (‘thickening of the extremities’)
occurs as one of the extra-thyroid
manifestations of auto-immune thyroid
disease.
Graves’ disease, Hashimoto’s thyroiditis .
seen in patients treated with radioiodine
ablation for hyperthyroidism-common in
smokers.
61. Solid periosteal new bone formation usually
bilateral, relatively symmetric and painless,
and involves the diaphyseal tubular bones of
the hands and feet.
62. Radiograph of the right hand showing
thick ‘feathery’ periosteal reaction of the
index and middle fingers.
The mid-portions of the diaphyses are
typically affected.
63. Rickets- vitamin D deficiency
decreased mineralization at the growth plate
resulting in growth retardation and delayed
skeletal maturation.
Defective mineralization of trabecular bone is
called osteomalacia.
Rickets can only be seen in children before
closure of growth plates, while osteomalacia
can occur at any age
64. Radiological features -widening, cupping and
fraying of metaphyses, craniotabes
bowing of long bones, genu valgum, scoliosis,
triradiatepelvis, rachitic rosary and periosteal
reaction. Knees, wristsmand ankles are
affected predominantly.
65. Hand radiograph shows
widening, cupping, and
fraying of distal metaphyses of
the ulna and radius.
There is reduction in bone
density with prominence of
trabeculae and thinning of cortex.
Findings are typical for rickets.
Follow-up radiograph 3 weeks after
initiation of
vitamin D therapy shows dense
metaphyseal band of provisional zone
of calcification (arrows), suggestive of
healing rickets
66. Miscellaneous
Hypertrophic Osteoarthropathy
triad of digital clubbing, symmetric arthritis and
periostitis -visceral disorder, usually intrathoracic
in location.
MC males in 4th-6th decades.
MC is hypertrophic pulmonary osteoarthropathy
(HPOA), a paraneoplastic syndrome secondary to
carcinoma of the lung
Radiographs show bilateral, symmetric, linear
periostitis (most common in the tibia, fibula, radius
and ulna), joint effusions, digital clubbing visible
as a bulbous enlargement of the distal fingertips
67. Radiograph of the ring finger of the left
hand
widespread irregular periosteal proliferation
of the phalanges (arrows).
There is cortical thickening without
narrowing of the medulla.
.
68. Radiograph of the right thumb shows
smooth laminar periosteal
proliferation of the proximal
metacarpal (arrows).
Mc site of hand involvement is the
ulnar aspect, peri-metaphyseal region
of the proximal phalanx.
69. Scleroderma (or Progressive
Systemic Sclerosis
multi-system connective tissue disorder of
unknown aetiology.
Musculoskeletal symptoms -fatigue and myalgia
accompanying arthralgia.
hand radiographs will show absorption of the
distal phalangeal tuft (acro-osteolysis).
The result is thinning of the bone distally. Peri-
articular osteopaenia and erosions are typical.
Subcutaneous calcifications are also seen,
particularly on the extensor surfaces of the hands.
70. Radiograph of the radial aspect of the right
hand shows acro-osteolysis of the
phalangeal tufts (arrow A), and soft tissue
calcifications (arrow B).
There is peri-articular osteopaenia.
Additionally, erosions are commonly seen
at the interphalangeal and
metacarpophalangeal joints.
71. references
RADIOLOGY OF HAND-MIRROR OF
VARIOUS SYSTEMIC DISEASES Sadashiva
Gowda H1
Twenty classic hand radiographs that lead to
diagnosis Govind B. Chavhan & Elka Miller &
Erika H. Mann .
Sutton