1) Heterotopic ossification is the formation of bone in soft tissues where bone is not normally present, usually occurring after injury or surgery.
2) It has three stages - early inflammatory phase with swelling, intermediate consolidation phase with calcification visible on x-rays, and late maturation phase where the bone hardens.
3) Risk factors include trauma, surgery, burns, and genetic conditions. It most commonly occurs around the elbow and hip.
4) Excision surgery aims to remove the ectopic bone, with different approaches depending on the location. Prophylaxis with indomethacin or radiation can decrease rates of recurrence after hip surgery.
Myositis ossificans is a condition where bone forms within muscle tissue, caused by severe trauma or repetitive minor injuries. There are two main types: traumatic myositis ossificans typically affects young males around the elbow, thigh, or hip joints, while myositis ossificans progressiva is a rare genetic disorder causing progressive bone growth in soft tissue from a young age. Diagnosis involves x-rays or MRI to detect the characteristic zonal ossification. Treatment focuses on rest, immobilization, and NSAIDs for traumatic cases or steroids and other medications to reduce flare-ups for the progressive form.
Morton's neuroma is a compressive neuropathy of the interdigital nerve in the forefoot caused by compression at the plantar aspect of the transverse intermetatarsal ligament. It commonly occurs between the second and third metatarsal bones and affects middle-aged women. Non-surgical treatments include wider shoes, padding, anti-inflammatories, and injections, but surgery may be required if conservative measures fail.
Heterotopic ossification (HO) is the formation of bone in soft tissues near a joint. It commonly occurs after injuries like traumatic brain or spinal cord injuries. Risk factors include older age, complete neurological lesions, male gender, and spasticity. While the exact cause is unknown, damage to sympathetic nerves may increase blood flow and promote HO. Diagnosis involves imaging like bone scans and x-rays. Treatment includes NSAIDs, bisphosphonates, radiation, surgery if limiting range of motion, and physical therapy to preserve joint mobility. Rehabilitation follows phases focusing on edema control, range of motion, and returning to prior activity levels.
Charcot joint or neuropathic joint are destructed joint occurs in Diabetes, syphilis, syringomyelia , leprosy, AMLS, Peripheral neuropathy and any condition leads to impair sensation of peripheral part of body
Myositis ossificans, now known as heterotopic ossification (HO), refers to the formation of bone within muscle or soft tissue. There are several classifications of HO, including heterotopic ossification per se, traumatic HO, neurogenic HO, and fibrodysplasia ossificans progressiva. Traumatic HO most commonly develops after musculoskeletal injuries and surgery and can lead to joint stiffness and loss of function. Neurogenic HO occurs after spinal cord or brain injuries. Fibrodysplasia ossificans progressiva is a rare genetic condition characterized by progressive HO.
Volkmann's ischemic contracture is caused by compartment syndrome leading to muscle and nerve necrosis in the forearm. It is characterized by contractures and neurological deficits. The condition typically results from untreated injuries that increase forearm compartment pressure, blocking blood flow. Clinical signs include pain, paresthesia, loss of pulses, and contractures. Treatment involves urgent fasciotomy to release pressure if compartment syndrome is present. Established contractures may be treated conservatively or with muscle sliding procedures like Inglis-Cooper or Williams-Haddad to release contracted flexor muscles and tendons.
This document discusses complex regional pain syndrome (CRPS), formerly known as reflex sympathetic dystrophy. It defines CRPS as a multi-symptom syndrome that usually affects one or more extremities and is characterized by disproportionate pain, vasomotor instability, trophic skin changes, and regional osteoporosis. Trauma is a common precipitating factor. Management involves a multidisciplinary approach including physical therapy, medications to relieve symptoms, and in some cases surgical or injection-based treatments.
This document summarizes rheumatoid hand deformities. It begins by describing the pathology of rheumatoid arthritis which principally affects synovial joints and tendon sheaths, destroying ligaments and tendons. This can lead to several hand deformities including ulnar deviation of fingers, swan neck deformity of the fingers, andboutonniere deformity. Deformities of the thumb can also occur. Late stage deformities involve destruction of joints of the wrist and fingers. Several classification systems are provided to characterize the various deformities.
Myositis ossificans is a condition where bone forms within muscle tissue, caused by severe trauma or repetitive minor injuries. There are two main types: traumatic myositis ossificans typically affects young males around the elbow, thigh, or hip joints, while myositis ossificans progressiva is a rare genetic disorder causing progressive bone growth in soft tissue from a young age. Diagnosis involves x-rays or MRI to detect the characteristic zonal ossification. Treatment focuses on rest, immobilization, and NSAIDs for traumatic cases or steroids and other medications to reduce flare-ups for the progressive form.
Morton's neuroma is a compressive neuropathy of the interdigital nerve in the forefoot caused by compression at the plantar aspect of the transverse intermetatarsal ligament. It commonly occurs between the second and third metatarsal bones and affects middle-aged women. Non-surgical treatments include wider shoes, padding, anti-inflammatories, and injections, but surgery may be required if conservative measures fail.
Heterotopic ossification (HO) is the formation of bone in soft tissues near a joint. It commonly occurs after injuries like traumatic brain or spinal cord injuries. Risk factors include older age, complete neurological lesions, male gender, and spasticity. While the exact cause is unknown, damage to sympathetic nerves may increase blood flow and promote HO. Diagnosis involves imaging like bone scans and x-rays. Treatment includes NSAIDs, bisphosphonates, radiation, surgery if limiting range of motion, and physical therapy to preserve joint mobility. Rehabilitation follows phases focusing on edema control, range of motion, and returning to prior activity levels.
Charcot joint or neuropathic joint are destructed joint occurs in Diabetes, syphilis, syringomyelia , leprosy, AMLS, Peripheral neuropathy and any condition leads to impair sensation of peripheral part of body
Myositis ossificans, now known as heterotopic ossification (HO), refers to the formation of bone within muscle or soft tissue. There are several classifications of HO, including heterotopic ossification per se, traumatic HO, neurogenic HO, and fibrodysplasia ossificans progressiva. Traumatic HO most commonly develops after musculoskeletal injuries and surgery and can lead to joint stiffness and loss of function. Neurogenic HO occurs after spinal cord or brain injuries. Fibrodysplasia ossificans progressiva is a rare genetic condition characterized by progressive HO.
Volkmann's ischemic contracture is caused by compartment syndrome leading to muscle and nerve necrosis in the forearm. It is characterized by contractures and neurological deficits. The condition typically results from untreated injuries that increase forearm compartment pressure, blocking blood flow. Clinical signs include pain, paresthesia, loss of pulses, and contractures. Treatment involves urgent fasciotomy to release pressure if compartment syndrome is present. Established contractures may be treated conservatively or with muscle sliding procedures like Inglis-Cooper or Williams-Haddad to release contracted flexor muscles and tendons.
This document discusses complex regional pain syndrome (CRPS), formerly known as reflex sympathetic dystrophy. It defines CRPS as a multi-symptom syndrome that usually affects one or more extremities and is characterized by disproportionate pain, vasomotor instability, trophic skin changes, and regional osteoporosis. Trauma is a common precipitating factor. Management involves a multidisciplinary approach including physical therapy, medications to relieve symptoms, and in some cases surgical or injection-based treatments.
This document summarizes rheumatoid hand deformities. It begins by describing the pathology of rheumatoid arthritis which principally affects synovial joints and tendon sheaths, destroying ligaments and tendons. This can lead to several hand deformities including ulnar deviation of fingers, swan neck deformity of the fingers, andboutonniere deformity. Deformities of the thumb can also occur. Late stage deformities involve destruction of joints of the wrist and fingers. Several classification systems are provided to characterize the various deformities.
This document discusses the sequelae and management of septic arthritis. Septic arthritis results in inflammation and destruction of the joint space. This can lead to several orthopedic sequelae including joint destruction, bony or fibrous ankylosis, fractures, limb length discrepancy, and persistent infection. The management depends on factors like the patient's age, delay in treatment, and extent of joint involvement. Treatment may include conservative measures, surgical stabilization, deformity correction, lengthening procedures, or arthrodesis to achieve a stable, mobile joint without pain. Classification systems help guide treatment, with the goal of optimizing long term function and quality of life.
The document discusses knee instability and describes the structure of the knee including the osseous, extra-articular, and intra-articular structures. It provides details on the menisci, ligaments including the ACL and PCL, and muscles. The document also covers causes of meniscal injuries, diagnostic tests, treatment options including non-operative treatment and surgical procedures like meniscectomy and repair.
This document discusses congenital vertical talus (CVT), a rare foot deformity. It begins by defining CVT and providing background information. It then describes the anatomy and pathoanatomy of CVT. Key points include that CVT results in an almost vertical talus bone and rigid flatfoot deformity. Treatment involves serial casting and manipulation to prepare for surgery, with the goal of restoring normal anatomical relationships in the foot. Surgical techniques described include open reduction and percutaneous fixation of the talonavicular joint with K-wires. Complications of surgery can include wound issues and stiffness.
Jean-Martin Charcot first described neuropathic arthropathy in 1868. It is a progressive joint condition characterized by dislocations, fractures, and deformities that results from sensory or autonomic neuropathy from various conditions like diabetes, MS, alcoholism, etc. The pathophysiology involves both repetitive microtrauma from loss of sensation and an inflammatory process induced by neurovascular changes. It commonly affects the foot, knee, and hip. Diagnosis is made clinically and radiographically, showing features like joint destruction and deformity. Treatment involves casting, bracing, and surgery like fusion for advanced cases.
This document discusses the anatomy and clinical assessment of the rotator cuff. It describes the four muscles that make up the rotator cuff, their innervation and attachments. Common rotator cuff injuries like impingement syndrome and ruptures are explained. The physical exam involves assessing range of motion and performing special tests like Neer's, Hawkins-Kennedy, and lift-off to identify injuries.
A Lisfranc injury involves fracture or ligament disruption of the tarsometatarsal joint complex of the midfoot. It results from high-energy twisting or axial loading injuries and often requires surgical fixation to achieve proper anatomical reduction. Non-operative treatment may be considered for non-displaced or minimally displaced injuries. Proper diagnosis involves weight-bearing radiographs to assess joint congruity, and sometimes CT or MRI. Surgical management focuses on anatomical reduction and stable fixation of the joints to allow early weight bearing and prevent post-traumatic arthritis.
CORA (center of rotation of angulation)Morshed Abir
This document discusses the concept of the center of rotation of angulation (CORA) in orthopedic surgery. The CORA is the point about which a deformed bone may be rotated to achieve correction of an angular deformity without introducing a translational deformity. Proper identification of the CORA allows selection of the optimal correction axis and type of osteotomy, such as opening, closing, or dome osteotomy, to realign the bone. Correction along the bisector line passing through the CORA ensures pure angular correction without residual translation. Identification of multiple CORAs indicates more complex multi-apical or translational deformities requiring different surgical techniques.
The document provides information on anterior cruciate ligament (ACL) injuries, including:
1. The ACL originates from the femur and inserts into the tibia, resisting anterior tibial translation and medial rotation. ACL injuries most commonly result from rapid changes in direction during sports.
2. Physical examination of ACL injuries involves tests like the Lachman test and anterior drawer test to assess knee stability. MRI is also used for diagnosis.
3. Treatment involves RICE initially, followed by either nonsurgical rehabilitation with bracing or surgical reconstruction using grafts like the patellar tendon. Reconstruction aims to restore stability and function to prevent further knee damage.
This document provides an overview of hallux valgus, including its anatomy, causes, symptoms, diagnosis, and treatment options. Key points include:
- Hallux valgus is a lateral deviation of the great toe and medial deviation of the first metatarsal. It can cause pain over the bunion.
- Risk factors include heredity, footwear, ligament laxity, and pes planus. Diagnosis involves examining range of motion, deformity, and taking x-rays to measure angles.
- Treatment progresses from footwear modifications and stretching to various surgical procedures depending on severity, including distal soft tissue procedures, osteotomies, and joint fusion or replacement in severe cases.
Rotator cuff tear is a very common orthopedic condition, which causes shoulder pain and stiffness. The slides are on rotator cuff tears and its management by open repair, mini open repair & by arthroscopy
Loose bodies are fragments of bone or cartilage that float freely in the joint space, causing symptoms like knee pain, swelling, and locking. They are classified as stable or unstable. Individuals with joint diseases like arthritis are more at risk, as are athletes. Loose bodies are diagnosed by x-ray, CT, MRI or arthrography. Treatment options include NSAIDs, arthroscopic removal of large loose bodies, or open surgery. The focus of rehabilitation is controlling pain and restoring function through gait training and avoiding prolonged immobilization.
Morton's neuroma is a common foot condition that causes pain in the ball of the foot, usually between the third and fourth toes. It occurs when a nerve in the foot is compressed, causing pain, numbness, and tingling. Symptoms include pain that gets worse with walking and is relieved by removing shoes. Treatments may include shoe inserts, steroid injections, and surgery. The condition is often caused by wearing narrow, tight shoes that squeeze the toes together.
This document provides an overview of traumatic paraplegia and spinal cord injury. It discusses the classification, epidemiology, mechanisms of injury, assessment, diagnostic modalities, management of complications like bladder dysfunction, and considerations for thoracolumbar injuries. Key points include that spinal cord injury results in changes to motor, sensory or autonomic function, most injuries occur in the cervical spine from motor vehicle accidents in young males, and diagnostic workup involves plain films, CT scans and potentially MRI to evaluate injury extent and neurological status.
This document provides an overview of clubfoot (congenital talipes equinovarus), including:
1. The definition, incidence, causes, and typical deformities seen in clubfoot.
2. Evaluation methods like the Pirani scoring system and radiographic assessment.
3. Treatment approaches like the Ponseti method of serial casting and bracing, as well as surgical options like the McKay procedure when non-operative treatment fails.
4. Post-operative casting protocols and complications that can arise from treatment.
Trigger finger is a condition where the finger or thumb gets stuck when bent, caused by inflammation of the tendons. Symptoms include a tender lump, catching, and pain when bending the finger. It is often caused by repetitive motions and can be treated with rest, splinting, corticosteroid injections, or surgery to release the tendon sheath if other treatments don't help. Recovery from surgery usually takes a few weeks but may be up to 6 months to fully resolve swelling and stiffness.
This document defines and discusses pigmented villonodular synovitis (PVNS), a benign tumor of the synovium. It most commonly affects large joints like the knee and hip in adults. While the exact cause is unknown, repetitive trauma is thought to play a role in many cases. PVNS can be either localized or diffuse. Treatment involves complete synovectomy, which can be performed either arthroscopically or via open surgery, with the goal of removing all affected synovial tissue. Radiation therapy may also be used in some cases. Prognosis is generally good for localized PVNS but recurrence is more common when disease is diffuse.
This document provides an overview of Monteggia fracture dislocations, beginning with definitions, history, epidemiology, classification, mechanisms of injury, clinical features, management, complications, and recent updates. Monteggia fractures, first described in 1814, constitute 1-2% of forearm fractures. Bado's 1958 classification divides them into four types based on the direction of radial head dislocation and location of the ulna fracture. Type I is the most common, involving anterior radial head dislocation and ulna fracture. Nonoperative treatment typically involves closed reduction and casting, while surgery is indicated for failed reductions. Complications can include nerve injuries, ossification, and compartment syndrome.
This document discusses myositis ossificans, a condition where bone forms in muscle tissue or other soft tissues. It presents two main types - non-hereditary myositis ossificans, which usually occurs after trauma in adolescents and young adults, and myositis ossificans progressiva (also called fibrodysplasia ossificans progressiva or stone man syndrome), a rare genetic disorder where muscle and connective tissues are gradually replaced by bone. The document outlines the etiology, clinical features, diagnosis, histopathology, and treatment of both conditions. Surgical excision may be indicated if the condition causes intolerable pain, neurological compression, or limited range of motion.
This document discusses the evaluation and treatment of temporomandibular joint disorders (TMDs). It begins by outlining the most common causes of TMDs, which are muscular disorders like myofascial pain. It then describes how to evaluate patients through history, examination, and various radiographic imaging techniques. Key findings on imaging include conditions like disc displacement, degenerative joint disease, and arthritis. The document concludes by discussing reversible conservative treatments like splint therapy and medications, as well as surgical options for issues like ankylosis, hypermobility, and internal derangements.
This document discusses the sequelae and management of septic arthritis. Septic arthritis results in inflammation and destruction of the joint space. This can lead to several orthopedic sequelae including joint destruction, bony or fibrous ankylosis, fractures, limb length discrepancy, and persistent infection. The management depends on factors like the patient's age, delay in treatment, and extent of joint involvement. Treatment may include conservative measures, surgical stabilization, deformity correction, lengthening procedures, or arthrodesis to achieve a stable, mobile joint without pain. Classification systems help guide treatment, with the goal of optimizing long term function and quality of life.
The document discusses knee instability and describes the structure of the knee including the osseous, extra-articular, and intra-articular structures. It provides details on the menisci, ligaments including the ACL and PCL, and muscles. The document also covers causes of meniscal injuries, diagnostic tests, treatment options including non-operative treatment and surgical procedures like meniscectomy and repair.
This document discusses congenital vertical talus (CVT), a rare foot deformity. It begins by defining CVT and providing background information. It then describes the anatomy and pathoanatomy of CVT. Key points include that CVT results in an almost vertical talus bone and rigid flatfoot deformity. Treatment involves serial casting and manipulation to prepare for surgery, with the goal of restoring normal anatomical relationships in the foot. Surgical techniques described include open reduction and percutaneous fixation of the talonavicular joint with K-wires. Complications of surgery can include wound issues and stiffness.
Jean-Martin Charcot first described neuropathic arthropathy in 1868. It is a progressive joint condition characterized by dislocations, fractures, and deformities that results from sensory or autonomic neuropathy from various conditions like diabetes, MS, alcoholism, etc. The pathophysiology involves both repetitive microtrauma from loss of sensation and an inflammatory process induced by neurovascular changes. It commonly affects the foot, knee, and hip. Diagnosis is made clinically and radiographically, showing features like joint destruction and deformity. Treatment involves casting, bracing, and surgery like fusion for advanced cases.
This document discusses the anatomy and clinical assessment of the rotator cuff. It describes the four muscles that make up the rotator cuff, their innervation and attachments. Common rotator cuff injuries like impingement syndrome and ruptures are explained. The physical exam involves assessing range of motion and performing special tests like Neer's, Hawkins-Kennedy, and lift-off to identify injuries.
A Lisfranc injury involves fracture or ligament disruption of the tarsometatarsal joint complex of the midfoot. It results from high-energy twisting or axial loading injuries and often requires surgical fixation to achieve proper anatomical reduction. Non-operative treatment may be considered for non-displaced or minimally displaced injuries. Proper diagnosis involves weight-bearing radiographs to assess joint congruity, and sometimes CT or MRI. Surgical management focuses on anatomical reduction and stable fixation of the joints to allow early weight bearing and prevent post-traumatic arthritis.
CORA (center of rotation of angulation)Morshed Abir
This document discusses the concept of the center of rotation of angulation (CORA) in orthopedic surgery. The CORA is the point about which a deformed bone may be rotated to achieve correction of an angular deformity without introducing a translational deformity. Proper identification of the CORA allows selection of the optimal correction axis and type of osteotomy, such as opening, closing, or dome osteotomy, to realign the bone. Correction along the bisector line passing through the CORA ensures pure angular correction without residual translation. Identification of multiple CORAs indicates more complex multi-apical or translational deformities requiring different surgical techniques.
The document provides information on anterior cruciate ligament (ACL) injuries, including:
1. The ACL originates from the femur and inserts into the tibia, resisting anterior tibial translation and medial rotation. ACL injuries most commonly result from rapid changes in direction during sports.
2. Physical examination of ACL injuries involves tests like the Lachman test and anterior drawer test to assess knee stability. MRI is also used for diagnosis.
3. Treatment involves RICE initially, followed by either nonsurgical rehabilitation with bracing or surgical reconstruction using grafts like the patellar tendon. Reconstruction aims to restore stability and function to prevent further knee damage.
This document provides an overview of hallux valgus, including its anatomy, causes, symptoms, diagnosis, and treatment options. Key points include:
- Hallux valgus is a lateral deviation of the great toe and medial deviation of the first metatarsal. It can cause pain over the bunion.
- Risk factors include heredity, footwear, ligament laxity, and pes planus. Diagnosis involves examining range of motion, deformity, and taking x-rays to measure angles.
- Treatment progresses from footwear modifications and stretching to various surgical procedures depending on severity, including distal soft tissue procedures, osteotomies, and joint fusion or replacement in severe cases.
Rotator cuff tear is a very common orthopedic condition, which causes shoulder pain and stiffness. The slides are on rotator cuff tears and its management by open repair, mini open repair & by arthroscopy
Loose bodies are fragments of bone or cartilage that float freely in the joint space, causing symptoms like knee pain, swelling, and locking. They are classified as stable or unstable. Individuals with joint diseases like arthritis are more at risk, as are athletes. Loose bodies are diagnosed by x-ray, CT, MRI or arthrography. Treatment options include NSAIDs, arthroscopic removal of large loose bodies, or open surgery. The focus of rehabilitation is controlling pain and restoring function through gait training and avoiding prolonged immobilization.
Morton's neuroma is a common foot condition that causes pain in the ball of the foot, usually between the third and fourth toes. It occurs when a nerve in the foot is compressed, causing pain, numbness, and tingling. Symptoms include pain that gets worse with walking and is relieved by removing shoes. Treatments may include shoe inserts, steroid injections, and surgery. The condition is often caused by wearing narrow, tight shoes that squeeze the toes together.
This document provides an overview of traumatic paraplegia and spinal cord injury. It discusses the classification, epidemiology, mechanisms of injury, assessment, diagnostic modalities, management of complications like bladder dysfunction, and considerations for thoracolumbar injuries. Key points include that spinal cord injury results in changes to motor, sensory or autonomic function, most injuries occur in the cervical spine from motor vehicle accidents in young males, and diagnostic workup involves plain films, CT scans and potentially MRI to evaluate injury extent and neurological status.
This document provides an overview of clubfoot (congenital talipes equinovarus), including:
1. The definition, incidence, causes, and typical deformities seen in clubfoot.
2. Evaluation methods like the Pirani scoring system and radiographic assessment.
3. Treatment approaches like the Ponseti method of serial casting and bracing, as well as surgical options like the McKay procedure when non-operative treatment fails.
4. Post-operative casting protocols and complications that can arise from treatment.
Trigger finger is a condition where the finger or thumb gets stuck when bent, caused by inflammation of the tendons. Symptoms include a tender lump, catching, and pain when bending the finger. It is often caused by repetitive motions and can be treated with rest, splinting, corticosteroid injections, or surgery to release the tendon sheath if other treatments don't help. Recovery from surgery usually takes a few weeks but may be up to 6 months to fully resolve swelling and stiffness.
This document defines and discusses pigmented villonodular synovitis (PVNS), a benign tumor of the synovium. It most commonly affects large joints like the knee and hip in adults. While the exact cause is unknown, repetitive trauma is thought to play a role in many cases. PVNS can be either localized or diffuse. Treatment involves complete synovectomy, which can be performed either arthroscopically or via open surgery, with the goal of removing all affected synovial tissue. Radiation therapy may also be used in some cases. Prognosis is generally good for localized PVNS but recurrence is more common when disease is diffuse.
This document provides an overview of Monteggia fracture dislocations, beginning with definitions, history, epidemiology, classification, mechanisms of injury, clinical features, management, complications, and recent updates. Monteggia fractures, first described in 1814, constitute 1-2% of forearm fractures. Bado's 1958 classification divides them into four types based on the direction of radial head dislocation and location of the ulna fracture. Type I is the most common, involving anterior radial head dislocation and ulna fracture. Nonoperative treatment typically involves closed reduction and casting, while surgery is indicated for failed reductions. Complications can include nerve injuries, ossification, and compartment syndrome.
This document discusses myositis ossificans, a condition where bone forms in muscle tissue or other soft tissues. It presents two main types - non-hereditary myositis ossificans, which usually occurs after trauma in adolescents and young adults, and myositis ossificans progressiva (also called fibrodysplasia ossificans progressiva or stone man syndrome), a rare genetic disorder where muscle and connective tissues are gradually replaced by bone. The document outlines the etiology, clinical features, diagnosis, histopathology, and treatment of both conditions. Surgical excision may be indicated if the condition causes intolerable pain, neurological compression, or limited range of motion.
This document discusses the evaluation and treatment of temporomandibular joint disorders (TMDs). It begins by outlining the most common causes of TMDs, which are muscular disorders like myofascial pain. It then describes how to evaluate patients through history, examination, and various radiographic imaging techniques. Key findings on imaging include conditions like disc displacement, degenerative joint disease, and arthritis. The document concludes by discussing reversible conservative treatments like splint therapy and medications, as well as surgical options for issues like ankylosis, hypermobility, and internal derangements.
This document summarizes several types of benign bone tumors and tumor-like conditions. It describes the characteristics, presentation, diagnosis and treatment for conditions such as osteoid osteoma, enchondroma, osteochondroma, peristeal chondroma, haemangioma of bone, simple bone cyst, and fibrous dysplasia. These lesions are generally classified based on their ability to invade surrounding tissue or spread elsewhere in the body, with benign lesions not invading or spreading, intermediate lesions potentially destroying bone and recurring, and rare intermediate lesions having a potential to metastasize. Diagnosis involves imaging such as x-ray, CT, MRI and biopsy. Treatment ranges from observation to surgical resection depending on symptoms, risk of fracture
Osteochondroma is a benign bone tumor that projects from the external surface of bones. It consists of a bony projection capped with cartilage. The majority of osteochondromas are solitary lesions that present during childhood in long bones like the femur or humerus. Multiple or hereditary osteochondromas can occur as part of genetic syndromes. Osteochondromas are usually asymptomatic but can cause pain or neurological symptoms from local effects. Malignant transformation is rare in solitary lesions but higher in hereditary forms. Imaging plays a key role in diagnosis and follow up, with plain radiographs, CT and MRI used to characterize lesions. Surgical excision is reserved for symptomatic osteochondromas.
This document discusses several conditions that should be considered in the differential diagnosis of subacute osteomyelitis based on location and appearance of the lesion on imaging. These include Ewing sarcoma, Langerhans cell histiocytosis, and osteogenic sarcoma for diaphyseal lesions with onion skin periosteal reaction. Epiphyseal lesions may be confused with chondroblastoma, fungal osteomyelitis, tuberculous osteomyelitis, or aneurysmal bone cyst depending on patient age. Metaphyseal eccentric lesions could be mistaken for nonossifying fibroma. Brodie abscesses, osteoid osteoma, and intracortical hemangioma should also
Here are the answers to your questions:
1. Most common site of osteomyelitis - Metaphysis of long bones, especially distal femur and proximal tibia.
2. Most common organism causing osteomyelitis - Staphylococcus aureus.
3. Earliest radiographic and MRI findings of acute osteomyelitis - Soft tissue swelling and loss of fascial planes seen within 24-48 hours on radiographs. Bone marrow edema seen as low signal on T1 and high signal on T2/STIR sequences in MRI.
4. What is sequestrum - Avascular/necrotic bone fragment formed due to osteonecrosis in chronic osteomyelitis
MANAGEMENT OF TEMPEROMANDIBULAR JOINT DISLOCATIONBimmaNweze
An in depth presentation highlighting the anatomy,aetiology,pathogenesis and clinical presentation of TMJ dislocation in the clinical setting and how to effectively manage using proven strategies.
This document discusses several bone cysts and tumors that can occur in children, including:
- Unicameral/simple bone cysts, which typically occur in the metaphysis of long bones and cause pain or pathologic fractures. Treatment options include immobilization, aspiration with steroid injection, or curettage with bone grafting.
- Aneurysmal bone cysts, which are expansile and vascular lesions commonly found in the humerus, femur or tibia. Treatment involves curettage with burring or cryotherapy to reduce the high recurrence rate.
- Telangiectatic osteosarcoma, a rare but aggressive bone cancer that can be difficult to distinguish from aneurysmal
This document provides an overview of common benign bone lesions. It begins with an introduction to bone tumors and their classification as benign or malignant. Several common benign bone tumors are then described in detail, including their clinical features, radiological appearance, diagnosis, treatment, and prognosis. Examples discussed include osteoid osteoma, osteoblastoma, bone islands, chondromas, osteochondromas, chondromyxoid fibroma, chondroblastoma, non-ossifying fibroma, fibrous dysplasia, unicameral bone cyst, aneurysmal bone cyst, and hemangioma. For each lesion, the key presenting symptoms, diagnostic imaging findings, treatment approaches such as surgery or observation, and recurrence risks
This document discusses solitary lytic bone lesions and provides descriptions and key distinguishing features of several possible diagnoses, including:
- Fibrous dysplasia presents as a long lesion in long bones with ground-glass appearance and bone expansion. Discriminator is presence of pain or periosteal reaction.
- Enchondroma frequently presents in hand phalanges with fracture. Must have calcification except in phalanges. No periostitis.
- Eosinophilic granuloma should be considered in patients under 30 with osteolytic or sclerotic lesions. Must be under age 30.
- Giant cell tumor typically presents as an eccentric lytic lesion in long bone epiphyses abutting the joint
This document provides an overview of osteochondroma, which is a benign bone tumor characterized by a bony projection with a cartilage cap. It summarizes the definition, epidemiology, pathogenesis, clinical presentation, imaging features, complications, and risk of malignant transformation. Osteochondroma most commonly involves the long bones such as the femur and humerus during childhood. Imaging plays an important role in the diagnosis and surveillance for complications or malignant degeneration.
This document summarizes several types of benign bone tumors including osteoid osteoma, osteoblastoma, chondroma, osteochondroma, fibrous dysplasia, and cystic lesions like unicameral bone cyst and aneurysmal bone cyst. It describes the classification, clinical features, radiographic findings, pathology, diagnosis and treatment of these tumors. Malignant tumors like giant cell tumor are also briefly discussed.
benign and malignant tumors of connective tissue originmadhusudhan reddy
This document discusses various connective tissue tumors that can occur in the oral cavity. It describes benign fibrous lesions like fibroma and giant cell fibroma. It also discusses benign adipose tissue lesions like lipoma. Various benign vascular lesions are described, including hemangiomas and lymphangiomas. Finally, it summarizes benign bone tissue tumors like osteoma and osteoid osteoma. For each lesion, the clinical features, histopathology, radiographic appearance, and treatment are summarized.
This document discusses imaging patterns of cystic bone tumors. Plain radiography is usually the initial imaging modality used. CT and MRI help further characterize lesions by assessing extraosseous extension, tumor relationships and content. Eosinophilic granuloma commonly appears lytic under 30 years of age. Enchondromas typically contain punctate calcification except in the hands/feet. Fibrous dysplasia has a ground glass appearance with no periostitis or pain unless fractured. Differential diagnoses are considered based on location, margins, expansion and other characteristics.
CLASSIFICATION OF BONE TUMORS & PRINCIPLES OF LIMB.pptxSalman Syed
The document discusses the classification and principles of bone tumors and limb salvage surgery. It begins by classifying bone tumors based on cell type and aggressiveness as benign, intermediate, or malignant. Examples are provided for common tumor types. Principles of limb salvage surgery are then outlined, including indications, surgical techniques like modular endoprostheses and allografts, complications, and margins. Surgical margins are classified as intralesional, marginal, or wide based on the dissection plane in relation to the tumor.
This document summarizes fractures of the femur bone, including intertrochanteric and shaft fractures. Intertrochanteric fractures typically occur due to falls in elderly patients and result in the distal fragment riding up. They are usually comminuted and displaced. Shaft fractures result from high-energy trauma and can occur anywhere along the shaft. Treatment involves restoring alignment through conservative or operative methods like internal fixation. Complications include malunion, osteoarthritis, delayed healing, and infection.
Chondroblastoma is a benign bone tumor caused by rapid division of chondroblast cells in long bone epiphyses. It most commonly affects males in their second decade of life. While the cause is idiopathic, chromosomal abnormalities on chromosomes 5 and 6 have been associated. Clinically, patients experience pain, swelling and limping. Imaging shows a well-defined lytic lesion near the bone cortex, often with surrounding sclerosis or mottled appearance from calcification. Treatment involves surgical curettage and bone grafting for small lesions or excision for large lesions.
This document discusses cubitus varus and cubitus valgus deformities of the elbow. Cubitus varus is a reduced carrying angle, most commonly caused by malunion of a supracondylar humerus fracture. Cubitus valgus is an increased carrying angle, most often due to non-union of a lateral condylar humerus fracture. Both conditions are typically corrected surgically through osteotomies if causing cosmetic issues, with cubitus valgus at risk of tardy ulnar nerve palsy requiring nerve transposition.
Rickets is a disease of growing bone caused by unmineralized bone matrix at the growth plates, occurring only in children before fusion of the epiphyses. It is caused by vitamin D disorders, calcium deficiency, renal losses, or phosphorous deficiency. Clinical features include failure to thrive, bowed legs, widened wrists and ankles, and bone pain. X-rays show widened growth plates and fraying and cupping of the metaphysis. Treatment involves high dose vitamin D and calcium supplementation.
The document summarizes information about the meniscus. It describes the meniscus' location and functions in the knee joint, including preventing impingement, distributing synovial fluid, and providing stability. It discusses patterns of collagen in the meniscus and its vascular supply. Common types of meniscal tears are described such as longitudinal tears in the posterior horn. Classification systems for tears and imaging appearances of normal and torn menisci are presented. Treatment options are covered including non-operative care for minor tears and operative procedures like meniscal repair and resection.
This document summarizes information about post-polio residual palsy. It discusses that polio is caused by enterovirus infection that affects motor neurons in the spinal cord. While most polio infections are asymptomatic, it can cause acute flaccid paralysis. After the initial infection, patients enter the residual palsy stage where muscles remain paralyzed and deformities develop over time due to muscle imbalance, spasm, growth issues, and lack of movement. The management of residual palsy involves physical therapy, orthotics, and sometimes surgery to address deformities and improve function and mobility.
The cervical spine is made up of 7 vertebrae. C3-C6 are typical vertebrae with bifid spinous processes and facets while C1-C2 and C7 have distinguishing features. The joints in the cervical spine include intervertebral joints between vertebral bodies, joints of Lushka between vertebral arches, and craniovertebral joints. Important ligaments like the atlantoaxial and zygohypophyseal joints allow flexion, extension, lateral flexion and rotation of the cervical spine.
Congenital pseudoarthrosis of tibia is a failure of normal bone formation in the distal half of the tibia, often leading to a segmental defect and bowing of the bone. It is most commonly caused by neurofibromatosis, which is present in 40-80% of cases. Pathology shows thickened periosteum and fibrous tissue surrounding the tibia, preventing callus formation and bone healing. Treatment aims to fully excise the soft tissue, correct angular deformity, stimulate bone healing, and properly fixate bone fragments, often through the Ilizarov technique or intramedullary nailing with bone grafting. Complications can include non-union, refracture, malalignment and
Screws and plates are commonly used implants in orthopedic surgery. There are different types of screws designed for either cortical or cancellous bone. Cortical screws have a finer pitch while cancellous screws have a coarser pitch. Plates can serve different functions, including as neutralization plates to bridge a fracture, compression plates to compress bone fragments, and buttress plates to strengthen weakened bone. Proper screw and plate selection depends on the bone type and fracture characteristics.
External fixation is a method of stabilizing fractures using pins connected to an external frame. It is indicated for open fractures with soft tissue injury, long bone and pelvic fractures, and in multiple trauma patients. The basic components are pins inserted through bones, clamps connecting pins to rods or rings, and external rods or rings. Proper pin placement and construct are important for stability. Complications can include pin site infections, loosening, and breakage. Care includes daily inspection and cleaning of pins.
1) Intramedullary nailing has evolved over the past 75 years from early wooden and ivory implants to modern interlocking nails made of titanium.
2) Reaming improves nail stability and increases the use of larger nails but also disrupts endosteal blood supply, so newer reamer designs like the Reamer-Irrigator-Aspirator aim to minimize this.
3) Nail characteristics like diameter, length, curvature and interlocking screws influence stability, with larger diameter nails providing greater bending stiffness and interlocking screws enhancing torsional stability.
The Krukenberg surgery converts the forearm into a forceps-like structure by separating the radius and ulna into opposing rays that can act against each other like chopsticks. This allows amputees, especially in areas without modern prosthetics, to regain some hand function. The procedure involves longitudinally splitting the flexor and extensor muscles of the forearm into radial and ulnar groups and severing the interosseous membrane to separate the radius and ulna at their tips while maintaining motion at their proximal ends. Reconstructing the forearm in this way provides a more useful alternative to amputees than a mechanical prosthesis.
This document provides an overview of patellofemoral disorders, including the anatomy and biomechanics of the patellofemoral joint. It describes several common patellofemoral conditions such as patellar instability, excessive lateral patellar compression syndrome, chondromalacia patellae, bipartite patella, and patellofemoral arthritis. For each condition, it discusses symptoms, physical exam findings, imaging features, and treatment options both non-surgical and surgical. Surgical procedures discussed include lateral retinacular release, tibial tubercle elevation, drilling/abrasion techniques, and patellectomy.
Osteonecrosis is the death of bone tissue due to a lack of blood supply. It can be caused by trauma or other events that disrupt blood flow, such as fractures or dislocations. Imaging like x-rays and MRIs are used to stage osteonecrosis and monitor for signs of bone death and structural damage over time. The femoral head, humeral head, and scaphoid bone are particularly susceptible to osteonecrosis due to their vascular anatomy. Long term complications can include bone collapse and osteoarthritis. Prevention focuses on minimizing corticosteroid use and maintaining circulation for patients with conditions like sickle cell disease.
Osteochondroma is a benign bone tumor that presents as a cartilage-capped bony projection on the external surface of bones. It is caused by aberrant growth plate development and is associated with mutations in EXT1 and EXT2 genes. Osteochondroma typically presents in childhood as multiple lesions near joints and can cause deformities. Complications include fractures, bursa formation, arthritis and rare malignant transformation into chondrosarcoma. Diagnosis involves radiology and biopsy. Treatment involves surgery to remove painful or deforming lesions. It has an autosomal dominant inheritance pattern and carriers have a 50% risk of passing the condition to offspring.
Dupuytren contracture is a condition characterized by nodules and cords in the subcutaneous palmar tissue, resulting in progressive and irreversible finger joint flexion contractures. It is caused by increased proliferation of fibroblasts and deposition of type III collagen in the palmar fascia. The pathogenesis involves uncontrolled growth of the palmar fascia leading to flexion contractures. Treatment options include clostridial collagenase injections for mild contractures or surgical procedures like fasciotomy or fasciectomy for more severe contractures.
This document describes the Chopart amputation procedure, which removes the forefoot and midfoot while preserving the talus and calcaneus bones. It notes that this is an unstable amputation due to loss of tendon insertion points, often requiring a prosthesis extending to the patellar tendon level. The technique involves excising the Achilles tendon, creating skin flaps, disarticulating the transverse tarsal joints, and transferring the anterior tibial tendon for fixation. Post-op, the patient wears a splint and ankle-foot orthosis to prevent equinus deformity. Complications can include progressive equinovarus, which a modified procedure aims to address through additional steps like tendon transfers and flap
This document provides detailed information about the anatomy of the anterior cruciate ligament (ACL). It describes the ACL's embryology, histology, blood supply, nerve supply, measurements, biomechanics, and variations. It discusses ACL injuries and reconstruction procedures. Key points include that the ACL attaches to oval footprints on the femur and tibia, has a spiral arrangement that allows it to tuck under the intercondylar notch, and is most commonly reconstructed using a bone-patellar tendon-bone autograft.
The document discusses the innervation of the urinary bladder. It describes how the bladder develops from three sources and its anatomy. The bladder has a detrusor muscle layer and two sphincters. Micturition is controlled by higher cortical and brainstem centers that coordinate sympathetic, parasympathetic, and somatic nerve pathways. The sympathetic pathway relaxes the detrusor and contracts the internal sphincter during bladder filling. The parasympathetic pathway contracts the detrusor and relaxes the internal sphincter during voiding. The somatic pathway controls the external urethral sphincter voluntarily. Neurogenic bladder can occur due to nerve damage and is classified based on the lesion level.
This document provides information about Maduramycosis, also known as Madura foot or mycetoma. It is a chronic fungal or bacterial infection that enters through the skin, usually on the foot, and causes swelling, draining sinuses, and grain-like structures. It is most common in tropical areas and affects adult males. Diagnosis involves examining these grains microscopically and through cultures. Treatment involves long-term antifungal medications for fungal causes or antibiotic regimens for bacterial causes. Surgery may be needed for extensive or bone-involved cases. Prevention focuses on protecting the feet from minor skin trauma.
Adult-acquired flatfoot deformity is caused by posterior tibial tendon dysfunction and results in collapse of the medial longitudinal arch. It is classified into stages based on deformity severity and joint involvement.
Conservative management is recommended for stages 1 and 2, involving rest, orthotics, physical therapy and bracing to correct deformities. Surgery is considered if conservative measures fail for over 4-6 months. Joint-sparing procedures are preferred, such as posterior tibial tendon repair/transfer and medializing calcaneal osteotomy. For more severe stage 2 cases, lateral column lengthening procedures like calcaneocuboid fusion or Evan's osteotomy may be used. Stages 3 and
Pictorial and detailed description of patellar instability with sign and symptoms and how to diagnose , what investigations you should go with and how to approach with treatment options . I have presented this slide in my 2nd year junior residency in orthopedics at LLRM medical college Meerut and got good reviews for it
After getting it read you will definitely understand the topic.
The biomechanics of running involves the study of the mechanical principles underlying running movements. It includes the analysis of the running gait cycle, which consists of the stance phase (foot contact to push-off) and the swing phase (foot lift-off to next contact). Key aspects include kinematics (joint angles and movements, stride length and frequency) and kinetics (forces involved in running, including ground reaction and muscle forces). Understanding these factors helps in improving running performance, optimizing technique, and preventing injuries.
This presentation gives information on the pharmacology of Prostaglandins, Thromboxanes and Leukotrienes i.e. Eicosanoids. Eicosanoids are signaling molecules derived from polyunsaturated fatty acids like arachidonic acid. They are involved in complex control over inflammation, immunity, and the central nervous system. Eicosanoids are synthesized through the enzymatic oxidation of fatty acids by cyclooxygenase and lipoxygenase enzymes. They have short half-lives and act locally through autocrine and paracrine signaling.
The Children are very vulnerable to get affected with respiratory disease.
In our country, the respiratory Disease conditions are consider as major cause for mortality and Morbidity in Child.
Travel Clinic Cardiff: Health Advice for International TravelersNX Healthcare
Travel Clinic Cardiff offers comprehensive travel health services, including vaccinations, travel advice, and preventive care for international travelers. Our expert team ensures you are well-prepared and protected for your journey, providing personalized consultations tailored to your destination. Conveniently located in Cardiff, we help you travel with confidence and peace of mind. Visit us: www.nxhealthcare.co.uk
Computer in pharmaceutical research and development-Mpharm(Pharmaceutics)MuskanShingari
Statistics- Statistics is the science of collecting, organizing, presenting, analyzing and interpreting numerical data to assist in making more effective decisions.
A statistics is a measure which is used to estimate the population parameter
Parameters-It is used to describe the properties of an entire population.
Examples-Measures of central tendency Dispersion, Variance, Standard Deviation (SD), Absolute Error, Mean Absolute Error (MAE), Eigen Value
5-hydroxytryptamine or 5-HT or Serotonin is a neurotransmitter that serves a range of roles in the human body. It is sometimes referred to as the happy chemical since it promotes overall well-being and happiness.
It is mostly found in the brain, intestines, and blood platelets.
5-HT is utilised to transport messages between nerve cells, is known to be involved in smooth muscle contraction, and adds to overall well-being and pleasure, among other benefits. 5-HT regulates the body's sleep-wake cycles and internal clock by acting as a precursor to melatonin.
It is hypothesised to regulate hunger, emotions, motor, cognitive, and autonomic processes.
Discover the benefits of homeopathic medicine for irregular periods with our guide on 5 common remedies. Learn how these natural treatments can help regulate menstrual cycles and improve overall menstrual health.
Visit Us: https://drdeepikashomeopathy.com/service/irregular-periods-treatment/
PGx Analysis in VarSeq: A User’s PerspectiveGolden Helix
Since our release of the PGx capabilities in VarSeq, we’ve had a few months to gather some insights from various use cases. Some users approach PGx workflows by means of array genotyping or what seems to be a growing trend of adding the star allele calling to the existing NGS pipeline for whole genome data. Luckily, both approaches are supported with the VarSeq software platform. The genotyping method being used will also dictate what the scope of the tertiary analysis will be. For example, are your PGx reports a standalone pipeline or would your lab’s goal be to handle a dual-purpose workflow and report on PGx + Diagnostic findings.
The purpose of this webcast is to:
Discuss and demonstrate the approaches with array and NGS genotyping methods for star allele calling to prep for downstream analysis.
Following genotyping, explore alternative tertiary workflow concepts in VarSeq to handle PGx reporting.
Moreover, we will include insights users will need to consider when validating their PGx workflow for all possible star alleles and options you have for automating your PGx analysis for large number of samples. Please join us for a session dedicated to the application of star allele genotyping and subsequent PGx workflows in our VarSeq software.
Congestive Heart failure is caused by low cardiac output and high sympathetic discharge. Diuretics reduce preload, ACE inhibitors lower afterload, beta blockers reduce sympathetic activity, and digitalis has inotropic effects. Newer medications target vasodilation and myosin activation to improve heart efficiency while lowering energy requirements. Combination therapy, following an assessment of cardiac function and volume status, is the most effective strategy to heart failure care.
Dr. Tan's Balance Method.pdf (From Academy of Oriental Medicine at Austin)GeorgeKieling1
Home
Organization
Academy of Oriental Medicine at Austin
Academy of Oriental Medicine at Austin
Academy of Oriental Medicine at Austin
About AOMA: The Academy of Oriental Medicine at Austin offers a masters-level graduate program in acupuncture and Oriental medicine, preparing its students for careers as skilled, professional practitioners. AOMA is known for its internationally recognized faculty, award-winning student clinical internship program, and herbal medicine program. Since its founding in 1993, AOMA has grown rapidly in size and reputation, drawing students from around the nation and faculty from around the world. AOMA also conducts more than 20,000 patient visits annually in its student and professional clinics. AOMA collaborates with Western healthcare institutions including the Seton Family of Hospitals, and gives back to the community through partnerships with nonprofit organizations and by providing free and reduced price treatments to people who cannot afford them. The Academy of Oriental Medicine at Austin is located at 2700 West Anderson Lane. AOMA also serves patients and retail customers at its south Austin location, 4701 West Gate Blvd. For more information see www.aoma.edu or call 512-492-303434.
2. Definition:
Heterotropic ossification – formation of mature cellular bone in
non – osseous tissue or presence of bone formation at a place
where it should not be present[ heterotopic] that is usually soft
tissue.
3. HETEROTOPIC OSSIFICATION
• HO – 1st described in 1883 by Riedel.
• HO may be traumatic or non-traumatic
• Types of HO:
- HO per se / Myositis ossificans circumscripta
- Traumatic HO/ Myositis ossificans traumatica
- Neurogenic HO
4. • Causes?? Evolution of disease :
- It has early, intermediate and late presentations and pts may
present anytime during the disease evolution.
- Fever, swelling, erythema and joint stiffness typically seen in
early HO may mimic the presentation of cellulitis, osteomyelitis
or thrombophlebitis
Idiopathic
Tetanus
Hemophilia
DISH
5. • MRI –
- T1 – isointense to hyperintense
- T2 – intermediate to high signal
These features though suggestive of HO may be confused with
focal myositis so confirmation comes only when the lesion
matures with time.
6. PATHOGENESIS
• Early disease[ inflammatory phase]:
- Early there is swelling & pain similar to an infection or soft tissue
aggressive tumor
- Radiographs??
- Usg – hypoechoic mass with central reflective core is seen that may
have a lamellar hyperreflectivity at the periphery of the mass
- CT scan ??
Radiographs are normal or show a soft tissue density
CT scan reveals enlarged m/s group with normal attenuation
7. • INTERMEDIATE STAGE [ CONSOLIDATION STAGE ]:
- Clinically ?
- Radiographs shows dotted veil calcificaton confusing with
rhabdomyosarcoma or synovial sarcoma
- There may be continuous or discontinuous peripheral
calcification.
8. • The lesion becomes clinically firm with constant pain
• There may b limitation of movements at adjacent joints if the lesion
is large
• CT SCAN is a better modality & reveals zonal phenomenon with rim
of calcification of varying thickness at periphery while central area
similar to m/s
• MRI – more non specific with variable signal at the center &
decreased signal intensity at periphery on all pulses
• d/d – calcific tendinitis- if mass is small as in tendinitis the mass is
small with asso.calcification
9. • Late stage [ maturation phase]
• Mass – bony hard & easily discernable from its surrounding
tissue.
• Pain reduces dramatically but the swelling & deformity is
concern for most pts
• Mass may mere with adjacent bone resembling
osteochondroma
10. • Movts at the asso. Jts may be limited in a large mass.
• pattern of mineralization --periphery -more mature than
central region that is still evolving [ zonation phenonmenon]
11. • This helps in differentiating it from extraskeletal osteosarcoma
• Os- hav immature periphery mature dense calcification
centrally
• d/d – osteomyelitis, osteochondroma,osteosarcoma,myositis,
pentazosine induced myopathy,hematoma formation,
intramuscular parasitic cysts, rhabdomyosarcoma,synovial
sarcoma
12. Rx
• Early stage ?
• Prognosis is good & the lesion usually does not recur after sx
excision if performed adequately
13. Traumatic HO/ myositis ossificans traumatica .
• m/c form
• Can occur after any type of musculoskeletal trauma
- characterized by
heterotopic calcification & ossification in muscle tissue.
Injury is an important factor in its pathogenesis.
Usually there is a h/o severe single injury.
It is only seen in children with # or d/l of elbow. In our
country, usually the patient has taken massage treatment.
14. • Clinical Features
• Rapid enlargement and severe pain are
the cardinal
• symptoms usually 1 or 2 weeks following
trauma.
In our country after trauma or injury, the
bonesetter/quack massages the injured
part daily, often vigorously. This leads to
calcification.
• Patient usually presents with stiff painful
joint.
• h/o injury 1 to 2 weeks back.
• Patient may come even months after the
injury.
15. • O/E:
-palpable swelling.
-Mass is initially ill defined, then becomes better circumscribed.
The part becomes grossly swollen.
-lesion - self-limited and usually matures into a hard
mass, or it may totally regress.
-Most common location is the post-traumatic elbow
16. myositis ossificans is
• diaphyseal , lying parallel to surface of bone &
often separated from it by a distinct lucent area
in which cortex & periosteum have abn’l
appearance
Osteogenic sarcoma is likely to show some
evidence of involvement of the cortex &
periosteum, & it is metaphyseal .
• Occasionally, the differentiation is difficult &
even the histologic ex. may be misinterpreted
Differential
Diagnosis
Myositis ossificans
must be
distinguished
from calcifying
hematoma,
interstitial
calcinosis, and
osteogenic
sarcoma.
17. • Treatment
• Rest of the affected part during the period while the
process is active is the basic principle of Rx.
-Aspirin is known to inhibit calcification.
-Passive movts & vigorous exercises must be stopped.
No massage.
Very gentle exercises must be started.
Surgery is contraindicated during the period when calcification matures.
Usually it takes more than 8 months one
ossification to mature and if it interferes with function, it may be excised
18. 43% rate of HO
in operatively
treated fracture
–d/l
half of these
requiring sx
intervention.
was asso. with
clinically
relevant
motion
deficits
20 % of 130 elbow HOForuria et al
Shukla et
al
19. Risk Factors for Developing Heterotopic
Ossification about the Elbow
Trauma
■ Open elbow D/L requiring extensive or
multiple débridements
■ Elbow D/L asso with # that require ORIF
■ Radial head # treated with surgery > 24
hrs after injury
Surgery :
■ Distal biceps tendon repair
■ Repeated procedures with improper
exposure in first 2 wks
■ CNS injury
■ Traumatic brain injury
■ Elbow trauma + traumatic brain injury
Burns
■ 3rd-degree burns over 20% of
TBA
■ 3rd-degree burns over elbow
■ Long periods of bed
confinement
Genetic Conditions
■FOP
■ H/O heterotopic bone
formation
20. Location of Heterotopic Ossification Related to
Associated Pathological Process
• Traumatic
• ■ Most often posterolateral elbow
• ■ Bone bridge between lateral humeral condyle and posterolateral
olecranon
• ■ Bone may fill olecranon fossa
• ■ Anterolateral compartment second most common location
• ■ Bone may extend from distal humerus to radius and ulna at level
of bicipital tuberosity
• ■ Coronoid frequently enlarged, blocking elbow flexion
21. • Burn-Related
• ■ Most often posteromedial
• ■ Cubital tunnel often obliterated
• ■ Ulnar nerve may be completely encased in bone
• Neurogenic
• ■ M/C anteriorly in flexor muscles or posteriorly in extensors
• ■ Ossification tends to occur within the muscle and follow a single
plane
• ■ Forearm and proximal radioulnar joint also may be involved
22. EXCISION OF HETEROTOPIC OSSIFICATION
• Usually a posterior skin incision is made, and subcutaneous
dissection is carried laterally or medially depending on the
location of the heterotopic ossification. Care must be taken to
identify and protect the ulnar nerve.
23. • POSTEROLATERAL EXCISION
• ■ For posterolateral resection, retract the triceps mechanism
medially without disturbing its insertion and expose the ectopic
bone subperiosteally. Resect the central portion of the bony bridge.
• ■ Flex the elbow and remove the attachments of the ectopic bone
to the humerus and olecranon. Anterior capsular release is not
necessary.
• ■ Excise any ectopic bone in the olecranon fossa to reduce
olecranon impingement
24. • MEDIAL EXCISION
• ■ When the posterior ectopic bone extends to the medial aspect of
the elbow, ulnar nerve transposition is necessary.
• ■ Identify the ulnar nerve, which may be completely surrounded by
bone.
• ■ Expose the triceps expansion and incise it distal to its insertion.
• ■ Expose the ectopic bone subperiosteally and resect it.
• ■ If the ectopic bone interferes with ulnar nerve function,
decompress the nerve or transfer it anteriorly if necessary.
25. • ANTERIOR EXCISION
• ■ If anterior excision is necessary, elevate the origins of the brachioradialis
and brachialis muscles from the lateral supracondylar ridge to expose the
ectopic bone.
• ■ Identify the radial nerve and retract it laterally.
• ■ Resect the bone subperiosteally.
• CLOSURE
• ■ Deflate the tourniquet and obtain hemostasis before routine layered
closure over a suction drain. Do not close the capsule. Apply a soft dressing
that will allow immediate postoperative range of motion.
26. THA
High risk for HO
male
hypertrophic OA
and h/o of HO or
posttraumatic
arthritis with
hypertrophic
osteophytosis
Moderate risk is
associated with
ankylosing
spondylitis,
DISH, Paget
disease, &
unilateral
hypertrophic
osteoarthritis
According to Iorio
and Healy
29. indomethacin (25
mg three times a
day for 4 to 6
weeks)
occasionally
radiation therapy
with a one-time
dose of in patients
in whom
indomethacin is
contraindicated
700 cGy
KOCHER-LANGENBECK
APPROACH
or
30. THA HO
Calcification can be seen radiographically the 3rd or 4thwk; however,
the bone does not mature fully for 1 to 2 years.
classification of Brooker et al. is useful in describing the extent of
bone formation:
• Grade I: islands of bone within soft tissues
• Grade II: bone spurs from the proximal femur or pelvis with at least
1 cm between opposing bone surfaces
• Grade III: bone spurs from the proximal femur or pelvis with less
than 1 cm between opposing bone surfaces
• Grade IV: ankylosis
31. Brooker grade IV heterotopic ossification occurred
despite postoperative irradiation.
32. THA HO
prevalence of
HO: 2% to
90%
Mostly HO: asymptomatic
Brooker grade III or grade IV
:restricted ROM & pain.
Marked limitation of motion
or bony ankylosis is
uncommon,
but significant loss of
function - 10% pts
33. Controversy on prophylaxis
• Multiple authors have found indomethacin to be effective in
decreasing significant HO after acetabular fracture surgery,
although this has been called into question by others who
found indomethacin to be ineffective in their prospective
series.
• Low-dose irradiation has been shown to be effective in
decreasing the incidence of significant heterotopic ossification,
and an additive effect has been noted when the two regimens
were combined.
34. • Radiation exposure is limited to the soft tissues immediately
around the hip joint, and ingrowth surfaces must be
appropriately shielded
• Hedley et al. reported no clinical evidence of loosening,
subsidence, or radiolucent lines around cementless prostheses
after irradiation
35. • Kennedy et al. also reported no increase in radiolucent lines
and no revisions for aseptic loosening in a group of cementless
total hip arthroplasties treated with radiation prophylaxis
• Delayed union or nonunion of trochanteric osteotomy is a
potential problem with radiation therapy. Malignant
transformation after radiation has not been reported with
dosages currently recommended for prophylaxis.
36. • NSAIDs have been shown to reduce the formation of heterotopic bone in
many studies.
• Historically, nonselective cyclooxygenase-1 (COX-1) and cyclooxygenase-2
(COX-2) inhibitors for 6 weeks have been recommended, although courses
of administration of 7 days have been reported as successful.
• Compliance is limited by medical contraindications to the drug and by
patient intolerance.
• Cella et al. found that 37% of patients were unable to complete a course of
treatment with indomethacin.
• More recently, a meta-analysis by Xue et al. of four randomized trials
comparing selective COX-2 inhibitors with nonselective COX-1 inhibitors
showed no difference in efficacy in preventing heterotopic ossification.
37. • In light of a more favorable gastrointestinal safety profile for
the COX-2 inhibitors, they were recommended for heterotopic
ossification.
• Similar to irradiation, NSAIDs have been shown to diminish
bone ingrowth into porous implants; however, no method
exists to shield the implant, in contrast to radiation treatment
38. • An operation to remove heterotopic bone rarely is indicated because pain
usually is not severe, and excision of established heterotopic bone is a difficult
procedure.
• Extensile exposure is required, and the ectopic bone obscures normal
landmarks.
• The abnormal bone is not easily shelled out of the surrounding soft tissues.
• Substantial blood loss can be anticipated.
• Radiation and NSAIDs have been used successfully to prevent recurrence.
Decreased technetium bone scan activity indicates that the heterotopic bone is
mature and that excision can take place safely.
• Range of motion should improve with excision, but pain may not be reliably
alleviated.
39. After shoulder arthroplasty
• Bridging heterotopic bone of glenohumeral jt or glenoacromial
space can occur in extreme situations.
• No correlation is evident, however, b/w HO and the
development of shoulder pain.
• Low grade HO, is present early in postop period, is
nonprogressive, and does not adversely affect clinical results
10% to
45% -HO
Risk factors:
Male gender
& OA
40. After total ankle arthroplasty
freq. HO (42%
to 82%)
HO pts had limited
dorsiflexion and
plantar flexion and
lower (AOFAS)
• Male
• limited preop
ROM
• previous
heterotopic
bone
formation,
• posttraumatic
OA,
• ankylosing
spondylitis
• infection
42. Classification of Heterotopic Ossification After
Total Ankle Arthroplasty
• CLASS CRITERIA
• 0 No HO
• I Islands of bone within the soft tissue around the ankle
• II Bone spurs from the tibia or talus, reducing the posterior joint
space by < 50%
• III Bone spurs from the tibia or talus, reducing the posterior joint
space by ≥ 50%
• IV Bridging bone continuous between the tibia & the talus
43. After total ankle arthroplasty
Currently, NSAIDs
most freq. used method for prophylaxis .
• Do not routinely administer NSAIDs before total ankle
arthroplasty, but prophylactic therapies (e.g., NSAIDs,
radiation) may be used in patients who require
excision of symptomatic HO.
• Noting the lack of strong asso. b/w HO &
postoperative ankle pain & functional limitation, Choi
and Lee cautioned against attributing these symptoms
to HO in posterior ankle when considering its excision.
Meticulous
soft tissue
dissection,
adequate
implant size
&
shortened
operative
time.
To reduce
risk of HO
44. CASE SCENARIO
• Three years after total knee arthroplasty, a 66-year-old male
patient presents with right knee stiffness and swelling for 6
months after being struck in the anterior thigh by a baseball.
Range of active motion is 10 to 40 degrees.??
45.
46.
47.
48.
49.
50. Fibrodysplasia ossificans progressiva (FPP, Stone
Man Disease/ Munchmeyer’s disease/MOP]
• Rare progressive disease
• It involves the ACVR1 gene (activin A type I receptor gene, a BMP
type-1 receptor).
• hallmark characteristics:
- progressive heterotopic ossification (muscles, fascia, tendons,
ligaments and joint capsules)
- congenital malformation of the great toe (hallux valgus, malformed
first metatarsal and monophalangism)
• BMP4, which contributes to the formation of the skeleton in the
normal embryo, is implicated in this disease.
51. muscles of
face, larynges,
tongues and
diaphragm -
spared.
Characteristically muscles
involved are those of the
hand and back, then the
shoulder
muscles and hips
52. • . Probably excessive proliferation
• of collagenoblast sets the pace. The collagen accepts
• calcium a salt, i.e. dystrophic calcification occurs. This is
• followed by metaplasia of collagenoblasts into osteoblast
• and chondroblast which eventually transform into
• mature bone. It progresses along with muscle sheaths and
55. heterotopic ossification around the left hip.
ossification of soft tissues and paraspinal ligaments
and fusion of the vertebral bodies give rise to a
“bamboo spine” appearance
HO is m/c extrinsic cause of elbow contracture
Periarticular calcification – collection of calcium pyrophosphate ..lacks trabecular organisation ..occurs in distinct structures like colleteral ligaments..capsule
Myositis ossificans – Formation of HO in inflammed muscle
Early stage bisphonates & or nsaids can be started to limit the extension
Ackerman has described four histologic zones:
(i) the central, undifferentiated zone, which is highly cellular, with mitotic figures and with extreme variation in the
size and shape of the cells (cytologic differentiation of
this zone from sarcoma is extremely difficult),
(ii) an adjacent zone in which there are well-oriented zones of
cellular osteoid separated by loose cellular stroma,
(iii) A more peripheral zone showing new bone formation with
osteoblasts and fibrous tissue undergoing trabecular
organization, and
(iv) an outermost zone of well delimited and oriented bone encapsulated by the
presence of the zone phenomenon, i.e. the innermost
undifferentiated are a merging into oriented osteoid
formation and finally into well-formed bone in the
periphery. As the bone matures, the area involved
Extensive heterotopic ossification after fracture-dislocation of elbow and radial head excision
TOTAL BODY AREA
Fibrodysplasia ossificans progressiva
diffuse idiopathic skeletal hyperostosis
Kocher- posterior approach
Debride gluteus medius m/s to decrease incidence of HO{ rath et al}
ILIOINGUINAL APPROACH rare - unless the external surface of the ilium is stripped.
allows exposure to entire internal iliac fossa& pelvic brim from SI joint to pubic symphysis – indi – anterior wall # anterior column #
Centigray
radiation therapy more frequently in patients with extensile exposures
Try not to use routine radiation therapy in very young patients
Routine prophylaxis is not recommended for all pts, but some form of prophylaxis is warranted in high-risk patients
American Orthopaedic Foot and Ankle Score
Most descriptions of HO after total ankle arthroplasty place it in the posterior aspect of the ankle
a classification system for heterotopic ossification after total ankle arthroplasty based on the Brooker classification of heterotopic ossification after total hip arthroplasty but made no treatment or prophylaxis recommendations based on the classificati
AP and lateral radiographs showing mature, well formed bone in the suprapatellar pouch
axial and sagittal CT images showing mature bone with no underlying cortical destruction or connection with the medullary cavity proper.
The left T2-weighted image demonstrates diffuse intramuscular edema. The right T1-weighted image demonstrates an indistinct lesion within the anterior thigh mostly isointense to muscle with areas of low signal, likely corresponding to mineralized regions.
shows the intraoperative appearance
Here a patient with a mineralized mass in the soft tissues.Notice that the mineralization is predominantly in the periphery of the mass and that there is a lucent zone between the mass and the cortical bone.
Contrast-enhanced T1-weighted MR image demonstrates heterogeneous enhancement of the mass with extensive surrounding edema.This is consistent with the diagnosis of a reactive process like myositis ossificans.