Imaging of Focal Sclerotic Bone Lesions Omer Awan, MD, Jim Wu, MD, and Ronald Eisenberg, MD
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Benign Fibro-Osseous Lesions Plus…
“Vision is the art of seeing things invisible.” Jonathan Swift 1667 - 1745 Benign Fibro-osseous Lesions Plus… Steven R. Singer, DDS [email protected] 212.305.5674 Benign Fibro-osseous Lesions Fibrous Dysplasia A group of lesions in which normal bone is Localized change in bone metabolism replaced initially by fibrous connective tissue Normal cancellous bone is replaced by Over time, the lesion is infiltrated by osteoid fibrous connective tissue and cementoid tissue The connective tissue contains varying amounts of abnormal bone with irregular This is a benign and idiopathic process trabeculae Trabeculae are randomly oriented. (Remember that normal trabeculae are aligned to respond to stress) Fibrous Dysplasia Fibrous Dysplasia Lesions may be solitary (monostotic) or Fibrous dysplasia is non-hereditary involve more than one bone (polyostotic) Caused by a mutation in a somatic cell. Monostotic form accounts for 70% of all Extent of lesions depends on the timing of cases the mutation. Polyostotic form is more common in the first If the mutation occurs earlier, the disease decade will be more widespread throughout the M=F except in McCune-Albright syndrome, body. An example is McCune-Albright which is almost exclusively found in females Syndrome 1 Fibrous Dysplasia Fibrous Dysplasia McCune-Albright Syndrome • Monostotic and polyostotic forms usually -Almost exclusively begins in the second decade of life females -Polyostotic fibrous • Slow, painless expansion of the jaws dysplasia • Patients may complain of swelling or have -
Diagnosis and Treatment of Intramedullary Osteosclerosis
Abe et al. BMC Musculoskeletal Disorders (2020) 21:762 https://doi.org/10.1186/s12891-020-03758-5 CASE REPORT Open Access Diagnosis and treatment of intramedullary osteosclerosis: a report of three cases and literature review Kensaku Abe, Norio Yamamoto, Katsuhiro Hayashi, Akihiko Takeuchi* , Shinji Miwa, Kentaro Igarashi, Takashi Higuchi, Yuta Taniguchi, Hirotaka Yonezawa, Yoshihiro Araki, Sei Morinaga, Yohei Asano and Hiroyuki Tsuchiya Abstract Background: Intramedullary osteosclerosis (IMOS) is a rare condition without specific radiological findings except for the osteosclerotic lesion and is not associated with family history and infection, trauma, or systemic illness. Although the diagnosis of IMOS is confirmed after excluding other osteosclerotic lesions, IMOS is not well known because of its rarity and no specific feature. Therefore, these situations might result in delayed diagnosis. Hence, this case report aimed to investigate three cases of IMOS and discuss imaging findings and clinical outcomes. Case presentation: All three cases were examined between 2015 and 2019. The location of osteosclerotic lesions were femoral diaphyses in the 60-year-old man (Case 1) and 41-year-old woman (Case 2) and tibial diaphysis in the 44-year-old woman (Case 3). All cases complained of severe pain and showed massive diaphyseal osteosclerotic lesions in plain radiograms and computed tomography (CT) scans. Cases 2 and 3 were examined using the triphasic bone scan, and a fusiform-shaped intense area of the tracer uptake on delayed bone image was detected in both cases without (Case 2) or slightly increased vascularity (Case 3) on the blood pool image, which was reported as a specific finding of IMOS. -
Orthopedic-Conditions-Treated.Pdf
Orthopedic and Orthopedic Surgery Conditions Treated Accessory navicular bone Achondroplasia ACL injury Acromioclavicular (AC) joint Acromioclavicular (AC) joint Adamantinoma arthritis sprain Aneurysmal bone cyst Angiosarcoma Ankle arthritis Apophysitis Arthrogryposis Aseptic necrosis Askin tumor Avascular necrosis Benign bone tumor Biceps tear Biceps tendinitis Blount’s disease Bone cancer Bone metastasis Bowlegged deformity Brachial plexus injury Brittle bone disease Broken ankle/broken foot Broken arm Broken collarbone Broken leg Broken wrist/broken hand Bunions Carpal tunnel syndrome Cavovarus foot deformity Cavus foot Cerebral palsy Cervical myelopathy Cervical radiculopathy Charcot-Marie-Tooth disease Chondrosarcoma Chordoma Chronic regional multifocal osteomyelitis Clubfoot Congenital hand deformities Congenital myasthenic syndromes Congenital pseudoarthrosis Contractures Desmoid tumors Discoid meniscus Dislocated elbow Dislocated shoulder Dislocation Dislocation – hip Dislocation – knee Dupuytren's contracture Early-onset scoliosis Ehlers-Danlos syndrome Elbow fracture Elbow impingement Elbow instability Elbow loose body Eosinophilic granuloma Epiphyseal dysplasia Ewing sarcoma Extra finger/toes Failed total hip replacement Failed total knee replacement Femoral nonunion Fibrosarcoma Fibrous dysplasia Fibular hemimelia Flatfeet Foot deformities Foot injuries Ganglion cyst Genu valgum Genu varum Giant cell tumor Golfer's elbow Gorham’s disease Growth plate arrest Growth plate fractures Hammertoe and mallet toe Heel cord contracture -
(Osgood- Schlatter Disease): a Review
Open Access Review Article DOI: 10.7759/cureus.780 Apophysitis of the Tibial Tuberosity (Osgood- Schlatter Disease): A Review Raju Vaishya 1 , Ahmad Tariq Azizi 2 , Amit Kumar Agarwal 1 , Vipul Vijay 1 1. Orthopaedics, Indraprastha Apollo Hospitals 2. Orthoapedics, Herat Regional Hospital, Herat, Afghanistan Corresponding author: Amit Kumar Agarwal, [email protected] Abstract Osgood-Schlatter disease (OSD) is a condition in which the patellar tendon insertion on the tibial tuberosity becomes inflamed. It is a well-known condition in late childhood characterized by pain and a bony prominence over the tibial tuberosity. The pain is usually exacerbated by physical activities like running, jumping, and climbing stairs. In the acute stage, the margins of the patellar tendon become blurred in radiographs due to the soft tissue swelling. After three to four months, bone fragmentation at the tibial tuberosity is viewed. In the sub-acute stage, soft tissue swelling resolves, but the bony ossicle remains. In the chronic stage, the bone fragment may fuse with the tibial tuberosity which can appear normal. The primary goal in the treatment of OSD is the reduction of pain and swelling over the tibial tuberosity. The patient should limit physical activities until the symptoms are resolved. In some cases, the patient should restrict physical activities for several months. The presence of pain with kneeling because of an ossicle that does not respond to conservative measures is the indication for surgery. In these cases, the removal of the ossicle, surrounding bursa, and the bony prominence is the treatment of choice. Categories: Orthopedics Keywords: tibial tuberosity, osgood-schlatter disease, apophysitis Introduction And Background Osgood-Schlatter disease (OSD, also called Lannelongue’s disease) is a condition in which the patellar tendon insertion on the tibial tuberosity becomes inflamed [1-2]. -
Knee Pain in Children, Part II: Limb- and Life-Threatening Conditions, Hip Pathology, and Effusion
Knee Pain in Children, Part II: Limb- and Life-threatening Conditions, Hip Pathology, and Effusion Michael Wolf, MD* *Pediatrics and Orthopedic Surgery, St Christopher’s Hospital for Children, Philadelphia, PA. Practice Gap Clinicians who evaluate knee pain must be able to recognize limb- and life-threatening conditions, hip pathology, or joint effusion and pursue the appropriate management. Objectives After reading the article, the reader should be able to: 1. Describe the presentation and treatment of common limb- and life-threatening conditions that can cause knee pain in children. 2. Delineate how hip pathology can contribute to knee pain in children and how such conditions should be diagnosed and treated. 3. Explain the diagnosis and treatment of conditions that may cause effusion in conjunction with knee pain in children. INTRODUCTION As noted in the first part of this three-part review of knee pain in children, the clinician can use the information gained from the history and physical examination in an algorithm to establish a working diagnosis and direct subsequent evaluation and management. The initial priorities are to identify emergent limb- and life-threatening conditions, hip pathology, or effusion (Table). LIMB- AND LIFE-THREATENING CONDITIONS Bacterial Infections Septic Arthritis. The knee is the most common site of septic arthritis in children. Usually, septic arthritis is characterized by the acute onset of steadily progressive knee pain with fever and a physical examination demonstrating effusion, warmth, AUTHOR DISCLOSURE Dr Wolf has disclosed fi erythema, and limited motion. Concern for septic bacterial arthritis in children no nancial relationships relevant to this article. This commentary does not contain a warrants emergent evaluation, including knee radiographs (anteroposterior [AP] discussion of an unapproved/investigative and lateral) and laboratory studies (complete blood cell [CBC] count with use of a commercial product/device. -
Musculoskeletal Radiology
MUSCULOSKELETAL RADIOLOGY Developed by The Education Committee of the American Society of Musculoskeletal Radiology 1997-1998 Charles S. Resnik, M.D. (Co-chair) Arthur A. De Smet, M.D. (Co-chair) Felix S. Chew, M.D., Ed.M. Mary Kathol, M.D. Mark Kransdorf, M.D., Lynne S. Steinbach, M.D. INTRODUCTION The following curriculum guide comprises a list of subjects which are important to a thorough understanding of disorders that affect the musculoskeletal system. It does not include every musculoskeletal condition, yet it is comprehensive enough to fulfill three basic requirements: 1.to provide practicing radiologists with the fundamentals needed to be valuable consultants to orthopedic surgeons, rheumatologists, and other referring physicians, 2.to provide radiology residency program directors with a guide to subjects that should be covered in a four year teaching curriculum, and 3.to serve as a “study guide” for diagnostic radiology residents. To that end, much of the material has been divided into “basic” and “advanced” categories. Basic material includes fundamental information that radiology residents should be able to learn, while advanced material includes information that musculoskeletal radiologists might expect to master. It is acknowledged that this division is somewhat arbitrary. It is the authors’ hope that each user of this guide will gain an appreciation for the information that is needed for the successful practice of musculoskeletal radiology. I. Aspects of Basic Science Related to Bone A. Histogenesis of developing bone 1. Intramembranous ossification 2. Endochondral ossification 3. Remodeling B. Bone anatomy 1. Cellular constituents a. Osteoblasts b. Osteoclasts 2. Non cellular constituents a. -
Intramuscular Myxoma Associated with Fibrous Dysplasia
Mazabraud’s Syndrome: Intramuscular Myxoma Associated with Fibrous Dysplasia Authors: Dr Fevziye Kabukcuoglu and Dr Yavuz Kabukcuoglu Creation date: January 2005 Scientific Editor: Prof Loic Guillevin Department of Pathology and Department of Orthopedics and Traumatology. Sisli Etfal Training and Research Hospital, Istanbul Turkey. [email protected] Abstract Key words Definition and disease name Differential Diagnosis Incidence Etiology Clinical Description Radiologic findings Histopathology Treatment Unresolved Questions References Abstract Mazabraud’s syndrome is a rare disease known as the association of intramuscular myxoma with fibrous dysplasia. The number of reported cases in 2004 is 55. Myxomas generally occur as multiple masses and fibrous dysplasia most commonly appear with its polyostotic form. Both lesions tend to involve the same anatomical region. Patients usually present with a painless mass with a history of long duration due top lack of symptoms. Most fibrous dysplasias are asymptomatic while some may appear with pain, skeletal deformities or fractures. Generally fibrous dysplasias occur during the growth period and the myxomas appear during adult life. The relationship between fibrous dysplasia and myxoma remains unclear, where an underlying localized error in tissue metabolism has been proposed. Molecular genetic analysis has shown activating mutations in GNAS1 gene. Several benign lesions as well as richly myxoid malignant lesions may be confused with myxoma. Histopathologic examination should be carried out to exclude malignancy. Treatment is dependent on the extent of the lesions. Malignant transformation of myxoma is not reported, although local recurrence may be expected if incompletely resected. While sarcomatous transformation is uncommon for fibrous dysplasia, greater risk has been reported for Mazabraud’s syndrome. -
Radionuclide Bone Scintigraphy in Sports Injuries
Radionuclide Bone Scintigraphy in Sports Injuries Hans Van der Wall, MBBS, PhD, FRACP,* Allen Lee, MBBS, MMed, FRANZCR, FRAACGP, DDU,† Michael Magee, MBBS, FRACP,* Clayton Frater, PhD, ANMT, BHSM,† Harindu Wijesinghe, MBBS, FRCP,‡ and Siri Kannangara, MBBS, FRACP†,§ Bone scintigraphy is one of the mainstays of molecular imaging. It has retained its relevance in the imaging of acute and chronic trauma and sporting injuries in particular. The basic reasons for its longevity are the high lesional conspicuity and technological changes in gamma camera design. The implementation of hybrid imaging devices with computed tomography scanners colocated with the gamma camera has revolutionized the technique by allowing a host of improvements in spatial resolution and anatomical registration. Both bone and soft-tissue lesions can be visualized and identified with greater and more convincing accuracy. The additional benefit of detecting injury before anatomical changes in high-level athletes has cost and performance advantages over other imaging modalities. The applications of the new imaging techniques will be illustrated in the setting of bone and soft-tissue trauma arising from sporting injuries. Semin Nucl Med 40:16-30 © 2010 Elsevier Inc. All rights reserved. he uptake characteristics of the bone-seeking radiophar- Scintigraphy is also capable of detecting bone bruising, an Tmaceuticals are highly conducive to the localization of acute injury resulting from direct trauma that leads to trabec- trauma to bone or its attached soft-tissue structures. Bone ular microfractures without frank cortical disruption.1 The scintigraphy has an inherently high contrast-resolution, greater force transmission involved in cortical fracture en- which enables the detection of the pathophysiology of sures early detection by three-phase scintigraphy. -
Bone Scan in Tumor-Induced Osteomalacia
Bone Scan in Tumor-Induced Osteomalacia Hee K. Lee, Wei Wen Sung, Paul Solodnik and Mona Shimshi Section of Nuclear Medicine, Department of Medicine and Department of Radiology, Mount Sinai School of Medicine and Elmhurst Hospital Center, Elmhurst, New York revealed markedly improved focal lesions while diffusely in A 66-yr-old female was admitted with a 3-yr history of general creased activity, especially in the skull remained (Fig. 2). ized bone pain and nasal obstruction. CT and MRI of the head revealed a large nasal mass. A whole-body bone scan revealed multifocal lesions of increased activity. Surgical removal of the DISCUSSION nasal tumor revealed hemangiopericytoma. The patient im Tumor-induced osteomalacia or oncogenic osteomalacia proved clinically and a repeat bone scan 10 mo after surgery is a rare phenomenon with less than 100 reported cases in revealed markedly improved findings. the literature. Most of the tumors are benign, mesenchymal Key Words: oncogenous;osteomalacia;bone scan in origin and highly vascular (1,2). Benign tumors associ ated with osteomalacia include giant-cell granuloma, J NucÃMed 1995; 36:247-249 cavernous hemangioma, nonossifying fibroma, benign ossifying mesenchymal tumors, fibrous xanthoma, heman giopericytoma, angiosarcoma, osteoblastoma and fibroan- 'ncogenous osteomalacia is a rarely described clinical gioma. Malignant tumors associated with oncogenic osteo o, malacia are extremely rare with less than 10reported cases entity that may mimic metastatic bone lesions in bone (3). There is one reported case each of prostate cancer (4) scanning. It is most commonly associated with benign tu and oat-cell lung cancer (5). More common are the malig mors of mesenchymal origin and can be cured after surgical nant soft-tissue sarcomas and malignant neurinoma. -
Injuries and Normal Variants of the Pediatric Knee
Revista Chilena de Radiología, año 2016. ARTÍCULO DE REVISIÓN Injuries and normal variants of the pediatric knee Cristián Padilla C.a,* , Cristián Quezada J.a,b, Nelson Flores N.a, Yorky Melipillán A.b and Tamara Ramírez P.b a. Imaging Center, Hospital Clínico Universidad de Chile, Santiago, Chile. b. Radiology Service, Hospital de Niños Roberto del Río, Santiago, Chile. Abstract: Knee pathology is a reason for consultation and a prevalent condition in children, which is why it is important to know both the normal variants as well as the most frequent pathologies. In this review a brief description is given of the main pathologies and normal variants that affect the knee in children, not only the main clinical characteristics but also the findings described in the different, most used imaging techniques (X-ray, ultrasound, computed tomography and magnetic resonance imaging [MRI]). Keywords: Knee; Paediatrics; Bone lesions. Introduction posteromedial distal femoral metaphysis, near the Pediatric knee imaging studies are used to evaluate insertion site of the medial twin muscle or adductor different conditions, whether traumatic, inflammatory, magnus1. It is a common finding on radiography and developmental or neoplastic. magnetic resonance imaging (MRI), incidental, with At a younger age the normal evolution of the more frequency between ages 10-15 years, although images during the skeletal development of the distal it can be present at any age until the physeal closure, femur, proximal tibia and proximal fibula should be after which it resolves1. In frontal radiography, it ap- known to avoid diagnostic errors. Older children and pears as a radiolucent, well circumscribed, cortical- adolescents present a higher frequency of traumatic based lesion with no associated soft tissue mass, with and athletic injuries. -
Effectiveness of Ultraporous Β-Tricalcium Phosphate (Vitoss) As Bone Graft Substitute for Cavitary Defects in Benign and Low-Grade Malignant Bone Tumors
An Original Study Effectiveness of Ultraporous β-Tricalcium Phosphate (Vitoss) as Bone Graft Substitute for Cavitary Defects in Benign and Low-Grade Malignant Bone Tumors Corey Van Hoff, MD, Julie Balch Samora, MD, MPH, PhD, Michael J. Griesser, MD, Martha K. Crist, RN, BSH, Thomas J. Scharschmidt, MD, and Joel L. Mayerson, MD the graft to promote eventual bone growth into the cavity. Abstract Given their osteogenic, inductive, and conductive proper- We retrospectively evaluated healing with ultrapor- ties, autologous bone grafts have been the gold standard ous β-tricalcium phosphate (β-TCP [Vitoss; Orthovida, of management.3 However, harvesting these grafts can lead Malvern, Pennsylvania]) bone graft in patients who to higher morbidity, including infections, hematomas, neu- underwent surgical excision or curettage of benign bone rovascular injuries, wound healing problems, heterotopic lesions subsequently filled with bone void filler. Twenty- nine patients were treated with curettage and ultrapor- bone formation, cosmetic deformities, pain, and prolonged 4,5 ous β-TCP morsels. Radiologic defect size at initial anesthesia time. postoperative presentation and subsequent visits (mini- Cancellous or cortical bone allografts, which can be mum follow-up, 6 months) was evaluated. Results sug- fresh-frozen or freeze-dried, are a successful alternative to gested that an ultraporous β-TCP synthetic bone graft is autografts, as they have osteoconductive properties and effective in managing bone voids. The vast majority of provide comparable results.6,7 Banked allograft bone, how- patients who undergo curettage for benign bone lesions ever, is slow to incorporate, has the potential for immunoge- can expect to have complete or near complete healing of nicity, and has been known to carry bacteria and viruses.8-10 these defects within 6 months of their surgical procedure Tomford and colleagues8 reported allograft infection rates with use of ultraporous β-TCP morsels. -
Evaluation of Anterior Knee Pain Kristin M Houghton*
Pediatric Rheumatology BioMed Central Review Open Access Review for the generalist: evaluation of anterior knee pain Kristin M Houghton* Address: Division of Rheumatology, British Columbia's Children's Hospital, K4-119 Ambulatory CareBuilding, 4480 Oak Street, Vancouver British Columbia, Canada V6H 3V4 and Allan McGavin Sports Medicine Centre, University of British Columbia, 3055 Wesbrook Mall, Vancouver British Columbia, V6T 1Z3, Canada Email: Kristin M Houghton* - [email protected] * Corresponding author Published: 4 May 2007 Received: 28 December 2006 Accepted: 4 May 2007 Pediatric Rheumatology 2007, 5:8 doi:10.1186/1546-0096-5-8 This article is available from: http://www.ped-rheum.com/content/5/1/8 © 2007 Houghton; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Abstract Anterior knee pain is common in children and adolescents. Evaluation and management is challenging and requires a thorough history and physical exam, and understanding of the pediatric skeleton. This article will review common causes of chronic anterior knee pain in the pediatric population with a focus on patellofemoral pain. Background Clinical history Anterior knee pain (see Figure 1) is one of the most com- The clinical history should include a thorough description mon musculoskeletal complaints seen in the pediatric of the pain characteristics (location, character, onset, population. A fairly extensive differential diagnosis exists duration, change with activity or rest, aggravating and as anterior knee pain is a fairly nonspecific phenomenon.