Inflammation of the Bone Inflammation of the Bone Periapical Inflammatory Lesions
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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. -
(Xgeva®) Related Osteonecrosis of the Jaw: a Retrospective Study
Journal of Clinical Medicine Article A Comparison of the Clinical and Radiological Extent of Denosumab (Xgeva®) Related Osteonecrosis of the Jaw: A Retrospective Study Zineb Assili 1, Gilles Dolivet 2, Julia Salleron 3 , Claire Griffaton-Tallandier 4, Claire Egloff-Juras 1 and Bérengère Phulpin 1,2,* 1 Faculty of Odontology, Lorraine University, 7 Avenue de la Forêt de Haye, 54505 Vandoeuvre les Nancy, France; [email protected] (Z.A.); [email protected] (C.E.-J.) 2 Department of Head and Neck and Dental Surgery, Institut de Cancérologie de Lorraine, 54519 Vadoeuvre-lès-Nancy, France; [email protected] 3 Cellule Data-Biostatistiques, Institut de Cancérologie de Lorraine, 54519 Vandoeuvre-lès-Nancy, France; [email protected] 4 Cabinet de Radiologie RX125, 125 Rue Saint-Dizier, 54000 Nancy, France; [email protected] * Correspondence: [email protected]; Tel.: +33-3-83-59-84-46 Abstract: Medication-related osteonecrosis of the jaw (MRONJ) is a severe side effect of antiresorptive medication. The aim of this study was to evaluate the incidence of denosumab-related osteonecrosis of the jaw and to compare the clinical and radiological extent of osteonecrosis. A retrospective study of patients who received Xgeva® at the Institut de Cancérologie de Lorraine (ICL) was performed. Patients for whom clinical and radiological (CBCT) data were available were divided into two groups: Citation: Assili, Z.; Dolivet, G.; “exposed” for patients with bone exposure and “fistula” when only a fistula through which the bone Salleron, J.; Griffaton-Tallandier, C.; could be probed was observed. The difference between clinical and radiological extent was assessed. -
Chronic Osteomyelitis of Jaw
Chronic Osteomyelitis of Jaw Dr. Dhawal Goyal, 1 Dr. Nilima Malik, 2 Dr. Neha Gupta, 3 Dr. Manoj Agarwal, 4 Dr. Rajani Kalla, 5 Dr. Sanyam Agarwal 6 1. Dr. Dhawal Goyal MDS, Oral Private Practitioner 2. Dr. Nilima Malik MDS Oral and Maxillofacial Surgery 3. Dr. Neha Gupta Assistant Professor, Dept. of Prosthodontics, RUHS College of Dental Sciences, Jaipur 4. Dr. Manoj Agarwal Assistant Professor, Dept. of Conservative Dentistry & Endodontics, RUHS College of Dental Sciences, Jaipur 5. Dr. Rajani Kalla Assistant Professor, Dept. of Prosthodontics, RUHS College of Dental Sciences, Jaipur 6. Dr. Sanyam Agarwal Medical Officer, Dept. of Conservative Dentistry & Endodontics, RUHS College of Dental Sciences, Jaipur The prevalence of osteomyelitis of jaws in third Cultures, bone biopsy, conventional radiography, world country is still at a higher rate despite newer scintigraphy, CT scan are used to diagnose chronic and powerful antibiotics and advances in dental osteomyelitis of jaws. Computed Tomograph helps care. This may be due to low socio-economical in determination of cortex and medullary status, unavailability of primary health care involvement of diseased bone better as compared to services, and poor nutritional status in the rural conventional radiograph. areas. Therapy for osteomyelitis of jaws requires a Osteomyelitis may be defined as an inflammatory multidisciplinary approach. A precise condition of the bone that usually begins as an microbiologic diagnosis and adequate debridement infection of the medullary cavity, rapidly involves of necrotic tissue are essential. Acute the Haversian system and quickly extends to hematogenous osteomyelitis usually responds to periosteum of the affected area. The infection then antimicrobial therapy. -
WHO Manual of Diagnostic Imaging Radiographic Anatomy and Interpretation of the Musculoskeletal System
The WHO manual of diagnostic imaging Radiographic Anatomy and Interpretation of the Musculoskeletal System Editors Harald Ostensen M.D. Holger Pettersson M.D. Authors A. Mark Davies M.D. Holger Pettersson M.D. In collaboration with F. Arredondo M.D., M.R. El Meligi M.D., R. Guenther M.D., G.K. Ikundu M.D., L. Leong M.D., P. Palmer M.D., P. Scally M.D. Published by the World Health Organization in collaboration with the International Society of Radiology WHO Library Cataloguing-in-Publication Data Davies, A. Mark Radiography of the musculoskeletal system / authors : A. Mark Davies, Holger Pettersson; in collaboration with F. Arredondo . [et al.] WHO manuals of diagnostic imaging / editors : Harald Ostensen, Holger Pettersson; vol. 2 Published by the World Health Organization in collaboration with the International Society of Radiology 1.Musculoskeletal system – radiography 2.Musculoskeletal diseases – radiography 3.Musculoskeletal abnormalities – radiography 4.Manuals I.Pettersson, Holger II.Arredondo, F. III.Series editor: Ostensen, Harald ISBN 92 4 154555 0 (NLM Classification: WE 141) The World Health Organization welcomes requests for permission to reproduce or translate its publications, in part or in full. Applications and enquiries should be addressed to the Office of Publications, World Health Organization, CH-1211 Geneva 27, Switzerland, which will be glad to provide the latest information on any changes made to the text, plans for new editions, and reprints and translations already available. © World Health Organization 2002 Publications of the World Health Organization enjoy copyright protection in accordance with the provisions of Protocol 2 of the Universal Copyright Convention. All rights reserved. -
Periapical Radiopacities
2016 self-study course two course The Ohio State University College of Dentistry is a recognized provider for ADA CERP credit. ADA CERP is a service of the American Dental Association to assist dental professionals in identifying quality providers of continuing dental education. ADA CERP does not approve or endorse individual courses or instructors, nor does it imply acceptance of credit hours by boards of dentistry. Concerns or complaints about a CE provider may be directed to the provider or to the Commission for Continuing Education Provider Recognition at www.ada.org/cerp. The Ohio State University College of Dentistry is approved by the Ohio State Dental Board as a permanent sponsor of continuing dental education. This continuing education activity has been planned and implemented in accordance with the standards of the ADA Continuing Education Recognition Program (ADA CERP) through joint efforts between The Ohio State University College of Dentistry Office of Continuing Dental Education and the Sterilization Monitoring Service (SMS). ABOUT this COURSE… FREQUENTLY asked QUESTIONS… . READ the MATERIALS. Read and Q: Who can earn FREE CE credits? review the course materials. COMPLETE the TEST. Answer the A: EVERYONE - All dental professionals eight question test. A total of 6/8 in your office may earn free CE questions must be answered correctly credits. Each person must read the contact for credit. course materials and submit an online answer form independently. SUBMIT the ANSWER FORM ONLINE. You MUST submit your answers ONLINE at: Q: What if I did not receive a confirmation ID? us http://dentistry.osu.edu/sms-continuing-education A: Once you have fully completed your . -
Tuberculosis of the Hip Joint Region in Children
SAOJ Autumn 2013_Orthopaedics Vol3 No4 2013/03/20 3:06 PM Page 38 Page 38 SA Orthopaedic Journal Autumn 2013 | Vol 12 • No 1 Tuberculosis of the hip joint region MAFin Mohideen children MBChB(Medunsa) Registrar MN Rasool MBChB(UKZN), FC(Ortho)SA Paediatric Orthopaedics Nelson Mandela School of Medicine, University of KwaZulu-Natal, Durban, South Africa Reprints requests: [email protected] Abstract Aim: To describe the clinical and radiological manifestations of tuberculosis of the hip joint and the resemblance to com- mon osteoarticular lesions in children. Methods: Thirty-six children (1 to 12 years) were reviewed retrospectively between 1990 and 2011. Clinical, laboratory and radiological features were assessed. The hips were classified and the outcome was graded as described by Shanmugasundaram. Results: Common clinical features were a limp, flexion, adduction and internal rotation contractures. Common radiologi- cal features were osteopaenia and cystic lesions in the neck and acetabulum. Permeative lesions, focal erosions, pathological fractures and sequestra were less common. Seven children had extra-articular lesions. Of the 29 with osteoarticular involvement, six had purely synovial involvement. Osteoarticular lesions mimicked benign bone and joint conditions. Follow-up was 1 to 6 years, 36% were graded as good, 36% fair and 28% had poor outcome with ankylosis. Other complications included avascular necrosis, coxa vara, coxa magna, growth arrest and flex- ion-adduction contractures. Conclusion: Tuberculosis of the hip can mimic various benign conditions. Biopsy from a bony lesion is important. The initial radiological appearance predicts the outcome, especially in the ‘normal’ type of hip. Key words: tuberculosis, hip joint, children Most of the literature on tuberculosis of the hip in children Introduction is over 40 years old.6-11 The lesions were mainly destructive. -
Hematological Diseases and Osteoporosis
International Journal of Molecular Sciences Review Hematological Diseases and Osteoporosis , Agostino Gaudio * y , Anastasia Xourafa, Rosario Rapisarda, Luca Zanoli , Salvatore Santo Signorelli and Pietro Castellino Department of Clinical and Experimental Medicine, University of Catania, 95123 Catania, Italy; [email protected] (A.X.); [email protected] (R.R.); [email protected] (L.Z.); [email protected] (S.S.S.); [email protected] (P.C.) * Correspondence: [email protected]; Tel.: +39-095-3781842; Fax: +39-095-378-2376 Current address: UO di Medicina Interna, Policlinico “G. Rodolico”, Via S. Sofia 78, 95123 Catania, Italy. y Received: 29 April 2020; Accepted: 14 May 2020; Published: 16 May 2020 Abstract: Secondary osteoporosis is a common clinical problem faced by bone specialists, with a higher frequency in men than in women. One of several causes of secondary osteoporosis is hematological disease. There are numerous hematological diseases that can have a deleterious impact on bone health. In the literature, there is an abundance of evidence of bone involvement in patients affected by multiple myeloma, systemic mastocytosis, thalassemia, and hemophilia; some skeletal disorders are also reported in sickle cell disease. Recently, monoclonal gammopathy of undetermined significance appears to increase fracture risk, predominantly in male subjects. The pathogenetic mechanisms responsible for these bone loss effects have not yet been completely clarified. Many soluble factors, in particular cytokines that regulate bone metabolism, appear to play an important role. An integrated approach to these hematological diseases, with the help of a bone specialist, could reduce the bone fracture rate and improve the quality of life of these patients. -
Molecular Characterization of Three Canine Models of Human Rare Bone Diseases: Caffey, Van Den Ende-Gupta, and Raine Syndromes
RESEARCH ARTICLE Molecular Characterization of Three Canine Models of Human Rare Bone Diseases: Caffey, van den Ende-Gupta, and Raine Syndromes Marjo K. Hytönen1,2,3, Meharji Arumilli1,2,3, Anu K. Lappalainen4, Marta Owczarek-Lipska5, Vidhya Jagannathan5, Sruthi Hundi1,2,3, Elina Salmela1,2,3, Patrick Venta6, Eva Sarkiala4, Tarja Jokinen1,4, Daniela Gorgas7, Juha Kere2,3,8, Pekka Nieminen9, Cord Drögemüller5☯, a11111 Hannes Lohi1,2,3☯* 1 Department of Veterinary Biosciences, University of Helsinki, Helsinki, Finland, 2 Research Programs Unit, Molecular Neurology, University of Helsinki, Helsinki, Finland, 3 The Folkhälsan Institute of Genetics, Helsinki, Finland, 4 Department of Equine and Small Animal Medicine, University of Helsinki, Helsinki, Finland, 5 Institute of Genetics, Vetsuisse Faculty, University of Bern, Bern, Switzerland, 6 Department of Microbiology and Molecular Genetics, Michigan State University, East Lansing, Michigan, United States of America, 7 Division of Clinical Radiology, Department of Clinical Veterinary Medicine, Vetsuisse Faculty, OPEN ACCESS University of Bern, Bern, Switzerland, 8 Department of Biosciences and Nutrition, Karolinska Institutet, Huddinge, Sweden, 9 Department of Oral and Maxillofacial Diseases, University of Helsinki, Helsinki, Citation: Hytönen MK, Arumilli M, Lappalainen AK, Finland Owczarek-Lipska M, Jagannathan V, Hundi S, et al. ☯ (2016) Molecular Characterization of Three Canine These authors contributed equally to this work. * [email protected] Models of Human Rare Bone Diseases: Caffey, van den Ende-Gupta, and Raine Syndromes. PLoS Genet 12(5): e1006037. doi:10.1371/journal. pgen.1006037 Abstract Editor: Leigh Anne Clark, Clemson University, UNITED STATES One to two percent of all children are born with a developmental disorder requiring pediatric hospital admissions. -
Tuberculosis – the Masquerader of Bone Lesions in Children MN Rasool FCS(Orth) Department of Orthopaedics, University of Kwazulu-Natal
SAOJ Autumn 2009.qxd 2/27/09 11:11 AM Page 21 CLINICAL ARTICLE SA ORTHOPAEDIC JOURNAL Autumn 2009 / Page 21 C LINICAL A RTICLE Tuberculosis – the masquerader of bone lesions in children MN Rasool FCS(Orth) Department of Orthopaedics, University of KwaZulu-Natal Reprint requests: Dr MN Rasool Department of Orthopaedics University of KwaZulu-Natal Private Bag 7 Congella 4001 Tel: (031) 260 4297 Fax: (031) 260 4518 Email: [email protected] Abstract Fifty-three children with histologically confirmed tuberculous osteomyelitis were treated between 1989 and 2007. The age ranged from 1–12 years. There were 65 osseous lesions (excluding spinal and synovial). Seven had mul- tifocal bone involvement. Four basic types of lesions were seen: cystic (n=46), infiltrative (n=7), focal erosions (n=6) and spina ventosa (n=7). The majority of lesions were in the metaphyses (n=36); the remainder were in the diaphysis, epiphysis, short tubular bones, flat bones and small round bones. Bone lesions resembled chronic infections, simple and aneurysmal bone cysts, cartilaginous tumours, osteoid osteoma, haematological bone lesions and certain osteochondroses seen during the same period of study. Histological confirmation is man- datory to confirm the diagnosis of tuberculosis as several bone lesions can mimic tuberculous osteomyelitis. Introduction The variable radiological appearance of isolated bone Tuberculous osteomyelitis is less common than skeletal lesions in children can resemble various bone lesions tuberculosis involving the spine and joints. The destruc- including subacute and chronic osteomyelitis, simple and tive bone lesions of tuberculosis, the disseminated and the aneurysmal bone cysts, cartilaginous tumours, osteoid multifocal forms, are less common now than they were 50 osteoma, granulomatous lesions, haematological disease, 6,7,12 years ago.1-7 However, in recent series, solitary involve- and certain malignant tumours. -
Core Decompression for Avascular Necrosis (For North Carolina Only) – Community Plan Medical Policy
UnitedHealthcare® Community Plan Medical Policy Core Decompression for Avascular Necrosis (for North Carolina Only) Policy Number: CSNCT0219.01 Effective Date: July 1, 2021 Instructions for Use Table of Contents Page Related Policies Application.......................................................................................... 1 None Coverage Rationale ........................................................................... 1 Applicable Codes .............................................................................. 1 Description of Services ..................................................................... 2 Clinical Evidence ............................................................................... 3 U.S. Food and Drug Administration ................................................ 7 References ......................................................................................... 7 Policy History/Revision Information................................................ 8 Instructions for Use ........................................................................... 8 Application This Medical Policy only applies to the state of North Carolina. Coverage Rationale Core decompression is proven and medically necessary for treating early (pre-collapse stage I and II) avascular necrosis of the femoral head. Core decompression is unproven and not medically necessary for treating late avascular necrosis of the femoral head or for avascular necrosis elsewhere, including the humeral head, the distal femur, the talus, or the -
Ewing's Sarcoma and Primary Osseous Lymphoma
36 Ewing’s Sarcoma and Primary Osseous Lymphoma: Spectrum of Imaging Appearances Marc-André Weber, MD, MSc1 Olympia Papakonstantinou, MD2 Violeta Vasilevska Nikodinovska, MD, PhD3 Filip M. Vanhoenacker, MD, PhD4 1 Institute of Diagnostic and Interventional Radiology, University Address for correspondence Marc-André Weber, MD, MSc, Institute Medical Center Rostock, Rostock, Germany of Diagnostic and Interventional Radiology, University Medical Center 2 Second Department of Radiology, National and Kapodistrian Rostock, Ernst-Heydemann-Str. 6, 18057 Rostock, Germany University of Athens “Attikon” Hospital, Athens, Greece (e-mail: [email protected]). 3 Department of Radiology, University Surgical Clinic “St. Naum Ohridski,” University “Ss. Cyril and Methodius,” Skopje, Macedonia 4 Department of Radiology, AZ Sint-Maarten Mechelen, University Hospital Antwerp, Ghent University, Mechelen, Belgium Semin Musculoskelet Radiol 2019;23:36–57. Abstract Ewing’s sarcoma (ES) is a rare, highly malignant anaplastic stem cell tumor. Histolo- gically, the tumor consists of uniform densely packed small monomorphic cells with round nuclei. The typical appearance at hematoxylin and eosin (H&E) staining is small blue round cells without any matrix formation. On conventional radiography, ES typically presents as a permeative lesion in the diaphysis of a long bone in a child. A Keywords large soft tissue component is another characteristic feature, best depicted by ► Ewing’sSarcoma magnetic resonance imaging. ► primary osseous Primary osseous lymphomas are most commonly highly malignant B-cell lymphomas. lymphoma At H&E histologic staining, the tumor stroma consists of diffuse round-cell infiltrates ► radiography that resembles the appearance of ES. Although there is no typical imaging appearance ► magnetic resonance of an osseous lymphoma, it should be considered in an adult presenting with a Lodwick imaging grade II or III lesion in the metaphysis or diaphysis of a large long bone, the pelvis, or the ► review vertebral column. -
Sclerosing Bone Dysplasias: Genetic, Clinical and Radiology Update of Hereditary and Non-Hereditary Disorders
BJR © 2016 The Authors. Published by the British Institute of Radiology Received: Revised: Accepted: http://dx.doi.org/10.1259/bjr.20150349 26 April 2015 14 December 2015 17 February 2016 Cite this article as: Boulet C, Madani H, Lenchik L, Vanhoenacker F, Amalnath DS, De Mey J, et al. Sclerosing bone dysplasias: genetic, clinical and radiology update of hereditary and non-hereditary disorders. Br J Radiol 2016; 89: 20150349. REVIEW ARTICLE Sclerosing bone dysplasias: genetic, clinical and radiology update of hereditary and non-hereditary disorders 1CEDRIC BOULET, MD, 2HARDI MADANI, FRCR, 3LEON LENCHIK, MD, 4FILIP VANHOENACKER, MD, PhD, 5DEEPAK S AMALNATH, MD, 1JOHAN DE MEY, MD, PhD and 1MICHEL DE MAESENEER, MD, PhD 1Department of Radiology, Universitair Ziekenhuis Brussel, Brussel, Belgium 2Department of Radiology, Royal Free Hospital, London, UK 3Department of Radiology, Wake Forest University, Winston Salem, NC, USA 4Department of Radiology, Universitair Ziekenhuis Anwerpen, Antwerpen, Belgium 5Department of Medicine, Indira Gandhi Medical College and Research Institute, Pondicherry, India Address correspondence to: Dr Michel De Maeseneer E-mail: [email protected] ABSTRACT There is a wide variety of hereditary and non-hereditary bone dysplasias, many with unique radiographic findings. Hereditary bony dysplasias include osteopoikilosis, osteopathia striata, osteopetrosis, progressive diaphyseal dysplasia, hereditary multiple diaphyseal sclerosis and pyknodysostosis. Non-hereditary dysplasias include melorheostosis, intramedullary osteosclerosis and overlap syndromes. Although many of these dysplasias are uncommon, radiologists should be familiar with their genetic, clinical and imaging findings to allow for differentiation from acquired causes of bony sclerosis. We present an overview of hereditary and non-hereditary bony dysplasias with focus on the pathogenesis, clinical and radiographic findings of each disorder.