Osteoid Osteoma: Contemporary Management
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Bone and Soft Tissue Tumors Have Been Treated Separately
EPIDEMIOLOGY z Sarcomas are rare tumors compared to other BONE AND SOFT malignancies: 8,700 new sarcomas in 2001, with TISSUE TUMORS 4,400 deaths. z The incidence of sarcomas is around 3-4/100,000. z Slight male predominance (with some subtypes more common in women). z Majority of soft tissue tumors affect older adults, but important sub-groups occur predominantly or exclusively in children. z Incidence of benign soft tissue tumors not known, but Fabrizio Remotti MD probably outnumber malignant tumors 100:1. BONE AND SOFT TISSUE SOFT TISSUE TUMORS TUMORS z Traditionally bone and soft tissue tumors have been treated separately. z This separation will be maintained in the following presentation. z Soft tissue sarcomas will be treated first and the sarcomas of bone will follow. Nowhere in the picture….. DEFINITION Histological z Soft tissue pathology deals with tumors of the classification connective tissues. of soft tissue z The concept of soft tissue is understood broadly to tumors include non-osseous tumors of extremities, trunk wall, retroperitoneum and mediastinum, and head & neck. z Excluded (with a few exceptions) are organ specific tumors. 1 Histological ETIOLOGY classification of soft tissue tumors tumors z Oncogenic viruses introduce new genomic material in the cell, which encode for oncogenic proteins that disrupt the regulation of cellular proliferation. z Two DNA viruses have been linked to soft tissue sarcomas: – Human herpes virus 8 (HHV8) linked to Kaposi’s sarcoma – Epstein-Barr virus (EBV) linked to subtypes of leiomyosarcoma z In both instances the connection between viral infection and sarcoma is more common in immunosuppressed hosts. -
The Health-Related Quality of Life of Sarcoma Patients and Survivors In
Cancers 2020, 12 S1 of S7 Supplementary Materials The Health-Related Quality of Life of Sarcoma Patients and Survivors in Germany—Cross-Sectional Results of A Nationwide Observational Study (PROSa) Martin Eichler, Leopold Hentschel, Stephan Richter, Peter Hohenberger, Bernd Kasper, Dimosthenis Andreou, Daniel Pink, Jens Jakob, Susanne Singer, Robert Grützmann, Stephen Fung, Eva Wardelmann, Karin Arndt, Vitali Heidt, Christine Hofbauer, Marius Fried, Verena I. Gaidzik, Karl Verpoort, Marit Ahrens, Jürgen Weitz, Klaus-Dieter Schaser, Martin Bornhäuser, Jochen Schmitt, Markus K. Schuler and the PROSa study group Includes Entities We included sarcomas according to the following WHO classification. - Fletcher CDM, World Health Organization, International Agency for Research on Cancer, editors. WHO classification of tumours of soft tissue and bone. 4th ed. Lyon: IARC Press; 2013. 468 p. (World Health Organization classification of tumours). - Kurman RJ, International Agency for Research on Cancer, World Health Organization, editors. WHO classification of tumours of female reproductive organs. 4th ed. Lyon: International Agency for Research on Cancer; 2014. 307 p. (World Health Organization classification of tumours). - Humphrey PA, Moch H, Cubilla AL, Ulbright TM, Reuter VE. The 2016 WHO Classification of Tumours of the Urinary System and Male Genital Organs—Part B: Prostate and Bladder Tumours. Eur Urol. 2016 Jul;70(1):106–19. - World Health Organization, Swerdlow SH, International Agency for Research on Cancer, editors. WHO classification of tumours of haematopoietic and lymphoid tissues: [... reflects the views of a working group that convened for an Editorial and Consensus Conference at the International Agency for Research on Cancer (IARC), Lyon, October 25 - 27, 2007]. 4. ed. -
Leg Pain and Swelling in a 22-Year-Old Man
CLINICAL ORTHOPAEDICS AND RELATED RESEARCH Number 448, pp. 259–266 © 2006 Lippincott Williams & Wilkins Orthopaedic • Radiology • Pathology Conference Leg Pain and Swelling in a 22-Year-Old Man Mustafa H. Khan, MD*; Ritesh Darji, MD†; Uma Rao, MD‡; and Richard McGough, MD* HISTORY AND PHYSICAL EXAMINATION which precluded him from participating in any sports, and night pain. The patient localized the pain over the anterior The patient was a 22-year man who presented with right aspect of the midtibia. He denied any history of trauma. He leg pain and swelling that had increased during the last 6 required regular doses of oxycodone for the past year to years. He complained of pain with walking and running, achieve adequate pain relief. His past medical history was unremarkable. From the *Departments of Orthopedic Surgery, †Radiology, and ‡Pathology; On physical examination a large anterior pretibial bony University of Pittsburgh Medical Center, Pittsburgh, PA. mass was palpable. No other masses were palpable in the Each author certifies that he or she has no commercial associations (eg, consultancies, stock ownership, equity interest, patent/licensing arrange- extremities and there was no evidence of lymphadenopa- ments, etc) that might pose a conflict of interest in connection with the thy. Active and passive range of motion testing and neu- submitted article. rovascular examination was in normal limits. Each author certifies that his or her institution has approved the reporting of this case report and that all investigations were conducted in conformity with Plain radiographs and MRI scans of the leg, along ethical principles of research. with CT scan of the leg and chest, were obtained Correspondence to: Richard McGough, MD, Department of Orthopedic Sur- (Figs 1–3). -
The Role of Cytogenetics and Molecular Diagnostics in the Diagnosis of Soft-Tissue Tumors Julia a Bridge
Modern Pathology (2014) 27, S80–S97 S80 & 2014 USCAP, Inc All rights reserved 0893-3952/14 $32.00 The role of cytogenetics and molecular diagnostics in the diagnosis of soft-tissue tumors Julia A Bridge Department of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, NE, USA Soft-tissue sarcomas are rare, comprising o1% of all cancer diagnoses. Yet the diversity of histological subtypes is impressive with 4100 benign and malignant soft-tissue tumor entities defined. Not infrequently, these neoplasms exhibit overlapping clinicopathologic features posing significant challenges in rendering a definitive diagnosis and optimal therapy. Advances in cytogenetic and molecular science have led to the discovery of genetic events in soft- tissue tumors that have not only enriched our understanding of the underlying biology of these neoplasms but have also proven to be powerful diagnostic adjuncts and/or indicators of molecular targeted therapy. In particular, many soft-tissue tumors are characterized by recurrent chromosomal rearrangements that produce specific gene fusions. For pathologists, identification of these fusions as well as other characteristic mutational alterations aids in precise subclassification. This review will address known recurrent or tumor-specific genetic events in soft-tissue tumors and discuss the molecular approaches commonly used in clinical practice to identify them. Emphasis is placed on the role of molecular pathology in the management of soft-tissue tumors. Familiarity with these genetic events -
View Presentation Notes
When is a musculoskeletal condition a tumor? Recognizing common bone and soft tissue tumors Christian M. Ogilvie, MD Assistant Professor of Orthopaedic Surgery University of Pennsylvania University of Pennsylvania Department of Orthopaedic Surgery Purpose • Recognize that tumors can present in the extremities of patients treated by athletic trainers • Know that tumors may present as a lump, pain or both • Become familiar with some bone and soft tissue tumors University of Pennsylvania Department of Orthopaedic Surgery Summary • Introduction – Pain – Lump • Bone tumors – Malignant – Benign • Soft tissue tumors – Malignant – Benign University of Pennsylvania Department of Orthopaedic Surgery Summary • Presentation • Imaging • History • Similar conditions –Injury University of Pennsylvania Department of Orthopaedic Surgery Introduction •Connective tissue tumors -Bone -Cartilage -Muscle -Fat -Synovium (lining of joints, tendons & bursae) -Nerve -Vessels •Malignant (cancerous): sarcoma •Benign University of Pennsylvania Department of Orthopaedic Surgery Introduction: Pain • Malignant bone tumors: usually • Benign bone tumors: some types • Malignant soft tissue tumors: not until large • Benign soft tissue tumors: some types University of Pennsylvania Department of Orthopaedic Surgery Introduction: Pain • Bone tumors – Not necessarily activity related – May be worse at night – Absence of trauma, mild trauma or remote trauma • Watch for referred patterns – Knee pain for hip problem – Arm and leg pains in spine lesions University of Pennsylvania -
Osteoid Osteoma and Your Everyday Practice
n Review Article Instructions 1. Review the stated learning objectives at the beginning cme ARTICLE of the CME article and determine if these objectives match your individual learning needs. 2. Read the article carefully. Do not neglect the tables and other illustrative materials, as they have been selected to enhance your knowledge and understanding. 3. The following quiz questions have been designed to provide a useful link between the CME article in the issue Osteoid Osteoma and your everyday practice. Read each question, choose the correct answer, and record your answer on the CME Registration Form at the end of the quiz. Petros J. Boscainos, MD, FRCSEd; Gerard R. Cousins, MBChB, BSc(MedSci), MRCS; 4. Type or print your full name and address and your date of birth in the space provided on the CME Registration Form. Rajiv Kulshreshtha, MBBS, MRCS; T. Barry Oliver, MBChB, MRCP, FRCR; 5. Indicate the total time spent on the activity (reading article and completing quiz). Forms and quizzes cannot be Panayiotis J. Papagelopoulos, MD, DSc processed if this section is incomplete. All participants are required by the accreditation agency to attest to the time spent completing the activity. educational objectives 6. Complete the Evaluation portion of the CME Regi stration Form. Forms and quizzes cannot be processed if the Evaluation As a result of reading this article, physicians should be able to: portion is incomplete. The Evaluation portion of the CME Registration Form will be separated from the quiz upon receipt at ORTHOPEDICS. Your evaluation of this activity will in no way affect educational1. -
What Is New in Orthopaedic Tumor Surgery?
15.11.2018 What is new in orthopaedic tumor surgery? Marko Bergovec, Andreas Leithner Department of Orhtopaedics and Trauma Medical University of Graz, Austria 1 15.11.2018 Two stories • A story about the incidental finding • A scary story with a happy end The story about the incidental finding • 12-year old football player • Small trauma during sport • Still, let’s do X-RAY 2 15.11.2018 The story about the incidental finding • Panic !!! • A child has a tumor !!! • All what a patient and parents hear is: – bone tumor = death – amputation – will he ever do sport again? • Still – what now? 3 15.11.2018 A scary story with a happy end • 12-year old football player • Small trauma during sport • 3 weeks pain not related to physical activity • “It is nothing, just keep it cool, take a rest” 4 15.11.2018 A scary story with a happy end • A time goes by • After two weeks of rest, pain increases... • OK, let’s do X-RAY 5 15.11.2018 TUMORS benign vs malign bone vs soft tissue primary vs metastasis SARCOMA • Austria – cca 200 patients / year – 1% of all malignant tumors • (breast carcinoma = 5500 / year) 6 15.11.2018 Distribution of the bone tumoris according to patients’ age and sex 250 200 150 100 broj bolesnika broj 50 M Ž 0 5 10 15 20 25 30 35 40 45 50 55 60 65 70 75 80 80+ dob 7 15.11.2018 WHO Histologic Classification of Bone Tumors Bone-forming tumors Benign: Osteoma; Osteoid osteoma; Osteoblastoma Intermediate; Aggressive (malignant) osteoblastoma Malignant: Conventional central osteosarcoma; Telangiectatic osteosarcoma; Intraosseous well -
Ewing-Like Adamantinoma
Orthopaedics & Traumatology: Surgery & Research (2012) 98, 845—849 View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Elsevier - Publisher Connector Available online at www.sciencedirect.com CASE REPORT Ewing-like adamantinoma a,∗ a a b a M.M. Hamdane , L. Charfi , M. Driss , H. Nouri , R. Sellami-Dhouib , a b a K. Mrad ,M. Mestiri , K. Ben Romdhane a Histopathology Department, Salah Azaiez Institute, Bab Saâdoun, 1006 Tunis, Tunisia b Adult Orthopaedics Department, Mohamed-Kassab Orthopaedics Institute, Ksar Saïd, 2010 Mannouba, Tunisia Accepted: 6 June 2012 KEYWORDS Summary The Ewing-like variation of adamantinoma is a rare entity, leading to challenge its Adamantinoma; differential diagnosis, notably with Ewing’s sarcoma. We are reporting a case of a 20-year-old Sarcoma; male who presented with swelling in the left leg that had progressed over a 2-year period. X-rays Ewing; revealed a tumour in the tibia that was intracortical, osteolytic, multilocular and invaded the Pathology; soft tissues. A surgical biopsy was performed. Histopathology examination showed a tumour Immunohistochemistry growth with small round cells expressing CD99. A diagnosis of Ewing’s sarcoma was made. Since the patient declined surgical treatment, chemotherapy was administered. Tw o years later, the patient returned because the tumour had grown in size. A second biopsy was performed. Microscopic evaluation showed a tumour growth with osteofibrous and epithelial components, which expressed pankeratin and vimentin, but was negative for CD99. A diagnosis of Ewing-like adamantinoma was made. © 2012 Published by Elsevier Masson SAS. Introduction We are reporting here on a rare case of Ewing-like adamanti- noma. -
Adamantinoma
Cancer Association of South Africa (CANSA) Fact Sheet on Adamantinoma Introduction Bone cancer develops in the skeletal system and destroys tissue. It can spread to distant organs, such as the lungs. The usual treatment for bone cancer is surgery, and it has a good outlook following early diagnosis and management. Adamantinoma The two main types are primary and secondary bone cancer. In primary bone cancer, cancer develops in the cells of the bone. Secondary bone cancer occurs when cancers that develop elsewhere spread, or metastasize, to the bones. Adamantinoma Adamantinoma is a rare bone cancer. It makes up less than 1% of bone cancers. Most of the time, adamantinoma grows in the lower leg. It often starts as a lump in the middle of the shinbone (tibia) or the calf bone (fibula). Adamantinoma can also occur in the jaw bone (mandible) or, sometimes, the forearm, hands, or feet. An adamantinoma lump can be painful, swollen and red, and can cause movement problems. [Picture Credit: Adamantinoma] Adamantinoma mostly occurs in the second to fifth decade. The median patient age is 25 to 35 years, with a range from 2 years to 86 years. It is slightly more common in men than women, with a ratio of 5:4. It rarely occurs in children. Adamantinoma is a serious condition. Treatment is important for survival but it is possible to make a full recovery. Limaiem, F., Tafti, D. & Malik, A. 2020. “Adamantinoma is a rare low-grade malignant bone tumor of uncertain histogenesis which occurs commonly in the diaphyses and metaphyses of the tibia. -
Primary Tumors of the Spine
280 Primary Tumors of the Spine Sebnem Orguc, MD1 Remide Arkun, MD1 1 Department of Radiology, Celal Bayar University, Manisa, Türkiye Address for correspondence Sebnem Orguc, MD, Department of 2 Department of Radiology, Ege University, İzmir, Türkiye Radiology, Celal Bayar University, Manisa, Türkiye (e-mail: [email protected]; [email protected]). Semin Musculoskelet Radiol 2014;18:280–299. Abstract Spinal tumors consist of a large spectrum of various histologic entities. Multiple spinal lesions frequently represent known metastatic disease or lymphoproliferative disease. In solitary lesions primary neoplasms of the spine should be considered. Primary spinal tumors may arise from the spinal cord, the surrounding leptomeninges, or the extradural soft tissues and bony structures. A wide variety of benign neoplasms can involve the spine including enostosis, osteoid osteoma, osteoblastoma, aneurysmal bone cyst, giant cell tumor, and osteochondroma. Common malignant primary neo- plasms are chordoma, chondrosarcoma, Ewing sarcoma or primitive neuroectodermal Keywords tumor, and osteosarcoma. Although plain radiographs may be useful to characterize ► spinal tumor some spinal lesions, magnetic resonance imaging is indispensable to determine the ► extradural tumor extension and the relationship with the spinal canal and nerve roots, and thus determine ► magnetic resonance the plan of management. In this article we review the characteristic imaging features of imaging extradural spinal lesions. Spinal tumors consist of a large spectrum of various histo- Benign Tumors of the Osseous Spine logic entities. Primary spinal tumors may arise from the spinal cord (intraaxial or intramedullary space), the sur- Enostosis rounding leptomeninges (intradural extramedullary space), Enostosis, also called a bone island, is a frequent benign or the extradural soft tissues and bony structures (extra- hamartomatous osseous spinal lesion with a developmental dural space). -
Peripheral Osteoma of the Mandible a Report of Two Cases and Review of Literature
Journal of Research in Medical and Dental Science 2020, Volume 8, Issue 6, Page No: 176-179 Copyright CC BY-NC 4.0 Available Online at: www.jrmds.in eISSN No. 2347-2367: pISSN No. 2347-2545 Peripheral Osteoma of the Mandible a Report of Two Cases and Review of Literature Jawahar Anand*, Anil Kumar Desai, Sayali Desai Department of Oral and Maxillofacial Surgery, Craniofacial Unit and Research Centre, SDM College of Dental Sciences, Dharwad, Karnataka, India ABSTRACT Osteoma is a benign osteogenic tumour, commonly involving the craniofacial bones. It is characterized by excessive proliferation of cortical or cancellous bone. It can be of the central, peripheral or extraskeletal variety. Peripheral osteoma arises from the periosteum and is usually asymptomatic, however, can attain large size in the involved bone. In this paper, we report two cases of peripheral osteoma and review the literature related to the pathological condition. Two patients reported with a chief complaint of asymptomatic slow-growing swelling over the mandibular body region. Radiographic examination revealed a lobulated pedunculated radiopaque mass. It was excised surgically, and no recurrence was noted on follow-up visits. Osteoma involving the jaws is not common and can be associated with Gardner’s syndrome thereby requiring regular follow-up and thorough examination. Surgical excision is the treatment of choice and recurrence is rare. Key words: Peripheral osteoma, Mandibular osteoma, Benign tumour, Osteogenic tumour. HOW TO CITE THIS ARTICLE Review of Literature, J Res Med Dent Sci, 2020, 8 (6): 176-179. : Jawahar Anand, Anil Kumar Desai, Sayali Desai, Peripheral Osteoma of the Mandible a Report of Two Cases and Corresponding author: Jawahar Anand purpose of this paper is to report two cases of e-mail: [email protected] osteomas involving the mandibular body and Received: 27/08/2020 present a review of the literature. -
Osteoid Osteoma of Mandibular Bone Case Report and Review of The
Journal of Oral and Maxillofacial Surgery, Medicine, and Pathology 31 (2019) 322–326 Contents lists available at ScienceDirect Journal of Oral and Maxillofacial Surgery, Medicine, and Pathology journal homepage: www.elsevier.com/locate/jomsmp Osteoid osteoma of mandibular bone: Case report and review of the T literature ⁎ Takashi Maeharaa, ,1, Yuka Murakamia,1, Shintaro Kawanoa, Yurie Mikamia, Tamotsu Kiyoshimab, Toru Chikuic, Noriko Kakizoea, Ryusuke Munemuraa, Seiji Nakamuraa a Section of Oral and Maxillofacial Oncology, Division of Maxillofacial Diagnostic and Surgical Sciences, Faculty of Dental Science, Kyushu University, Fukuoka, Japan b Laboratory of Oral Pathology, Division of Maxillofacial Diagnostic and Surgical Sciences, Faculty of Dental Science, Kyushu University, Fukuoka, Japan c Department of Oral and Maxillofacial Radiology, Faculty of Dental Science, Ktyushu University, Fukuoka, Japan ARTICLE INFO ABSTRACT Keywords: Osteoid osteoma is a benign bone-forming tumor and characterized by its limited growth potential, not Osteoid osteoma exceeding 2 cm. The radiological hallmark of this tumor is a nidus, which is a small round area of relative Osteoblastoma radiolucency. Osteoid osteoma can involve any bone but is most commonly found in long bones and is Osteosarcoma extremely rare in the head and neck region. This disease characteristically presents with dull pain, worse Nidus at night, and sometimes relieved with NSAIDs. A 24-year-old Japanese woman presented with spontaneous Mandible pain and tenderness on the lingual side of her mandibular second molar on the right side. The patient reported that her pain had gradually increased, becoming more continuous and severe and no longer responding to NSAIDs. An initial panoramic radiograph revealed an oval, internally non-uniform, some- what obscure boundaries in the right mandible.