245 results match your criteria Chondromyxoid Fibroma Imaging


Chondromyxoid fibroma of the temporal bone: A case report and review of the literature.

World J Clin Cases 2018 Dec;6(16):1210-1216

Department of Radiology, the Affiliated Hospital of Qingdao University, Qingdao 266000, Shandong Province, China.

Background: Chondromyxoid fibroma (CMF) is a rare benign bone tumour of cartilaginous origin, which usually affects the metaphysis of the long bone. Involvement of the temporal bone is extremely rare. Patients with CMF in the temporal bone can present some neurological deficits due to involvement of surrounding neural structures. Read More

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http://dx.doi.org/10.12998/wjcc.v6.i16.1210DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6306630PMC
December 2018

Surface-type chondromyxoid fibroma in an elderly patient: a case report and literature review.

Skeletal Radiol 2018 Nov 29. Epub 2018 Nov 29.

Department of Musculoskeletal Radiology, NYU Langone Health, New York, NY, USA.

Chondromyxoid fibroma (CMF) is a rare benign bone neoplasm that typically occurs in young adults. Juxtacortical or surface-type CMF are rarer still and we present the case of a surface-type CMF in a 78-year-old woman, with only one other case described in a patient of a similar age previously. This patient was an otherwise healthy woman who presented for evaluation of a palpable lump in the anterior proximal tibia. Read More

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http://dx.doi.org/10.1007/s00256-018-3120-4DOI Listing
November 2018
2 Reads

Huge chondromyxoid fibroma of the right iliac wing with tremendous soft tissue extensions.

BJR Case Rep 2018 21;4(1):20170014. Epub 2017 Oct 21.

Department of Radiology, Benha University, Benha, Egypt.

This report describes a huge chondromyxoid fibroma (CMF) that developed in the right iliac crest and wing. The tumour is rare, perhaps the rarest of all bone tumours, and its occurrence in the iliac crest and wing of a 63-year-old male is extraordinarily uncommon. The patient complained of gradual onset of right groin pain over a period of more than 2 years and low back pain and tender swelling of the right gluteal region over a period of another 1 year. Read More

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http://dx.doi.org/10.1259/bjrcr.20170014DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6159151PMC
October 2017
9 Reads

Peering beneath the surface: Juxtacortical tumors of bone (part I).

Clin Imaging 2018 Sep - Oct;51:1-11. Epub 2018 Feb 3.

Department of Radiology, Cleveland Medical Center, University Hospitals of Cleveland, Case Western Reserve University, Cleveland, OH, USA.

Juxtacortical or surface tumors of bone are neoplasms arising from or just outside the cortex, and are composed of different histologic types. Although the imaging appearances of these lesions have similarities to their intramedullary counterparts, their location alters their radiographic and MR characteristics, creating difficulties in diagnosis. Meanwhile, several non-neoplastic lesions, such as stress reaction/stress fracture and indolent infectious processes, compound the differential diagnosis. Read More

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http://dx.doi.org/10.1016/j.clinimag.2018.01.009DOI Listing
December 2018
29 Reads

Benign Chondromyxoid Fibroma of the Iliac Crest.

J Orthop Sports Phys Ther 2018 Feb;48(2):122

A 23-year-old woman initiated a running program and after 2 months began experiencing right hip joint pain and sharp pain at the iliac crest. Following evaluation by her primary care physician, she was referred to a physical therapist. Eighteen months later, the patient had developed a bony prominence at the iliac crest that was painful to touch. Read More

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http://dx.doi.org/10.2519/jospt.2018.7551DOI Listing
February 2018
5 Reads

Peering beneath the surface: juxtacortical tumors of bone (part II).

Clin Imaging 2018 Jul - Aug;50:113-122. Epub 2018 Jan 11.

Department of Radiology, Cleveland Medical Center, University Hospitals of Cleveland, Case Western Reserve University, Cleveland, OH, USA.

Juxtacortical or surface tumors of bone are neoplasms arising from or just outside the cortex, and are composed of different histologic types. Although the imaging appearances of these lesions have similarities to their intramedullary counterparts, their location alters their radiographic and MR characteristics, creating difficulties in diagnosis. Meanwhile, several non-neoplastic lesions, such as stress reaction/stress fracture and indolent infectious processes, compound the differential diagnosis. Read More

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http://dx.doi.org/10.1016/j.clinimag.2018.01.005DOI Listing
October 2018
17 Reads

Chondromyxoid Fibroma Arising in Craniofacial Sites: A Clinicopathologic Analysis of 25 Cases.

Am J Surg Pathol 2018 03;42(3):392-400

Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA.

Chondromyxoid fibroma (CMF) is a rare benign tumor, usually arising in the metaphysis of long bones in young adults. Occurrence in craniofacial bones presents a particular diagnostic challenge given its unusual location and resemblance to malignant mimics. We describe the clinicopathologic features of 25 cases of craniofacial CMF identified between 1999 and 2017. Read More

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http://dx.doi.org/10.1097/PAS.0000000000001019DOI Listing
March 2018
7 Reads

Radiological presentation of chondromyxoid fibroma in the sellar region: A CARE-compliant article and literature review.

Medicine (Baltimore) 2017 Dec;96(49):e9049

aDepartment of Neurology, Shengjing Hospital of China Medical University, Shenyang, Liao Ning, ChinabDepartment of Pathology, Duke University Medical Center, Durham, NCcDepartment of Pathology, First Affiliated Hospital of China Medical University and College of Basic Medical Sciences, Shenyang, Liao Ning, China.

Rationale: Chondromyxoid fibroma (CMF) is a rare benign bone neoplasm which often occurs in the lower extremities. Little is known about the radiological and histological presentation of CMF in the sellar region.

Patient Concerns: A 16-year-old Asian male presented to the hospital 12 months ago with bilateral diplopia involving right visual fields, intermittent headaches, and dizziness. Read More

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http://dx.doi.org/10.1097/MD.0000000000009049DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5728922PMC
December 2017
17 Reads

An intracortical chondromyxoid fibroma in the diaphysis of the metatarsal.

Skeletal Radiol 2017 Dec 15;46(12):1757-1762. Epub 2017 Aug 15.

Department of Pathology, Korea University Ansan Hospital, Ansan-si, Republic of Korea.

Chondromyxoid fibromas (CMFs) are rare, benign, primary tumors of bones, and occur in the metaphyses of the medullary canals of the long bones. The occurrence of intracortical CMFs is extremely rare. Very few cases of intracortical CMFs located in the long tubular bones have been reported to date. Read More

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http://dx.doi.org/10.1007/s00256-017-2743-1DOI Listing
December 2017
3 Reads

Chondromyxoid fibroma of the distal fibula treated by percutaneous radiofrequency ablation.

J Orthop Surg (Hong Kong) 2017 May-Aug;25(2):2309499017720830

4 Department of Orthopedic Surgery, Hadassah-Hebrew University School of Medicine, Shaare Zedek Medical Center, Jerusalem, Israel.

Background: Percutaneous radiofrequency ablation (RFA) has been shown to be an effective treatment for soft tissue lesions and also benign bone tumors, especially osteoid osteoma. There are limited data regarding this technique in other bone tumors, specifically larger and more aggressive ones.

Purposes: To describe the use of RFA as a definitive treatment and an alternative to traditional open surgery for the treatment of chondromyxoid fibroma (CMF), a benign but locally aggressive bone tumor. Read More

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http://dx.doi.org/10.1177/2309499017720830DOI Listing
March 2018
4 Reads

Benign Bone Conditions That May Be FDG-avid and Mimic Malignancy.

Semin Nucl Med 2017 07 12;47(4):322-351. Epub 2017 Apr 12.

Department of Radiology and Nuclear Medicine, Deventer Ziekenhuis, Deventer, The Netherlands.

Positron emission tomography with the radiotracer F-fluoro-2-deoxy-d-glucose (FDG) plays an important role in the evaluation of bone pathology. However, FDG is not a cancer-specific agent, and knowledge of the differential diagnosis of benign FDG-avid bone alterations that may resemble malignancy is important for correct patient management, including the avoidance of unnecessary additional invasive tests such as bone biopsy. This review summarizes and illustrates the spectrum of benign bone conditions that may be FDG-avid and mimic malignancy, including osteomyelitis, bone lesions due to benign systemic diseases (Brown tumor, Erdheim-Chester disease, Gaucher disease, gout and other types of arthritis, Langerhans cell histiocytosis, and sarcoidosis), benign primary bone lesions (bone cysts, chondroblastoma, chondromyxoid fibroma, desmoplastic fibroma, enchondroma, giant cell tumor and granuloma, hemangioma, nonossifying fibroma, and osteoid osteoma and osteoblastoma), and a group of miscellaneous benign bone conditions (post bone marrow biopsy or harvest status, bone marrow hyperplasia, fibrous dysplasia, fractures, osteonecrosis, Paget disease of bone, particle disease, and Schmorl nodes). Read More

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http://dx.doi.org/10.1053/j.semnuclmed.2017.02.004DOI Listing
July 2017
31 Reads

[Chondromyxoid fibroma of the mandible: a case report].

Hua Xi Kou Qiang Yi Xue Za Zhi 2016 Dec;34(6):654-656

Dept. of Oral and Maxillofacial Surgery, General Hospital of Ningxia Medical University, Yinchuan 750004, China.

Chondromyxoid fibroma (CMF) is a rare benign bone tumor. This tumor mostly affects the long bones of the appendicular skeleton but rarely grows in the craniofacial region. In this article, a case of CMF of the mandible was presented to enhance our understanding of CMF. Read More

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http://dx.doi.org/10.7518/hxkq.2016.06.020DOI Listing
December 2016
6 Reads

Chondromyxoid Fibroma of the Skull Base: Our Experience with an Elusive Disease.

J Neurol Surg A Cent Eur Neurosurg 2017 Nov 2;78(6):576-581. Epub 2017 Mar 2.

Rome Army Hospital "Celio," Neurosurgery Division, Sapienza University Rome, Dipartimento Scienze Neurosensoriali, Rome, Italy.

Chondromyxoid fibroma (CMF) is an extremely rare lesion of the skull base. This histologic type typically predilects metaphysis of the long bones. It is locally invasive/infiltrative, and this tendency is more concerning in the skull base, where a radical resection is often technically impossible because of the presence of vital neurovascular structures. Read More

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http://dx.doi.org/10.1055/s-0037-1599137DOI Listing
November 2017
4 Reads

Primary Orbital Chondromyxoid Fibroma: A Rare Case.

Ophthalmic Plast Reconstr Surg 2017 May/Jun;33(3S Suppl 1):S114-S116

Departments of *Ophthalmology and †Neurosurgery, Maywood, Illinois, U.S.A.

A 56-year-old male with history of chronic sinusitis was found to have a 3 cm left orbital lesion on CT. Subsequent MRI demonstrated a multilobulated enhancing soft tissue lesion at the superotemporal region of the left orbit. Initial biopsy was reported as a low-grade sarcoma. Read More

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http://dx.doi.org/10.1097/IOP.0000000000000857DOI Listing
September 2017
7 Reads

Exceptional Rare Giant Craniofacial Chondroid Tumor in Adult.

World Neurosurg 2017 Feb 18;98:867.e1-867.e3. Epub 2016 Dec 18.

Department of Neurosurgery, West China Hospital of Sichuan University, Chengdu, Sichuan, China. Electronic address:

We present a rare case of giant soap bubble-shaped cystic lesion in the craniofacial region in an adult female. Histopathologic examination revealed the tumor consisted of 3 components including chondroblastoma, chondromyxoid fibroma, and hemorrhagic aneurysmal bone cyst. The present case is rare in terms of size, location, and histopathologic diagnosis, which is probably the result of underdeveloped health care in the remote place. Read More

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http://dx.doi.org/10.1016/j.wneu.2016.12.032DOI Listing
February 2017
10 Reads

Pediatric Chondromyxoid Fibroma-Like Osteosarcoma.

Fetal Pediatr Pathol 2017 Apr 9;36(2):154-161. Epub 2016 Dec 9.

a Department of Pathology , Children's Hospital New Orleans , New Orleans , LA , USA.

Chondromyxoid fibroma-like osteosarcoma (CMF-OS) is a low-grade osteosarcoma, often misdiagnosed on initial biopsy as a benign lesion, with five cases previously described. We report a 13-year-old male with an intramedullary lytic CMF-OS of the right tibial proximal metaphysis with cortical destruction and soft tissue extension. Diagnosis was based on malignant new bone formation, increased mitotic figures, lamellar bone permeation with bony destruction, and correlation with imaging studies. Read More

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https://www.tandfonline.com/doi/full/10.1080/15513815.2016.1
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http://dx.doi.org/10.1080/15513815.2016.1259376DOI Listing
April 2017
8 Reads

Chondromyxoid fibroma of the sacrum: A case report and literature review.

Surg Neurol Int 2016 17;7(Suppl 13):S370-4. Epub 2016 May 17.

Department of Neurosurgery, Arrowhead Regional Medical Center, Colton, CA, USA; Department of Neurosurgery, Kaiser Permanente Fontana Medical Center, Fontana, CA, USA.

Background: Chondromyxoid fibroma (CMF) is an extremely rare, benign cartilaginous tumor that makes up <0.5% of all bone tumors, typically presenting in the second or third decade of life. CMF of the sacrum is exceedingly rare, with only seven documented cases reported in the neurosurgical literature. Read More

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http://dx.doi.org/10.4103/2152-7806.182547DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4879845PMC
June 2016
36 Reads

[EFFICACY OF BIOACTIVE GLASS AND ALLOGENIC BONE IN REPAIR OF BONE DEFECT AFTER BENIGN BONE TUMOR CURETTAGE].

Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi 2016 Jun;30(6):675-679

Department of Orthopaedic Oncology Surgery, Beijing Jishuitan Hospital, Beijing, 100035, P.R.China.

Objective: To compare the healing process and clinical results of bioactive glass and allogenic bone in the repair of bone defects after benign bone tumor curettage.

Methods: Between November 2011 and December 2012, 20 patients with benign bone tumor received bioactive glass and allogenic bone for repair of bone defects after benign bone tumor curettage. There were 17 males and 3 females, aged 9-68 years (median, 18. Read More

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http://www.rrsurg.com/article/10.7507/1002-1892.20160137
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http://dx.doi.org/10.7507/1002-1892.20160137DOI Listing
June 2016
4 Reads

Imaging features of chondromyxoid fibroma: report of 15 cases and literature review.

Br J Radiol 2016 Jun 13:20160088. Epub 2016 Jun 13.

2 Department of Pathology, University Hospital Leuven and KU Leuven, Leuven, Belgium.

Objective: Chondromyxoid fibroma (CMF) is a rare benign bony tumour. Our objectives are three-fold: first, comparing MRI, conventional radiography (CR) and CT characteristics of CMF; second, providing a literature review; and third, summarizing the role of imaging landmarks in the differential diagnosis with other bony lesions.

Methods: 15 patients with histopathologically proven CMF were retrospectively included. Read More

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http://dx.doi.org/10.1259/bjr.20160088DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5124884PMC
June 2016
1 Read

Rare case of sacral mass due to chondromyxoid fibroma.

BMJ Case Rep 2016 Mar 9;2016. Epub 2016 Mar 9.

Department of Orthopaedics and Traumatology, İstanbul Medeniyet University, Istanbul, Turkey.

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http://dx.doi.org/10.1136/bcr-2015-214145DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4785414PMC
March 2016
2 Reads

Congenital bizarre parosteal osteochondromatous proliferation in unusual location and age: a case report.

Acta Orthop Traumatol Turc 2016 ;50(1):120-4

Baltalimanı Bone Diseases Training and Research Hospital, Department of Orthopaedic Oncology, İstanbul, Turkey.

Bizarre parosteal osteochondromatous proliferation (BPOP, also known as Nora's lesion) is a rare, benign, locally aggressive condition defined as osteochondromatous exostosis arising from the bony cortex. BPOP presents predominantly in the 2nd and 3rd decades of life, and commonly arises from the periosteum of metacarpals and metatarses, though rare locations have been reported, including the long bones, the maxillae, the bones of calvaria, and the sesamoids. The case of an osteochondromatous lesion in an infant with an intra-abdominal mass arising from the iliac wing, an atypical location of benign solitary lesions, is reported. Read More

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http://dx.doi.org/10.3944/AOTT.2016.13.0141DOI Listing
December 2016
24 Reads

Chondromyxoid fibroma of the pubic ramus: a case report and literature review.

Acta Orthop Traumatol Turc 2016 ;50(1):115-9

Ankara Oncology Training and Research Hospital, Department of Orthopaedics and Traumatology, Ankara, Turkey.

Chondromyxoid fibromas (CMF) are benign cartilaginous bone tumors which are found most frequently in the metaphyses of long bones. They comprise less than 1% of primary bone neoplasms. We report an interesting incidental case of a 43-year-old woman with a CMF of the left pubic ramus, presenting with complaints of gradual onset of left groin pain over a period of 2 years. Read More

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http://dx.doi.org/10.3944/AOTT.2016.14.0232DOI Listing
December 2016
13 Reads

Chondromyxoid Fibroma of Pelvis, Surgical Management of 8 Cases.

Arch Iran Med 2015 Jun;18(6):367-70

Bone and Joint Reconstruction Research Center, Shafa Yahyaeian hospital, Iran University of Medical Sciences, Tehran, Iran.

Background: Chondromyxoid fibroma is a rare benign primary bone tumor of cartilaginous origin, which most commonly involves the metaphyseal bone of proximal tibia and distal femur. The purpose of the study is to report our experience with diagnosis and surgical management of Chondromyxoid fibroma in the pelvic region.

Methods: Eight consecutive patients with a final diagnosis of pelvic Chondromyxoid fibroma were treated from 2001 to 2010. Read More

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http://www.aimjournal.ir/pdffiles/62_june2015_008.pdf
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http://dx.doi.org/015186/AIM.008DOI Listing
June 2015
19 Reads

Chondromyxoid fibroma of the frontal bone mimicking meningioma.

J Craniofac Surg 2015 Mar;26(2):e179-81

From the *Department of Neurosurgery, The Second Hospital Affiliated Bengbu Medical School, Bengbu, and †Department of Neurosurgey, Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

Chondromyxoid fibroma (CMF) is a rare benign cartilaginous tumor that usually arises from lower-extremity long-bone metaphyses, with approximately 5.4% of all CMFs presenting in the craniofacial bones. Chondromyxoid fibroma of the frontal bone is exceedingly rare, with only a few cases reported. Read More

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http://pdfs.journals.lww.com/jcraniofacialsurgery/2015/03000
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http://content.wkhealth.com/linkback/openurl?sid=WKPTLP:land
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http://dx.doi.org/10.1097/SCS.0000000000001447DOI Listing
March 2015
5 Reads

Inferior displacement of the lower belly of the lateral pterygoid muscle: a sign of temporomandibular joint lesions.

J Comput Assist Tomogr 2015 May-Jun;39(3):340-2

From the *Department of Radiology, Hospital Pablo Tobón Uribe, Medellín, Colombia; and †Massachusetts Eye and Ear Infirmary and Harvard Medical School, Boston, MA.

Objective: The purposes of this article are to report the imaging finding of inferior displacement of the lower belly of the lateral pterygoid muscle (LPM) in patients with lesions arising from the temporomandibular joint (TMJ) and to propose that this imaging finding is suggestive of the presence of a TMJ lesion.

Materials And Methods: We reviewed computed tomographic and magnetic resonance images of 9 patients with lesions involving the TMJ. Images were evaluated for identification of an inferiorly displaced lower belly of the LPM. Read More

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http://pdfs.journals.lww.com/jcat/2015/05000/Inferior_Displa
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http://content.wkhealth.com/linkback/openurl?sid=WKPTLP:land
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http://dx.doi.org/10.1097/RCT.0000000000000225DOI Listing
July 2015
4 Reads

Management of craniofacial chondroid tumors.

J Craniofac Surg 2015 Jan;26(1):10-8

From the *Department of Skull Base and Craniofacial Surgery, Burdenko Neurosurgical Institute; †Department of Neurosurgery, N.N. Blokhin Cancer Research Centre; and ‡Department of Neuropathology, and §Department of Medical Statistics, Burdenko Neurosurgical Institute, Moscow, Russia.

Background: Craniofacial chondroid tumors (CFCTs) constitute less than 1% of all intracranial mass lesions. No protocol for evaluation and management of CFCTs is developed at the moment.

Materials And Methods: We analyzed 51 patients with CFCTs operated on in Burdenko Neurosurgical Institute from 1980 until 2012, which included chondroma (15), chondroblastoma (3), chondromyxoid fibroma (11), and chondrosarcoma (22). Read More

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http://pdfs.journals.lww.com/jcraniofacialsurgery/2015/01000
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http://content.wkhealth.com/linkback/openurl?sid=WKPTLP:land
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http://dx.doi.org/10.1097/SCS.0000000000001307DOI Listing
January 2015
10 Reads

Clival lesion incidentally discovered on cone-beam computed tomography: A case report and review of the literature.

Imaging Sci Dent 2014 Jun 11;44(2):165-9. Epub 2014 Jun 11.

Department of Oral and Maxillofacial Radiology, University of Connecticut School of Dental Medicine, Farmington, CT, USA.

An osteolytic lesion with a small central area of mineralization and sclerotic borders was discovered incidentally in the clivus on the cone-beam computed tomography (CBCT) of a 27-year-old male patient. This benign appearance indicated a primary differential diagnosis of non-aggressive lesions such as fibro-osseous lesions and arrested pneumatization. Further, on magnetic resonance imaging (MRI), the lesion showed a homogenously low T1 signal intensity with mild internal enhancement after post-gadolinium and a heterogeneous T2 signal intensity. Read More

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http://dx.doi.org/10.5624/isd.2014.44.2.165DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4061302PMC
June 2014
8 Reads

An intraosseous lipoma of the calcaneus: a case report.

J Foot Ankle Surg 2014 Sep-Oct;53(5):638-42. Epub 2014 May 27.

Residency Director, West Houston Medical Center, Houston, TX.

Intraosseous lipomas are one of the rarest bone tumors found in the body. The incidence has been reported to be <0.1% of all primary bone tumors. Read More

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https://linkinghub.elsevier.com/retrieve/pii/S10672516140010
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http://dx.doi.org/10.1053/j.jfas.2014.03.007DOI Listing
June 2015
23 Reads

Chondromyxoid fibroma of the mandible in an adolescent: case report and microsurgical reconstructive option.

Cleft Palate Craniofac J 2015 Mar 13;52(2):223-8. Epub 2014 Mar 13.

Chondromyxoid fibroma is a rare bony tumor that usually presents in the lower extremities of middle-aged adults. Involvement of the craniofacial skeleton is extremely rare. We present the unique case of an adolescent boy with a chondromyxoid fibroma of the mandible. Read More

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http://dx.doi.org/10.1597/13-243DOI Listing
March 2015
2 Reads

A false positive finding on the PET of somatostatin receptor due to a chondromyxoid fibroma.

Rev Esp Med Nucl Imagen Mol 2014 Jul-Aug;33(4):245-6. Epub 2013 Oct 16.

Department of Nuclear Medicine and PET/CT Center, Oncology Institute of Southern Switzerland, Bellinzona, Switzerland.

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http://dx.doi.org/10.1016/j.remn.2013.09.003DOI Listing
March 2016
1 Read

Surface chondromyxoid fibroma of the distal ulna: unusual tumor, site, and age.

Skeletal Radiol 2014 Feb 21;43(2):243-6. Epub 2013 Sep 21.

Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Chondromyxoid fibroma (CMF) is a rare benign cartilage congener tumor comprising less than 1 % of primary bone tumors. Although the age range is wide, it is most commonly seen in the second and third decades. The most frequent location of CMF is in the long tubular bones of the lower extremities, particularly the proximal tibia and distal femur. Read More

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http://link.springer.com/content/pdf/10.1007%2Fs00256-013-17
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http://link.springer.com/10.1007/s00256-013-1720-6
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http://dx.doi.org/10.1007/s00256-013-1720-6DOI Listing
February 2014
6 Reads

Chondromyxoid fibroma of the second rib.

J Pediatr Surg 2013 Jun;48(6):1442-4

Department of Surgery, University of Kentucky, Lexington, KY 40536, USA.

Chondromyxoid fibromas are benign tumors which are found most frequently in the metaphyses of long bones. They comprise less than 1% of primary bone neoplasms and display a hypermetabolic appearance on PET imaging. Oftentimes, they are misdiagnosed as chondrosarcomas and are excised due to concern for malignancy. Read More

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http://dx.doi.org/10.1016/j.jpedsurg.2013.04.016DOI Listing
June 2013
6 Reads

Epiphyseal chondromyxoid fibroma with prominent adipose tissue: an unusual radiologic and histologic presentation.

Am J Orthop (Belle Mead NJ) 2013 Apr;42(4):175-8

University of Alabama at Birmingham, Birmingham, AL 35249-7331, USA.

Chondromyxoid fibroma (CMF) is a rare benign tumor that typically develops in the metaphyseal intramedullary portion of long bones. The tumor may extend into the diaphysis or, seldom, into the epiphysis, but purely epiphyseal lesions are extremely rare, with only 2 cases having been reported in the literature. In this article, we report the case of a 51-year-old African American woman. Read More

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April 2013
5 Reads

Chondromyxoid fibroma of the mastoid portion of the temporal bone: MRI and PET/CT findings and their correlation with histology.

Ear Nose Throat J 2013 Apr-May;92(4-5):201-3

Department of Radiology, Beth Israel Medical Center, 10 Union Square East, New York, NY 10003, USA.

We report a very rare case of a chondromyxoid fibroma of the mastoid portion of the temporal bone in a 38-year-old woman who presented with left-sided hearing loss. Magnetic resonance imaging identified an expansile mass in the left mastoid bone with a heterogeneous hyperintense signal on T2-weighted imaging and peripheral enhancement. Subsequent positron emission tomography/computed tomography identified erosive bony changes associated with hypermetabolism. Read More

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February 2014
2 Reads

Calcaneal myxoid chondrosarcoma: a rare case.

JNMA J Nepal Med Assoc 2012 Jul-Sep;52(187):130-2

Department of orthopedics, Shree Birendra Hospital, Chhauni, Kathmandu, Nepal.

Skeletal myxoid chondrosarcoma is an extraordinarily rare neoplasm with a distinct histological morphology. Although it grows slowly, the clinical course was found to be worse than usual chondrosarcoma. We report a case of a skeletal myxoid chondrosarcoma in the calcaneus of a 21-year-old female who presented to us with a feature of gradually increasing benign swelling left foot for last two years. Read More

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March 2014
2 Reads

Chondromyxoid fibroma of the calcaneus: two case reports and literature review.

J Foot Ankle Surg 2013 Sep-Oct;52(5):643-9. Epub 2013 Apr 13.

Hofstra North Shore Long Island Jewish School of Medicine/North Shore Long Island Jewish Health System-Forest Hills Hospital, Forest Hills, NY, USA.

Chondromyxoid fibroma occurs primarily in the long tubular bones of the lower extremity, with the foot representing the second most frequent location after the knee. This benign cartilaginous tumor of bone is currently the rarest reported neoplasm of cartilaginous origin. This mass can mimic other benign and malignant bone tumors owing to its variable histologic features. Read More

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http://dx.doi.org/10.1053/j.jfas.2013.02.014DOI Listing
April 2014
10 Reads

Chondromyxoid fibroma of the temporal bone: A rare entity.

J Pediatr Neurosci 2012 Sep;7(3):211-4

Department of Neurosurgery, Grant Medical College and Sir J.J Group of Hospitals, Byculla, Mumbai, India.

Chondromyxoid fibroma (CMF) is the least common benign tumor of the cartilaginous origin. It is very unusual to find these tumors in the skull bones. We report one such case involving the temporal bone. Read More

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http://dx.doi.org/10.4103/1817-1745.106483DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3611914PMC
September 2012
4 Reads

Chondromyxoid fibroma of the clavicle extending to the adjacent joint: a case report.

J Orthop Surg (Hong Kong) 2012 Dec;20(3):402-5

Department of Orthopaedics, Postgraduate Institute of Medical Education and Research, Chandigarh, India.

Chondromyxoid fibroma is a rare benign bone tumour usually involving bones of the lower extremity in young adults. We present a case of chondromyxoid fibroma of the left clavicle extending to the adjacent joint in a 84-year-old man. The tumour had breached the hyaline cartilage of acromioclavicular joint. Read More

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http://dx.doi.org/10.1177/230949901202000330DOI Listing
December 2012
2 Reads

Primary juxtacortical myoepithelioma/mixed tumor of the bone: a report of 3 cases with clinicopathologic, immunohistochemical, ultrastructural, and molecular characterization.

Hum Pathol 2013 Apr 15;44(4):566-77. Epub 2012 Oct 15.

Division of Anatomic Pathology, Department of Critical Care Medicine and Surgery, University of Florence Medical School, 50134, Florence, Italy.

We describe the clinicopathological, immunohistochemical, and molecular features of 3 primary juxtacortical myoepithelioma/mixed tumor of bone. The patients were 2 males (13 and 23 years of age) and a 15-year-old female. The juxtacortical lesions were all located in the femur, and were surgically removed, 2 with wide margins and one with marginal margins. Read More

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http://dx.doi.org/10.1016/j.humpath.2012.06.020DOI Listing
April 2013
6 Reads

Chondromyxoid fibroma with secondary aneurysmal bone cyst of the rib.

Ann Thorac Cardiovasc Surg 2013 20;19(3):250-2. Epub 2012 Aug 20.

Department of General Thoracic Surgery, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Kyoto, Japan.

Chondromyxoid fibroma (CMF) is a rare, benign cartilaginous tumor, comprising less than 1% of primary bone tumors, and usually occurs in the metaphysis of a long tubular bone around the knee. We report a rare case of CMF of the rib. The patient was a 25-year-old man who visited the hospital for left upper back pain. Read More

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October 2013
9 Reads

Fibromyxoma of the axis.

Orthopedics 2012 Jul;35(7):e1133-5

First Department of Orthopaedics, Athens University Medical School, Athens, Greece.

Fibromyxoma of bone is a rare benign tumor of fibrous tissue origin. The typical location is the jaws. Sporadic extragnathic cases have been reported, but fibromyxoma of the spine has not been reported. Read More

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http://dx.doi.org/10.3928/01477447-20120621-40DOI Listing
July 2012
9 Reads

Chondromyxoid fibroma of the temporal bone.

Otol Neurotol 2012 Oct;33(8):e71-2

Department of Otolaryngology, New York University School of Medicine, New York, New York 10016, USA.

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http://dx.doi.org/10.1097/MAO.0b013e31825f21e2DOI Listing
October 2012
1 Read

Chondromyxoid fibroma of the orbit.

Ophthalmic Plast Reconstr Surg 2012 Sep-Oct;28(5):e105-6

Department of Ophthalmology, Hamilton Eye Institute, Memphis, Tennessee 38163, USA.

A 51-year-old woman with a history of migraine headaches was found to have an incidental right orbital mass on MRI during neurologic evaluation for headaches. The orbital mass was a well-defined, lobulated, intraosseous soft tissue lesion with circumscribed margins. Clinically, there was noted proptosis, tenderness to palpation, and slight limitation to right abduction. Read More

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http://dx.doi.org/10.1097/IOP.0b013e31823bd1e0DOI Listing
December 2012
3 Reads

The imaging of cartilaginous bone tumours. I. Benign lesions.

Authors:
H Douis A Saifuddin

Skeletal Radiol 2012 Sep 17;41(10):1195-212. Epub 2012 Jun 17.

Department of Radiology, The Royal National Orthopaedic Hospital NHS Trust, Brockley Hill, Stanmore, Middlesex HA7 4LP, UK.

Benign cartilage tumours of bone are the most common benign primary bone tumours and include osteochondroma, (en)chondroma, periosteal chondroma, chondroblastoma and chondromyxoid fibroma. These neoplasms often demonstrate typical imaging features, which in conjunction with lesion location and clinical history, often allow an accurate diagnosis. The aim of this article is to review the clinical and imaging features of benign cartilage neoplasms of bone, as well as the complications of these lesions. Read More

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http://link.springer.com/10.1007/s00256-012-1427-0
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http://dx.doi.org/10.1007/s00256-012-1427-0DOI Listing
September 2012
7 Reads

Chondromyxoid fibroma of the anterior skull base invading the orbit in a pediatric patient: case report and review of the literature.

Neuropediatrics 2012 Jun 2;43(3):140-5. Epub 2012 Apr 2.

Department of Neurosurgery, Arad Hospital, Tehran, Islamic Republic of Iran.

Chondromyxoid fibroma (CMF) is a rare bone tumor of cartilaginous derivation representing less than 1% of all benign bone neoplasms. It is a slow-growing, locally destructive tumor that usually affects the metaphyseal region of long bones of patients in their second or third decade of life. Involvement of the skull base and orbit is extremely rare. Read More

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http://www.thieme-connect.de/DOI/DOI?10.1055/s-0032-1307460
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http://dx.doi.org/10.1055/s-0032-1307460DOI Listing
June 2012
4 Reads

A t(1;9)(q10;q10) translocation with additional 6q23 and 9q22 rearrangements in a case of chondromyxoid fibroma.

Cancer Genet 2011 Dec;204(12):666-70

Department of Pathology, University of Texas Medical Branch, Galveston, USA.

Chondromyxoid fibroma (CMF) is a rare cartilaginous tumor of bone. It typically presents in the long tubular bones and to a lesser extent in the small bones of the hands and feet of young adults. To date, several cytogenetic abnormalities have been described in association with CMF. Read More

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http://dx.doi.org/10.1016/j.cancergen.2011.11.005DOI Listing
December 2011
1 Read

Chondromyxoid fibroma of the rib with prominent exophytic configuration.

Jpn J Radiol 2012 Jan 10;30(1):81-5. Epub 2011 Dec 10.

Department of Radiology, Teikyo University School of Medicine, 2-11-1 Kaga, Itabashiku, Tokyo 173-8606, Japan.

Chondromyxoid fibroma (CMF) of the rib is exceedingly unusual and few detailed image findings have been reported. Plain radiograph, computed tomography (CT), and magnetic resonance (MR) imaging findings and pathological aspects of a case of CMF of the right 2nd rib in a 15-year-old woman are reported, which was difficult to diagnose preoperatively. Though it is challenging to diagnose CMF preoperatively, it is important to be aware that CMF can exhibit atypical prominent exophytic features in unexpected locations such as the ribs. Read More

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http://dx.doi.org/10.1007/s11604-011-0013-zDOI Listing
January 2012
4 Reads

Chondromyxoid fibroma of the lumbar spine: case report and literature review.

Eur Spine J 2012 Jun 18;21 Suppl 4:S458-62. Epub 2011 Nov 18.

Department of Neurosurgery, Puerta de Hierro University Hospital, Manuel de Falla 1, 28222, Madrid, Spain.

Purpose: Chondromyxoid fibroma (CMF) is a benign tumour of the bone that typically occurs in long bone metaphysis. Spinal involvement is uncommon, but more frequent in the cervical and thoracic segments. Lumbar involvement is extremely rare. Read More

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http://dx.doi.org/10.1007/s00586-011-2078-xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3369062PMC
June 2012
3 Reads

Chondromyxoid fibroma of the second metacarpal bone--a case report.

Coll Antropol 2011 Sep;35(3):929-31

University of Rijeka, Rijeka University Hospital Center, Department of Traumatology, Rijeka, Croatia.

This report describes a chondromyxoid fibroma of the second metacarpal bone in a 32-year-old female patient. Chondromyxoid fibroma is a rare, benign, slow-growing bone tumor of cartilaginous origin. Tumor has a high recurrance rate. Read More

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September 2011
6 Reads

A rare case of epiphyseal chondromyxoid fibroma of the proximal tibia.

Korean J Radiol 2011 Nov-Dec;12(6):761-4. Epub 2011 Sep 27.

Department of Radiology, Eulji Hospital, Eulji University, Seoul 139-711, Korea.

Chondromyxoid fibroma is an uncommon benign cartilaginous tumor of the bone. It occurs most frequently in the metaphysis of long tubular bones, and an epiphyseal location is exceedingly rare. We present here an unusual case of a chondromyxoid fibroma that occurred in the epiphysis of the proximal tibia with an open growth plate. Read More

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http://dx.doi.org/10.3348/kjr.2011.12.6.761DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3194784PMC
March 2012
2 Reads