Articles de revues : « Ollier disease »

1

D’Angelo, Luca, Luca Massimi, Alessandro Narducci et Concezio Di Rocco. « Ollier disease ». Child's Nervous System 25, n^o 6 (27 mars 2009) : 647–53. http://dx.doi.org/10.1007/s00381-009-0873-z.

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Ali, Mohammed Iftekar. « Ollier disease ». Apollo Medicine 14, n^o 1 (mars 2017) : 72–74. http://dx.doi.org/10.1016/j.apme.2017.01.006.

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Cerny, Milena, Hannes A. Rudiger, Berengere Aubry-Rozier, Eric Dugert et Fabio Becce. « Enchondromatosis (Ollier disease) ». Arthritis & ; Rheumatism 65, n^o 11 (28 octobre 2013) : 2886. http://dx.doi.org/10.1002/art.38115.

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Choh, Suhil A., et Naseer A. Choh. « Multiple enchondromatosis (Ollier disease) ». Annals of Saudi Medicine 29, n^o 1 (janvier 2009) : 65–67. http://dx.doi.org/10.5144/0256-4947.2009.65.

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P, Correa Bellido, et Wadhwani WJ. « Ollier´s disease : Multiple enchondromatosis ». International Journal of Orthopaedics Sciences 7, n^o 4 (1 octobre 2021) : 409–11. http://dx.doi.org/10.22271/ortho.2021.v7.i4f.2910.

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Koc, Filiz, et Zafer Koc. « Ollier Disease Anaplastic Mixed Oligoastrocytoma ». Neurosurgery Quarterly 16, n^o 4 (décembre 2006) : 195–97. http://dx.doi.org/10.1097/01.wnq.0000214039.38720.b4.

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Le, Bryan B., et Ba D. Nguyen. « Ollier Disease With Digital Enchondromatosis ». Clinical Nuclear Medicine 39, n^o 8 (août 2014) : e375-e378. http://dx.doi.org/10.1097/rlu.0000000000000284.

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Laios, Konstantinos, Konstantinos Markatos et George Androutsos. « Louis-Léopold-Xavier-Édouard Ollier (1830-1900) : An Innovative Orthopedic Surgeon ». Surgical Innovation 24, n^o 4 (9 avril 2017) : 402–4. http://dx.doi.org/10.1177/1553350617702310.

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Louis-Léopold-Xavier-Édouard Ollier (1830-1900) was a pioneer in orthopedics considered as the founder of modern orthopedic surgery. He was a skillful and experimenter surgeon. He invented many new surgical techniques in orthopedic surgery and many new surgical instruments. His most known discovery is Ollier’s disease.

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Kumar, Avinash, Vijay Kumar Jain, Minakshi Bharadwaj et Rajendra Kumar Arya. « Ollier Disease : Pathogenesis, Diagnosis, and Management ». Orthopedics 38, n^o 6 (1 juin 2015) : e497-e506. http://dx.doi.org/10.3928/01477447-20150603-58.

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Saleh, M., J. A. Fernandes, M. J. Bell, S. S. Madan, K. Robinson et P. D. Kasliwal. « Limb reconstruction in Ollier\'s disease ». Strategies in Trauma and Limb Reconstruction 10, n^o 1 (10 avril 2015) : 49–54. http://dx.doi.org/10.1007/s11751-015-0223-5.

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Markevičiūtė, Vėtra, Medeinė Šilenė Markevičiūtė et Mindaugas Stravinskas. « Ollier Disease : A Case Series and Literature Review ». Acta medica Lituanica 28, n^o 1 (19 février 2021) : 8. http://dx.doi.org/10.15388/amed.2021.28.1.8.

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Background. Ollier disease is the most common nonhereditary type of enchondromatosis. Enchondromas are common, usually benign intraosseous cartilaginous tumors that form near the growth plate cartilage predominantly unilaterally in the metaphyses and diaphyses of tubular bones. They usually affect the long bones of the hand, the humerus, and the tibia, followed by flat bones, such as the pelvis. The estimated prevalence of Ollier disease is 1 in 100,000 and while it is linked with somatic heterozygous mutations in IDH1 or IDH2 genes, exact etiology is unknown. The risk of malignant transformation towards chondrosarcoma is up to 30–35% and it is clinically suspected when pain and a rapid increase in the size of the lesions is seen.Case presentations. We report two clinical cases of patients diagnosed with Ollier disease. In both cases transformation to chondrosarcoma was observed.Conclusions. Ollier disease is a rare disorder, defined by the presence of multiple enchondromas and an asymmetric distribution of the cartilage lesions that can be extremely variable in terms of size, location, age, gender. Constant monitoring of patients is important due to the high risk of malignancy. Because the disease is very rare and the manifestations vary widely, each patient’s case must be evaluated, and the treatment strategy adopted individually.

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Chen, Chunyan, Jian Li, Ting Jiang, Juan Tang, Zhichang Zhang, Yanli Luo, Xinpei Wang et al. « IDH Mutations Are Potentially the Intrinsic Genetic Link among the Multiple Neoplastic Lesions in Ollier Disease and Maffucci Syndrome : A Clinicopathologic Analysis from a Single Institute in Shanghai, China ». Diagnostics 12, n^o 11 (11 novembre 2022) : 2764. http://dx.doi.org/10.3390/diagnostics12112764.

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Background: This study aims to investigate isocitrate dehydrogenase gene mutations in patients with the non-hereditary skeletal disorders of Ollier disease and Maffucci syndrome, particularly in the extraosseous tumours. Methods: A total of 16 tumours from three patients with Ollier disease and three patients with Maffucci syndrome were collected. Sanger sequencing was applied to determine the hotspot mutations of IDH1 and IDH2 genes in multiple neoplastic tissues. Results: A majority of the tumours displayed an IDH1 mutation (p.R132C in 11 tumours including the paediatric ovarian tumour from one patient with Ollier disease, 4 cutaneous haemangiomas from three patients with Maffucci syndrome, 5 enchondromas and 1 chondrosarcoma; p.R132H in 2 cartilaginous tumours from one patient). Conclusions: IDH1 mutations were demonstrated in multiple cartilaginous tumours and extraskeletal neoplasms in this case series. Specifically, identical IDH1 mutations were confirmed in the separate lesions of each patient. These results are in concordance with findings that have been reported. However, here, we additionally reported the first case of Ollier disease with an ovarian tumour, which harboured the identical IDH1 mutation with the corresponding cartilaginous tumour. We further provided evidence that IDH mutations are the potential genetic links among the multiple neoplastic lesions of Ollier disease and Maffucci syndrome.

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Ida Ayu Made Pradnyanini et I Putu Gde Surya Adhitya. « Physical Therapy Management in Femoral Ollier Disease ». Physical Therapy Journal of Indonesia 1, n^o 1 (15 mai 2020) : 1–4. http://dx.doi.org/10.51559/ptji.v1i1.1.

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Introduction: Ollier disease (OD) is a non-hereditary, an uncommon bone disorder that typically presented by multiple or unilateral enchondromatosis associated with the deformity of the extremities. This article describes a case of a patient with OD that contribute endochondral ossification of the femoral bone and the physical therapy management.Case Description: An eight years old female patient referred to physical therapy unit after resection of right femur enchondroma, had undergone surgery for bone lengthening with external fixation. Further, the patient has been undergone surgical intervention for the tibial enchondromatosis. Physical therapy management aimed to improve the range of motion, pain, gait pattern, and activity of daily living. After three sessions of intervention, the patient reported the improvement in the pain and range of motion of the right lower limb.Conclusion: The physical therapy management might improve the pain and lower limb range of motion after the surgical intervention in femoral OD.

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Moussa, Mohammed, Anwar Ul-Haque et Ake Ahlberg. « Ehlers-Danlos Syndrome Associated with Ollier Disease ». Annals of Saudi Medicine 14, n^o 3 (mai 1994) : 260–62. http://dx.doi.org/10.5144/0256-4947.1994.260.

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Fridirici, Zachary C., Jeffrey J. Petrusek, Eric J. Thorpe et John P. Leonetti. « Ollier Disease of the Lateral Skull Base ». Otology & ; Neurotology 39, n^o 1 (janvier 2018) : e52-e53. http://dx.doi.org/10.1097/mao.0000000000001651.

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Porto Matias, Michelle Danielle, Alessandro Oliveira De Jesus, Gustavo Marques De Oliveira Chiavaioli, Guilherme Lacerda De Toledo, Ricardo Alves Mesquita et Marcio Bruno Figueiredo Amaral. « Management of Facial Alterations in Ollier Disease ». Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology 126, n^o 3 (septembre 2018) : e84. http://dx.doi.org/10.1016/j.oooo.2018.02.255.

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Elsayed, Hany, et Ahmed Mostafa. « Ollier Disease With Sole Chest Wall Involvement ». Annals of Thoracic Surgery 100, n^o 1 (juillet 2015) : 327. http://dx.doi.org/10.1016/j.athoracsur.2015.02.131.

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White, Matthew S., Paul L. Martin et Thomas W. McLean. « Acute myelogenous leukemia associated with Ollier disease ». Pediatric Blood & ; Cancer 50, n^o 3 (2008) : 645–46. http://dx.doi.org/10.1002/pbc.21050.

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Ranger, Adrianna, Artur Szymczak, Robert R. Hammond et Shayna Zelcer. « Pediatric thalamic glioblastoma associated with Ollier disease (multiple enchondromatosis) : a rare case of concurrence ». Journal of Neurosurgery : Pediatrics 4, n^o 4 (octobre 2009) : 363–67. http://dx.doi.org/10.3171/2009.5.peds08422.

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Ollier disease and Maffucci syndrome are rare syndromes in which there is deforming dysplasia of cartilage, primarily but not exclusively involving the metaphyses and diaphyses of long bones. In a minority of patients, dysplasia can lead to sarcomatous degeneration, producing chondrosarcomas. There also appears to be an association with other neoplasms. Little has been written about the association between Ollier disease and intracranial tumors, and these papers have largely consisted of case reports in adults. The authors present the case of a 6-year-old girl with left arm osseous changes consistent with Ollier disease and a biopsy-proven thalamic glioblastoma multiforme. They then examine the co-occurrence of brain tumors in conjunction with a dyschondroplasia syndrome in children and adolescents to assess the presentation, treatment offered, and disease course of similar cases. Eight other such cases were identified, 6 in patients with Ollier disease (ranging in age from 7 to 18 years), and 2 with Maffucci syndrome (both in late adolescence). Including our own patient, 7 of the 9 cases of comorbid dyschondroplasia and intracranial malignancy occurred in girls. Some patients presented soon after the acute onset of symptoms, and others had a more subtle, protracted course over as many as 2 years. Some tumors were deemed resectable and others not. In only 1 instance was follow-up beyond 1 year reported.

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Sampagar, AbhilashaAshok, RahulR Jahagirdar, VibhaSanjay Bafna et SandipP Bartakke. « Juvenile granulosa cell tumor associated with Ollier disease ». Indian Journal of Medical and Paediatric Oncology 37, n^o 4 (2016) : 293. http://dx.doi.org/10.4103/0971-5851.195749.

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Kotrych, Daniel, Jakub Pawlik, Radomir Czajka, Karina Szczypiór-Piasecka, Paweł Łęgosz, Andrzej Bohatyrewicz, Łukasz Kołodziej et Paweł Ziętek. « Surgical Management of Multifocal Chondrosarcoma in Ollier Disease ». Ortopedia Traumatologia Rehabilitacja 22, n^o 5 (31 octobre 2020) : 373–82. http://dx.doi.org/10.5604/01.3001.0014.4227.

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Ollier disease is a rare congenital disease in which multiple enchondromas occur. The tumors can transform to malignant chondrosarcomas of various histologic grades. The patient we described has been treated in our orthopedic department six times, always being referred on account of new lesions. The tumors were excised with margins of healthy tissue. Each tumor was subjected to a histological examination to determine its type and grade. Chondroid tumors should be diagnosed carefully, because the treatment depends on their histologic features. If surgery is performed, removal of the tumor with a margin of healthy tissue is crucial for the patient’s well-being and good prognosis.

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Atanasova, Stela, Sevdzhan Osman, Boyan Balev, Ara Kaprelyan et Ivan Dimitrov. « Ollier disease and neurological complications—a clinical case ». Varna Medical Forum 10, n^o 1 (18 juin 2021) : 73. http://dx.doi.org/10.14748/vmf.v10i1.7721.

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Mitchell, Ruth A., Joshua Mingsheng Ye, Simone Mandelstam et Patrick Lo. « Gliomatosis cerebri in a patient with Ollier disease ». Journal of Clinical Neuroscience 18, n^o 11 (novembre 2011) : 1564–66. http://dx.doi.org/10.1016/j.jocn.2011.03.025.

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Gouk, C., L. Daniele et C. Buchan. « Ollier disease in a 6-year-old child ». Case Reports 2015, apr21 1 (21 avril 2015) : bcr2015210057. http://dx.doi.org/10.1136/bcr-2015-210057.

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Moser, T., X. Z. Lin, G. Bazille, M. Fleury, J. L. Dietemann et S. Kremer. « Progressive hemianopsia caused by intracranial enchondroma in Ollier disease ». Neurology 71, n^o 24 (8 décembre 2008) : 2018. http://dx.doi.org/10.1212/01.wnl.0000336976.07237.17.

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Kim, Eugene, Junichi Miyake, Toshiyuki Kataoka, Kunihiro Oka, Hisao Moritomo et Tsuyoshi Murase. « Corticoplasty for Improved Appearance of Hands With Ollier Disease ». Journal of Hand Surgery 37, n^o 11 (novembre 2012) : 2294–99. http://dx.doi.org/10.1016/j.jhsa.2012.08.006.

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Klausmeyer, Melissa A., Myles J. Cohen et David A. Kulber. « Reconstruction of Ollier Disease in a Severely Involved Hand ». Annals of Plastic Surgery 71, n^o 6 (décembre 2013) : 646–48. http://dx.doi.org/10.1097/sap.0b013e318255a3ce.

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Candas, Fatih, Akin Yildizhan et Rauf Gorur. « Different appearance of Ollier disease : enchondromatosis of the ribs ». ANZ Journal of Surgery 87, n^o 12 (22 avril 2015) : E305—E306. http://dx.doi.org/10.1111/ans.13141.

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Walid, Mohammad Sami, et Earl Christopher Troup. « Cerebellar anaplastic astrocytoma in a teenager with Ollier Disease ». Journal of Neuro-Oncology 89, n^o 1 (15 avril 2008) : 59–62. http://dx.doi.org/10.1007/s11060-008-9583-8.

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Diezi, Manuel, Pierre‐Yves Zambelli, Andrea Superti‐Furga, Sheila Unger et Raffaele Renella. « Cancer surveillance in children with Ollier Disease and Maffucci Syndrome ». American Journal of Medical Genetics Part A 185, n^o 4 (12 janvier 2021) : 1338–40. http://dx.doi.org/10.1002/ajmg.a.62078.

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Sashida Mendez, Hirosi, Maria de los Angeles Mendoza Velez, Luisa Hurtado Diaz, Jorge Rojas Ortiz et Edgardo Araiza Gomez. « Ollier disease : multiple enchondromatosis : case report and review of literature ». International Journal of Research in Medical Sciences 9, n^o 6 (27 mai 2021) : 1770. http://dx.doi.org/10.18203/2320-6012.ijrms20212250.

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Multiple enchondromatosis is a rare disease in which cartilage tumors appear at the level of the skeleton. The incidence is unknown due to the very few cases reported in world literature. We presented the case of a patient at the plastic surgery department at General hospital Dr. Ruben Leñero, otherwise healthy, referring first clinical manifestations at childhood with an increase in volume and deformity at the second and third fingers of the left hand.

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Bathla, Girish, KangOng Cheng et Sarika Gupta. « Multifocal intracranial astrocytoma in a pediatric patient with Ollier disease ». Indian Journal of Radiology and Imaging 22, n^o 1 (2012) : 58. http://dx.doi.org/10.4103/0971-3026.95406.

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Khan, ShoukatH, TanveerA Rather, ParvaizA Koul, Rumana Makhdoomi, AbdulRashid Bhat, Dharmender Malik et Ram Manohar. « Bone scintigraphy in Ollier′s disease : A rare case report ». Indian Journal of Nuclear Medicine 28, n^o 4 (2013) : 226. http://dx.doi.org/10.4103/0972-3919.121968.

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Piai, A., A. Loria, P. G. Esposito, A. Mazzilli, P. Tiberio, L. M. Sconfienza et A. del Vecchio. « Organ dose evaluation in radiological monitoring of paediatric Ollier disease ». Physica Medica 92 (décembre 2021) : S112. http://dx.doi.org/10.1016/s1120-1797(22)00238-1.

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Nguyen, Ba D. « Ollier Disease With Synchronous Multicentric Chondrosarcomas : Scintigraphic and Radiologic Demonstration ». Clinical Nuclear Medicine 29, n^o 1 (janvier 2004) : 45–47. http://dx.doi.org/10.1097/01.rlu.0000103230.58596.73.

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Kaya, Halil, Halil Komek, Sevim Sureyya Cerci et Sadiye Altun Tuzcu. « Bilateral Symmetrical Ollier Disease and Tc-99m MDP Bone Scintigraphy ». Clinical Nuclear Medicine 29, n^o 7 (juillet 2004) : 456. http://dx.doi.org/10.1097/01.rlu.0000129272.94309.d1.

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Oestreich, A., C. Mitchell et J. Akeson. « Both Trevor and Ollier disease limited to one upper extremity ». Skeletal Radiology 31, n^o 4 (9 février 2002) : 230–34. http://dx.doi.org/10.1007/s00256-001-0473-9.

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Corvino, Sergio, Giuseppe Mariniello, Giuseppe Corazzelli, Raduan Ahmed Franca, Marialaura Del Basso De Caro, Rosa Della Monica, Lorenzo Chiariotti et Francesco Maiuri. « Brain Gliomas and Ollier Disease : Molecular Findings as Predictive Risk Factors ? » Cancers 14, n^o 14 (16 juillet 2022) : 3464. http://dx.doi.org/10.3390/cancers14143464.

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Background: Ollier disease (OD) is a rare nonhereditary type of dyschondroplasia characterized by multiple enchondromas, with typical onset in the first decade of life. Surgery is the only curative treatment for primary disease and its complications. Patients with OD are at risk of malignant transformation of enchondromas and of occurrence of other neoplasms. Methods: A wide literature review disclosed thirty cases of glioma associated with OD, most of them belonging to the pre-molecular era. Our own case was also included. Demographic, clinical, pathologic, molecular, management, and outcome data were analyzed and compared to those of sporadic gliomas. Results: Gliomas associated with OD more frequently occur at younger age, present higher rates of multicentric lesions (49%), brainstem localizations (29%), and significantly lower rates of glioblastomas (7%) histotype. The IDH1 R132H mutation was detected in 80% of gliomas of OD patients and simultaneously in enchondromas and gliomas in 100% of cases. Conclusions: The molecular data suggest a higher risk of occurrence of glioma in patients with enchondromas harboring the IDH1 R132H mutation than those with the IDH1 R132C mutation. Thus, we suggest considering the IDH1 R132H mutation in enchondromas of patients with OD as a predictive risk factor of occurrence of glioma.

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Huk, Yu M., A. M. Zima, R. V. Luchko et I. A. Molnar. « Sonographic Diagnosis of the Acroform Types in Ollier Disease in Children ». TRAUMA 17, n^o 5 (9 décembre 2016) : 81–84. http://dx.doi.org/10.22141/1608-1706.5.17.2016.83882.

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Rawlings, C. E., D. E. Bullard, P. C. Burger et A. H. Friedman. « A case of Ollier??s disease associated with two intracranial gliomas ». Neurosurgery 21, n^o 3 (septembre 1987) : 400???3. http://dx.doi.org/10.1097/00006123-198709000-00023.

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Pearce, P., T. Robertson, J. D. Ortiz-Gomez, T. Rajah et G. Tollesson. « Multifocal supratentorial diffuse glioma in a young patient with Ollier disease ». Journal of Clinical Neuroscience 19, n^o 3 (mars 2012) : 477–78. http://dx.doi.org/10.1016/j.jocn.2011.06.019.

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Oushy, Soliman, Maria Peris-Celda et Jamie J. Van Gompel. « Skull Base Enchondroma and Chondrosarcoma in Ollier Disease and Maffucci Syndrome ». World Neurosurgery 130 (octobre 2019) : e356-e361. http://dx.doi.org/10.1016/j.wneu.2019.06.087.

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Balcer, Laura J., Steven L. Galetta, Wayne T. Cornblath et Grant T. Liu. « Neuro-Ophthalmologic Manifestations of Maffucci??s Syndrome and Ollier??s Disease ». Journal of Neuro-Ophthalmology 19, n^o 1 (mars 1999) : 62???66. http://dx.doi.org/10.1097/00041327-199903000-00021.

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Krishnappa, Santosh Kumar, Ramesh R. L. et Prakash Vemgal. « Fortuitous enchondroma of hand in a traumatic fracture : a case report of Ollier’s disease ». International Journal of Contemporary Pediatrics 5, n^o 1 (21 décembre 2017) : 257. http://dx.doi.org/10.18203/2349-3291.ijcp20175596.

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Enchondromas are benign cartilage forming tumors most commonly involving the marrow cavity of the long bones. Ollier disease is one of the subtypes of Enchondromatosis associated with lesions in the center of the bone. Most commonly presenting in 2nd and 3rd decade of life. Radiological evidence is adequate for the diagnosis. Exact etiology is unknown with increasing genetic predilection. Regular follow up with conservative management remains the mainstay of treatment.

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Gurbani, Barkha, Matthew Igbinigie, Aristides Koutrouvelis, Jack B. Alperin et Ronald W. Lindsey. « Bilateral Forearm Pseudotumors in an Adult with Hemophilia A and Ollier Disease ». JBJS Case Connector 8, n^o 3 (25 juillet 2018) : e54-e54. http://dx.doi.org/10.2106/jbjs.cc.17.00234.

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Couvineau, Alain, Vinciane Wouters, Guylène Bertrand, Christiane Rouyer, Bénédicte Gérard, Laurence M. Boon, Bernard Grandchamp, Miikka Vikkula et Caroline Silve. « PTHR1 mutations associated with Ollier disease result in receptor loss of function ». Human Molecular Genetics 17, n^o 18 (17 juin 2008) : 2766–75. http://dx.doi.org/10.1093/hmg/ddn176.

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Pansuriya, Twinkal C., Jan Oosting, Tibor Krenács, Antonie HM Taminiau, Suzan HM Verdegaal, Luca Sangiorgi, Raf Sciot, Pancras CW Hogendoorn, Karoly Szuhai et Judith VMG Bovée. « Genome-wide analysis of Ollier disease : Is it all in the genes ? » Orphanet Journal of Rare Diseases 6, n^o 1 (2011) : 2. http://dx.doi.org/10.1186/1750-1172-6-2.

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Klein, Céline, Tiphanie Delcourt, Arielle Salon, Georges Finidori, Christophe Glorion et Stéphanie Pannier. « Surgical Treatment of Enchondromas of the Hand During Childhood in Ollier Disease ». Journal of Hand Surgery 43, n^o 10 (octobre 2018) : 946.e1–946.e5. http://dx.doi.org/10.1016/j.jhsa.2018.02.010.

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Hughes, Marion Alicia, William Delfyett, Paul Gardner, Leonidas Arvanitis et Tanya Rath. « Hemorrhagic chondrosarcoma in a patient with Ollier disease : Case report and literature review ». Radiology Case Reports 9, n^o 1 (2014) : 889. http://dx.doi.org/10.2484/rcr.v9i1.889.

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Rietveld, Lieke, Theodoor E. Nieboer, Kirsten B. Kluivers, Hendrik W. B. Schreuder, Johannes Bulten et Leon F. A. G. Massuger. « First Case of Juvenile Granulosa Cell Tumor in an Adult With Ollier Disease ». International Journal of Gynecological Pathology 28, n^o 5 (septembre 2009) : 464–67. http://dx.doi.org/10.1097/pgp.0b013e3181a05af4.

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Articles de revues sur le sujet « Ollier disease »

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