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Journal articles on the topic 'Ollier'

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Published: 4 June 2021
Last updated: 4 February 2022

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1

Ali, Mohammed Iftekar. "Ollier disease." Apollo Medicine 14, no. 1 (March 2017): 72–74. http://dx.doi.org/10.1016/j.apme.2017.01.006.

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2

D’Angelo, Luca, Luca Massimi, Alessandro Narducci, and Concezio Di Rocco. "Ollier disease." Child's Nervous System 25, no. 6 (March 27, 2009): 647–53. http://dx.doi.org/10.1007/s00381-009-0873-z.

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3

Rexach Fumanya, Maria, Antoni Castro Guardiola, and Ferran García-Bragado Dalmau. "Enfermedad de Ollier." Medicina Clínica 139, no. 3 (June 2012): e5. http://dx.doi.org/10.1016/j.medcli.2011.10.016.

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4

Cerny, Milena, Hannes A. Rudiger, Berengere Aubry-Rozier, Eric Dugert, and Fabio Becce. "Enchondromatosis (Ollier disease)." Arthritis & Rheumatism 65, no. 11 (October 28, 2013): 2886. http://dx.doi.org/10.1002/art.38115.

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5

Laios, Konstantinos, Konstantinos Markatos, and George Androutsos. "Louis-Léopold-Xavier-Édouard Ollier (1830-1900): An Innovative Orthopedic Surgeon." Surgical Innovation 24, no. 4 (April 9, 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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6

Choh, Suhil A., and Naseer A. Choh. "Multiple enchondromatosis (Ollier disease)." Annals of Saudi Medicine 29, no. 1 (January 2009): 65–67. http://dx.doi.org/10.5144/0256-4947.2009.65.

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7

Bertina, Arnaud. "L'atelier de Claude Ollier." Critique 677, no. 10 (2003): 737. http://dx.doi.org/10.3917/criti.677.0737.

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8

Wörner, B., and M. Schumacher. "Querschnittssyndrom bei Morbus Ollier." Klinische Neuroradiologie 7, no. 2 (June 1997): 93–97. http://dx.doi.org/10.1007/bf03044249.

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9

Schwarz, W., J. Hardes, and M. Schulte. "Multiple Enchondromatose: Morbus Ollier." Der Unfallchirurg 105, no. 12 (December 1, 2002): 1139–42. http://dx.doi.org/10.1007/s00113-002-0430-7.

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10

Silva, Luis Manuel. "Encondromatosis múltiple (Enfermedad de Ollier)." Acta Médica Colombiana 35, no. 1 (November 29, 2019): 36. http://dx.doi.org/10.36104/amc.2010.1583.

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Paciente de 36 años con antecedente conocido de encondromatosis múltiple quien consulta por cuadro de tres días de evolución de dolor en la pierna derecha posterior a trauma. Se realizan radiografías de rodillas comparativas y pierna derecha en las que se observan múltiples encondromas que comprometen la diáfisis distal del fémur (Panel A) y las metáfisis y diáfisis proximal; y distal de la tibia y el peroné (Panel B). Existe importante deformidad y acortamiento de esta extremidad
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11

Nahaboo, Zaki. "Rémy Ollier and Imperial Citizenship." Interventions 20, no. 5 (June 21, 2018): 717–33. http://dx.doi.org/10.1080/1369801x.2018.1487317.

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12

Le, Bryan B., and Ba D. Nguyen. "Ollier Disease With Digital Enchondromatosis." Clinical Nuclear Medicine 39, no. 8 (August 2014): e375-e378. http://dx.doi.org/10.1097/rlu.0000000000000284.

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13

Koc, Filiz, and Zafer Koc. "Ollier Disease Anaplastic Mixed Oligoastrocytoma." Neurosurgery Quarterly 16, no. 4 (December 2006): 195–97. http://dx.doi.org/10.1097/01.wnq.0000214039.38720.b4.

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14

Tejada Gallego, Javier, and Carmen Martinez-Gonzalez. "Encondromatosis múltiple, enfermedad de Ollier." Anales de Pediatría 87, no. 3 (September 2017): 176–77. http://dx.doi.org/10.1016/j.anpedi.2016.04.011.

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15

Kalbermatten, N. T., M. F. Müller, and D. F. Kalbermatten. "Thorakale Raumforderung bei Morbus Ollier." Der Radiologe 37, no. 10 (November 3, 1997): 839–41. http://dx.doi.org/10.1007/s001170050291.

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16

Markevičiūtė, Vėtra, Medeinė Šilenė Markevičiūtė, and Mindaugas Stravinskas. "Ollier Disease: A Case Series and Literature Review." Acta medica Lituanica 28, no. 1 (February 19, 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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17

Kumar, Avinash, Vijay Kumar Jain, Minakshi Bharadwaj, and Rajendra Kumar Arya. "Ollier Disease: Pathogenesis, Diagnosis, and Management." Orthopedics 38, no. 6 (June 1, 2015): e497-e506. http://dx.doi.org/10.3928/01477447-20150603-58.

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18

Saleh, M., J. A. Fernandes, M. J. Bell, S. S. Madan, K. Robinson, and P. D. Kasliwal. "Limb reconstruction in Ollier\'s disease." Strategies in Trauma and Limb Reconstruction 10, no. 1 (April 10, 2015): 49–54. http://dx.doi.org/10.1007/s11751-015-0223-5.

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19

Bricco, Elisa. "Arnaud Bertina, L’atelier de Claude Ollier." Studi Francesi, no. 144 (XLVIII | III) (December 15, 2004): 652. http://dx.doi.org/10.4000/studifrancesi.38357.

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20

Ranger, Adrianna, Artur Szymczak, Robert R. Hammond, and Shayna Zelcer. "Pediatric thalamic glioblastoma associated with Ollier disease (multiple enchondromatosis): a rare case of concurrence." Journal of Neurosurgery: Pediatrics 4, no. 4 (October 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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21

Moussa, Mohammed, Anwar Ul-Haque, and Ake Ahlberg. "Ehlers-Danlos Syndrome Associated with Ollier Disease." Annals of Saudi Medicine 14, no. 3 (May 1994): 260–62. http://dx.doi.org/10.5144/0256-4947.1994.260.

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22

Houppermans, Sjef. "Transculturalité : Verne, Le Clézio, Ollier, Dicker, Mauvignier." RELIEF - REVUE ÉLECTRONIQUE DE LITTÉRATURE FRANÇAISE 9, no. 1 (June 22, 2015): 119. http://dx.doi.org/10.18352/relief.911.

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23

Porto Matias, Michelle Danielle, Alessandro Oliveira De Jesus, Gustavo Marques De Oliveira Chiavaioli, Guilherme Lacerda De Toledo, Ricardo Alves Mesquita, and Marcio Bruno Figueiredo Amaral. "Management of Facial Alterations in Ollier Disease." Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology 126, no. 3 (September 2018): e84. http://dx.doi.org/10.1016/j.oooo.2018.02.255.

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24

Gökhan;SENEN, ADANALI. "Nadir Görülen Bir Ollier Hastalığı (Vaka Sunumu)." Ankara Üniversitesi Tıp Fakültesi Mecmuası 55, no. 1 (2002): 1. http://dx.doi.org/10.1501/tipfak_0000000695.

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25

Engelhardt, T., and W. Schultz. "Maligne Entartung bei multipler Enchondromatose (M. Ollier)." Osteologie/Osteology 13, no. 03 (2004): 123–28. http://dx.doi.org/10.1024/1019-1291.13.3.123.

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26

White, Matthew S., Paul L. Martin, and Thomas W. McLean. "Acute myelogenous leukemia associated with Ollier disease." Pediatric Blood & Cancer 50, no. 3 (2008): 645–46. http://dx.doi.org/10.1002/pbc.21050.

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27

Bowler, J. M. "Clifford david ollier: His life and times." Earth Surface Processes and Landforms 17, no. 4 (June 1992): 319–22. http://dx.doi.org/10.1002/esp.3290170403.

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28

Fridirici, Zachary C., Jeffrey J. Petrusek, Eric J. Thorpe, and John P. Leonetti. "Ollier Disease of the Lateral Skull Base." Otology & Neurotology 39, no. 1 (January 2018): e52-e53. http://dx.doi.org/10.1097/mao.0000000000001651.

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29

Elsayed, Hany, and Ahmed Mostafa. "Ollier Disease With Sole Chest Wall Involvement." Annals of Thoracic Surgery 100, no. 1 (July 2015): 327. http://dx.doi.org/10.1016/j.athoracsur.2015.02.131.

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30

Ida Ayu Made Pradnyanini and I Putu Gde Surya Adhitya. "Physical Therapy Management in Femoral Ollier Disease." Physical Therapy Journal of Indonesia 1, no. 1 (May 15, 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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31

Woo, Seunghun, Su-Young Bae, Hyung Jin Chung, and Tae Sik Goh. "Radiologic and Clinical Outcomes of Ollier Approach with Screw Fixation for Displaced Intra-Articular Calcaneal Fractures – Comparative Study with Extensile Lateral Approach with Lateral Plating." Foot & Ankle Orthopaedics 2, no. 3 (September 1, 2017): 2473011417S0004. http://dx.doi.org/10.1177/2473011417s000412.

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Category: Trauma Introduction/Purpose: This study aims to assess the detailed radiologic outcomes which used uninjured side weight-bearing radiograph as a template as well as clinical results to compare the Ollier approach with screw fixation and the extensile lateral approach with lateral plating. Methods: We performed a retrospective review of intra-articular calcaneal fractures treated operatively in our hospital from January 2009 to November 2014. Radiologic outcomes were assessed using radiologic parameters such as Böhler angle, calcaneal height, and talar sagittal angles represent calcaneal deformation by the comparison of the final follow-up bilateral weight-bearing lateral radiograph. Functional outcome was assessed through the American Orthopaedic Foot and Ankle Society (AOFAS) scores and Visual Analog Scale (VAS) pain scores. Postoperative complications were investigated. Results: Ninety-seven unilateral fractures were appeared to match our inclusion criteria: forty-six fractures were treated by using the extensile lateral approach with lateral plating (the ELP group), and fifty-one fractures were treated with the Ollier approach and screw fixation (the OS group). The operation time was significantly shorter in the OA group (p<0.05). There were no significant difference of the final follow-up radiologic parameters between two groups. The mean AOFAS scores were significantly higher in the OS group (p = 0.020) and both groups showed similarity in the VAS pain scores (p = 0.175). Overall soft-tissue complications were 28.3% in the ELP group and 9.8% in the OS group (p = 0.034). Conclusion: No difference could be shown in the postoperative and final follow-up radiological outcomes between the Ollier approach and the extensile lateral approach, but the Ollier approach had better functional score and lower soft tissue complication rate with shorter operative time.
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32

Kotrych, Daniel, Jakub Pawlik, Radomir Czajka, Karina Szczypiór-Piasecka, Paweł Łęgosz, Andrzej Bohatyrewicz, Łukasz Kołodziej, and Paweł Ziętek. "Surgical Management of Multifocal Chondrosarcoma in Ollier Disease." Ortopedia Traumatologia Rehabilitacja 22, no. 5 (October 31, 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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33

Mitchell, Ruth A., Joshua Mingsheng Ye, Simone Mandelstam, and Patrick Lo. "Gliomatosis cerebri in a patient with Ollier disease." Journal of Clinical Neuroscience 18, no. 11 (November 2011): 1564–66. http://dx.doi.org/10.1016/j.jocn.2011.03.025.

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34

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

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35

Climent Alcalá, F. J., J. Guerrero-Fernández, C. Melcón Crespo, I. González Casado, F. Carceller Benito, and R. Gracia Bouthelier. "Encondroma intraselar en niña con enfermedad de Ollier." Anales de Pediatría 71, no. 6 (December 2009): 582–84. http://dx.doi.org/10.1016/j.anpedi.2009.08.010.

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36

Sampagar, AbhilashaAshok, RahulR Jahagirdar, VibhaSanjay Bafna, and SandipP Bartakke. "Juvenile granulosa cell tumor associated with Ollier disease." Indian Journal of Medical and Paediatric Oncology 37, no. 4 (2016): 293. http://dx.doi.org/10.4103/0971-5851.195749.

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37

Décarie, David. "Thème du traître et du complot : La mise en scène de Claude Ollier." Études françaises 38, no. 3 (July 22, 2004): 109–33. http://dx.doi.org/10.7202/008387ar.

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Résumé Ba Iken, l’interprète de Lassalle, le « héros » de La mise en scène de Claude Ollier, s’avérant être un « traître », l’authenticité de sa traduction doit être remise en question. La « trahison » de l’interprète révèle en fait la fragilité de toute « interprétation ». L’essentiel, chez Ollier, réside cependant dans ce que masque la trahison de Ba Iken : soit ce que l’auteur, dans un texte de Navettes intitulé « Thème du texte et du complot », appelle le « complot ». Le « complot », ce « mode majeur » de la trahison, étant le rapport du texte au monde, il faut, pour en rendre compte, revenir au concept de mimêsis. Alors seulement, ajoutant à l’idée d’une « inspiration » dans le réel, celle d’une « expiration » dans un « réel » constamment remis en scène et en jeu, peut-on commencer à percevoir la « respiration » complète de la littérature dont rend compte La mise en scène.
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38

Walid, Mohammad Sami, and Earl Christopher Troup. "Cerebellar anaplastic astrocytoma in a teenager with Ollier Disease." Journal of Neuro-Oncology 89, no. 1 (April 15, 2008): 59–62. http://dx.doi.org/10.1007/s11060-008-9583-8.

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39

Ito, Hiroshi, Takeo Matsuno, and Akio Minami. "Rotational Acetabular Osteotomy Through an Ollier Lateral U Approach." Clinical Orthopaedics and Related Research 459 (June 2007): 200–206. http://dx.doi.org/10.1097/blo.0b013e31803b942a.

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40

Klausmeyer, Melissa A., Myles J. Cohen, and David A. Kulber. "Reconstruction of Ollier Disease in a Severely Involved Hand." Annals of Plastic Surgery 71, no. 6 (December 2013): 646–48. http://dx.doi.org/10.1097/sap.0b013e318255a3ce.

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41

Moser, T., X. Z. Lin, G. Bazille, M. Fleury, J. L. Dietemann, and S. Kremer. "Progressive hemianopsia caused by intracranial enchondroma in Ollier disease." Neurology 71, no. 24 (December 8, 2008): 2018. http://dx.doi.org/10.1212/01.wnl.0000336976.07237.17.

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42

Candas, Fatih, Akin Yildizhan, and Rauf Gorur. "Different appearance of Ollier disease: enchondromatosis of the ribs." ANZ Journal of Surgery 87, no. 12 (April 22, 2015): E305—E306. http://dx.doi.org/10.1111/ans.13141.

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43

Kim, Eugene, Junichi Miyake, Toshiyuki Kataoka, Kunihiro Oka, Hisao Moritomo, and Tsuyoshi Murase. "Corticoplasty for Improved Appearance of Hands With Ollier Disease." Journal of Hand Surgery 37, no. 11 (November 2012): 2294–99. http://dx.doi.org/10.1016/j.jhsa.2012.08.006.

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44

Khan, ShoukatH, TanveerA Rather, ParvaizA Koul, Rumana Makhdoomi, AbdulRashid Bhat, Dharmender Malik, and Ram Manohar. "Bone scintigraphy in Ollier′s disease: A rare case report." Indian Journal of Nuclear Medicine 28, no. 4 (2013): 226. http://dx.doi.org/10.4103/0972-3919.121968.

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45

Solterer, Helen. "Masques et déguisements dans la littérature médiévale. Marie-Louise Ollier." Speculum 65, no. 2 (April 1990): 472–75. http://dx.doi.org/10.2307/2864351.

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46

Bathla, Girish, KangOng Cheng, and Sarika Gupta. "Multifocal intracranial astrocytoma in a pediatric patient with Ollier disease." Indian Journal of Radiology and Imaging 22, no. 1 (2012): 58. http://dx.doi.org/10.4103/0971-3026.95406.

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47

Nguyen, Ba D. "Ollier Disease With Synchronous Multicentric Chondrosarcomas: Scintigraphic and Radiologic Demonstration." Clinical Nuclear Medicine 29, no. 1 (January 2004): 45–47. http://dx.doi.org/10.1097/01.rlu.0000103230.58596.73.

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48

Kaya, Halil, Halil Komek, Sevim Sureyya Cerci, and Sadiye Altun Tuzcu. "Bilateral Symmetrical Ollier Disease and Tc-99m MDP Bone Scintigraphy." Clinical Nuclear Medicine 29, no. 7 (July 2004): 456. http://dx.doi.org/10.1097/01.rlu.0000129272.94309.d1.

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49

Oestreich, A., C. Mitchell, and J. Akeson. "Both Trevor and Ollier disease limited to one upper extremity." Skeletal Radiology 31, no. 4 (February 9, 2002): 230–34. http://dx.doi.org/10.1007/s00256-001-0473-9.

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50

Diezi, Manuel, Pierre‐Yves Zambelli, Andrea Superti‐Furga, Sheila Unger, and Raffaele Renella. "Cancer surveillance in children with Ollier Disease and Maffucci Syndrome." American Journal of Medical Genetics Part A 185, no. 4 (January 12, 2021): 1338–40. http://dx.doi.org/10.1002/ajmg.a.62078.

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