scholarly journals Erratum: Translated Article: Resection of a Rare Proximal Radius Malignant Chondrosarcoma (Grade III) Bone Tumor and Reconstruction of the Forearm Functionality: A Case Report

2020 ◽  
Vol 7 (4) ◽  
pp. 193-194
Author(s):  
Sayed Abdulla Jami ◽  
◽  
Shi Jiandang ◽  

N/A

2020 ◽  
Vol 7 (2) ◽  
pp. 79-86
Author(s):  
Sayed Abdulla Jami ◽  
◽  
Shi Jiandang ◽  

Background: Chondrosarcoma is one of the common malignant bone tumors and is characterized by thin tumors. The cells produce tumor cartilage. It occur usually 3rd decade of life, affected more men than women. Objectives: To perform alternate surgical procedures for remove tumor and obtain fully forearm functionality by reconstruction.  Methods: A patient affected by a rare proximal radius chondrosarcoma bone tumor and it became malignant (grade III). Resection the tumor along with chemotherapy and radiotherapy was done. Surgical treatments are mainly recommended for most types of chondrosarcoma treatment. However, the treatment of chondrosarcoma clinically and surgically is controversial due to different techniques. Results: Patients was fully recovered with excellent wrist and elbow joint functionality. Reconstruction of bones were fused by the support of metallic implants. There was no tumor recurrence occur during post-operative follow-up period. Conclusion: Chondrosarcoma of bone generally has an excellent prognosis when optimal diagnosed and treated by an experienced team of specialists. Its clinical treatment is always challenging due to of the rarity of these lesions and few institutions having enough patients to study about it.


2021 ◽  
Vol 82 ◽  
pp. 105910
Author(s):  
Anderson S.M. Leung ◽  
Maximus C.F. Yeung ◽  
Raymond C.H. Yau ◽  
Kenneth W.Y. Ho ◽  
Tony W.H. Shek ◽  
...  

2021 ◽  
pp. 29-32
Author(s):  
Elsiddig E. Mahmoud

Congenital bilateral humeroradial synostosis (HRS) is a rare condition. It is generally divided into 2 categories. In the first group, which is mainly sporadic, additional upper limb hypoplasia typically coexists. In the second group, which is classically familial, HRS is commonly an isolated upper extremity anomaly. HRS can lead to variable degrees of functional disability. The clinical case reported here illustrates a possibly avoidable presentation of this uncommon condition. In this case report, we present a 6-week-old male who presented with bilateral radius fractures. Radiography revealed congenital HRS at both elbows. No other associated congenital abnormalities were detected, and there was no family history of similar conditions in any first-degree relatives. In cases of congenital HRS, movement at the elbow joint is not possible. Parents who are unaware of this information might try to straighten their infant’s elbows, which in turn may result in fractures of the proximal radius. Hence, early diagnosis and proper parental education could prevent fractures as a sequela of HRS.


2007 ◽  
Vol 42 (5) ◽  
pp. 696 ◽  
Author(s):  
Dong-Soo Kim ◽  
Yong-Min Kim ◽  
Eui-Sung Choi ◽  
Hyun-Chul Shon ◽  
Kyoung-Jin Park ◽  
...  

2007 ◽  
Vol 01 (01) ◽  
pp. 060-063 ◽  
Author(s):  
Esra Yeşilovaa ◽  
Faruk Akgünlü ◽  
Doğan Dolanmazc ◽  
Füsun Yaşar ◽  
Sevgi Şenere

ABSTRACTAlthough osteosarcoma of the head and neck is a relatively rare disease, it is a highly malignant bone tumor. Diagnosis of the tumor is important especially in early stages for improving prognosis. The patients with orofacial pain firstly prefer to go to dentists. Such kind of pain may be associated with an oral or maxillofacial cancer. The dentists must be careful for evaluating the clinical and radiologic clues. These clues determine the biopsy necessity, type and management plan. The aim of this case presentation is to emphasize the importance of dentists on diagnosis and prognosis of oral malignancies. (Eur J Dent 2007;1:60-63)


2018 ◽  
Vol 23 (4) ◽  
pp. 697-700
Author(s):  
Yu Toda ◽  
Motoki Sonohata ◽  
Kazuyoshi Uchihashi ◽  
Hiroko Mine ◽  
Toshiyuki Tsuruta ◽  
...  

2015 ◽  
Vol 15 (6) ◽  
pp. 638-640 ◽  
Author(s):  
Scott A. Wallace ◽  
Romeo C. Ignacio ◽  
Arnett Klugh ◽  
Gregory Gates ◽  
Marion C. W. Henry

Osteoblastoma is an uncommon primary bone tumor that usually presents as a painful lesion in a long bone or in the spine. Osteoblastoma has been reported only twice in the literature in conjunction with systemic fibromatosis. The authors report the case of an 8-year-old girl with suspected Klippel-Trenaunay-Weber syndrome, a rare syndrome of systemic fibromatosis, who presented with a painless thoracic rib lesion that was found to be an osteoblastoma.


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