Case Reports in Orthopedics最新文献

筛选
英文 中文
Bilateral Lumbar Facet Synovial Cysts as a Cause of Radiculopathy. 双侧腰椎关节突滑膜囊肿是神经根病的病因。
Case Reports in Orthopedics Pub Date : 2022-11-07 eCollection Date: 2022-01-01 DOI: 10.1155/2022/2519468
Pawin Kasempipatchai, Verapan Kuansongtham, Monchai Ruangchainikom, Khin Myat Myat Lwin
{"title":"Bilateral Lumbar Facet Synovial Cysts as a Cause of Radiculopathy.","authors":"Pawin Kasempipatchai,&nbsp;Verapan Kuansongtham,&nbsp;Monchai Ruangchainikom,&nbsp;Khin Myat Myat Lwin","doi":"10.1155/2022/2519468","DOIUrl":"https://doi.org/10.1155/2022/2519468","url":null,"abstract":"<p><p>Remarkable advancements in endoscopic spinal surgery have led to successful outcomes comparable to those of conventional open surgery with the benefits of less traumatization and postoperative spinal instability. Bilateral lumbar facet cysts are rarely found in the spinal canal. We report a rare case of L4-L5 bilateral lumbar facet cysts compressing the nerve root in a patient who presented with L5 radiculopathy. Endoscopic decompression and removal of the cysts without fusion were performed. Histopathology revealed synovial cysts. Postoperatively, the patient showed a total resolution of symptoms with sustained benefits at the final evaluation. No recurrence of pain and no further segmental instability were observed at the 1-year follow-up.</p>","PeriodicalId":30287,"journal":{"name":"Case Reports in Orthopedics","volume":" ","pages":"2519468"},"PeriodicalIF":0.0,"publicationDate":"2022-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9663226/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40709286","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Spinal Epidural Lipoma on the Ventral Dura Side and Intervertebral Foramen Causing Lumbar Radiculopathy. 硬脑膜腹侧及椎间孔的硬膜外脂肪瘤引起腰椎神经根病。
Case Reports in Orthopedics Pub Date : 2022-10-27 eCollection Date: 2022-01-01 DOI: 10.1155/2022/7502552
Hiroshi Noguchi, Masao Koda, Tetsuya Abe, Toru Funayama, Hiroshi Takahashi, Kousei Miura, Kentaro Mataki, Mamoru Kono, Fumihiko Eto, Yosuke Shibao, Masashi Yamazaki
{"title":"Spinal Epidural Lipoma on the Ventral Dura Side and Intervertebral Foramen Causing Lumbar Radiculopathy.","authors":"Hiroshi Noguchi,&nbsp;Masao Koda,&nbsp;Tetsuya Abe,&nbsp;Toru Funayama,&nbsp;Hiroshi Takahashi,&nbsp;Kousei Miura,&nbsp;Kentaro Mataki,&nbsp;Mamoru Kono,&nbsp;Fumihiko Eto,&nbsp;Yosuke Shibao,&nbsp;Masashi Yamazaki","doi":"10.1155/2022/7502552","DOIUrl":"https://doi.org/10.1155/2022/7502552","url":null,"abstract":"<p><p>A 56-year-old obese man with a body mass index of 30.9 kg/m<sup>2</sup> presented with left sciatica and intermittent claudication. Computed tomography scans showed a posterior vertebral scalloping change in L3, L4, and L5. Meanwhile, magnetic resonance imaging revealed epidural mass posterior to the L3, L4, and L5 vertebral bodies. The solitary mass was isosignal to subcutaneous fat and asymmetrically compressed to the left side of the dural sac and L4 nerve root, as observed on axial T1- and T2-weighted images. To the best of our knowledge, there have been few reports of a solitary epidural lipoma causing lumbar radiculopathy. The patient underwent transforaminal lumbar interbody fusion at L4-L5, and his symptoms then resolved. Thus, we recommend decompression and fixation as appropriate management for lumbar radiculopathy caused by epidural lipoma located on the ventral side of the dura and intervertebral foramen.</p>","PeriodicalId":30287,"journal":{"name":"Case Reports in Orthopedics","volume":" ","pages":"7502552"},"PeriodicalIF":0.0,"publicationDate":"2022-10-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9633206/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40456251","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Arthroscopic Treatment of Pigmented Villonodular Synovitis of the Elbow. 关节镜下治疗肘关节色素绒毛结节性滑膜炎。
Case Reports in Orthopedics Pub Date : 2022-10-13 eCollection Date: 2022-01-01 DOI: 10.1155/2022/7956167
Hatem B Afana, Thomas Nau
{"title":"Arthroscopic Treatment of Pigmented Villonodular Synovitis of the Elbow.","authors":"Hatem B Afana,&nbsp;Thomas Nau","doi":"10.1155/2022/7956167","DOIUrl":"https://doi.org/10.1155/2022/7956167","url":null,"abstract":"<p><p>Pigmented villonodular synovitis (PVNS) is a benign proliferative disorder of synovium that surrounds the joints, tendon sheaths, and bursae. The elbow is rarely affected, making it difficult to establish treatment guidelines. This article relates on a case of a male patient who presented with elbow pain and decreased range of motion. Diagnosis was established with magnetic resonance imaging (MRI) and biopsy, followed by arthroscopic removal and synovectomy. The patient was pain free shortly after surgery and gained free range of motion after six weeks. At the most recent follow-up after six months, he remained clinically well. The most recent MRI did not reveal any recurrence.</p>","PeriodicalId":30287,"journal":{"name":"Case Reports in Orthopedics","volume":" ","pages":"7956167"},"PeriodicalIF":0.0,"publicationDate":"2022-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9584726/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40568332","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Metatarsophalangeal Joint Reconstruction Using Talar Osteochondral Allograft following a Failed Dorsal Cheilectomy. 背侧颧骨切除术失败后距骨软骨异体移植重建跖趾关节。
Case Reports in Orthopedics Pub Date : 2022-09-19 eCollection Date: 2022-01-01 DOI: 10.1155/2022/6359108
Alexandria J Lichtl, Kelly L Vittetoe, Connie P Friedman, Hardik P Parikh, Christopher S Lee
{"title":"Metatarsophalangeal Joint Reconstruction Using Talar Osteochondral Allograft following a Failed Dorsal Cheilectomy.","authors":"Alexandria J Lichtl,&nbsp;Kelly L Vittetoe,&nbsp;Connie P Friedman,&nbsp;Hardik P Parikh,&nbsp;Christopher S Lee","doi":"10.1155/2022/6359108","DOIUrl":"https://doi.org/10.1155/2022/6359108","url":null,"abstract":"<p><p>Dorsal cheilectomy is often used as a first-line surgical treatment for hallux rigidus; however, revision surgery is needed in nearly 9% of cases. One option for revision surgery is interpositional arthroplasty, which is designed to preserve joint motion and is favorable in young, active populations. This case discusses a young female patient with persistent, painful hallux rigidus and a large osteochondral defect despite prior dorsal cheilectomy. We performed an interpositional arthroplasty of the first metatarsophalangeal joint using an osteochondral allograft from the talus. At three-year follow-up, she had greatly improved function and was able to run without pain. To our knowledge, this is the first documented use of an osteochondral allograft from the talus in conjunction with metatarsophalangeal joint interpositional arthroplasty for treatment of hallux rigidus and a severe osteochondral defect. This technique introduces osseous subchondral scaffolding as well as mature hyaline cartilage into an osteochondral lesion, thereby reestablishing proper joint architecture and congruent articulation and ultimately improving range of motion and reducing pain. We present this technique as an experimental treatment option for restoring both the integrity and function of the metatarsophalangeal joint following trauma, osteochondritis dissecans, or prior operative failure in patients who wish to delay metatarsophalangeal joint fusion.</p>","PeriodicalId":30287,"journal":{"name":"Case Reports in Orthopedics","volume":" ","pages":"6359108"},"PeriodicalIF":0.0,"publicationDate":"2022-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9512608/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40381194","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Malignant Diffuse-Type Tenosynovial Giant Cell Tumor in the Subcutaneous Tissue of the Midthigh: A Report of a Rare Tumor in an Unusual Location. 大腿中部皮下组织恶性弥漫性腱鞘巨细胞瘤:一罕见部位肿瘤报告。
Case Reports in Orthopedics Pub Date : 2022-09-19 eCollection Date: 2022-01-01 DOI: 10.1155/2022/6986741
Omar Salem, Khalid Kurdi, Amani Joudeh, Ahmad Al-Dhafiri, Zahra Alkhunaizi, Emad Al Absi
{"title":"Malignant Diffuse-Type Tenosynovial Giant Cell Tumor in the Subcutaneous Tissue of the Midthigh: A Report of a Rare Tumor in an Unusual Location.","authors":"Omar Salem,&nbsp;Khalid Kurdi,&nbsp;Amani Joudeh,&nbsp;Ahmad Al-Dhafiri,&nbsp;Zahra Alkhunaizi,&nbsp;Emad Al Absi","doi":"10.1155/2022/6986741","DOIUrl":"https://doi.org/10.1155/2022/6986741","url":null,"abstract":"<p><p>Malignant TS-GCT is an extremely rare and aggressive tumor with only few cases published in the literature, due to the small number of cases is not completely understood and is diagnostically challenging. Although surgical treatment is the primary treatment modality, there is no consensus regarding adjuvant treatment. Regardless of mode of treatment, the tumor still caries unfavorable prognosis. In this paper, we reviewed the literature for cases of malignant TS-GCT. We also would like to present an additional case of malignant TS-GCT that was found in an unusual location in subcutaneous tissue of the midthigh.</p>","PeriodicalId":30287,"journal":{"name":"Case Reports in Orthopedics","volume":" ","pages":"6986741"},"PeriodicalIF":0.0,"publicationDate":"2022-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9512598/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40381195","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Peroneal Nerve Palsy Caused by Proximal Fibular Solitary Osteochondroma: Case Report and Literature Review. 腓骨近端孤立性骨软骨瘤致腓神经麻痹1例并文献复习。
Case Reports in Orthopedics Pub Date : 2022-09-13 eCollection Date: 2022-01-01 DOI: 10.1155/2022/5865040
Takashi Kozu, Masayoshi Machida, Katsuaki Taira, Noboru Oikawa, Naho Nemoto, Kazuyoshi Nakanishi
{"title":"Peroneal Nerve Palsy Caused by Proximal Fibular Solitary Osteochondroma: Case Report and Literature Review.","authors":"Takashi Kozu,&nbsp;Masayoshi Machida,&nbsp;Katsuaki Taira,&nbsp;Noboru Oikawa,&nbsp;Naho Nemoto,&nbsp;Kazuyoshi Nakanishi","doi":"10.1155/2022/5865040","DOIUrl":"https://doi.org/10.1155/2022/5865040","url":null,"abstract":"<p><p>Osteochondroma is a relatively common benign tumor of the bone, and compressive neuropathies due to osteochondroma are comparatively rare. Here, we present a rare case of osteochondroma of the fibular head that caused peroneal nerve palsy in an 8-year-old girl. Physical examination revealed 0/5 tibialis anterior, 1/5 extensor hallucis longus, and 1/5 peroneal brevis muscle power-according to the manual muscle testing grading system, as well as numbness on the lateral side of the right leg and the back of the foot. Radiological examination and ultrasound revealed a bone tumor in the head of the right fibula. Magnetic resonance imaging ruled out spinal nerve root compression. It was discovered that the bone tumor in the fibular head had compressed and displaced the common peroneal nerve. The patient underwent surgical decompression of the right peroneal nerve. A bone region measuring 22 × 14 × 8 mm was removed. Three months postoperatively, the preoperative neurological deficits were found to be nearly resolved. The patient presented with a foot drop for 1 year, but symptoms resolved 3 months after surgery. Conventional wisdom states that surgery should be performed within 3 months, but we recommend that surgery be performed as soon as diagnosis is made even in cases with a long history, as it may improve patient symptoms and outcomes.</p>","PeriodicalId":30287,"journal":{"name":"Case Reports in Orthopedics","volume":" ","pages":"5865040"},"PeriodicalIF":0.0,"publicationDate":"2022-09-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9489407/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33478243","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Treatment of Severe Hip Dysplasia with Leg Length Discrepancy Using Spherical Periacetabular Osteotomy. 髋臼周围球形截骨术治疗伴腿长不齐的严重髋关节发育不良。
Case Reports in Orthopedics Pub Date : 2022-09-05 eCollection Date: 2022-01-01 DOI: 10.1155/2022/3930806
Yu Takeda, Tomokazu Fukui, Shigeo Fukunishi
{"title":"Treatment of Severe Hip Dysplasia with Leg Length Discrepancy Using Spherical Periacetabular Osteotomy.","authors":"Yu Takeda,&nbsp;Tomokazu Fukui,&nbsp;Shigeo Fukunishi","doi":"10.1155/2022/3930806","DOIUrl":"https://doi.org/10.1155/2022/3930806","url":null,"abstract":"<p><p><i>Case</i>. A 20-year-old woman with severe subluxation of the hip displayed a leg length discrepancy of approximately 20 mm. The proposed treatment was a spherical periacetabular osteotomy (SPO) for joint preservation and postoperative leg length maintenance. SPO is a novel periacetabular osteotomy procedure. At her 3-year follow-up, the patient had functional, pain-free motion and high satisfaction. In this case, the SPO technique was able to achieve satisfactory clinical results without further exacerbating the leg length discrepancy after surgery.</p>","PeriodicalId":30287,"journal":{"name":"Case Reports in Orthopedics","volume":" ","pages":"3930806"},"PeriodicalIF":0.0,"publicationDate":"2022-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9467771/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40358853","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Transtibial Pullout Repair of Lateral Meniscus Posterior Root Tear with Tissue Loss: A Case with Anterior Cruciate Ligament Injury and Medial Meniscus Tear. 经胫骨拔出修复外侧半月板后根撕裂伴组织缺损:前交叉韧带损伤合并内侧半月板撕裂1例。
Case Reports in Orthopedics Pub Date : 2022-08-31 eCollection Date: 2022-01-01 DOI: 10.1155/2022/9776388
Masanori Tamura, Takayuki Furumatsu, Takaaki Hiranaka, Keisuke Kintaka, Naohiro Higashihara, Yusuke Kamatsuki, Eiji Nakata, Toshifumi Ozaki
{"title":"Transtibial Pullout Repair of Lateral Meniscus Posterior Root Tear with Tissue Loss: A Case with Anterior Cruciate Ligament Injury and Medial Meniscus Tear.","authors":"Masanori Tamura,&nbsp;Takayuki Furumatsu,&nbsp;Takaaki Hiranaka,&nbsp;Keisuke Kintaka,&nbsp;Naohiro Higashihara,&nbsp;Yusuke Kamatsuki,&nbsp;Eiji Nakata,&nbsp;Toshifumi Ozaki","doi":"10.1155/2022/9776388","DOIUrl":"https://doi.org/10.1155/2022/9776388","url":null,"abstract":"<p><p>Lateral meniscus (LM) posterior root tear (LMPRT) is mainly caused by trauma, especially trauma associated with anterior cruciate ligament (ACL) injuries. Although a transtibial pullout repair or a side-to-side repair is commonly performed for LMPRT, to the best of our knowledge, there is no clinical report of LMPRT with tissue loss using the pullout technique. Thus, the purpose of this report was to describe a clinical, radiographic, and arthroscopic outcome after pullout repair for a case of LMPRT with a large defect with a chronic ACL tear and complex medial meniscus (MM) tears. A 31-year-old man complained of knee pain and restricted range of motion after twisting his knee when he stepped on an iron pipe. The patient had a football-related injury to his right knee 14 years before presentation, and since then, the patient's knee has given out more than 10 times but was left unassessed. Magnetic resonance imaging showed LMPRT with tissue loss, ACL tears, and complex MM tears. Transtibial pullout repair of the LMPRT with ACL reconstruction and MM repairs were performed. Following the pullout repair of the LMPRT, an approximately 6 mm gap remained between the LM posterior root and root insertion. However, magnetic resonance imaging and second-look arthroscopy at 1 year postoperatively revealed meniscal healing, gap filling with some regeneration tissue, of the LM posterior root. Furthermore, the lateral meniscus extrusion in the coronal plane improved from 3.1 mm (preoperative) to 1.6 mm (1 year postoperatively). Transtibial pullout repair with the remaining gap could be a viable treatment option for LMPRT with tissue loss, combined with ACL reconstruction.</p>","PeriodicalId":30287,"journal":{"name":"Case Reports in Orthopedics","volume":" ","pages":"9776388"},"PeriodicalIF":0.0,"publicationDate":"2022-08-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9453023/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33466659","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Preaxial Polydactyly in an Elderly Woman. 老年妇女前轴多指畸形1例。
Case Reports in Orthopedics Pub Date : 2022-08-31 eCollection Date: 2022-01-01 DOI: 10.1155/2022/7031401
Barkha Chhabra, Richy Charls, John J Faillace
{"title":"Preaxial Polydactyly in an Elderly Woman.","authors":"Barkha Chhabra,&nbsp;Richy Charls,&nbsp;John J Faillace","doi":"10.1155/2022/7031401","DOIUrl":"https://doi.org/10.1155/2022/7031401","url":null,"abstract":"<p><p>A 70-year-old woman born and raised in India presented with Wassel type IV preaxial polydactyly of the right thumb and difficulty performing daily activities. She elected for surgical reconstruction after postponing the procedure for many years due to cultural norms. Her postoperative course was unremarkable. At her 3-month follow-up, she was diagnosed with carpal tunnel syndrome and underwent open carpal tunnel release. Preaxial polydactyly repair is unusual in patients older than 25 years. Though the duplication is considered lucky in South Asia, indications for this case were arthritic pain, cosmesis, and function. This case report details a unique indication for polydactyly reconstruction, arthritic pain, which may benefit hand surgeons when discussing the literature on adult polydactyly with their patients.</p>","PeriodicalId":30287,"journal":{"name":"Case Reports in Orthopedics","volume":" ","pages":"7031401"},"PeriodicalIF":0.0,"publicationDate":"2022-08-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9453009/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33466658","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Isolated Infraspinatus Myositis after Intramuscular Vaccine Administration. 肌肉注射疫苗后孤立性冈下肌炎。
Case Reports in Orthopedics Pub Date : 2022-08-05 eCollection Date: 2022-01-01 DOI: 10.1155/2022/1363462
Eric R Samuelson, Joseph M Bano, Heath P Gould, Richard G Levine
{"title":"Isolated Infraspinatus Myositis after Intramuscular Vaccine Administration.","authors":"Eric R Samuelson,&nbsp;Joseph M Bano,&nbsp;Heath P Gould,&nbsp;Richard G Levine","doi":"10.1155/2022/1363462","DOIUrl":"https://doi.org/10.1155/2022/1363462","url":null,"abstract":"<p><strong>Case: </strong>A 74-year-old female developed left shoulder pain after receiving an influenza vaccine. Her initial physical exam was suggestive of subacromial bursitis, and a corticosteroid injection into the subacromial space resulted in a 50% improvement in her pain. Subsequent MRI demonstrated myositis isolated to the infraspinatus muscle. She was successfully treated with anti-inflammatory medication and physical therapy.</p><p><strong>Conclusion: </strong>Shoulder injury related to vaccine administration (SIRVA) is a rare clinical complication, and myositis in the rotator cuff musculature has not been previously reported. Proper administration of intramuscular vaccinations should be emphasized to prevent injury to structures surrounding the shoulder joint.</p>","PeriodicalId":30287,"journal":{"name":"Case Reports in Orthopedics","volume":" ","pages":"1363462"},"PeriodicalIF":0.0,"publicationDate":"2022-08-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9410995/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33443782","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
相关产品
×
本文献相关产品
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信