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1دورية أكاديمية
المؤلفون: Kir, Mustafa C.1 drcaglarkir@gmail.com, Ozdemir, Mehmet T.2
المصدر: Indian Journal of Orthopaedics. Nov/Dec2011, Vol. 45 Issue 6, p573-575. 3p. 2 Color Photographs, 2 Black and White Photographs.
مصطلحات موضوعية: *FIBRODYSPLASIA ossificans progressiva, *MILITARY education, *RADIOGRAPHIC films, *SHOULDER, *TOMOGRAPHY, *DIAGNOSIS
مستخلص: The myositis ossificans around shoulder in military recruits are not reported yet. Three young male soldiers presented with complaints of palpable mass at the anterior aspect of shoulder; tenderness around the superior part of deltopectoral groove close to acromioclavicular joint; and restriction of shoulder motion. They also noticed ecchymosis and pain around the coracoid process and anterior shoulder region during regular firing exercises. Plain X-rays and computerized tomography showed extra-capsular, dense, irregular structure in the space between pectoralis and deltoid muscles which correlated with heterotopic bone. One patient refused surgical intervention because of the completion of his military serving period. Surgical excision was performed for the other two patients. During surgical exploration, both ossified masses were found in deltopectoral region and mostly in fibers of clavicular and acromial parts of deltoid muscle. Pathological reports confirmed the structure of masses as mature trabecular bone. Postoperatively indomethacin treatment and active shoulder exercises were started until the full range of motion was regained. Mini soft bag was used on the rifle contact area of the shoulder. No complications or recurrences were observed during the 24 months of followup period. [ABSTRACT FROM AUTHOR]
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2
المصدر: Indian Journal of Orthopaedics, Vol 49, Iss 3, Pp 361-364 (2015)
Indian Journal of Orthopaedicsمصطلحات موضوعية: mesh:heterotopic, medicine.medical_specialty, Pathology, Case Report, genetic analysis, lcsh:Orthopedic surgery, Medicine, Orthopedics and Sports Medicine, genetic analysis MeSH terms: Ossification, genetic predisposition to disease, business.industry, Ossification, heterotropic, Heterotopic bone, medicine.disease, mesh:genetic predisposition to disease, lcsh:RD701-811, progressive ossific heteroplasia, heterotopic ossification, Fibrodysplasia ossificans progressiva, Orthopedic surgery, Heterotopic ossification, mesh:Ossification, medicine.symptom, business
الوصف: Fibrodysplasia ossificans progressiva (FOP) and progressive ossific heteroplasia (POH) are rare genetic disorders characterized by heterotopic bone formation leading to progressive loss of mobility and function. We report three cases of these rare disorders (two cases of FOP and one case of POH), which were clinically diagnosed and underwent genetic analysis. The aim of this report is to highlight the clinical features and the differences between these two conditions. We would also like to emphasize on the morbidity that can arise from unnecessary invasive investigations for diagnostic purposes.
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5bcb6de7d9de3bee2e8ef6c318c9fdeTest
http://www.ijoonline.com/article.asp?issn=0019-5413;year=2015;volume=49;issue=3;spage=361;epage=364;aulast=SankarTest -
3
المؤلفون: Vikas Verma, Girish Kumar Singh
المصدر: Indian Journal of Orthopaedics, Vol 45, Iss 3, Pp 280-282 (2011)
Indian Journal of Orthopaedicsمصطلحات موضوعية: Pathology, medicine.medical_specialty, biology, business.industry, Ossification, Case Report, medicine.disease, Progressive osseous heteroplasia, GNAS1 mutation, lcsh:RD701-811, subcutaneous ossification, heterotopic ossification, lcsh:Orthopedic surgery, Fibrodysplasia ossificans progressiva, GNAS complex locus, biology.protein, Medicine, Orthopedics and Sports Medicine, Pseudopseudohypoparathyroidism, Heterotopic ossification, medicine.symptom, business, Paternal Inheritance, Pseudohypoparathyroidism
الوصف: We report a sporadic case of progressive osseous heteroplasia (POH) in a 10-year-old male child who developed progressive ossification of the skin and deep connective tissue. The condition needs to be distinguished from other causes of childhood heterotopic ossification, such as fibrodysplasia ossificans progressiva, pseudohypoparathyroidism, and pseudopseudohypoparathyroidism. The cause of POH is an inactivating GNAS1 (guanine nucleotide-binding protein alpha-stimulating activity polypeptide 1) mutation caused only by paternal inheritance of the mutant allele. Most cases are sporadic and only 2 instances of familial transmission have been documented, suggesting an autosomal dominant mode of inheritance with possible somatic mosaicism. The condition is associated with progressive superficial to deep ossification, progressive restriction of range of motion, bleak prognosis, and recurrence if excised.
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b442e7aa5181246a72762626909f860Test
https://doi.org/10.4103/0019-5413.80050Test -
4دورية أكاديمية
المصدر: Indian Journal of Orthopaedics; Jan-Mar2009, Vol. 43 Issue 1, p97-98, 2p, 1 Black and White Photograph
مصطلحات موضوعية: GENETIC disorders, SURGICAL excision, FIBRODYSPLASIA ossificans progressiva, PELVIC injuries
مستخلص: Described as asymptomatic and an incidental finding on a plain x-ray film, the "pelvic digit" is a rare congenital anomaly. A 35-year-old man is of a rare symptomatic pelvic digit that warranted surgical excision. Its importance lies in its differentiation from acquired abnormalities due to trauma such as myositis ossificans and avulsion injuries of pelvis. If this entity is kept in mind, unnecessary investigations or interventions can be avoided. [ABSTRACT FROM AUTHOR]
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