Traumatic sacralization of L5 vertebra with severe extension type spinopelvic dissociation: A case report
نویسندگان
چکیده
منابع مشابه
Minimally Traumatic Spinopelvic Dissociation With Prolonged Bisphosphonate Use.
Bisphosphonates have become the first-line treatment for diseases involving excessive osteoclast-mediated bone resorption. However, evidence suggests that elevated doses or prolonged treatment may impair normal skeletal mineralization and may be associated with fractures. The majority of these fractures are located in the subtrochanteric region. This article presents the first described case of...
متن کاملTraumatic Scapholunate Dissociation--case Report.
Perilunate injuries occur after an impact trauma to the wrist. The recognition of these lesions and immediate treatment are the two essential conditions to ensure the best possible outcome. The first therapeutic step is the restoration of anatomical joint relationships of the carpus followed by percutaneous pinning or internal fixation required for maintaining the congruence this segment. Despi...
متن کاملL5 vertebrectomy for the surgical treatment of tumoral and traumatic lesions of L5 vertebra
We retrospectively reviewed the clinical characteristics and the surgical results of seven patients treated with L5 vertebrectomy. The pathologies, clinical characteristics, preoperative and postoperative radiological findings, surgical techniques, and instrumentation for seven patients operated on between 1998 and 2009 are presented in this article. Biopsies were performed on all patients exce...
متن کاملReport of a Case of Histiocytosis X with Severe Jaundice
A case report of histiocytosis X in a 2 years old infaut, primarily admitted a for jaundice is discussed. Major clinical manifestations included: Jaundice, bilateral otitis media. pallor and loss of weight. Clinical examination revealed hepatosplenomegaly. lymphadenopathies and sever anemia. Seborrr.eic eruptions and ptechias appeared over the scalp and other parts of body surface a few days ...
متن کاملReport of a case of Proteus syndrome with severe anemia
Proteus syndrome is a rare congenital disorder comprised of subcutaneous and internal hamartomas, miscellaneous skin and vascular nevi, skeletal and nervous system and eye malformations, with characteristic manifestations including hemihypertrophy, local gigantism, macrodactyly and cerebriform thickness of soles and palms. A 23 year-old man with diagnosis of proteus syndrome had sever ane...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Trauma Case Reports
سال: 2020
ISSN: 2352-6440
DOI: 10.1016/j.tcr.2020.100338