Chondromyxoid Fibroma of the Cervical Spine—a Case Report with a Review of the Literature and a Description of an Operative Approach to the Lower Anterior Cervical Spine

Neurosurgery ◽  
1982 ◽  
Vol 11 (2) ◽  
pp. 288-292 ◽  
Author(s):  
Michael Standefer ◽  
Russell W. Hardy ◽  
Kenneth Marks ◽  
D. M. Cosgrove

Abstract A case of chondromyxoid fibroma arising from the C-7 vertebral body and involving the epidural space and paraspinal soft tissues is presented. The surgical treatment of this tumor is described, and the pertinent literature is reviewed.

2010 ◽  
Vol 13 (03) ◽  
pp. 147-151 ◽  
Author(s):  
Nasir A. Siddiqui ◽  
Emad Almusa ◽  
Cynthia A. Britton

Introduction: Cervical pneumatocyst is an important entity that has been rarely reported in the literature. Less than 20 cases have been reported in the English literature. This entity is an important differential consideration when evaluating cervical spine lesions. The purpose of our study is to characterize the imaging features of cervical pneumatocysts. Methods: We report a case of a cervical pneumatocyst in a 51-year-old female patient, which mimicked a sclerotic lesion on magnetic resonance evaluation. Additionally, a dedicated literature review was performed evaluating the location, signal alterations, and imaging characteristics of 16 cervical pneumatocysts. Results: Fifteen of the sixteen cases in the cervical spine were found in the vertebral body. One case was identified in the lateral mass of the cervical spine. Two pneumatocysts were identified in C4, eight in C5, four in C6, and one in C7. Nine of the sixteen cases demonstrated disruption of the endplate with likely communication with either the spinal canal or intravertebral disc, with the remaining seven cases appearing isolated from the vertebral body. Conclusions: Cervical pneumatocysts are benign lesions that do not require urgent treatment. Based on their imaging appearance alone, they can be differentiated from more serious lesions such as neoplasms or osteomyelitis.


The Foot ◽  
2021 ◽  
pp. 101796
Author(s):  
Elias S. Vasiliadis ◽  
Christos Vlachos ◽  
Angelos Antoniades ◽  
Eftychios Papagrigorakis ◽  
Matthaios Bakalakos ◽  
...  

Author(s):  
Núria Carreras ◽  
Cristian de Guirior ◽  
Meritxell Munmany ◽  
Mariona Rius ◽  
Roser Nonell ◽  
...  

2021 ◽  
pp. 1-6
Author(s):  
Kadir Oktay ◽  
Dogu Cihan Yildirim ◽  
Arbil Acikalin ◽  
Kerem Mazhar Ozsoy ◽  
Nuri Eralp Cetinalp ◽  
...  

<b><i>Introduction:</i></b> Extraneural metastases of glioblastoma are very rare clinical entities, especially in pediatric patients. Because of their rarity, they can be confused with other pathological processes. <b><i>Case Presentation:</i></b> We report a case of 16-year-old boy with extensive extraneural metastases of glioblastoma. Lung, liver, cervical lymph nodes, skin, and bone metastases were detected in the patient. <b><i>Conclusion:</i></b> We describe the presentation, evaluation, and diagnosis of this rare condition with regard to pertinent literature.


2000 ◽  
Vol 16 (8) ◽  
pp. 522-524 ◽  
Author(s):  
H. Ilhan ◽  
Baran Tokar ◽  
Metin Ant Atasoy ◽  
Alparslan Kulali

2016 ◽  
Vol 17 (5) ◽  
pp. 607-611 ◽  
Author(s):  
Wei Qu ◽  
Dingjun Hao ◽  
Qining Wu ◽  
Zongrang Song ◽  
Jijun Liu

Unilateral facet dislocation at the subaxial cervical spine (C3–7) in children younger than 8 years of age is rare. The authors describe a surgical approach for irreducible subaxial cervical unilateral facet dislocation (SCUFD) at C3–4 in a 5-year-old boy and present a literature review. A dorsal unilateral approach was applied, and a biodegradable plate was used for postreduction fixation without fusion after failed conservative treatment. There was complete resolution of symptoms and restored cervical stability. Two years after surgery, the patient had recovered range of motion in C3–4. In selected cases of cervical spine injury in young children, a biodegradable plate can maintain reduction until healing occurs, obviate the need to remove an implant, and recover the motion of the injured segment.


Neurosurgery ◽  
1991 ◽  
Vol 29 (4) ◽  
pp. 599-602 ◽  
Author(s):  
B. Aesch ◽  
E. Lioret ◽  
B. de Toffol ◽  
M. Jan

Abstract A 25-year-old man was hospitalized after suffering a subarachnoid hemorrhage. Arteriograms disclosed two arteriovenous malformations, one of which was asymptomatic. Rendu-Osler-Weber disease was suspected because of the concomitant existence of cutaneous telangiectases, Review of the literature shows that in 12 previously published cases involving multiple arteriovenous malformations, this diagnosis was established five times. The indications for surgical treatment are discussed.


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