scholarly journals SPASTIC PARAPARESIS IN YOUNG MEN WITH SPINAL MENINGIOMA AND SPINAL ARTERIOVENOUS MALFORMATION: A CASE REPORT

Author(s):  
Leonard Christianto Singjie ◽  
Ivan Jeremia ◽  
Esdras Ardi Pramudita

Background: Compared to trauma cases, the publication of non-traumatic events is much less, although the incidence is estimated to be as much as a traumatic event. This case report presents spinal cord tumors together with arteriovenous malformation (AVM) in young men, where there are no previous case reports that the authors can find.Case Report: A 22-year-old male patient with complaints of pain in the back (NPRS 8-9), followed by difficulty moving the lower limb accompanied by a burning sensation, problem in defecation, and urination. We found motor weakness in the lower extremities (1/1), positive pathological reflexes, and sensibility disorders on physical examination.Discussion: According to history taking, physical examination, and MR Imaging, the spastic paraparesis symptom in this patient is likely due to a spinal cord tumor, which is meningioma (according to histopathological examination). Where back pain rarely presents in the patient with spinal AVM. Laminectomy and tumor destruction were the gold standards of therapy, and the symptom was relieved.Conclusion: A complete examination is the main key in determining the appropriate therapy for the patient's disease. In this case, the manifestation of spastic paraparesis was likely to be caused by meningioma rather than spinal AVM. Laminectomy and extirpation of the spinal meningioma were done as the gold standard of therapy, and the symptom was relieved. In contrast, spinal AVM was not performed­ and is still under observation.

2002 ◽  
Vol 11 (1) ◽  
pp. 1-5
Author(s):  
Taichi Tsuji ◽  
Yukihiro Matsuyama ◽  
Koji Sato ◽  
Hisashi Iwata

Author(s):  
Madan Basnet ◽  
Suman Gaire ◽  
Abisha Phudong ◽  
Kamal Gautam ◽  
Prarthana Subedhi ◽  
...  

Perimedullary spinal AVM is a rare type of spinal arteriovenous malformations. We present a case of 70 yrs female who presented with motor weakness in her bilateral limbs. Initial MRI was misinterpreted as ependymal myxoma; however, histopathology revealed spinal AVM. MRA or DSA should be conducted if AVM is suspected.


2007 ◽  
Vol 65 (3b) ◽  
pp. 838-840 ◽  
Author(s):  
Helio A. Oliveira ◽  
Alan Chester F. de Jesus ◽  
Roberto César P. Prado ◽  
Augusto César E. Santos ◽  
Paulo Marcelo S. Sobral ◽  
...  

Spinal cord compressing syndrome due to synovial cyst (SC) of the thoracic spine is a rare clinic condition. We report a case of SC located in the thoracic spine causing spastic paraparesis in a 14 year-old female patient. The SC was removed thoroughly by laminectomy. The patient had an excellent recovery. The etiological and therapeutic aspects are discussed.


2021 ◽  
Vol 1 ◽  
pp. 100459
Author(s):  
E. Abdulla ◽  
H. Luther ◽  
T. Shah ◽  
N. Chandran

Neurosurgery ◽  
1989 ◽  
Vol 24 (1) ◽  
pp. 118-124 ◽  
Author(s):  
Kazuhiko Tokoro ◽  
Yasuhiro Chiba ◽  
Saburo Yagishita ◽  
Yumiko Kunimi

Abstract The case of a 40-year-old man with syringobulbo-myelia secondary to an unresectable spinal extramedullary tumor is described. Fifteen years previously, the patient had undergone a laminectomy of T8 through T12 for a “benign” spinal cord tumor at another hospital and had become paraplegic; the tumor (neurinoma) had been neglected for 12 years. Magnetic resonance imaging demonstrated a large thoracolumbar spinal tumor with syringobulbo-myelia. Polysomnography showed central-, peripheral-, and mixed-type sleep apneas. After the failure of an attempted syringoperitoneal shunt, cordectomy at the level of T6 was performed with a good result. The mechanisms of the formation of syringomyelia and sleep apnea secondary to a caudal spinal extramedullary tumor are discussed.


2016 ◽  
Vol 18 (2) ◽  
pp. 177-182 ◽  
Author(s):  
Eslam M. Samak ◽  
Assem M. Abdel Latif ◽  
Walid Abdel Ghany ◽  
Iman H. Hewedi ◽  
Aboubakr Amer ◽  
...  

True hamartomas of the spinal cord are very rare, and although several have been reported in the literature, there are few detailed radiological and pathological descriptions of the condition. There is also considerable overlap with other entities, the most common being spinal cord teratomas. The authors report the case of a 13-month-old child with a supragluteal sacral dimple who presented with acute neurological deterioration. MRI of the spine revealed a big intramedullary lesion with heterogeneous signal intensity. A near-total resection was performed, and histopathological examination demonstrated findings consistent with a spinal cord hamartoma. The authors believe that careful preoperative evaluation and rigorous pathological examination are mandatory to establish diagnosis and direct further management of cases in which such a lesion is suspected.


2011 ◽  
Vol 31 (6) ◽  
pp. 632-638 ◽  
Author(s):  
Takeshi Iwasaki ◽  
Masako Kato ◽  
Yasushi Horie ◽  
Shinsuke Kato ◽  
Keiichi Akatsuka ◽  
...  

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