scholarly journals Schwannoma of Dorsal spine: A case report of a 25 year old female with Schwannoma at D10-11 level

Author(s):  
Dr. Piyush Mittal ◽  
Dr. Deepak Agrawal ◽  
Dr. Sagar Usdadia ◽  
Dr. Harsh Vyas ◽  
Dr. Deep Shah
Keyword(s):  
2021 ◽  
Vol 16 (4) ◽  
pp. 886
Author(s):  
SauravNarayan Nanda ◽  
Gurudip Das ◽  
NabinKumar Sahu ◽  
DokiSunil Kumar ◽  
BishnuPrasad Patro

2017 ◽  
Vol 8 (4) ◽  
pp. 378
Author(s):  
Satyashiva Munjal ◽  
Amit Srivastava ◽  
Shivya Tucker ◽  
Neha Bakshi ◽  
Sunita Bhalla ◽  
...  

2019 ◽  
Vol 08 (02) ◽  
pp. 136-138
Author(s):  
Musali Siddartha Reddy ◽  
Gollapudi Prakash Rao ◽  
Mohammed Imran ◽  
Uday Goutam Nookathota

AbstractA rare case of monostotic ossifying fibroma of the dorsal spine in a postpartum woman is being described. Ossifying fibromas of the spine are very rare tumors. They are components of benign fibro-osseous lesions. We report a case of an 18-year-old woman, who presented with complaints of weakness of both the lower limbs in the immediate postpartum period and was diagnosed with ossifying fibroma of the dorsal [D3] vertebral body. The tumor was excised followed by spinal stabilization. Histopathologic findings were consistent with ossifying fibroma. Postoperative period was uneventful. Monostotic variant of ossifying fibroma in the dorsal spine is an extremely rare tumor, and its presence in the postpartum period adds on to the diagnostic dilemma. Hence this case report can be kept in mind while evaluating a case presenting with complaints of weakness of both the lower limbs in the immediate postpartum period.


2015 ◽  
Vol 0 (0) ◽  
pp. 0
Author(s):  
Shilpa Garg ◽  
Ketan Khurjekar ◽  
Hrutvij Bhatt ◽  
Rohit Singla ◽  
Rajiv Goyal

2020 ◽  
Vol 8 (3) ◽  
Author(s):  
S.H TOUIMI ◽  
S DAOUDI ◽  
I MBARKI ◽  
I ADRIF ◽  
H ELKACEMI ◽  
...  

2016 ◽  
Vol 4 (1) ◽  
pp. 137-139
Author(s):  
Dr. Lohit kumar Kalita ◽  
◽  
Dr. Chayanika Kalita ◽  
Dr Tralukya Nandan Sonowal ◽  
Dr. Umesh Ch. Sarma ◽  
...  

2021 ◽  
Vol 27 (4) ◽  
pp. 38-42
Author(s):  
Tamajyoti Ghosh ◽  
Ajay Sebastian Carvalho

Introduction: Hemangiopericytomas are rare CNS Neoplasms constituting <1% of CNS tumours. They are more commonly seen in cranium than in spine where they present as Intradural extramedullary in location. They rarely metastasize to Lung and Bone.World Health Organization Classification of Tumors of the Central Nervous System (CNS WHO) assigned the combined term solitary fibrous tumor/ hemangiopericytoma (SFT/HPC) to such lesions in 2016 due to their same genetic makeup. Case report: Our case is about a 61-year-old diabetic male who presented with insidious onset, gradually progressive thoracic backache and asymmetric weakness with tightness and numbness of both lower limbs for last 6 months with no sphincter incontinence and bed bound for last 15 days. Clinically he had asymmetric spastic paraparesis of lower limb. His MRI Dorsal spine showed a 1.5 ґ 2 cm heterogeneously contrast enhancing Intradural lesion at D6-D7 compressing the cord from dorsolaterally with extensive cord edema from C5 to L2. Preoperative diagnosis of Meningioma/ Metastasis was made and patient underwentD5-D7 laminectomy and tumour excision. Intraoperative findings, there was no dural attachment, there were multiple tortuous blood vessels overlying greyish pink, fleshy, suckable, highly vascular, capsulated tumor posterolateral to cord. The superior aspect of tumor was adherent to cord with no clear interface. Tumor was seen separate from Left D7 nerve root. Post operatively patient improved symptomatically and neurologically. His HPE was suggestive of Hemangiopericytoma WHO Grade II (IHC markers CD34 and CD 31 was positive and KI 67% index of 10-15%). Patient has been on follow up and planned for metastatic workup. Conclusion: Spinal Hemangiopericytoma are rare disease with nonspecific radiological features making preoperative diagnosis difficult. Differential diagnosis of hemangiopericytoma should be kept in case of atypical and high - grade radiological features. Gross total resection without compromising the neurological status should be the goal to prevent local recurrence. Proper consensus regarding the follow up and adjuvant therapies of spinal Hemangiopericytoma are still lacking.


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