Spontaneous Vertebral Column Dislocation in Neurofibromatosis - A Case Report -

2007 ◽  
Vol 42 (6) ◽  
pp. 822 ◽  
Author(s):  
Ki-Tack Kim ◽  
Sang-Hun Lee ◽  
Kyung-Soo Suk ◽  
Jung-Hee Lee ◽  
Eun-Min Seo ◽  
...  
Keyword(s):  
BMC Surgery ◽  
2010 ◽  
Vol 10 (1) ◽  
Author(s):  
Despoina Georgiadou ◽  
George N Zografos ◽  
Dennis Vaidakis ◽  
Spiridon Avlonitis ◽  
Angeliki Katopodi ◽  
...  
Keyword(s):  

2021 ◽  
pp. 509-511
Author(s):  
Mohd Monis ◽  
Shagufta Wahab ◽  
Divyashree Koppal ◽  
Aiman Ibbrahim

This is a rare case report of a 5-month-old child with a complex spinal dysraphic state, and an accessory limb (tripedus morphology), accessory genitalia, and anal dimple. The child was brought to the hospital with an accessory limb arising from the back. On clinical examination, an accessory limb arising from the lower back with a partially developed foot with the presence of toes and nails was noted. Spinal MRI was advised which revealed dysraphic features including spina bifida with the low lying and posteriorly tethered cord with diastematomyelia along with a supernumerary appendage attached to the vertebral column having rudimentary bones resembling those of extremities. The presence of an accessory limb with spinal dysraphism is quite a rare anomaly. The condition can be treated by surgical intervention and involves excision of the accessory limb with adequate dural and paraspinal muscle cover.


2020 ◽  
Vol 15 (2) ◽  
Author(s):  
Nik Qisti F ◽  
Shahrun Niza AS ◽  
Razrim R

Aberrant right subclavian artery is a rare cause of dysphagia. This is a congenital anomaly with the right subclavian artery originating from the dorsal part of the aortic arch and coursing through the mediastinum between the esophagus and the vertebral column. We report a case of a patient with chronic dysphagia caused by this condition. We further discuss the case with regards to its clinical features and options of management.


Neurospine ◽  
2020 ◽  
Vol 17 (4) ◽  
pp. 941-946
Author(s):  
Venkat Boddapati ◽  
Joseph M. Lombardi ◽  
Lawrence G. Lenke

2019 ◽  
Vol 70 (5) ◽  
pp. 1856-1858
Author(s):  
Mihai Musteata ◽  
Diana Mocanu ◽  
Eusebiu Sindilar ◽  
Mihai Mares ◽  
Ramona Florina Moraru ◽  
...  

A 6-year-old, neutered female Doberman Pinscher was presented with acute progressive paraparesis consistent with T3-L3 myelopathy. For 5 months prior to the admission, the dog had multiple recurrent hyperthermic episodes treated with antibiotics and intermittent corticosteroids for a Borrelia and Ehrlichia co-infection. On survey radiographs and CT of the spine, severe osteoproliferative changes were extensively seen throughout the thoracolumbar vertebral column, and were suggestive of discospondylitis. After cytological and microbiological examinations of the vertebral aspirate a severe Staphylococcus aureus methicillin-resistant discospondylitis was established as a final diagnosis. This is the first case report of discospondylitis due to MRSA in dog without vertebral spine surgery. Treatment with corticosteroids can cover the evolution of discospondylitis until the condition became severe and untreatable.


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