Intraosseous Schwannoma of the Fourth Lumbar Vertebra: Case Report

Neurosurgery ◽  
1998 ◽  
Vol 43 (5) ◽  
pp. 1219-1222 ◽  
Author(s):  
Chih-Ju Chang ◽  
Jing-Shan Huang ◽  
Yung-Cheng Wang ◽  
Shih-Hung Huang
2020 ◽  
Vol 16 (1) ◽  
Author(s):  
Gerlinde J. Wunderink ◽  
Ursula E. A. Bergwerff ◽  
Victoria R. Vos ◽  
Mark W. Delany ◽  
Dorien S. Willems ◽  
...  

Abstract Background This case report describes the clinical signs of a calf with focal diplomyelia at the level of the fourth lumbar vertebra. Magnetic resonance imaging (MRI) images and histological findings of the affected spinal cord are included in this case report. This case differs from previously reported cases in terms of localization and minimal extent of the congenital anomaly, clinical symptoms and findings during further examinations. Case presentation The calf was presented to the Farm Animal Health clinic, Faculty of Veterinary Medicine, Utrecht University, with an abnormal, stiff, ‘bunny-hop’ gait of the pelvic limbs. Prominent clinical findings included general proprioceptive ataxia with paraparesis, pathological spinal reflexes of the pelvic limbs and pollakiuria. MRI revealed a focal dilated central canal, and mid-sagittal T2 hyperintense band in the dorsal part of the spinal cord at the level of the third to fourth lumbar vertebra. By means of histology, the calf was diagnosed with focal diplomyelia at the level of the fourth lumbar vertebra, a rare congenital malformation of the spinal cord. The calf tested positive for Schmallenberg virus antibodies, however this is not considered to be part of the pathogenesis of the diplomyelia. Conclusions This case report adds value to future clinical practice, as it provides a clear description of focal diplomyelia as a previously unreported lesion and details its diagnosis using advanced imaging and histology. This type of lesion should be included in the differential diagnoses when a calf is presented with a general proprioceptive ataxia of the hind limbs. In particular, a ‘bunny-hop’ gait of the pelvic limbs is thought to be a specific clinical symptom of diplomyelia. This case report is of clinical and scientific importance as it demonstrates the possibility of a focal microscopic diplomyelia, which would not be evident by gross examination alone, as a cause of hind-limb ataxia. The aetiology of diplomyelia in calves remains unclear.


2011 ◽  
Vol 55 (5) ◽  
pp. 473-477 ◽  
Author(s):  
Silvia J. Hernández Martínez ◽  
Hernán Campa Núñez ◽  
Gerardo Ornelas Cortinas ◽  
Raúl Garza Garza

2011 ◽  
Vol 117 (1) ◽  
pp. 72-77 ◽  
Author(s):  
Tomoaki Koakutsu ◽  
Naoki Morozumi ◽  
Takeshi Hoshikawa ◽  
Shinji Ogawa ◽  
Yushin Ishii ◽  
...  

2007 ◽  
Vol 28 (7) ◽  
pp. 845-848 ◽  
Author(s):  
R.M. Meek ◽  
H. Sharma ◽  
M.J. Jane ◽  
N. Raby ◽  
E. Macduff ◽  
...  

2013 ◽  
Vol 56 (3) ◽  
pp. 126-129
Author(s):  
George Paraskevas ◽  
Maria Tzika ◽  
Panagiotis Kitsoulis

Congenital malformations such as lumbosacral transitional vertebrae and spina bifida occulta constitute unrare anomalies and could affect the symptomatology of low back pain. A transitional vertebra is characterized by elongation of one or both transverse processes, leading to the appearance of a sacralized fifth lumbar vertebra or a lumbarized first sacral vertebra. Furthermore, sacral spina bifida occulta is a developmental anomaly that corresponds to the incomplete closure of the vertebral column. In the present case report, we describe a case of a dried sacrum presenting a partially sacralized fifth lumbar vertebra and total spina bifida, extended from first to fifth sacral vertebra. A pseudoarthrosis is formed on the left side and the specimen could be incorporated in Castellvi’s type IIa. Moreover, the incidence, morphology, clinical and surgical significance of these spinal malformations are discussed.


1990 ◽  
Vol 25 (4) ◽  
pp. 1276
Author(s):  
Chang Uk Choi ◽  
Yon Il Kim ◽  
Byung Il Lee ◽  
Byung Joon Shin ◽  
Hong Seop Kim

Author(s):  
Yuichiro Matsuoka ◽  
Asuka Iwamoto ◽  
Ryoji Yoshida ◽  
Taku Kojima ◽  
Masatoshi Hirayama ◽  
...  

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