scholarly journals Spinal dysraphism with neuropathic bladder and charcot joint

2022 ◽  
Author(s):  
Irvine Sihlahla
Keyword(s):  
Spinal Dysraphism ◽  
Neuropathic Bladder ◽  
Charcot Joint

scholarly journals Charcot joint in a case of syringomyelia with spinal dysraphism

2021 ◽  
Vol 14 (5) ◽  
pp. e239497
Author(s):  
Ashwini Sankhe ◽  
Ankita Shah ◽  
Sneha Deshpande ◽  
Radhika Kshirsagar
Keyword(s):  
Spinal Dysraphism ◽  
Charcot Joint

Neuropathic bladder and spinal dysraphism

1982 ◽  
Vol 17 (1) ◽  
pp. 103-104
Author(s):  
P.A.M. Raine
Keyword(s):  
Spinal Dysraphism ◽  
Neuropathic Bladder

Neuropathic Bladder and Spinal Dysraphism

2011 ◽  
pp. 396-409
Author(s):  
Sanjeev Kaul ◽  
Yegappan Lakshmanan
Keyword(s):  
Spinal Dysraphism ◽  
Neuropathic Bladder

Detrusorectomy for Neuropathic Bladder in Patients with Spinal Dysraphism

2003 ◽  
Vol 170 (4 Part 1) ◽  
pp. 1351-1354 ◽  
Author(s):  
P. DIK ◽  
G.D. TSACHOURIDIS ◽  
A.J. KLIJN ◽  
C.S.P.M. UITERWAAL ◽  
T.P.V.M. de JONG
Keyword(s):  
Spinal Dysraphism ◽  
Neuropathic Bladder

scholarly journals Neuropathic bladder and spinal dysraphism.

1981 ◽  
Vol 56 (9) ◽  
pp. 733-733
Author(s):  
R K Levick ◽  
W J Sharrard
Keyword(s):  
Spinal Dysraphism ◽  
Neuropathic Bladder

NEUROTROPHIC ARTHROPATHY CAUSED BY SPINAL DISORDERS

2001 ◽  
Vol 05 (01) ◽  
pp. 65-72
Author(s):  
Kazumasa Ueyama ◽  
Akihiro Okada ◽  
Naoki Echigoya ◽  
Toru Yokoyama ◽  
Seiko Harata
Keyword(s):  
Weight Bearing ◽  
Spinal Dysraphism ◽  
Posterior Longitudinal Ligament ◽  
Knee Joints ◽  
Surgical Removal ◽  
Spinal Disorders ◽  
Fibula Graft ◽  
Charcot Joint ◽  
Vascularized Fibula ◽  
Vascularized Fibula Graft

Neurotrophic arthropathy, also called Charcot joint, is caused by various diseases. We came across five cases associated with spinal disorders: two presented with syringomyelia with Chiari malformation, one presented with syringomyelia with arachnoiditis secondary to tuberculous meningitis, one presented with ossification of the posterior longitudinal ligament (OPLL) of the lumber spine, and one presented with spinal dysraphism. Neutrophic joints included two knees, two shoulders and one elbow. All spinal disorders were treated surgically but the Charcot joints were treated with arthrodesis in two knee cases and one shoulder case. Solid fusions of arthrodeses were completely achieved using intramedullary nailing to the knee joints and vascularized fibula graft to the shoulder joint. Pathological joints of the shoulder and elbow that did not undergo joint surgery could not be controlled by spinal surgery. Early diagnosis was important for prevention of trauma or sprains to the weight-bearing joints. MRI of the Charcot joint proved useful in confirming the pathological changes in the early destructive stage, and in determining the extent of surgical removal of it for arthrodesis.

scholarly journals Neuropathic bladder and spinal dysraphism.

1981 ◽  
Vol 56 (3) ◽  
pp. 176-180 ◽  
Author(s):  
M Borzyskowski ◽  
B G Neville
Keyword(s):  
Spinal Dysraphism ◽  
Neuropathic Bladder

Spinal Cord Anomalies: Spinal Dysraphism

2017 ◽  
Author(s):  
Tamas Fekete
Keyword(s):  
Spinal Cord ◽  
Spinal Dysraphism

Congenital Dermal Sinus Elements in Each Tethering Stalk of Coexisting Thoracic Limited Dorsal Myeloschisis and Retained Medullary Cord

2020 ◽  
pp. 1-8
Author(s):  
Takato Morioka ◽  
Nobuya Murakami ◽  
Masako Ichiyama ◽  
Takeshi Kusuda ◽  
Satoshi O. Suzuki
Keyword(s):  
Present Article ◽  
Dermoid Cyst ◽  
Spinal Dysraphism ◽  
Conus Medullaris ◽  
Dermal Sinus ◽  
Case Presentation ◽  
Upper Tract ◽  
Secondary Neurulation ◽  
Extradural Space ◽  
Congenital Dermal Sinus

<b><i>Introduction:</i></b> The embryogenesis of limited dorsal myeloschisis (LDM) likely involves impaired disjunction between the cutaneous and neural ectoderms during primary neurulation. Because LDM and congenital dermal sinus (CDS) have a shared origin in this regard, CDS elements can be found in the LDM stalk. Retained medullary cord (RMC) is a closed spinal dysraphism involving a robust, elongated, cord-like structure extending from the conus medullaris to the dural cul-de-sac. Because the RMC is assumed to be caused by impaired secondary neurulation, concurrent RMC and CDS cannot be explained embryologically. In the present article, we report a case in which CDS elements were noted in each tethering stalk of a coexisting LDM and RMC. <b><i>Case Presentation:</i></b> A 2.5-month-old boy with left clubfoot and frequent urinary and fecal leakage had 2 tethering tracts. The upper tract, which ran from the thoracic tail-like cutaneous appendage, had CDS elements in the extradural stalk and a tiny dermoid cyst in the intradural stalk immediately after the dural entry. In the lower tract, which ran from the lumbosacral dimple, the CDS as an extradural stalk continued to the RMC at the dural cul-de-sac. Both stalks were entirely resected through skip laminotomy/laminectomy at 1 stage to untether the cord and resect the CDS elements. <b><i>Conclusion:</i></b> Surgeons should be aware that CDS elements, in addition to LDM, may coexist with RMC that extends out to the extradural space.

Concurrent Thoracic Spinal Intradural Extramedullary Epidermoid and Neurenteric Cyst in a Spinal Dysraphism Child

2021 ◽  
pp. 1-7
Author(s):  
Rajeev Sharma ◽  
Swati Mahajan ◽  
Minakshi Bhardwaj ◽  
Laxmi Naraian Gupta ◽  
Deepak Gupta
Keyword(s):  
Surgical Planning ◽  
English Literature ◽  
Spinal Dysraphism ◽  
Neurenteric Cyst ◽  
Germ Layers ◽  
Case Presentation ◽  
Spinal Lesions ◽  
Congenital Origin ◽  
Thoracic Spinal ◽  
Intradural Extramedullary

<b><i>Introduction:</i></b> Intraspinal epidermoid cysts are congenital or acquired in origin; whereas intraspinal neurenteric cysts (NECs) are of congenital origin. Their individual association with spinal dysraphism and vertebral segmentation anomalies is very well known. <b><i>Case presentation:</i></b> We hereby report a case of concurrent intradural extramedullary epidermoid and NEC at adjacent vertebral levels in a spinal dysraphism child, not reported in English Literature till now. <b><i>Conclusion:</i></b> Multiple spinal lesions related to any/all of the 3 germ layers can coexist at same or adjacent vertebral levels in the same patient and surgical planning shown to be done accordingly.

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