Myelopathy due to Vitamin B12 Deficiency: Case Report
DOI:
https://doi.org/10.25759/spmfr.204Keywords:
Spinal Cord Diseases/rehabilitation, Vitamin B 12 DeficiencyAbstract
Vitamin B12 deficiency causes several neurological manifestations such as myelopathy, polyneuropathy, optic neuropathy and dementia. The most common etiology for vitamin B12 deficiency is pernicious anemia; however, other causes include strict vegan, post-gastrectomy and Crohn’s disease. Vitamin B12 deficiency-induced myelopathy (subacute combined degeneration) is characterized by affecting the posterior and lateral columns of the spinal cord, which may lead to severe and irreversible damage. Diagnosis is established by clinical features, serum cobalamin and homocysteine levels, urinary methylmalonic acid measurements and magnetic resonance imaging. Treatment is based on vitamin B12 injections and recovery depends on the severity and duration of the deficiency. Typically it requires Physical and Rehabilitation Medicine for patients suffering from lasting deficits. In this case report, authors show promising clinical and functional results after the administration of cobalamim and after following a rehabilitation program.
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References
Sethi N, Robilotti E, Sadan Y. Neurological manifestations of vitamin B12 deficiency. Internet J Nutrition Wellness. 2004;12.
Stabler SP, Savage DG, Lindenbaum J. Metabolic abnormalities in cobalamin (vitamin B-12) and folate deficiency. FASEB J. 1993; 7:1344-53.
Jacob A, Weinshenker BG. An approach to the diagnosis of acute transverse myelitis. Semin Neurol. 2008; 28:105–20.
Granados AM, Garcia LM, Ortega Toscano CA, López A. Enfoque diagnóstico de las mielopatías. Rev Colom Radiol. 2011; 21:1-21.
Garcia, A, Zanibbi K. Homocysteine and cognitive function in elderly people. CMJA. 2004; 171:897-904.
Wang H, Wahlin A, Basun H, Fastbom J, Fastbom J, Winblad B, Fratiglioni L. Vitamin B12 and folate in relation to the development of Alzheimer’s disease. Neurology. 2001; 56: 1188-1194.
Pruthi R, Tefferi A. Pernicious anemia revisited. Mayo Clin Proc. 1994; 69:144-50.
Incecik F, Hergüner M, Altunba
Christie C, Lepera S, Giacchino A, Giacchino A, Rey RC. Mielopatía cordonal posterior por déficit de vitamina B12 en el contexto de atrofia gástrica. Rev Neurol Arg 2010; 2: 55-7.
Bhuiyan A, Dash S, Shahriar S, Zak IT, Madhavan R. A case of sub-acute combined degeneration of the spinal cord with associated pernicious anemia. Pulse. 2014; 2: 61-3.
Nogales-Gaete J, Jiménez P, García P, David Sáez M, Rodrigo Aracena C, Jorge González V, et al. Mielopatía por déficit de vitamina B12: caracterización clínica de 11 casos. Rev Med Chile. 2004; 132: 1377-82.
Ertan T, Tanriverdi G, Kiziltan G. Complete resolution of myelopathy in a patient with vitamin B12 deficiency: A case report. Internet J Neurol. 2002;2.
Biçak N, Çelebisoy N. Sub acute combined degeneration: A case with spinal MRI findings improving before the clinical features. J Neurol Sci. 2007; 24:167-9.
Kuzminski A, Del Giacco E, Allen R, Stabler SP, Lindenbaum J.Effective treatment of Cobalamin deficiency with oral Cobalamin. Blood. 1998; 92:1191-8.
Vasconcelos O, Poehm E, McCarter, R, Campbell WW, Quezado ZM. Potential outcome factors in subacute combined degeneration: review of observational studies. J Gen Intern Med. 2006; 21:1063-8.
Vervoordeldonk JJ, Post MW, New P, Clin Epi M, Van Asbeck FW. Rehabilitation of patients with nontraumatic spinal cord injury in the Netherlands: etiology,length of stay, and functional outcome. Top Spinal Cord Inj Rehabil. 2013;19:195-201.
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