Vitamin B12 deficiency presenting with syringomyelia. Case report.

Sanaullah  Mudassir; Ankit  Panjwani

doi:10.51168/sjhrafrica.v6i9.2068

Authors

Dr. Sanaullah Mudassir Senior Consultant Neurologist, Department of Neurology, Jay Prabha Medanta Superspeciality Hospital, Patna, Bihar, India.
Dr. Ankit Panjwani Consultant Neurologist, Department of Neurology, Government Medical College and Superspeciality Hospital, Nagpur, India.

DOI:

https://doi.org/10.51168/sjhrafrica.v6i9.2068

Keywords:

vitamin b12 deficiency, syringomyelia, reversible

Abstract

Background:

Syringomyelia is characterized by the formation of a cyst or cavity (syrinx) within the spinal cord. It is typically associated with Chiari malformation, trauma, or other spinal cord abnormalities. Vitamin B12 deficiency can lead to various neurological and haematological manifestations, including myelopathy, neuropathy, cognitive impairment, and macrocytic anemia. This case highlights a rare or underreported association between vitamin B12 deficiency and syringomyelia.

Case presentation:

A 22-year-old young male, a vegetarian, presented with progressive gait disturbances for the last 4 months. He also had a history of imbalance on standing with closed eyes, with increased gait difficulty in the dark. There was also a history of numbness and paraesthesia of both upper and lower limbs. The neurological examination showed spasticity of both lower limbs, hyperreflexia, and gait ataxia with normal bulk and power, and increased deep tendon reflexes and absent bilateral ankle jerks. The plantar were flexors on both sides. Romberg’s test was positive. Blood investigation revealed pancytopenia (haemoglobin-4.6, total leucocyte count- 3900, Platelet count-62,000) with raised MCV- 118 fL. Serum vitamin B12 was found to be low (78 pg/ml) with elevated homocysteine levels (27 umol/l). MRI revealed prominence of the central canal in the cervical spinal cord at the C2-C3 vertebral level. The nerve conduction study showed inexcitable bilateral sural nerves. He was treated with intramuscular vitamin B12 injections. He was given 1000 μg of methylcobalamin initially daily for a week and then weekly for a month, and once-monthly injections for 6 months. After 9 months, he significantly recovered to his near-normal physical capacity with a normal gait. There was also almost complete regression of the syrinx cavity.

Conclusion:

Syrinx formation secondary to B12 deficiency is rarely reported in the literature. This case highlights the importance of treating the underlying vitamin B12 deficiency before planning for any interventional procedure.

Author Biographies

Dr. Sanaullah Mudassir , Senior Consultant Neurologist, Department of Neurology, Jay Prabha Medanta Superspeciality Hospital, Patna, Bihar, India.

is a Senior Consultant Neurologist in the Department of Neurology at Jay Prabha Medanta Hospital in Patna, India. His qualifications include MBBS, MD in General Medicine, and DM in Neurology. He has various national and international publications in his name.

Dr. Ankit Panjwani , Consultant Neurologist, Department of Neurology, Government Medical College and Superspeciality Hospital, Nagpur, India.

is a Consultant Neurologist in the Department of Neurology at Government Medical College and Super speciality Hospital, Nagpur, India. His qualifications include MBBS, MD in General Medicine, and DM in Neurology. He is a Gold Medallist in DM and has various research papers in his name

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