Thoracic ligamentum flavum ossification causing progressive myelopathy: a case report

Background: Ossified ligamentum flavum (OLF) in the thoracic segments is a rare but significant cause of progressive myelopathy characterized by spinal canal stenosis. While OLF is commonly reported in East Asian populations, it remains under-recognized in other regions, including India. Case presentation: We present a case of a 60-year-old Indian male laborer who developed progressive lower-limb weakness, sensory deficits, and immobility over several months. This case is notable for its occurrence in an Indian patient, within a population in which OLF remains significantly underreported, and for advanced neurological compromise (preoperative Medical Research Council [MRC] grade 2/5 bilaterally) and intraoperative dural ossification requiring complex surgical decision-making. Imaging revealed severe spinal cord compression at D10–D11 due to OLF, with associated dural calcification. Surgical decompression via laminectomy resulted in significant neurological improvement, with motor power improving to MRC grade 3/5 bilaterally and complete resolution of sensory deficits, highlighting the importance of timely intervention. Conclusion: This case highlights the need for increased awareness of OLF in underrepresented populations and emphasizes the critical role of advanced imaging and surgical management in achieving favorable outcomes. The rarity of reported cases of OLF from India and the presence of concurrent dural calcification further distinguish this report and highlight a diagnostic gap that warrants attention.

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Publication Details

Journal
International Journal of Surgery Case Reports
Published
2026-08-18
DOI
https://doi.org/10.1097/rc9.0000000000000859
Primary Topic
Cervical and Thoracic Myelopathy
Type
article
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article

Thoracic ligamentum flavum ossification causing progressive myelopathy: a case report

Bipin Chaurasia, Maryam Afifa -, Kıvanç Yangı, Kashif Qureshi et al.
International Journal of Surgery Case Reports
Cervical and Thoracic Myelopathy
article

Thoracic ligamentum flavum ossification causing progressive myelopathy: a case report

Bipin Chaurasia, Maryam Afifa -, Kıvanç Yangı, Kashif Qureshi, VenkatR Reddy, Rishesh Sharma
article en

Abstract

Background: Ossified ligamentum flavum (OLF) in the thoracic segments is a rare but significant cause of progressive myelopathy characterized by spinal canal stenosis. While OLF is commonly reported in East Asian populations, it remains under-recognized in other regions, including India. Case presentation: We present a case of a 60-year-old Indian male laborer who developed progressive lower-limb weakness, sensory deficits, and immobility over several months. This case is notable for its occurrence in an Indian patient, within a population in which OLF remains significantly underreported, and for advanced neurological compromise (preoperative Medical Research Council [MRC] grade 2/5 bilaterally) and intraoperative dural ossification requiring complex surgical decision-making. Imaging revealed severe spinal cord compression at D10–D11 due to OLF, with associated dural calcification. Surgical decompression via laminectomy resulted in significant neurological improvement, with motor power improving to MRC grade 3/5 bilaterally and complete resolution of sensory deficits, highlighting the importance of timely intervention. Conclusion: This case highlights the need for increased awareness of OLF in underrepresented populations and emphasizes the critical role of advanced imaging and surgical management in achieving favorable outcomes. The rarity of reported cases of OLF from India and the presence of concurrent dural calcification further distinguish this report and highlight a diagnostic gap that warrants attention.

International Journal of Surgery Case Reports
Nizam's Institute of Medical Sciences (IN), Government Nizamia General Hospital (IN), College of Medical Sciences (NP), Yale University (US), Istanbul Eye Hospital (TR)
Openalex Percentile: Top 8%
Cervical and Thoracic Myelopathy
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