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Case Report
2022
:13;
70
doi:
10.25259/SNI_101_2022

Symptomatic thoracic ossified ligamentum flavum in achondroplasia: A case report and literature review

Pars Advanced and Minimally Invasive Medical Manners Research Center, Pars Hospital, Iran University of Medical Sciences, Tehran, Iran.
Corresponding author: Abolfazl Rahimizadeh, Pars Advanced and Minimally Invasive Medical Manners Research Center, Pars Hospital, Iran University of Medical Sciences, Tehran, Iran. a_rahimizadeh@hotmail.com
Licence

This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, transform, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.

How to cite this article: Rahimizadeh A, Sami SH, Amirzadeh M, Rahimizadeh S, Asgari N. Symptomatic thoracic ossified ligamentum flavum in achondroplasia: A case report and literature review. Surg Neurol Int 2022;13:70.

Abstract

Background:

In a patient with achondroplasia, it is rare to encounter thoracic cord compression due to both spinal stenosis and ossification of the yellow ligament (OYL).

Case Description:

A 33-year-old achondroplastic female presented with a progressive spastic paraparesis attributed to thoracic stenosis combined with T10-T11 OYL. Following a laminectomy, the patient demonstrated a marked recovery of neurological function.

Conclusion:

This case and 12 others from the literature demonstrated that achondroplastic patients who present with myelopathy secondary to thoracic stenosis and OYL can be readily diagnosed with MR/CT and successfully treated utilizing decompressive laminectomies with/without fusions (i.e., for those crossing the thoracolumbar junction).

Keywords

Achondroplasia
Laminectomy
Lumbar canal stenosis
Ossification of the ligamentum flavum

INTRODUCTION

Ossification of yellow ligament (OYL) in the thoracic spine has only rarely been reported to result in severe myelopathy in achondroplastic patients with thoracic stenosis.[2-5,10-12] Here, the authors present a 33-year-old myelopathic Iranian female with achondroplasia, thoracic stenosis, and T10-T11 OYL whose spastic paraparesis successfully resolved following a laminectomy alone.

CASE REPORT

A 33-year-old achondroplastic female presented with a progressive spastic paraparesis/unsteady gait of 6 months’ duration. In addition to the characteristic features of spinal achondroplasia on routine X-rays, the thoracolumbar MRI and CT studies confirmed the presence of moderate thoracic stenosis plus T10/T11 OYL (i.e., dorsolateral hypodense masses) [Figures 1-3]. Following a two-level thoracic laminectomy for decompression and excision of OYL/stenosis, the patient’s myelopathy dramatically improved. The postoperative MR confirmed adequate decompression at the T10/T11 levels [Figures 4 and 5].

Figure 1:: Total spine radiographs. (a) Posteroanterior radiograph shows large pedicle cortex outline, note the interpedicular distance progressively decrease from thoracic to the lumbar spine. Mild coronal imbalance is also seen. (b) Lateral views demonstrate short, large pedicles, and lumbar canal stenosis along with mild sagittal imbalance.
Figure 2:: (a and b) Thoracolumbar sagittal MRI; T1- and T2-weighted images show a posteriorly located hypointense extradural mass compressing the spinal cord at T10-T11 level, compatible with ossified ligamentum flavum.
Figure 3:: CT scan, axial views at T10-T11 level shows bilateral fused type ossification of the ligamentum flavum.
Figure 4:: Photograph of the patient 6 months after surgery.
Figure 5:: Postoperative thoracolumbar MRI, (a and b) T1 and T2 sagittal weighted images show appropriate decompression of lumbar and low thoracic spine.

DISCUSSION

Ossification of the ligamentum flavum (OLF) is well-known that involves patients from all over the world, including Iran (i.e., the US).[1,6-9] Although rare, these patients typically had underlying congenital thoracic stenosis making them uniquely susceptible to myelopathy due to the additional superimposition OYL.[2-5,10-12] Further, we were able to identify 12 similar thoracic cases of myelopathic achondroplastic patients with stenosis/OYL in the medical literature [Table 1]. Putting our case together with those 12 from the literature, there were nine males and four females averaging 49.1 years of age; eight were Japanese, two were East Indian, one was Thai, one Turkish, and one was Iranian. Spastic paraparesis was evident within 11 cases, while two had cauda equina syndromes (i.e., with thoracolumbar stenosis/OYL). MRI is the diagnostic study of choice for identifying achondroplasia accompanied by OYL, lumbar canal stenosis, and wedge vertebra, but CT studies best define OYL’s exact shape, location, and extent of dural ossification.[2-5,10-12] The operations performed included nine thoracic laminectomies, one lumbar laminectomy, and three had thoracolumbar instrumented fusions [Table 1]. In all cases, meticulous detachment/excision of OYL required a microscope to avoid a cerebrospinal dural fistula and minimize trauma to the underlying cord/cauda equina.[1,6-9] Outcomes were good in 10 of 13 patients with minimal preoperative neurological deficits while with the three with more advance preoperative myelopathy exhibited only fair outcomes.

Table 1:: Summary of thoracic/thoracolumbar OYL with stenosis in achondroplastic adults with “PLEASE LOOK AT PREOP DEFICITS AND FILL IN ”

CONCLUSION

OLF should be considered among the differential diagnoses for achondroplastic patients with thoracic spinal cord compression and OYL. Following diagnostic MR/CT studies, these patients typically do well with laminectomies alone, only rarely requiring fusions.

Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

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