Journal List > J Korean Soc Spine Surg > v.24(2) > 1076129

Choi, Lee, Chun, Kim, and Shin: A Long, Solitary, Rosary-Shaped Spinal Neurofibroma

Abstract

Study Design

Case report.

Objectives

We report the case of a long, solitary, rosary-shaped neurofibroma that was misdiagnosed as another disease due to the patient's surgical history involving repetitive procedures and its abnormal appearance.

Summary of Literature Review

Neurofibroma is an intradural-extramedullary spinal tumor. It is generally not difficult to diagnose due to its frequent occurrence and specific magnetic resonance imaging (MRI) findings. However, to date, neurofibromatosis stigmata and long, solitary, rosary-shaped neurofibromas have rarely been reported.

Materials and Methods

A 60-year-old woman was admitted to our hospital due to persistent pain, despite previous surgery and repetitive procedures. On physical examination, vision loss, hearing loss, skin discoloration, or subcutaneous nodules were not observed. A neurologic examination revealed normal motor and sensory function and voiding sensation. No pathologic reflexes such as the Babinski sign were observed. Previous sequential MRIs revealed intradural lesions that progressed from the thoracic vertebra 11 to the lumbar vertebra 3. She had no signs of neurofibromatosis stigmata, and the neurologic examination was unremarkable. The initial diagnosis was based on serial MRIs, which revealed a parasite infestation, a spinal cord tumor (myxopapillary-type ependymoma with hemorrhage), arachnoiditis, and vascular malformations. Total mass excision was performed, and the final diagnosis was neurofibroma.

Results

There were no signs of a tumor remnants or local recurrence in a 1-year follow-up MRI study.

Conclusions

Although intradural spinal tumors are very rare, their clinical features are nonspecific and resemble other degenerative spinal diseases, including spinal stenosis and disc herniation. These diseases may easily be overlooked by physicians.

REFERENCES

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Fig. 1.
Serial T2-weighted sagittal magnetic resonance imaging revealed that the mass-like lesion grew or moved caudally. (A-B) 27 months, (B-C) 12 months, (C-D) 5 months.
jkss-24-109f1.tif
Fig. 2.
A post-myelographic computed tomography scan revealed multiple filling defects in the dural sac, from the T11 to L3-4 disc levels. (A, B) Coronal and sagittal images show a tortuous lesion in the spinal canal with an elongated shape.
jkss-24-109f2.tif
Fig. 3.
Preoperative sagittal magnetic resonance imaging demonstrated that the mass-like lesion extended from the T11 level to the L3-4 disc levels. It was shaped like a rosary or pea in the dural sac. (A) Isointensity on T1; (B) mixed or slightly low intensity on T2; (C) a heterogeneous well-enhanced image post-contrast.
jkss-24-109f3.tif
Fig. 4.
Photographic findings. The mass had a serpentine shape with firm consistency. It measured 1.0×1.5×14 cm and weighed 10 g. (A) Gross sur-face, (B) longitudinal cross-section.
jkss-24-109f4.tif
Fig. 5.
Histological findings. A high-power section revealed a proliferation of spindle cells with wavy nuclei, consistent with a neurofibroma (hematoxylin and eosin staining, ×400 magnification).
jkss-24-109f5.tif
Fig. 6.
Postoperative 1-year follow-up magnetic resonance imaging. There was no evidence of tumor remnants or local recurrence of the tumor.
jkss-24-109f6.tif
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