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. 2018 Sep;97(38):e12468.
doi: 10.1097/MD.0000000000012468.

Spinal paragangliomas: Surgical treatment and follow-up outcomes in eight cases

Affiliations

Spinal paragangliomas: Surgical treatment and follow-up outcomes in eight cases

Okan Turk et al. Medicine (Baltimore). 2018 Sep.

Abstract

Paragangliomas are neuro-endocrine tumors originating from the adrenal gland. They are usually benign and nonfunctioning, rarely seen in central nervous system. More than 90% of central nervous system paragangliomas are manifested as carotid and glomus jugulare tumors. Spinal paragangliomas are quite rare.The study was conducted through retrospective analysis of the files of the patients who had undergone surgery with pre-diagnosis of spinal intradural tumor between 2011 and 2017 and diagnosed with paraganglioma.A total of 8 patients (4 females and 4 males) were included in the study. Mean age of the patients was 51.1 years (28-64). Time to admission was mean 6.5 months (3 weeks-24 months). Recurrence was not observed in 7 patients, 1 patient is being followed up due to residual tumor.Treatment may be achieved through recognizing malignant transformation in patients who were not diagnosed histopathologically. We consider that quality of life of the patients may be improved through this way.

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Figures

Figure 1
Figure 1
(A–D) Preoperative spinal magnetic resonance imaging (MRI) images of the patient 4 in Table 1.
Figure 2
Figure 2
Postoperative spinal magnetic resonance imaging (MRI) images of the patient 4 in Table 1.
Figure 3
Figure 3
Peroperative images of the patient 4 in Table 1.
Figure 4
Figure 4
Histochemical pathology image of case 4 presented in Table 1. A. HEX200. B. HEX400 C. CD56 D. EMA.

References

    1. Ardon H, Plets C, Sciot R, et al. Paraganglioma of the cauda equina region: a report of three cases. Surg Neurol Int 2011;2:96. - PMC - PubMed
    1. Polman CH, Gijsbers CJ, Heimans JJ, et al. Rapid spontaneous resolution of an acute subdural hematoma. Neurosurgery 1986;19:446–8. - PubMed
    1. Yin M, Huan Q, Sun Z, et al. Clinical characteristics and surgical treatment of spinal paraganglioma: a case series of 18 patients. Clin Neurol Neurosurg 2017;158:20–6. - PubMed
    1. Mishra T, Goel NA, Goel AH. Primary paraganglioma of the spine. A clinicopathological study of eight cases. J Craniovertebr Junction Spine 2014;5:20–4. - PMC - PubMed
    1. Miller CA, Torack RM. Secretory ependymoma of the filum terminale. Acta Neuropathol 1970;15:240–50. - PubMed