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Masatoshi Yunoki, Kenta Suzuki, Atsuhito Uneda, Kimihiro Yoshino
  1. Department of Neurosurgery, Kagawa Rosai Hospital, Kagawa, Japan

Correspondence Address:
Masatoshi Yunoki
Department of Neurosurgery, Kagawa Rosai Hospital, Kagawa, Japan

DOI:10.4103/2152-7806.159378

Copyright: © 2015 Yunoki M. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

How to cite this article: Yunoki M, Suzuki K, Uneda A, Yoshino K. A case of dumbbell-shaped epidural cavernous angioma in the lumbar spine. Surg Neurol Int 25-Jun-2015;6:

How to cite this URL: Yunoki M, Suzuki K, Uneda A, Yoshino K. A case of dumbbell-shaped epidural cavernous angioma in the lumbar spine. Surg Neurol Int 25-Jun-2015;6:. Available from: http://surgicalneurologyint.com/surgicalint_articles/a-case-of-dumbbell%e2%80%91shaped-epidural-cavernous-angioma-in-the-lumbar-spine/

Date of Submission
23-Apr-2015

Date of Acceptance
08-May-2015

Date of Web Publication
25-Jun-2015

Abstract

Background:Most spinal cavernous haemangiomas occur in the vertebral body and purely extradural cavernous hemangiomas without any vertebral body involvement is rare and account for only 4% of all extradural spinal tumors. Dumbbell-shaped spinal cavernous angioma is extremely rare, only 10 cases have been reported in the literature.

Case Description:A 77-year-old female presented with a one-year history of lumbago and right-sided L3 dermatomal hypoesthesia. A dumbbell mass at the L2/3 vertebral level was identified on lumbar MRI. The lesion was irregularly shaped and isointense on T1W and hyperintense on T2W and DWI images with homogenous contrast enhancement. A presumptive diagnosis was schwannoma, but other malignant neoplasms were also considered because of its irregular shape, minimally dilated neural foramen and the involvement of the non-enhanced L3 nerve root. The patient underwent surgery with a lateral extracavitary approach. A histopathological examination revealed cavernous hemangioma.

Conclusion:Cavernous hemangioma should be included in the differential diagnosis of dumbbell-shaped spinal tumors when the intervertebral foramina is not highly dilated and non-enhanced nerve root is identified in the tumor.

Keywords: Cavernous hemangioma, differential diagnosis, dumbbell, epidural, lumbar

INTRODUCTION

Most spinal cavernous hemangiomas occur in the vertebral body and may sometimes extend into the epidural space.[ 7 ] Purely extradural cavernous hemangiomas without any vertebral body involvement are extremely rare, and account for only 4% of all extradural spinal tumors.[ 14 ] We herein present a rare case of a dumbbell-shaped epidural cavernous hemangioma at the level of L2/3. This case is reported because of its rarity, the unusual dumbbell shape of the lesion and the difficulty in making a preoperative diagnosis.

CASE REPORT

A 77-year-old female presented with a 1-year history of lumbago and right-sided L3 dermatomal hypoesthesia. Her muscle strength and deep tendon reflexes were normal. Magnetic resonance imaging (MRI) of the lumbar spine revealed an irregularly-shaped, well-circumscribed paraspinal mass with minor intraspinal extension through the L2/3 intervertebral foramen. The lesion was isointense on T1-weighted (T1W) and hyperintense on T2W and diffusion-weighted images, with strong homogenous enhancement in a gadolinium (Gd) contrast study [ Figure 1 ]. In the Gd-enhanced images, involvement of the nonenhanced right L3 nerve root in the tumor was identified [Figure 1d and e ]. Computed tomography (CT) demonstrated mild enlargement of the right neural foramen at L2–3, but there were no remarkable erosive changes of the vertebral body, pedicle or lamina [Figure 2a and b ]. All modalities of sensations (pin prick, touch, temperature, vibration) at the L3 dermatomes on the right side were observed. The bilateral lower limb power was normal. The results of the general examination were unremarkable, and no sensorimotor deficits were detected in the upper limbs. A presumptive diagnosis was schwannoma, but the possibility of a neurofibroma or other malignant neoplasm was considered because of the tumor's irregular shape, lack of an enlarged neural foramen and the involvement of the nonenhanced L3 nerve root. The patient underwent surgery with a lateral extracavitary approach.[ 18 ]


Figure 1

Preoperative magnetic resonance images at the level of L2/3 showing an irregularly-shaped, well-defined extradural lesion with paraspinal transforaminal extension that was hypointense on T1-weighted (T1W) (a) and hyperintense on T2W (b) and diffusion-weighted images. (c) Contrast-enhanced T1W images of transverse (d) and coronal sections showed the right L3 nerve root ventrally separated from the homogeneously enhanced tumor (arrow)

 

Figure 2

(a) A transverse computed tomography (CT) scan at the level of L2/3 showing a left-sided dumbbell-shaped mass (thick arrow). The posterior wall of the right intervertebral foramen was slightly eroded (thin arrow). (b) A coronal CT scan demonstrating the mildly enlarged right intervertebral foramen and dumbbell-shaped mass (thick arrow)

 

A longitudinal right paravertebral skin incision 15 cm in length at the L1–L3 level was made, followed by clear identification of the lumbodorsal fascia. The fascia was then incised in line, and a clear plane was identified between the multifidus medially and the longissimus laterally. The muscles were meticulously teased apart. The transverse processes of Th2 and Th3 were identified by fluoroscopy [ Figure 3 ], and were exposed with monopolar cautery. A Th3/4 external foraminotomy was performed and the transverse processes of Th2 and Th3 were removed, then a brownish-red, highly vascular mass was identified [ Figure 3 ]. The tumor was highly vascular and bled heavily upon the acquisition of a small biopsy. The capsule was coagulated to control the hemorrhage. An intraoperative histopathological examination indicated that the tumor was a hemangiomatous neoplasm, without evidence of malignancy. The tumor extended into the intrathecal region through the L2/3 neural foramen. The right L3 nerve root was identified in the ventral part of the tumor. The tumor adhesion to the nerve root was severe; therefore, we left the tumor around the nerve root behind due to concerns about possible nerve root damage. The tumor was removed subtotally. The patient's postoperative course was uneventful. She was discharged 2 weeks after surgery. The histological examination of the tumor showed it to be a cavernous hemangioma [ Figure 3 ].


Figure 3

A microscopic examination revealed numerous dilated vascular channels of variable sizes lined by a single layer of flattened epithelial cells that was filled with blood elements. The tumor stroma consisted of typical fibrous tissue. The histological findings were characteristic of cavernous hemangioma. (H and E, ×100)

 

DISCUSSION

Hemangiomas are congenital vascular malformations whose pathologies are considered to be hamartomatous malformations.[ 3 7 ] They are classified based on the predominant type of vascular channel (capillary, cavernous, arteriovenous or venous) observed during the histological examination. Spinal epidural hemangiomas account for 4% of all spinal epidural tumors, mostly occurring as a primary lesion in the vertebral bone.[ 2 ] Some authors have reported cases of purely epidural hemangiomas, most of which were of the cavernous type.[ 3 13 ] In contrast to the brain or spinal cord hemangiomas, the patterns of density on CT scans and signal intensity on MRI are more homogeneous in epidural hemangiomas. On CT studies, these neoplasms appear as intermediate or slightly hyperdense extradural masses. By MRI, they display high signal intensity on T2W images, which may be explained by the high content of stagnant blood. Slow blood flow may contribute substantially to the signal, conferring a low or intermediate signal intensity on T1W images, although there is no direct anatomical relationship with the intervertebral disk or exiting nerve root.[ 2 4 ]

About 80% of spinal epidural cavernous angiomas are in the thoracic spine, most of which are located posterior within the spinal canal and present with myelopathy.[ 2 ] In cases of lumbar epidural cavernous angiomas, they tend to be located in the ventral extradural space and cause lumbar radiculopathy, clinically and radiologically mimicking the presence of disk herniation.[ 15 ] These characteristics were also observed in 10 previously reported cases of dumbbell-shaped extradural cavernous angiomas[ 3 5 6 8 9 11 12 14 15 17 ] [ Table 1 ]. Seven of the 10 cases were in the thoracic spine and three were in the lumbar spine. The symptoms of the dumbbell-shaped hemangiomas in the thoracic spine were mainly myelopathy, while those in the lumbar spine mainly led to radicular pain.


Table 1

The reported cases of dumbbell-shaped epidural spinal hemangiomas

 

Dumbbell-shaped spinal tumors are usually thought to be schwannomas, neurofibromas or meningiomas.[ 10 ] Most of these tumors have enlarged intervertebral foramina, whereas cavernous angiomas do not tend to be dilated.[ 10 12 ] [ Table 1 ]. Some authors have reported that 10–40% of dumbbell-shaped spinal tumors are malignant tumors such as lymphoma, metastatic tumors, sarcoma, etc., which also tend to lack a dilated intervertebral foramina.[ 10 12 ] Cavernous hemangioma and malignant tumors should therefore be included in the differential diagnosis of dumbbell-shaped spinal tumors when the intervertebral foramina is not highly dilated.[ 10 ]

It has been suggested that a complete excision of the cavernous angioma is related to a favorable outcome. In the present case, however, we left a small amount of the tumor around the nerve root behind due to concerns about possible nerve root damage. When complete removal is not possible, radiosurgery is increasingly becoming an option, as advances in radiosurgical equipment are enabling safe and accurate targeting of lesions.[ 1 16 ] We are now considering adjuvant radiosurgery for the residual tumor.

References

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