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Jeong, Choi, Seong, and Roh: Thoracic Extradural Cavernous Hemangioma Mimicking a Dumbbell-Shaped Tumor

Abstract

Dumbbell-shaped spinal extradural cavernous hemangioma is rare. The differential diagnosis of dumbbell-shaped spinal tumors based on magnetic resonance imaging includes schwannoma and lymphoma. Here, we report a dumbbell-shaped spinal extradural cavernous hemangioma with intrathoracic growth on T2-3 in a 64-year-old man complaining of right side infrascapular area back pain with no neurologic deficit. The cavernous hemangioma was resected through combined video-assisted thoracoscopy and laminectomy without a fusion procedure. The patient had tolerable operative wound pain with no neurologic deficit after surgery. Based on magnetic resonance imaging findings and a review of the literature, we discuss cavernous hemangioma among the differential diagnosis of paravertebral dumbbell-shaped spinal tumors and the importance of complete resection.

INTRODUCTION

Cavernous hemangiomas of the central nervous system are vascular malformations that can affect any part of the neuraxis. Most of these lesions are found intracranially, with supratentorial sites being most commonly affected while vertebral locations are rare3). Cavernous hemangiomas constitute 5-12% of vascular lesions of the spine and are seen most frequently in the vertebral bodies17). The majority of extradural cavernous hemangiomas represent extension from a vertebral hemangioma into the spinal canal with purely extradural locations only representing 1-2% of spinal hemangiomas7,23). These tumors commonly affect the vertebral bodies and extend into the epidural space27), and are less commonly found within the thoracic cavity20). Here, we report our experience with a case of upper thoracic extradural cavernous hemangioma successfully treated by complete removal through combined approaches by video-assisted thoracoscopy and laminectomy.

CASE REPORT

A 64-year-old man was admitted to our hospital with a 6-month history of slowly progressive back pain in the right side infrascapular area. He was otherwise well. Physical examination on admission revealed no focal neurologic deficit. Preoperative magnetic resonance imaging showed a well-demarcated round-shaped abnormal high-signal intensity lesion with mottled low signal intensity on both T1- and T2-weighted sequences within the left half of the T2 vertebral body extending to the left pedicle. An associated left-sided dumbbell-shaped mass at the level of T2-3 was noted and comprised of an extradural mass causing mild cord compression without an intradural portion and extending through the left T2-3 neural foramen to form a 3.0×2.0×2.5-cm intrathoracic mass (Fig. 1). The mass demonstrated isosignal intensity on T1-weighted images (Fig. 1B) and high signal intensity on T2-weighted images (Fig. 1C). There was no contrast-enhanced T1-weighted sequence. The preoperative radiological diagnosis was an extradural dumbbell-shaped schwannoma and concomitant vertebral body hemangioma.
The patient underwent a planned combined posterior and thoracoscopic approach performed by the neurosurgery and cardiothoracic surgery teams, respectively. First, the neurosurgery team performed total laminectomies from T2 to T4. A pinkish, non-encapsulated tumor was found attached to the dura mater and extended through the left T2-3 intervertebral foramen (Fig. 2). Epidural portion of tumor was connected to the tumor of vertebral body portion which mainly involved the cancellous bony part. However, the margin of extradural hemangioma from vertebral body hemangioma was easily separated.
Gross total resection of the tumor was performed by piecemeal method. The left T2 nerve root was sacrificed after resection of the spinal cord-compressing tumor to have cardiothoracic team easily remove the paravertebral mass which was preoperatively diagnosed as an extradural schwannoma. The mass was hypervascular and entirely extradural. After changing the patient's position from prone to lateral, the cardiothoracic surgery team performed a video-assisted thoracoscopic surgery and completely removed the paravertebral mass by piecemeal method. There was no adhesion to the pleura.
Histopathological diagnosis of the extradural and paravertebral mass was cavernous hemangioma composed of irregular cavernous vascular spaces. The resected specimen contained fibrous connective tissue and many irregular thin-walled vessels filled with blood cells (Fig. 3). The postoperative course of the patient was uneventful. The right infrascapular area back pain was improved, and the patient showed tolerable operative wound pain without symptoms caused by the sacrifice of the left T2 nerve root. Follow-up magnetic resonance imaging performed on the following day after surgery showed no residual extradural cavernous hemangioma (Fig. 4). The patient was discharged on postoperative day 6.

DISCUSSION

Cavernous hemangiomas are benign vascular malformations that can affect any part of the neuraxis4). These masses are composed of packed and dilated sinusoidal vascular spaces lined by a single endothelial layer with no elastic or muscular tissue20). In addition, sinusoidal blood vessels are separated by the hyalinizing stroma with no normal neural connective tissue 3,27). Clinically, patients with spinal cavernous hemagniomas may present with symptoms of spinal cord or nerve root compression. Depending on the location and growth rate, symptoms include local pain, radiculopathy, and slow progressive or acute spinal cord compression8,11). Because these lesions do not grow by mitotic activity, sudden onset of symptoms usually result from trauma, exercise, change in posture, infection, pregnancy, or sprain, all of which may cause hemorrhage or microhemorrhages within the blood vessels and thrombotic occlusion resulting in secondary swelling10,1112,16).
Vertebral hemangioma is extraordinary common, the reported incidences ranged from 10 to 27% in adults. The incidence varies depending on the diagnostic modality used. 10.7% in one large autopsy report, 10-12% in a large population based study using plain X-ray and 27% in a cross sectional study using MRI as the diagnostic tool2).
It has been reported that cavernous hemagnioma developed purely at the spinal epidural space accounts for about 4% or less than that of the other tumors developed at the spinal epidural space and also reported about 1-2% of the cavernous hemangioma developed at the spine3,423,2527). Therefore, most published literatures about epidural cavernous hemangioma had to be case reports1,1213,1820,2224).
These masses can very rarely occur within the organs in the thoracic cavity such as, the anterior mediastinum or the lungs16). Posterior mediastinal cavernous hemangioma may also extend from an extradural spinal cavernous hemangioma through the intervertebral foramen, adopting a 'dumbbell' shape21).
Magnetic resonance imaging can help to differentiate posterior mediastinal cavernous hemangioma from other dumbbell-shaped lesions27), because the location, extent of vertebral hemangioma (intradural or extradural), and presence of neural compression can be visualized. Extradural cavernous hemangiomas show iso- or low-signal intensity on T1-weighted images and high signal intensity in T2-weighted images, with homogeneous or strong enhancement with contrast, although variable enhancement patterns such as slight or peripheral enhancement have also been reported6,723).
The differential diagnosis for paravertebral dumbbell-shaped spinal tumors commonly includes schwannomas, lymphomas, and rarely, meningiomas23). Schwannomas present as an epidural mass with extension to the intervertebral neural foramen; however, a smooth rather than lobulated contour and frequent cystic changes are indicative of this tumor in the differential diagnosis5,7). Lymphomas less frequently extend into the paravertebral or show intervertebral neural foraminal widening. In addition, lymphomas frequently show iso-signal intensity on T2-weighted magnetic resonance imaging14). Meningiomas rarely present with a dumbbell shape or epidural location; however, isosignal intensity of the spinal cord with frequent broad dural attachment can be indications for the differential diagnosis23).
Complete resection is recommended for the treatment for extradural cavernous hemangioma25,27), because incomplete resection of the tumor may lead to recurrence of symptoms27), although malignant transformation of extradural cavernous hemangioma has not been reported26). However, incomplete resection of cavernous hemangiomas often occurs because conventional piecemeal resection may lead to profuse bleeding during the surgery due to its friable, thin-walled vessels25). Laminectomy, either standard or combined with foraminotomy or costo-transversectomy, has also been used to treat these tumors20,27). However, these approaches only provide limited exposure of the posterior mediastinum and lead to incomplete resection in case of the intrathoracic extension of the tumor25). To achieve complete resection, sufficient exposure of both lesions is needed. Therefore, intrathoracic extraforaminal extension of an extradural cavernous hemangioma, including the other dumbbell-shaped tumors could be surgically treated through the combination of posterior laminectomy followed by thoracoscopic resection, because this approach maximizes visibility of the lesion, controls possible residual lesions, and minimizes operation time21). After incomplete resection, subsequent surgery can be performed on the residual lesion if symptoms recur. Radiation therapy may be indicated in cases of asymptomatic growth or persistent pain. However, the role of radiation therapy still remain controversial20,2527).

CONCLUSION

Cavernous hemangiomas should be considered in the differential diagnoses of paravertebral dumbbell-shaped spinal tumors and should be treated by complete resection using combined approaches of posterior laminectomy for resection of extradural part and video-assisted thoracoscopic removal of intrathoracic one.

References

1. A L H, T R, Chamarthy NP, Puri K : A pure epidural spinal cavernous hemangioma - with an innocuous face but a perilous behaviour!! J Clin Diagn Res 2013, 7 : 1434-1435,
crossref pmid pmc
2. Barzin M, Maleki I : Incidence of vertebral hemangioma on spinal magnetic resonance imaging in Northern Iran. Pak J Biol Sci 2009, 12 : 542-544,
crossref pmid
3. Carlier R, Engerand S, Lamer S, Vallee C, Bussel B, Polivka M : Foraminal epidural extra osseous cavernous hemangioma of the cervical spine : a case report. Spine (Phila Pa 1976) 2000, 25 : 629-631,
crossref pmid
4. Daneyemez M, Sirin S, Duz B : Spinal epidural cavernous angioma : case report. Minim Invasive Neurosurg 2000, 43 : 159-162,
crossref pmid
5. Demachi H, Takashima T, Kadoya M, Suzuki M, Konishi H, Tomita K, et al : MR imaging of spinal neurinomas with pathological correlation. J Comput Assist Tomogr 1990, 14 : 250-254,
crossref pmid
6. Feider HK, Yuille DL : An epidural cavernous hemangioma of the spine. AJNR Am J Neuroradiol 1991, 12 : 243-244,
pmid pmc
7. Golwyn DH, Cardenas CA, Murtagh FR, Balis GA, Klein JB : MRI of a cervical extradural cavernous hemangioma. Neuroradiology 1992, 34 : 68-69,
crossref pmid
8. Graziani N, Bouillot P, Figarella-Branger D, Dufour H, Peragut JC, Grisoli F : Cavernous angiomas and arteriovenous malformations of the spinal epidural space : report of 11 cases. Neurosurgery 1994, 35 : 856-863, discussion 863-864
crossref pmid
9. Guthkelch AN : Haemangiomas involving the spinal epidural space. J Neurol Neurosurg Psychiatry 1948, 11 : 199-210,
crossref pmid pmc
10. Hong SP, Cho DS, Kim MH, Shin KM : Spinal epidural cavernous hemangioma simulating a disc protrusion: a case report. J Korean Neurosurg Soc 2003, 33 : 509-511,

11. Lee JP, Wang AD, Wai YY, Ho YS : Spinal extradural cavernous hemangioma. Surg Neurol 1990, 34 : 345-351,
crossref pmid
12. Li TY, Xu YL, Yang J, Wang J, Wang GH : Primary spinal epidural cavernous hemangioma : clinical features and surgical outcome in 14 cases. J Neurosurg Spine 2015, 22 : 39-46,
crossref pmid
13. Luca D, Marta R, Salima M, Valentina B, Domenico D : Spinal epidural cavernous angiomas : a clinical series of four cases. Acta Neurochir (Wien) 2014, 156 : 283-284,
crossref pmid
14. Mascalchi M, Torselli P, Falaschi F, Dal Pozzo G : MRI of spinal epidural lymphoma. Neuroradiology 1995, 37 : 303-307,
crossref pmid
15. McCormick WF : The pathology of vascular ("arteriovenous") malformations. J Neurosurg 1966, 24 : 807-816,
crossref pmid
16. Padolecchia R, Acerbi G, Puglioli M, Collavoli PL, Ravelli V, Caciagli P : Epidural spinal cavernous hemangioma. Spine (Phila Pa 1976) 1998, 23 : 1136-1140,
crossref pmid
17. Padovani R, Tognetti F, Proietti D, Pozzati E, Servadei F : Extrathecal cavernous hemangioma. Surg Neurol 1982, 18 : 463-465,
crossref pmid
18. Rahman A, Hoque SU, Bhandari PB, Abu Obaida AS : Spinal extradural cavernous haemangioma in an elderly man. BMJ Case Rep 2012, 2012,
crossref
19. Saracen A, Kotwica Z : Thoracic spinal epidural cavernous haemangioma with an acute onset : case report and the review of the literature. Clin Neurol Neurosurg 2013, 115 : 799-801,
crossref pmid
20. Saringer W, Nöbauer I, Haberler C, Ungersböck K : Extraforaminal, thoracic, epidural cavernous haemangioma : case report with analysis of magnetic resonance imaging characteristics and review of the literature. Acta Neurochir 2001, 143(Wien):1293-1297,
crossref pmid
21. Saumench R, Barcia JA, Arnau A, Cantó A : Combined thoracotomy and laminectomy for spinal cavernomas with intrathoracic growth. Interact Cardiovasc Thorac Surg 2004, 3 : 76-78,
crossref pmid
22. Sharma MS, Borkar SA, Kumar A, Sharma MC, Sharma BS, Mahapatra AK : Thoracic extraosseous, epidural, cavernous hemangioma : case report and review of literature. J Neurosci Rural Pract 2013, 4 : 309-312,
crossref pmid pmc
23. Shin JH, Lee HK, Rhim SC, Park SH, Choi CG, Suh DC : Spinal epidural cavernous hemangioma : MR findings. J Comput Assist Tomogr 2001, 25 : 257-261,
crossref pmid
24. Shivaprasad S, Shroff G, Campbell GA : Thoracic epidural cavernous hemangioma imaging and pathology. JAMA Neurol 2013, 70 : 1196-1197,
crossref pmid
25. Talacchi A, Spinnato S, Alessandrini F, Iuzzolino P, Bricolo A : Radiologic and surgical aspects of pure spinal epidural cavernous angiomas. Report on 5 cases and review of the literature. Surg Neurol 1999, 52 : 198-203,
crossref pmid
26. Yettou H, Vinikoff L, Baylac F, Marchal JC : [Spinal epidural cavernous angioma. Apropos of 2 cases. Review of the literature]. Neurochirurgie 1996, 42 : 300-304, discussion 304-305
pmid
27. Zevgaridis D, Büttner A, Weis S, Hamburger C, Reulen HJ : Spinal epidural cavernous hemangiomas. Report of three cases and review of the literature. J Neurosurg 1998, 88 : 903-908,
crossref pmid
Fig. 1

Preoperative T2-weighted sequence (A and B) and T1-weighted sequence (C) magnetic resonance imaging showing an epidural mass compressing the spinal cord along the T2-3 disc level. The epidural mass revealed iso-signal intensity on T1-weight sequence and high signal intensity on T2-weighted sequence. Preoperative magnetic resonance imaging showed well-demarcated round-shaped abnormal high signal intensity with mottled low signal intensity on both T1- and T2-weighted sequences within the left half of the T2 vertebral body extending to the left pedicle.

jkns-58-72-g001.jpg
Fig. 2

Intraoperative microscopic photography. Laminectomy was performed from T2 to T4. A pinkish, non-encapsulated mass (white arrow) was found, which was attached to the dura mater and extended through the left T2-3 intervertebral foramen.

jkns-58-72-g002.jpg
Fig. 3

High-magnification (×40) of a haematoxylin and eosin (H&E) stained section showing the cavernous hemangioma composed of an irregular cavernous vascular space. Some of the vascular spaces contained blood. The walls of the vascular space were lined by a single layer of endothelium.

jkns-58-72-g003.jpg
Fig. 4

Postoperative day 1 magnetic resonance images of the patient. T2-weighted sequence (A and B) and T1-weighted sequence (C) images showing no residual extradural cavernous hemangioma. However, the T2 vertebral body cavernous hemagioma was still present.

jkns-58-72-g004.jpg
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