Accepted Manuscript Resection of a Posterior Mediastinal Mass: Lessons Learned from a Failed Exploration for Presumed Schwannoma Samuel Kim, MD, Brian Yoo, MD, Ali Baaj, MD, Alex G. Little, MD PII:
S0022-5223(16)30120-9
DOI:
10.1016/j.jtcvs.2016.04.030
Reference:
YMTC 10527
To appear in:
The Journal of Thoracic and Cardiovascular Surgery
Received Date: 20 October 2015 Revised Date:
28 March 2016
Accepted Date: 10 April 2016
Please cite this article as: Kim S, Yoo B, Baaj A, Little AG, Resection of a Posterior Mediastinal Mass: Lessons Learned from a Failed Exploration for Presumed Schwannoma, The Journal of Thoracic and Cardiovascular Surgery (2016), doi: 10.1016/j.jtcvs.2016.04.030. This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain.
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Resection of a Posterior Mediastinal Mass: Lessons Learned from a Failed Exploration for Presumed Schwannoma
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Samuel Kim MD1 , Brian Yoo MD1, Ali Baaj MD2,, Alex G. Little MD1
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1 Division of Cardiothoracic Surgery, University of Arizona, Tucson, AZ; 2 Department of Neurosurgery, New York-Presbyterian/ Weil Cornell Medical Center
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Running title: Considerations for resection of posterior mediastinal mass
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Keywords: chordoma, multi-disciplinary, considerations
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Word count= 750
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Corresponding author:
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Samuel Kim, MD
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1501 N. Campbell Ave., Rm 4302
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Tucson, AZ 85724
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Phone (520) 419-1535
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Fax (520) 626-4042
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All the authors have no conflict of interest and have nothing to disclose.
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No funding was provided for this work.
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Introduction Surgeons frequently proceed with surgical resection of a paraspinal tumor without biopsy for presumptive diagnosis of schwannoma.1-2 However, misdiagnosis
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and improper operative planning can have dire consequences for the patients. Here, we
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discuss our experience with perioperative management and resection of a large thoracic
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chordoma that was initially misdiagnosed as schwannoma.
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Clinical Presentation
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A 60-year old male underwent an attempted resection of a left-sided paraspinal mass spanning the level T7-T9 for a presumed diagnosis of schwannoma. A left
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posterolateral thoracotomy was performed, and a large paraspinal mass was found,
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invading the spine, abutting the descending aorta. An attempt was made to dissect the
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tumor off the spine, but “bleeding from intercostal arteries prevented further dissection.”
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The operation was aborted. An intraoperative incisional biopsy demonstrated chordoma.
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Magnetic resonance imaging (MRI) and positron emission tomography (PET) scan ruled
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out spinal cord involvement and distant metastasis, and a two-staged en-bloc surgical
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resection was recommended.
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Intervention and Technique
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Stage I involved a posterior midline approach to stabilize the thoracic spine by
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placing pedicle screws above (T6) and below the levels of the lesion (T10). The sagittal
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cuts were created along the lateral aspect of the lamina/pedicles and deep into the
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vertebral bodies (T7-T9). This in effect dissociated the vertebral segment with tumor
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from the remainder of the vertebral column.3 Stage II began with a left posterolateral thoracotomy at the sixth intercostal
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space. The 6th- 10th ribs were resected at a distance 4 cm lateral to the edge of the
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tumor to created a posterior and lateral margin. The descending aorta above and below
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the tumor was encircled to allow rapid vascular control in the event of bleeding.
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Medially, several intercostal arteries were ligated and the tumor was freed from the
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aorta. The dissection was carried dorsal to the ribs until the sagittal cut made from stage
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I was identified and remaining vertebral body attachments were cut. The lesion along
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with the lateral vertebral column was fractured out with delivery of the tumor en bloc.
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The chest wall was reconstructed using Goretex mesh.
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Clinical Outcome
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The patient was neurologically intact and discharged after 12 days. Initial pathology showed possible microscopic tumor at medical margin; however, re-
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examination of specimen by senior pathologist confirmed negative final margin. The
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patient did not receive adjuvant radiation treatment. A follow up MRI after 1 year
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demonstrated no evidence of recurrent disease.
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Discussion
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Paraspinal primary bone tumors, such as chordoma, are rare. Several
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procedures have been described for resection of thoracic paraspinal tumors including a
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single-staged midline approach or multiple stages.4-6 The technical operative details of
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the current case was published previously as well.3 However, most of these earlier
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reports focused on the neurosurgical techniques of operation. Yet, paraspinal primary
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bone tumors can be confused with more common schwannoma, and thoracic surgeons
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are often the first specialist the patients encounter. This case demonstrates the
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diagnostic and management dilemmas often confronted by thoracic surgeons and offers
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guidance in avoiding pitfalls.
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This case highlights two crucial errors that were made during our patient’s
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preoperative diagnosis and management: a wrong diagnosis made solely based on CT
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imaging and incomplete surgical planning. Both errors could have been prevented with
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multi-disciplinary team approach. The initial CT scan demonstrated an obliteration of the
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plane between the spine and the tumor (Figure 1B), which would be unusual for a
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benign schwannoma. Review of CT images and discussion between the oncologist,
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surgeon and radiologist could have led to a correct diagnosis. CT guided biopsy and
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further evaluation using MRI would have been invaluable in narrowing down the
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differential diagnosis and defining the anatomy for the surgical approach.
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A large chordoma involving the thoracic spine is challenging due to its proximity to descending aorta and requires careful planning by both thoracic surgery and
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neurosurgery. Major hemorrhage from intercostal arteries can be difficult to control
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especially if the tumor is large and near the aorta. Preparation for proximal and distal
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control of the aorta should be planned accordingly. We chose a 2-stage approach,
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because dissecting the tumor free from the aorta while controlling the intercostal artery
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branches was a key portion of the operation. The single stage posterior midline
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approach would have been difficulty if not impossible in our patient.
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Conclusion A presumed schwannoma with locally invasive features should be carefully worked up by a multi-disciplinary team to avoid misdiagnosis and pitfalls during the
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operation. A two-staged approach allows the surgeon to confirm the stability of the
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spine prior to the tumor resection and gives best exposure with minimal risk.
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primary bone tumors: technical note. J Neurosurg Spine. 2016: 24:2:223-227.
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4. Sciubba DM, Gokaslan ZL, Black JH, et al. 5-level spondylectomy for en bloc
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Figure 1: Side-by-side comparison of thoracic chordoma (A) vs. extradural schwannoma
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(B). Schwannoma is usually lobulated, encapsulated, and well demarcated as shown in
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Figure B. There is a loss of plane between the spine and tumor in chordoma as shown
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in Figure A.
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Figure 2: Intraoperative photograph of the resected tumor and the operative field after
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the resection. The arrows indicate ligated intercostal arteries
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Cranial
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Cranial
Posterior Anterior
Aorta
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Anterior
Caudal
Caudal
Spine Posterior