|Year : 2018 | Volume
| Issue : 4 | Page : 1182-1185
Adult thoracic intradural exophytic mature teratoma: Case report and literature review
Aaron P Danison, Dinesh Ramanathan, Mahan Matin, Kee Kim, Ripul R Panchal
Department of Neurosurgery, University of California, Davis, CA, USA
|Date of Web Publication||23-Oct-2018|
Dr. Ripul R Panchal
Department of Neurological Surgery, University of California, Davis Medical Center 4860 Y Street, Suite 3740, Sacramento 95817, CA
Source of Support: None, Conflict of Interest: None
Mature thoracic intraspinal teratomas are rare tumors in adults. In this case study, we present a case of intradural, extramedullary teratoma, which was surgically resected. A 50 year old man presented with progressive bilateral leg pain, severe myelopathy and weakness. Magnetic Resonance Imaging (MRI) revealed a cystic mass lesion in the T11-12 region region. Microsurgical resection of the tumor using CO2 laser with neuromonitoring was performed. Postoperatively, the patient had a remarkable clinical improvement. Mature spinal teratomas are rare, slow growing spinal tumors. Surgical resection provides excellent recovery, and recurrence rates are low.
Keywords: Spinal teratoma, teratoma, thoracic tumor
|How to cite this article:|
Danison AP, Ramanathan D, Matin M, Kim K, Panchal RR. Adult thoracic intradural exophytic mature teratoma: Case report and literature review. Asian J Neurosurg 2018;13:1182-5
|How to cite this URL:|
Danison AP, Ramanathan D, Matin M, Kim K, Panchal RR. Adult thoracic intradural exophytic mature teratoma: Case report and literature review. Asian J Neurosurg [serial online] 2018 [cited 2020 Jan 27];13:1182-5. Available from: http://www.asianjns.org/text.asp?2018/13/4/1182/231063
| Introduction|| |
Teratomas are rare in the spinal column representing <0.5% of spinal tumors. Most teratomas are identified in children and are even more rare in the adult population. These tumors are histologically made of one to all three germ layers.
Teratomas are classified as mature, immature, or malignant depending on the amount of cell differentiation. Most reported cases occurring in the pediatric population are the immature or malignant subtypes and are usually in the sacrococcygeal region. Teratomas in adults are typically the mature subtype and occur most commonly at the level of the conus., These tumors are slow-growing in adults and patients usually present with progressive pain and declining neurological function.
We present an unusual case of an intradural intramedullary mature teratoma in a 50-year-old male who presented with worsening back pain, urinary incontinence, and progressive lower extremity weakness. Clinical characteristics, pathological features, and surgical nuances for resection of these lesions will be discussed.
| Methods|| |
We conducted a retrospective review of initial clinical presentation, pathology, surgical treatment details, and clinical status of the patient at follow-up. An institutional review board approval was obtained, and the patient consented for the records to be reviewed and the findings to be published in this case report.
| Case Report|| |
A 50-year-old male presented with progressive bilateral leg pain, weakness, urinary retention, bowel and bladder dysfunction, and erectile dysfunction for 7 years. He developed progressive lower extremity weakness over a 2-month period, leading to him becoming wheelchair-bound. The motor function in the right hip flexion, knee extension, knee flexion, dorsiflexion, and plantar flexion was 2/5 and 1/5 strength in great toe extension. His left lower extremity strength was 4/5 in hip flexion, 4-/5 in knee extension, knee flexion, dorsiflexion, and 4/5 in plantar flexion and great toe extension. While his sensation was decreased on the right below the L2 dermatomal distribution, all other dermatomes of the bilateral upper and lower extremities were intact to pinprick. Bilateral upper extremity deep tendon reflexes were 2+, whereas lower extremity reflexes were absent. The Babinski reflex was absent bilaterally, whereas the patient had positive bilateral Hoffman's, Tromner and pectoralis reflexes.
Magnetic resonance imaging (MRI) imaging revealed the presence of a heterogeneous, intradural mass with cystic components, and expansion of the cord/thecal sac T11–T12. The findings on the MRI also suggested possible lumbarization of the sacral vertebra, making the case for cord to conus transition at the level of the mass. The lesion exhibited heterogeneous T1 enhancement [Figure 1].
|Figure 1: Magnetic resonance imaging. (a) Axial and (b) Sagittal T2 images show a heterogeneous cystic lesion at the level of the conus. The lesion appears intradural extramedullary|
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He was subsequently taken to the operating room for tumor debulking. Thoracic laminectomies at T11–T12 were performed, and a midline durotomy was made, exposing a yellow, fatty, exophytic intramedullary tumor with large cystic components. Neural motor units were found widespread over the lesion, which triggered electromyographic muscle activity (EMG) activity. A flexible CO2 laser was used to debulk the fatty components exophytic to the cord, from medial to lateral, carefully without causing any compression on the cord/conus, and traction on the surrounding nerve roots. The intramedullary cysts were subsequently exposed, revealing mucous products and hair [Figure 2]. A small amount of residual tumor was present that triggered EMG activity. This was left in place for concern of possible viable nervous tissue.
|Figure 2: Firm fatty tumor with cystic components containing mucous products and hair|
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Pathology confirmed the presence of a mature teratoma. The lesion consisted of disorganized, heterogeneous collections of tissue derived from all three germ layers. All elements were noted to be mature, which included skin and adnexal structures, adipose tissue and bone, disorganized fragments of peripheral nerve and ganglion, neuroglial tissue, squamous and columnar epithelium, mucous glands, hair shafts, and keratin debris. There was no evidence of immature elements or malignancy [Figure 3].
|Figure 3: (a) Adipose tissue, peripheral nerve, sebaceous glands, hair shaft, and columnar epithelium lining the cyst wall. (b) Disorganized fragments of peripheral nerve and ganglion, fragments of bone, and squamous epithelium|
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Postoperatively, the patient reported drastic improvement in pain. He continued to have lower extremity paresis, however, was able ambulate short distances with a walker. Both 1 and 6-month postoperative MRIs demonstrated small areas of residual tumor that remained stable compared to immediate postoperative imaging and no new recurrence was noted. At 1 year, his strength had improved and was able to walk with a walker up to five blocks. His right leg motor function was 4/5 throughout, except for 2–3/5 dorsiflexion and 0/5 Extensor hallucis longus (EHL). His left lower extremity was 4- to 4+/5 strength overall. The bladder motor function did not improve, and he continued to require intermittent catheterization at 1-year follow-up.
| Discussion|| |
Mature spinal teratomas are usually adherent to nervous tissues and at times are composed of cystic structures that compress the neural elements., These tumors have very low rates of recurrence in the setting of both gross (9%) and subtotal (11%) resection., The leading theory of teratoma development is cell migrational error. Misplaced germ lines migrate to the caudal mass that usually forms at the conus and lower thoracic regions of the developing embryo. This portends the common location of mature teratomas at or near the conus, the inclusion of several, but not all, well-differentiated germ cell layers and their relatively benign growth. However, intradural mature teratomas are rare, and the thoracic location has been described in the literature even less frequently.,,,,,,, Furthermore, these lesions usually present in isolation and unlike teratoma of childhood, association with spinal dysraphism is rare.
In contrast, immature teratomas usually originate in the sacrococcygeal region and are less well differentiated. These tumors exhibit rapid growth and secrete several biomarkers of proliferation. Immature teratomas are more commonly observed in the pediatric population and many case reports argue for a dysembryologic origin composed of chaotically differentiating pluripotent cells., These tumors require closer surveillance and more radical resection may be warranted.
Microsurgical techniques for tumor resection are used to dissect the tumor from the normal neural tissue. Intraoperative microscopy is used to develop a plane around the tumor. At times, as was the case in our patient, the tumor may invade the spinal cord parenchyma. The use of a CO2 laser has many advantages in this setting. The CO2 laser uses focused energy to coagulate and cut with pen-like precision without having to manipulate the tissues. Using the laser allows removal of infiltrating tumors in small areas next to critical structures. In addition, multiple adaptations have been made to the structure of the laser holder, including the neck, which resembles a pen and has the flexibility to allow alterations in the angle of use. Since no cleavage plane is present, the laser can be used to vaporize the tumor from the core to its periphery until white matter of the spinal cord is seen. A thin rim of tumor may be adherent to the parenchyma, which can be gently vaporized at a low voltage with the goal of disrupting viable tumor cells. The primary objective of surgical resection of intradural intramedullary spinal cord tumors is the decompression of neural elements without further damaging the neurological structures. Given the relatively benign nature of mature teratomas, we believe CO2 laser for intramedullary tumor cell vaporization with preservation of the surrounding nervous tissue is paramount.
There is a small risk of recurrence as has been shown by Stevens et al. and annual evaluation of neurological function and spinal imaging is recommended. Adjunctive radiation or chemotherapy is usually not recommended except in cases of malignant cell components. This underscores the importance of complete pathological analysis of the whole tumor species as these tumors are heterogeneous and malignant cell populations may be interspersed among benign tissue.
| Conclusion|| |
Thoracic spinal intradural mature teratomas are exceedingly rare, and thus, the prognosis for this disease following surgery has not been well defined. While these teratomas are typically slow-growing, neurological decline warrants surgical intervention. Here, we propose the use of the CO2 laser for microsurgical resection. As there is a risk of recurrence after surgery, routine clinical and MRI follow-up are necessary.
Declaration of patient consent
The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.
This manuscript was prepared by the authors without any funds or scholarships from any external sources.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| References|| |
Caruso R, Antonelli M, Cervoni L, Salvati M. Intramedullary teratoma: Case report and review of the literature. Tumori 1996;82:616-20.
Russel D, Rubinstein L. Pathology of Tumours of the Nervous System. 5th
ed. Baltimore: Williams and Wilkins; 1989.
Willis R. Teratomas. Atlas of Tumour Pathology. Washington, DC: Armed Forces Institute of Pathology; 1951. p. 9-58.
Caruso R, Colonnese C. Intramedullary teratomas: Two case reports and a review of the literature. Zentralbl Neurochir 2006;67:213-8.
Fernández-Cornejo VJ, Martínez-Pérez M, Polo-García LA, Martínez-Lage JF, Poza M. Cystic mature teratoma of the filum terminale in an adult. Case report and review of the literature. Neurocirugia (Astur) 2004;15:290-3.
Makary R, Wolfson D, Dasilva V, Mohammadi A, Shuja S. Intramedullary mature teratoma of the cervical spinal cord at C1-2 associated with occult spinal dysraphism in an adult. Case report and review of the literature. J Neurosurg Spine 2007;6:579-84.
Nonomura Y, Miyamoto K, Wada E, Hosoe H, Nishimoto H, Ogura H, et al.
Intramedullary teratoma of the Spine: Report of two adult cases. Spinal Cord 2002;40:40-3.
Allsopp G, Sgouros S, Barber P, Walsh AR. Spinal teratoma: Is there a place for adjuvant treatment? Two cases and a review of the literature. Br J Neurosurg 2000;14:482-8.
Li Y, Yang B, Song L, Yan D. Mature teratoma of the spinal cord in adults: An unusual case. Oncol Lett 2013;6:942-6.
al-Sarraj ST, Parmar D, Dean AF, Phookun G, Bridges LR. Clinicopathological study of seven cases of spinal cord teratoma: A possible germ cell origin. Histopathology 1998;32:51-6.
Rewcastle NB, Francoeur J. Teratomatous cysts of the spinal canal; with “sex chromatin” studies. Arch Neurol 1964;11:91-9.
Eneström S, von Essen C. Spinal teratoma. Acta Neurochir (Wien) 1977;39:121-6.
Rosenbaum TJ, Soule EH, Onofrio BM. Teratomatous cyst of the spinal canal. Case report. J Neurosurg 1978;49:292-7.
Padovani R, Tognetti F, Laudadio S, Manetto V. Teratoid cyst of the spinal cord. Neurosurgery 1983;13:74-7.
Poeze M, Herpers MJ, Tjandra B, Freling G, Beuls EA. Intramedullary spinal teratoma presenting with urinary retention: Case report and review of the literature. Neurosurgery 1999;45:379-85.
Hejazi N, Witzmann A. Spinal intramedullary teratoma with exophytic components: Report of two cases and review of the literature. Neurosurg Rev 2003;26:113-6.
Sharma MC, Jain D, Sarkar C, Suri V, Garg A, Singh M, et al.
Spinal teratomas: A clinico-pathological study of 27 patients. Acta Neurochir (Wien) 2009;151:245-52.
Koen JL, McLendon RE, George TM. Intradural spinal teratoma: Evidence for a dysembryogenic origin. Report of four cases. J Neurosurg 1998;89:844-51.
Stevens QE, Kattner KA, Chen YH, Rahman MA. Intradural extramedullary mature cystic teratoma: Not only a childhood disease. J Spinal Disord Tech 2006;19:213-6.
[Figure 1], [Figure 2], [Figure 3]