Bilateral VATS thymectomy in the treatment of myasthenia gravis
Review Article

Bilateral VATS thymectomy in the treatment of myasthenia gravis

Bianca Bromberger, Joshua Sonett

Department of Surgery, Columbia University Medical Center, Columbia University, New York 10032, USA

Contributions: (I) Conception and design: All authors; (II) Administrative support: All authors; (III) Provision of study materials or patients: All authors; (IV) Collection and assembly of data: All authors; (V) Data analysis and interpretation: All authors; (VI) Manuscript writing: All authors; (VII) Final approval of manuscript: All authors.

Correspondence to: Joshua Sonett. The Herbert Irving Pavilion, 161 Fort Washington Avenue, 3rd Floor, New York 10032, USA. Email: js2106@columbia.edu.

Abstract: Surgical removal of the thymus is an important tool in the treatment of myasthenia gravis. While there exist a number of different surgical approaches, the optimal thymectomy removes the most amount of thymic tissue in the least invasive manner, allowing for rapid recovery from the procedure and providing the best chance of remission of disease. The purpose of this paper is to review bilateral video-assisted thoracoscopic thymectomy with regard to both relevant anatomy and surgical technique, as well as in comparison to other existing methods of thymectomy in terms of safety, recovery and outcomes. Bilateral video-assisted thoracoscopic thymectomy appears to have improved recovery time and comparable rates of remission to more invasive approaches, though more high-quality long-term outcomes studies are needed.

Keywords: Thymectomy; video-assisted thoracoscopic surgery; myasthenia gravis


Received: 30 November 2016; Accepted: 05 January 2016; Published: 21 March 2017.

doi: 10.21037/vats.2017.02.02


Introduction

Myasthenia gravis (MG) is an autoimmune disorder characterized by skeletal muscle weakness, most commonly due to antibodies directed against acetylcholine receptors. The thymus is an immunogenic organ located in the anterior mediastinum and believed to be key to the pathogenesis of MG as a location of origin of these autoantibodies. Thymic abnormalities are prevalent in patients with MG; approximately 70% of patients have thymic hyperplasia and 15% have thymomas (thymic epithelial cell tumors that tend to be slow growing but have the potential to become invasive) (1).

Though still a source of debate, thymectomy is indicated for patients with myasthenia gravis with a thymoma and in non-thymomatous MG associated with certain autoantibodies (2,3). The purpose of thymectomy is to remove as much thymic tissue as possible in order to achieve remission and prevent tumor invasion in the setting of thymomas. However, the benefit of thymectomy for symptom remission is not immediate and may not be achieved until 5 to 10 years after surgery (4).

A number of issues regarding thymectomy in myasthenia gravis remain unresolved, including optimal surgical approach. The purpose of this paper is to provide an overview of bilateral video-assisted thoracic surgery (VATS) thymectomy in patients with myasthenia gravis, including a review of anatomic considerations, surgical technique, and evaluation of operative risk and disease outcomes in comparison to alternative methods of resection.


Anatomy

The thymus is a butterfly-shaped gland located in the anterior mediastinum. It reaches its maximal weight of approximately 30 to 40 gm during puberty, but subsequently involutes and eventually weighs between 20 to 28 gm in the normal adult. It is thought to be composed of multiple lobules, but typically maintains a distinct right and left bi-lobar shape. The upper left and right poles usually lie anterior to the brachiocephalic veins and have fibrous thyrothymic attachments at their superior ends. However, the thymic horns may be found under the brachiocephalic vein. The superior poles of the thymus may lie in close proximity to the recurrent laryngeal nerves as they course in the tracheoesophageal grooves. Inferiorly, the thymic lobules rest on the anterior aspect of the pericardium. The phrenic nerves run laterally to the thymus in the anterior mediastinum; thymic tissue may extend deep to these nerves, resting on the pericardium (5). Importantly, extracapsular islands of thymic tissue are found embedded in peri-thymic fat throughout the mediastinum and neck. Ectopic thymic tissue was found in the mediastinum and cervical neck in 98% and 32% of thymectomy specimens, respectively (6).

Arterial blood supply to the thymus is primarily derived from branches of the internal mammary arteries, but superior portions may also be supplied by branches of the inferior thyroid arteries. Venous drainage is predominantly achieved via a large draining vein on the posterior side of the thymus that enters the left brachiocephalic vein.


Surgical technique in bilateral VATS thymectomy

General principles

The goal of thymectomy in MG is to remove as much thymic tissue as is safely possible so as to reduce the number of immunogenic thymic cells responsible for the production of pathogenic antibodies, as well as achieving complete mass resection in cases associated with a thymoma. Care is taken to avoid directly grasping thymic tissue so as to reduce the risk of capsular disruption and spillage of thymic tissue. Thus, a “touch-free” approach is utilized throughout the operation, in which only peri-thymic tissue is grasped during the dissection. Capsular transgression of a thymoma should be considered a never event in any surgical approach.

Positioning and port placement

Patient is placed in the supine position and prepped such that both left and right sides may be accessed. The left side is accessed first with the left arm extended overhead. Once the left-sided portion of the operation is complete, the left arm is lower and the right arm extended, all while maintaining a sterile field. This avoids any brachial plexopathy from positioning. Additionally, the head is flexed so as to move the thymus inferiorly out of the cervical neck.

Three 5mm ports are placed on each side and 8 to 10 mmHg is used for insufflation. The initial port is placed in the mid-axillary line 2–3 ribs inferior to the inframammary crease, permitting direct visualization of the placement of the caudal-most port, located at the mid-axillary line at the level of the insertion of the diaphragm. The location of this second port facilitates dissection of mediastinal fat and allows for improved access to the cervical neck superior to the brachiocephalic vessels. The third port is placed is placed laterally and mid-way between the initial two.

Procedure overview (Figure 1)

Figure 1 Bilateral VATS thymectomy in the treatment of myasthenia gravis (7). Available online: http://www.asvide.com/articles/1417

Step 1: Release from diaphragm, sternum and pericardium

Thymic tissue is dissected free from attachments to the diaphragm inferiorly, sternum anteriorly and pericardium posteriorly until the right lung is visualized. Dissection is extended until the left internal mammary vein is identified and traced until it enters the inferior aspect of the left brachiocephalic vein.

Step 2: Release of left phrenic nerve

The left phrenic nerve should be visualized coursing on along the left lateral aspect of the pericardium; visceral pleural overlying the nerve is incised and thymic and peri-thymic tissue are resected deep to the phrenic nerve.

Step 3: Release from left brachiocephalic vein

Dissection is then continued laterally to medially along the inferior side of the left brachiocephalic vein, with continued removal of thymic and peri-thymic tissue anteriorly and posterior side of the brachiocephalic vein. A large venous branch draining the thymus is usually encountered on the inferior aspect of the brachiocephalic vein and may be clipped and transected.

Step 4: Cervical neck dissection

Dissection is then continued superiorly into the cervical neck until the thyrothymic ligaments are freed. Given the location of the thymic horn adjacent to the tracheoesophageal groove, care is taken to avoid injury to the recurrent laryngeal nerve, which runs in the same location. Additionally, inferior thyroid veins draining into the brachiocephalic vein may be identified and ligated.

Step 5: Release from right phrenic nerve and removal of specimen

The right anterior mediastinum in then accessed. The right phrenic nerve is freed in a similar manner to the left. Any thymic and peri-thymic tissue deep to the right phrenic nerve is dissected. Dissection is continued superiorly along the right internal mammary artery and vein while freeing and remaining thymic tissue. The thymus is placed in a bag and removed from the thoracic cavity.


Outcomes

As the goal of surgery in myasthenia gravis is to remove as much immunogenic thymic tissue as possible, the ideal thymectomy would maximize access to both the encapsulated thymus and ectopic islets of thymic tissue throughout the mediastinum and cervical neck while minimizing operative risks, recovery time, and postoperative pain.

A thymectomy classification system was developed by the Myasthenia Gravis Task Force in order to differentiate the variety of approaches that exist in practice (8). The basic transcervical approach (T-1a) is thought to provide inadequate exposure and sub-optimal remission rates, though more tissue may be resected with “extended” transcervical techniques (T-1b-d). Open transsternal approaches vary in the amount of thymic tissue estimated to be resected, ranging from 70–80% of thymic tissue resected during a “standard” transsternal resection of the lobular thymus (T-3a), to 98–100% of thymic tissue removed with a combined transcervical-transsternal approach (T-4), considered to be the “maximal” exposure and benchmark operation against which others are compared. “Extended” transsternal resections (median sternotomy with additional mediastinal dissection, T-3b), are estimated to resect the bulk of thymic tissue (85–95%), though vary in the extent of mediastinal tissue removal and may sacrifice removal of cervical thymic tissue, but minimize the risks associated with cervical neck dissection (such as recurrent laryngeal nerve injury) (9,10).

Within videoscopic-assisted thymectomy (T-2), there exists a range of surgical approaches, including unilateral (right or left) VATS (T-2a), bilateral VATS (T-2b), and robot-assisted thymectomy (T-2c-d). While the T-2b bilateral VATS, also known as “video-assisted thoracoscopic extended thymectomy” or VATET, is classically defined as a bilateral approach with a cervical neck incision to facilitate cervical lobe excision, the term is inconsistently used in the literature and may refer to a bilateral VATS thymectomy with or without additional cervical neck incision and transcervical dissection (10). In this paper, unless otherwise stated, “bilateral VATS thymectomy” refers to thoracoscopic resection alone without cervical neck dissection.

While much literature exists, definitive conclusions on if there exists a best surgical approach are limited by a number of issues: lack of prospective randomized controlled trials, reliance on retrospective data, heterogeneity of patient populations (with regard to disease severity and medical treatment pre- and post-surgery), as well as lack of use of a standardized classification system for MG disease severity and definition of remission (10). Nonetheless, the remainder of the discussion will review the existing evidence comparing bilateral VATS thymectomy (and its variations) to alternative approaches with regard to safety, recovery time and efficacy in disease treatment.

Perioperative safety and recovery

Numerous studies have reported low perioperative rates of morbidity and mortality for bilateral VATS thymectomy. A number of retrospective studies have demonstrated equivalent rates adverse events and faster recovery time in patients undergoing bilateral VATS thymectomy compared to open transsternal thymectomy (both T-3b and T-4 approaches) for myasthenia gravis. While respiratory and cardiac complications (such as pneumonia, need for prolonged ventilation, and arrhythmias) are similar between the two approaches, hospital and ICU length of stay, duration of need for chest tube, estimated blood loss, and postoperative pain are reported to be significantly less in patients undergoing bilateral VATS thymectomy (11-14). Reports of mean operative time for bilateral VATS compared to transsternal thymectomy range from equivalent (11-13) to increased (14).

Cervical neck exposure

As mentioned previously, bilateral VATS thymectomy may be performed with the addition of a cervical neck incision. Compared to extended transsternal thymectomy (T-3b), bilateral VATS thymectomy with transcervical dissection has been reported to have similar low perioperative mortality and morbidity (including laryngeal nerve injury), as well as equivalent amounts of thymic tissue resected (15). A study designed to evaluate bilateral VATS thymectomy with and without transcervical neck dissection observed that between 2–3% of thymic tissue may be left in the absence of additional cervical approach (16). However, as there is of yet no data reported on rates of operative complications and clinical measures of remission between bilateral VATS with and without cervical neck dissection, it is unknown if the additional dissection results in meaningful improvement in outcomes for all patients with MG undergoing thymectomy. While open cervical neck dissection may be not be necessary in all patients, it should be undertaken if the superior thymic horns are unable to be resected with the bilateral VATS approach; patients should be made aware of this possibility preoperatively (17).

Outcomes of bilateral VATS for nonthymomatous MG

While Kaplan-Meier time-to-event analyses are considered the ideal method for reporting rates of remission, they are not uniformly used in outcomes studies (18). Previous reviews utilizing studies that provided remission data with Kaplan-Meier analysis suggest comparable rates of remission at 5 years between bilateral VATS with cervical dissection and combined transcervical-transsternal (T-4) thymectomy (51% and 50% respectively), though inferences are limited by differences in the severity of symptoms between the study populations prior to surgery (18-20). Though utilizing less stringent measures of rates of remission, additional retrospective studies comparing bilateral VATS with and without cervical dissection to transsternal extended thymectomy (T-3b) report similar rates of remission between open and minimally invasive approaches (14,15).

Comparison to unilateral VATS

While unilateral VATS have been reported to have inferior rates of remission compared to maximal (T-4), extended transsternal (T-3b), and bilateral VATS thymectomy (10,21), recent data may suggest more equivalent outcomes. In order to address whether unilateral and bilateral VATS can achieve comparable outcomes, one retrospective study comparing right unilateral VATS to bilateral VATS without cervical incision in non thymomatous MG revealed similar rates of postoperative complications and recovery time; mean operative time was significantly longer in bilateral VATS. The weight of thymic specimens did not differ significantly between the two groups, nor did rates of remission at 5 years (47% vs. 52% in unilateral and bilateral VATS, respectively) (22).

Outcomes of bilateral VATS for MG with thymoma

Both unilateral and bilateral VATS are employed with success in the resection of early stage (Masaoka stage I or II) thymomas with or without concurrent MG (12,23-25). Successful resection of stage IIIA tumors (tumors that visibly invade adjacent organs) using bilateral VATS thymectomy has also been reported (26). There are no studies that directly address the superiority of one surgical approach versus another in MG associated with thymoma (25). However, given the heterogeneity of thymomas themselves, the stage and location of the thymoma associated with MG should dictate the optimal surgical approach on a case-by-case basis.


Conclusions

With a recent prospective randomized controlled study demonstrating the benefit of open transsternal thymectomy in myasthenia gravis, more attention may now be directed toward which surgical approach affords equally extensive dissection while minimizing post-operative recovery and complications (3). Results from retrospective data suggest that bilateral VATS thymectomy has the capacity to achieve similar rates of remission to the “maximal” thymectomy with improved recovery time and decreased invasiveness, but randomized prospective data with follow-up greater that 5 years is needed to address the question definitively. Additionally, given recent reports of similar outcomes between bilateral and unilateral VATS, differences in thymic tissue resection in bilateral VATS with and without a transcervical approach, and successful resection of more invasive thymomas with bilateral VATS, it may be that the unique anatomy and pathology of the patient dictates the optimal approach within the spectrum of minimally invasive thymectomies. Until such data is obtained, bilateral VATS thymectomy, with or without additional transcervical dissection, remains a safe and effective technique in the treatment of myasthenia gravis.


Acknowledgements

None.


Footnote

Conflicts of Interest: The authors have no conflicts of interest to declare.


References

  1. Drachman DB. Myasthenia gravis. N Engl J Med 1994;330:1797-810. [Crossref] [PubMed]
  2. Sanders DB, Wolfe GI, Benatar M, et al. International consensus guidance for management of myasthenia gravis: Executive summary. Neurology 2016;87:419-25. [Crossref] [PubMed]
  3. Wolfe GI, Kaminski HJ, Aban IB, et al. Randomized Trial of Thymectomy in Myasthenia Gravis. N Engl J Med 2016;375:511-22. [Crossref] [PubMed]
  4. Saperstein DS, Barohn RJ. Management of myasthenia gravis. Semin Neurol 2004;24:41-8. [Crossref] [PubMed]
  5. Shields TW. The Thymus. In: Shields TW, LoCicero III J, Reed CE, et al. (eds). General Thoracic Surgery. Philadelphia: Lippincott Williams & Wilkins 2009;2060-7. Available online: https://shop.lww.com/General-Thoracic-Surgery/p/9780781779821
  6. Jaretzki A 3rd, Wolff M. "Maximal" thymectomy for myasthenia gravis. Surgical anatomy and operative technique. J Thorac Cardiovasc Surg 1988;96:711-6. [PubMed]
  7. Bromberger B, Sonett J. Bilateral VATS thymectomy in the treatment of myasthenia gravis. Asvide 2017;4:109. Available online: http://www.asvide.com/articles/1417
  8. Jaretzki A 3rd, Barohn RJ, Ernstoff RM, et al. Myasthenia gravis: recommendations for clinical research standards. Task Force of the Medical Scientific Advisory Board of the Myasthenia Gravis Foundation of America. Ann Thorac Surg 2000;70:327-34. [Crossref] [PubMed]
  9. Jaretzki A, Steinglass KM, Sonett JR. Thymectomy in the management of myasthenia gravis. Semin Neurol 2004;24:49-62. [Crossref] [PubMed]
  10. Sonett JR, Jaretzki A 3rd. Thymectomy for nonthymomatous myasthenia gravis: a critical analysis. Ann N Y Acad Sci 2008;1132:315-28. [Crossref] [PubMed]
  11. Lee CY, Kim DJ, Lee JG, et al. Bilateral video-assisted thoracoscopic thymectomy has a surgical extent similar to that of transsternal extended thymectomy with more favorable early surgical outcomes for myasthenia gravis patients. Surg Endosc 2011;25:849-54. [Crossref] [PubMed]
  12. Jurado J, Javidfar J, Newmark A, et al. Minimally invasive thymectomy and open thymectomy: outcome analysis of 263 patients. Ann Thorac Surg 2012;94:974-81; discussion 981-2. [Crossref] [PubMed]
  13. Fiorelli A, Mazzella A, Cascone R, et al. Bilateral thoracoscopic extended thymectomy versus sternotomy. Asian Cardiovasc Thorac Ann 2016;24:555-61. [Crossref] [PubMed]
  14. Chang PC, Chou SH, Kao EL, et al. Bilateral video-assisted thoracoscopic thymectomy vs. extended transsternal thymectomy in myasthenia gravis: a prospective study. Eur Surg Res 2005;37:199-203. [Crossref] [PubMed]
  15. Shiono H, Kadota Y, Hayashi A, et al. Comparison of outcomes after extended thymectomy for myasthenia gravis: bilateral thoracoscopic approach versus sternotomy. Surg Laparosc Endosc Percutan Tech 2009;19:424-7. [Crossref] [PubMed]
  16. Shigemura N, Shiono H, Inoue M, et al. Inclusion of the transcervical approach in video-assisted thoracoscopic extended thymectomy (VATET) for myasthenia gravis: a prospective trial. Surg Endosc 2006;20:1614-8. [Crossref] [PubMed]
  17. Singh G, Glotzbach J, Costa J, et al. Minimally invasive radical thymectomy. Ann Cardiothorac Surg 2016;5:59-61. [PubMed]
  18. Sonett JR, Jaretzki A III. Evaluation of Results of Thymectomy for Nonthymomatous Myasthenia Gravis. In: Shields TW, LoCicero III J, Reed CE, et al. (eds). General Thoracic Surgery. Philadelphia: Lippincott Williams & Wilkins 2009:2314-21.
  19. Mantegazza R, Baggi F, Bernasconi P, et al. Video-assisted thoracoscopic extended thymectomy and extended transsternal thymectomy (T-3b) in non-thymomatous myasthenia gravis patients: remission after 6 years of follow-up. J Neurol Sci 2003;212:31-6. [Crossref] [PubMed]
  20. Jaretzki A 3rd, Penn AS, Younger DS, et al. "Maximal" thymectomy for myasthenia gravis. Results. J Thorac Cardiovasc Surg 1988;95:747-57. [PubMed]
  21. Huang CS, Cheng CY, Hsu HS, et al. Video-assisted thoracoscopic surgery versus sternotomy in treating myasthenia gravis: comparison by a case-matched study. Surg Today 2011;41:338-45. [Crossref] [PubMed]
  22. Liu Z, Yang J, Lin L, et al. Unilateral video-assisted thoracoscopic extended thymectomy offers long-term outcomes equivalent to that of the bilateral approach in the treatment of non-thymomatous myasthenia gravis. Interact Cardiovasc Thorac Surg 2015;21:610-5. [Crossref] [PubMed]
  23. Yuan ZY, Cheng GY, Sun KL, et al. Comparative study of video-assisted thoracic surgery versus open thymectomy for thymoma in one single center. J Thorac Dis 2014;6:726-33. [PubMed]
  24. Agasthian T, Lin SJ. Clinical outcome of video-assisted thymectomy for myasthenia gravis and thymoma. Asian Cardiovasc Thorac Ann 2010;18:234-9. [Crossref] [PubMed]
  25. Raza A, Woo E. Video-assisted thoracoscopic surgery versus sternotomy in thymectomy for thymoma and myasthenia gravis. Ann Cardiothorac Surg 2016;5:33-7. [PubMed]
  26. Zhang G, Li W, Chai Y, et al. Bilateral video-assisted thoracoscopic thymectomy for Masaoka stage IIIA thymomas. Thorac Cardiovasc Surg 2015;63:206-11. [Crossref] [PubMed]
doi: 10.21037/vats.2017.02.02
Cite this article as: Bromberger B, Sonett J. Bilateral VATS thymectomy in the treatment of myasthenia gravis. Video-assist Thorac Surg 2017;2:12.

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