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Giant thymoma successfully resected via anterolateral thoracotomy: a case report

  • Takahiro Saito1,
  • Takashi Makino1,
  • Yoshinobu Hata1,
  • Satoshi Koezuka1,
  • Hajime Otsuka1,
  • Kazutoshi Isobe2,
  • Naobumi Tochigi3,
  • Kazutoshi Shibuya3,
  • Sakae Homma2 and
  • Akira Iyoda1Email author
Journal of Cardiothoracic Surgery201510:110

https://doi.org/10.1186/s13019-015-0321-y

Received: 6 June 2015

Accepted: 24 August 2015

Published: 1 September 2015

Abstract

The appropriate surgical approach for a large mediastinal tumor is controversial. Median sternotomy is the standard approach for thymomas. We herein report the case of a giant thymoma, 13 cm in diameter, surgically resected via anterolateral incision. Subsequent thymectomy was performed via thoracoscopy. The resected specimen was a WHO type AB thymoma, Masaoka stage I, without capsular invasion. The anterolateral incision was less invasive and more versatile in the present case, as the incision could be extended to a hemiclamshell or posterolateral incision depending on exposure and relationship to adjacent organs and vascular structures.

Keywords

SurgeryGiant thymomaThymomaAnterolateral incision

Background

Thymomas are rare neoplasms with an indolent growth pattern and present with various clinical symptoms [1]. They are commonly found in the anterior mediastinum. Complete surgical resection is the mainstay of treatment. While median sternotomy has been the standard approach for thymectomy, the best incision is controversial for so-called giant thymomas [2]. Here we report the case of a giant thymoma in the anterior-inferior mediastinum successfully resected with additional thymectomy via anterolateral thoracotomy.

Case presentation

A 45-year-old man was referred to our hospital due to a routine chest x-ray showing an abnormal shadow in the right lower lung field (Fig. 1). He had no obvious symptoms, except for slight dyspnea on exertion for three months. He had no smoking history and no significant medical history. No previous chest x-rays were available. Chest CT-scan showed a well-defined mass 13 x 10 cm in diameter, in contact with the diaphragm, pericardium, right inferior pulmonary vein, and superior vena cava (Fig. 1). The tumor showed heterogenous contrast effect. F18-fluorodeoxyglucose positron emission tomography (FDG-PET) showed abnormal FDG uptake with maximum standardized uptake value of 4.2. Laboratory examination showed normal serum levels of alpha fetoprotein (2.4 ng/ml), human chorionic gonadotropin beta (<0.2 ng/ml) and anti-acetylcholine receptor antibody. Differential diagnosis included thymoma, thymic carcinoma, and a germ cell tumor; surgical resection was thus recommended. Preoperative needle biopsy was not performed because of the risk of dissemination or bleeding. As the tumor showed possible invasion into the superior vena cava, inferior pulmonary vein and diaphragm, we elected to perform an anterolateral thoracotomy in the fifth intercostal space in the semi-lateral decubitus position, which could be extended to a posterolateral thoracotomy or hemi-clamshell thoracotomy depending on the relationship of the tumor to the inferior pulmonary vein or superior vena cava, respectively.
Fig. 1

Chest x-ray shows a giant mass in the right lower lung field (left). Chest CT shows a mass measuring 13 x 10 cm in diameter, in contact with the right inferior pulmonary vein (right)

Thoracoscopic examination through the eighth intercostal space revealed no adhesions or pleural disease. An anterolateral incision, 20 cm in length, was made in the fifth intercostal space. The tumor was excised from the anterior mediastinal fat tissue and thymus. Dense adhesions of the tumor to the pericardium were sharply peeled off, and the tumor was resected without involvement of the superior vena cava or inferior pulmonary vein. Intraoperative frozen section diagnosed the tumor as a thymoma; thymectomy was thus performed through the same incision via thoracoscopy. The adherent portion of the pericardium was excised and reconstructed with the use of a Gore-Tex pericardial patch.

The resected specimen was 13 × 11.8 × 8 cm, showing a well encapsulated tumor with a lobulated appearance separated by fibrous bands. Microscopic examination revealed the tumor to be composed of a lymphocyte-associated area and a spindle cell-dominant area (Fig. 2), which was diagnosed as World Health Organization (WHO) Type AB thymoma without capsular invasion (Masaoka stage I). The postoperative course was uneventful and the patient is free of recurrence 12 months after the surgery.
Fig. 2

Microscopic examination revealed a WHO type AB thymoma, without capsular invasion

Discussion

The optimal surgical approach for giant thymomas is a point of controversy (Table 1). Two cases of giant thymoma resected via anterolateral thoracotomy have been reported [2, 3]. One case was an ectopic pleural thymoma measuring 20 cm in size located in the lower portion of the right thoracic cavity, with adhesions to the pulmonary pleura of the right lower lobe and central part of the diaphragm [3]. The other case was an anterio-inferior mass weighing 1705 g, which was attached to the mediastinal pleura via a small vascular bundle. This was easily removed after transection of the pedicle, and additional thymectomy was performed [2]. In the present case, we preferred the anterolateral approach because the incision could be extended to either a posterolateral approach in the case of adhesions to the inferior pulmonary vein, or a hemiclamshell approach in case of adhesions to the superior vena cava. Additional thymectomy was successfully performed via the same incision via thoracoscopy, thus avoiding the need for a second operation.
Table 1

Surgical approach for giant thymoma

Approach

n

Cases

Remarks

Median sternotomy [reference 46]

3

Anterior masses

Suitable for invasion into innominate vein

Possible blind spot caused by anterior mass

Hemiclamshell [reference 1214]

3

Large masses occupying more than half of thorax

Easy access to the mediastinum and hilum

Relatively invasive

Posterolateral [reference 8, 9]

2

Masses close to the diaphragm

Suitable for inferior mediastinal masses

Requires thymectomy at second operation

Unsuitable for antero-superior mediastinal masses

Anterolateral [reference 2, 3]

2

Antero-inferior masses

Possible to extend the incision posteriorly or with median sternotomy

Ectopic mass

Unsuitable in cases that are unstable in the decubitus position

Clamshell [reference 7]

1

Masses with bleeding

Quick access to the hilum and tumor control

Invasive

While median sternotomy is the standard approach for thymomas, only three cases of giant thymomas resected via median sternotomy have been reported [46]. Median sternotomy was suitable for one case with invasion into the innominate vein [4], but access to the hilum [7] or posterior thorax can be difficult in cases of giant thymomas. A hemiclamshell approach is a reasonable approach for giant thymomas [2], but is relatively more invasive compared with the other approaches. The clamshell incision, widely used in lung transplantation procedures, was selected in an emergency operation for a patient in shock secondary to spontaneous rupture of a giant thymoma, thought to be a giant sarcoma in close contact with the pulmonary artery [7]. The clamshell approach enables rapid tumor control and easy access to the hilum. A posterolateral approach was reported in two cases [8, 9]. One case was an ectopic pleural thymoma, preoperatively suspected to be a solitary fibrous tumor, and a subsequent transcervical thymectomy was not performed. In the other case, the remaining thymus gland portions were removed through a median sternotomy at a second operation [9]. Anterolateral thoracotomy is less invasive than the clamshell and hemiclamshell approaches, and may be appropriate for cases of giant thymoma.

While the size of the thymoma has been reported to be a significant prognostic factor from experienced single centers [10, 11], sporadic case reports of giant thymomas larger than 13 cm consisted of 4 cases of WHO type A, 6 cases of type AB (including the present case), and 2 cases of type B1 [29, 1214]. Although the five year survival for thymomas more than 10 cm is reported to be 72 % [10], successfully resected giant thymomas tend to be low-grade [12].

Conclusion

In the present case, surgical resection for a giant thymoma and additional thymectomy were successfully performed via an anterolateral approach, which is relatively less invasive and more versatile due to the ability to extend the incision posteriorly or to add a median sternotomy.

Consent

Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.

Abbreviations

FDG-PET: 

F18-fluorodeoxyglucose positron emission tomography

WHO: 

World Health Organization

Declarations

Acknowledgements

This study was supported in part by a Grant-in-aid for Scientific Research (C) 15 K10272 from the Japanese Ministry of Education, Culture, Sports, Science and Technology and The Research Promotion Grant from Toho University Graduate School of Medicine (No.15-02 to A.I.).

Disclosures

The authors have no funding, no financial relationships, and no conflicts of interests.

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Authors’ Affiliations

(1)
Division of Chest Surgery, Toho University School of Medicine
(2)
Division of Respiratory Medicine, Toho University School of Medicine
(3)
Department of Surgical Pathology, Toho University School of Medicine

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Copyright

© Saito et al. 2015

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