A giant tumor of the mediastinum mixed with thymocytes and adipocytes: a case report

Introduction

Lipoma is the most common soft tissue tumor in adults (1). It is characterized by asymptomatic soft tissue masses that can occur throughout the body, with subcutaneous lipomas being more common. Ultrasound, computed tomography (CT), and magnetic resonance imaging (MRI) are important methods for its diagnosis, but the gold standard is still based on histological results (2,3). Lipoma of the thymus is an extremely rare and slow-growing benign tumor, mostly originating from the anterior mediastinum (4). A patient with giant thymolipoma admitted to our department, chest CT showed tumor invasion of bilateral thorax, and the main symptoms were chest tightness and shortness of breath. In this paper, the clinical data of a patient with a giant thymolipoma treated in our department were analyzed, and the pathogenesis, clinical manifestation, and treatment of the disease were reviewed.

We present the following article in accordance with the CARE reporting checklist (available at https://dx.doi.org/10.21037/gs-21-651).

Case presentation

A 17-year-old male was hospitalized with chest tightness and shortness of breath for 6 months. Six months ago, there was no obvious cause of these symptoms, which were aggravated after activity. A chest CT scan was performed after admission, and it was found that there was a huge mixed density shadow in the anterior mediastinum, multiple patchy fat density shadows (Figure 1), left lower lung compression and atelectasis, partial compression of the right lung, and cardiac pressure to the front of the spine. The patient had no similar family history. After the admission blood biochemical examination (Table 1) and cardiac color ultrasound examination showed that there was no abnormality, the patient underwent median anterior mediastinal resection under general anesthesia. During the operation, no obvious adhesion was found between the tumor and the lung, pericardium, superior vena cava, and left innominate vein (Figure 2). The tumor was huge and was about 45×30×25 cm³ in size (Figure 3), with a soft and intact capsule. Postoperative pathology showed that the tumor tissue was consistent with thymolipoma (Figure 4), and there was no evidence of malignancy. The symptoms of chest tightness and shortness of breath were improved after the operation. One month later, the chest CT showed redilation of the left lower lung and the heart returned to the normal position (Figure 5).

Figure 1 Chest CT examination of the patient on admission.

Figure 2 Intraoperative photo of the patient (after tumor resection).

Figure 3 Gross tumor specimen.

Figure 4 Histopathological results, high power ×100 magnification, haematoxylin and eosin.

Figure 5 Reexamination of chest CT one month after the operation.

All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee(s) and with the Helsinki Declaration (as revised in 2013). Written informed consent was obtained from the patient’s parent for publication of this case report and accompanying images. A copy of the written consent is available for review by the editorial office of this journal.

Discussion

Thymolipoma is an extremely rare benign tumor of the anterior mediastinum, accounting for 2% to 9% of all thymic tumors (5). It was officially named thymolipoma in 1948 (6). The pathogenesis is unknown, and its most widely accepted pathogenesis is that adipose tissue replaces the proliferation of thymic tissue (7). Most thymolipomas are asymptomatic, but when the tumor tissue is significantly enlarged, the compression of nearby tissues and organs causes dyspnea, chest pain, weight loss, and other symptoms (4,8). Some patients with thymolipomas are associated with autoimmune diseases, such as myasthenia gravis, vitamin B12 deficiency, hypogammaglobulinemia, and aplastic anemia. These symptoms will be improved after the lipoma is removed (9,10). Therefore, early diagnosis and surgical intervention are very important to resect the symptoms of compression. Median incision or thoracoscopic resection is the first choice for the treatment of thymolipoma, but for large thymic tumors, median thoracotomy enables extensive contact with the tumor without difficulty. It is recommended that resection should not be reduced or compromised to perform the surgery in a minimally invasive manner (11,12). In this report, chest CT showed that the thymolipoma occupied most of the patient’s chest, significantly compressing the cardiopulmonary tube, and compression caused the mediastinum to move to the right. After median thoracotomy to remove the tumor, the symptoms of the patient were significantly improved, and no related myasthenia gravis, vitamin B12 deficiency, or other autoimmune diseases occurred.

Acknowledgments

Funding: This study was supported by the Science and Technology Project of Guizhou Province [Supported by Guizhou Science and Technology Combined (2021) General 073].

Footnote

Reporting Checklist: The authors have completed the CARE reporting checklist. Available at https://dx.doi.org/10.21037/gs-21-651

Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at https://dx.doi.org/10.21037/gs-21-651). The authors have no conflicts of interest to declare.

Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved. All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee(s) and with the Helsinki Declaration (as revised in 2013). Written informed consent was obtained from the patient’s parent for publication of this case report and accompanying images. A copy of the written consent is available for review by the editorial office of this journal.

Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.

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(English Language Editor: C. Betlazar-Maseh)