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01.12.2012 | Case report | Ausgabe 1/2012 Open Access

Journal of Medical Case Reports 1/2012

Unique presentation of a giant mediastinal tumor as kyphosis: a case report

Zeitschrift:
Journal of Medical Case Reports > Ausgabe 1/2012
Autoren:
Eleftherios D Spartalis, Theodore Karatzas, Petros Konofaos, Grigorios Karagkiouzis, Gregory Kouraklis, Periklis Tomos
Wichtige Hinweise

Electronic supplementary material

The online version of this article (doi:10.​1186/​1752-1947-6-99) contains supplementary material, which is available to authorized users.

Competing interests

The authors declare that they have no competing interests.

Authors' contributions

ES analyzed and interpreted the patient's files, wrote the paper, assisted at the operation and looked after the patient postoperatively. TK and PT were the surgeons responsible for the patient, performed the operation and critically revised the manuscript. PK and GKa contributed to the writing. GKo is the supervising professor. All authors read and approved the final manuscript.

Introduction

Thymomas are rare neoplasms with a largely indolent growth pattern and various clinical symptoms [1]. The successful treatment of thymomas relies largely on complete surgical resection [2]. The first transsternal thymectomy was performed in 1939 by Alfred Blalock, and since then, a median sternotomy has been the standard surgical approach [2, 3].

Case Presentation

An 83-year-old Caucasian woman was admitted to the Department of Orthopedics with a chief complaint of progressive kyphosis, which had worsened over the previous six months. The patient complained of a progressive dysphagia and had lost approximately 20 kg over the previous six months. Posteroanterior and lateral chest radiographs (Figures 1a and 1b) demonstrated a mediastinal homogenous opacity partially filling the left hemithorax and causing tracheal displacement. She was then referred to our department for further investigation.
A physical examination revealed marked prominence of the left hemithorax. This region was dull to percussion and did not move with respiration. The intercostal spaces were bulging, and no breath sounds were heard on the left. The right hemithorax was clear and moved well with respiration. The remainder of the physical examination was unremarkable. Her general condition was good. Physical examination of the heart as well as an electrocardiogram (ECG) revealed no abnormal findings. Routine laboratory tests were within normal limits. Liver and renal function was very good.
The presence of a giant tumor was confirmed by computed tomography (CT) (Figure 2a) (size 2 × 20 × 11 cm). The CT scan showed that the tumor caused bilateral lung compression and tracheal and esophageal displacement. No fluid accumulation was seen. A CT-guided fine needle aspiration identified the mediastinal mass lesion as a possible thymoma.
The patient subsequently underwent radical surgical excision of the tumor (Figure 3) via median sternotomy.
The total weight of the excised tumor was 2550 g (Table 1) [48]. Histological examination showed a thymoma [B1 according to the World Health Organization (WHO) classification, CD3(+), CD5(+), CD1(+), keratine(+), CD20(-) and CD30(-)]. The tumor was macroscopically and microscopically completely encapsulated (Masaoka stage I).
Table 1
Giant mediastinal thymomas in adults
Author
Year
Age (years)
Gender
Classification (WHO)
Tumor weight (g)
Sim
1992
83
Male
Type B1
n.d.
Selzner
1997
61
Female
Type A
1053
Agarwala
2003
65
Male
Type AB
1645
Gotte
2007
48
Female
Type A
1740
Yamazaki
2007
58
Female
Type A
n.d.
Santoprete
2007
73
Female
Type AB
n.d.
Moreno
2009
40
Male
Type AB
1725
Limmer
2009
52
Male
Type AB
1705
n.d., Not documented; WHO, World Health Organization
The patient was extubated in the operating room and then taken to the intensive care unit for two days of postoperative monitoring. The rest of her postoperative recovery was uneventful, and she was discharged on the tenth postoperative day.
Two years after the operation, the patient currently shows significant improvement of her posture, no pulmonary discomfort, and she has regained 20 kg of weight. Follow-up CT scans revealed no evidence of disease (Figure 2b). Her trachea and esophagus were returned to their anatomical location, the lungs were fully expanded and the mediastinum had returned to its normal width.

Discussion

Thymomas typically present in the fourth or fifth decade of life and exhibit no gender predilection [1]. The presenting clinical symptoms in patients with thymomas are varied. When symptoms are present, they most often consist of cough, dyspnea, and other upper respiratory complaints [3]. In this case, the patient reported a chief complaint of spinal distortion associated with progressive symptoms of dysphagia and weight loss.
It is a commonplace observation that carrying a heavy load causes the carrier to lean forwards, and that in general, the heavier the load, the further forward the carrier leans [9]. The manner in which the body alters its normal alignment to achieve stability under conditions of load carriage has been examined thoroughly [10]. The body treats the load on the back as essentially a problem in balancing [11]. Thomas et al. found that if the vertical projection of the center of gravity is kept in a more or less constant position, it follows that lowering the position of a heavy weight on the back must cause the trunk to lean further forwards to keep the combined center of gravity of the body plus the weight in the same position [12]. Once an asymmetric load or degeneration occurs, the pathomorphology and pathomechanism in adult scoliosis is quite predictable. Asymmetric degeneration leads to increased asymmetric load and, therefore, to a progression of the degeneration and deformity [13]. In this case, the chronic, asymmetric load on the spine led to a progressive vertebral deformity that manifested as kyphosis.
Half of all thymomas present asymptomatically and are detected incidentally on radiographic imaging [1]. Imaging is an essential part of the workup, and in conjunction with the history and physical examination, it is often the only investigation needed prior to treatment [2]. Following the identification of a mediastinal mass on chest x-ray, a CT scan of the chest should be obtained. CT allows for the characterization of tumors and the assessment of possible invasion into surrounding structures [14]. CT studies with intravenous contrast administration are the preferred method for assessing vascular invasion and cystic components of the tumor [2]. Dynamic magnetic resonance imaging (MRI) has been examined as a potential way to improve the staging and differential diagnosis. Positron emission tomography (PET) has been examined as a method of tumor detection and for differentiating between invasive and non-invasive thymomas with mixed results [14].
The successful treatment of thymomas (both invasive and non-invasive) largely depends on complete surgical resection, if possible [15]. If an induction strategy for more advanced disease is being considered, or a diagnosis other than thymoma is likely, biopsy is recommended to confirm the diagnosis. Thymomas are staged according to their histopathological features (WHO-classification) as well as their clinical stage (Masaoka) [16].
Although thymomas are responsive to both chemotherapy and radiation, the mainstay of treatment is surgical resection [17]. Patients with inoperable tumors warrant a strategy of induction chemotherapy followed by a surgical reassessment post-therapy [18]. Despite the lack of prospective studies, adjuvant radiation therapy is generally recommended for any evidence of invasive disease, regardless of the degree of resection obtained. Since the ability to resect thymomas is closely associated with the tumor stage, the improvement of long-term prognosis for patients with advanced thymomas may ultimately depend upon developing effective multidisciplinary neoadjuvant treatment protocols that can downstage unresectable disease, allowing most patients to undergo a complete resection [15]. Lasting responses can be obtained both in the metastatic and recurrent setting, and novel therapies are currently being explored [17].

Conclusions

Kyphosis in an adult with no previous history of any spinal curvature deformity should be considered as a possible symptom of an intrathoracic tumor. Imaging is an essential part of the investigation needed prior to surgical excision. CT-guided fine-needle aspiration biopsy is necessary for a definitive diagnosis and patient management. In the case of thymomas, complete surgical resection should be planned. Thymoma recurrence has been reported as late as 32 years after initial surgery [15]. As a result, patients with thymomas require life-long follow-up. The most important indicator of long-term prognosis is the completeness of resection [14]. Facing this case of a thymoma that presented as kyphosis, we achieved complete surgical excision of the tumor and improved the patient's posture and physical status.

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.
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://​creativecommons.​org/​licenses/​by/​2.​0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Competing interests

The authors declare that they have no competing interests.

Authors' contributions

ES analyzed and interpreted the patient's files, wrote the paper, assisted at the operation and looked after the patient postoperatively. TK and PT were the surgeons responsible for the patient, performed the operation and critically revised the manuscript. PK and GKa contributed to the writing. GKo is the supervising professor. All authors read and approved the final manuscript.

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Zusatzmaterial
Authors’ original file for figure 1
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Authors’ original file for figure 2
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Authors’ original file for figure 3
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