Combining surgery with 125I brachytherapy for recurrent mediastinal dedifferentiated liposarcoma:A case report and review of literature

Hui-Guo Chen,Kai Zhang,Wei-Bin Wu,Yong-Hui Wu,Jian Zhang,Li-Jia Gu,Xiao-Jun Li

Abstract

Key words: Dedifferentiated liposarcoma; Mediastinal neoplasms; Recurrence;Reoperation; 125I brachytherapy; Case report

INTRODUCTION

Liposarcoma is a malignant adipocytic neoplasm with varying degrees of atypia.According to the 2019 NCCN classification,liposarcoma has been classified into four types:Well-differentiated,myxoid,pleomorphic,and dedifferentiated.Dedifferentiated liposarcoma is a common form of liposarcoma,accounting for the most pleomorphic sarcoma in the retroperitoneum[1],but rarely occurs in the mediastium,and the exact frequency is unknown[2].Thus far,limited cases of mediastinal dedifferentiated liposarcoma have been reported,and its clinical characteristics,optimal treatment and clinical outcomes remain unclear.

The present study reports a case of primary multifocal recurrent dedifferentiated liposarcomas in the posterior mediastinum treated by combining surgery with125I brachytherapy following recurrence.In addition,38 cases of primary mediastinal dedifferentiated liposarcoma from the English literature are reviewed to illustrate the clinical characteristics,treatment and outcomes of the disease.To our knowledge,our literature review covers the largest number of cases compared to any prior reviews,and is the first report of dedifferentiated liposarcomas treated by125I brachytherapy.

CASE PRESENTATION

Chief complaints

Progressive dysphagia for one year.

History of present illness

A 75-year-old male was admitted in December 2013 due to gradually progressive dysphagia,and the symptoms became more aggravated 3 mo before admission.He had no chest pain,acid reflux or weight loss.

History of past illness

Atrial fibrillation had been diagnosed eight years prior,but had been left untreated.There was no history of trauma,thoracic disease,thoracic surgery or abdominal disease.

Physical examination

No remarkable abnormality was found upon physical examination,with the exception of atrial fibrillation with a heart rate of approximately 80 beats per minute.

Laboratory examinations

Tumor markers were in the normal range,including α-fetoprotein,carcinoembryonic antigen,β-human chorionic gonadotropin,cytokeratin 19-fragments (CYFRA21-1),neuron specific enolase,cancer antigens 19-9 and squamous cell carcinoma antigen.

Imaging examination

Chest contrast-enhance computed tomography (CT) revealed several large cystic-solid masses that compressed the left atrium,left ventricular and esophagus in the posterior-inferior mediastinum.The largest mass was about 10.5 cm × 9 cm in size and had three attenuation components,namely a lipomatous element,a soft tissue density component and a high attenuation calcified area (Figure 1A and B).The other masses had only two attenuation components without calcification.All of the masses had a relatively distinct margin,and the CT value was 19 HU.A small amount of pericardial effusion and bilateral pleural effusion were present.No obvious enhancement was found in any of the stages after enhancement,and no obviously enlarged lymph nodes were found.The 18F-fluorodeoxyglucose positron emission tomography (PET) showed an maximum standardized uptake value (SUVmax) of 1.8(Figure 1C) and no metastasis.Esophageal dynamic radiography and fibergastroscopy showed that the lower esophagus was significantly compressed.No obvious changes were observed on the mucosal surface of the esophagus,and no tumorous lesion was seen.

Preoperative diagnosis

Teratoma in the posterior mediastinum.

FINAL DIAGNOSIS

Grossly,all tumors had an integrated capsule,and there was some adipose tissues between adjacent tumors (Figure 2A).Within the tumor,the cut interface presented as variegated tan-yellow to brown,and had a partial myxoid appearance.Haematoxylin and eosin staining showed proliferating fat cells and well-differentiated liposarcoma,as well as spindle cell sarcoma with spindle nuclei and nuclear fission (Figure 2B and C).Immunohistochemical analysis showed that the tumor was positive for vimentin,S100 (Figure 2D),CD34,CD68 (diffused),and Desmin (partial),but negative for SMA,and the ki-67 index was 5%.Finally,a diagnosis of dedifferentiated liposarcoma was made.

TREATMENT

The patient immediately underwent wide excision by video-assisted thoracoscopic surgery,with a small incision (8 cm) made in the right thoracic cavity.The tumors presented as encapsulated and smooth,and occupied a large part of the left pleural cavity.There were mild adhesions,with fat tissue between tumors and lung,esophagus,descending aorta,left atrium,and left ventricular,but no direct invasion.Finally,a total of eight tumors were resected completely.The largest tumor was about 10.5 cm × 9 cm × 8.9 cm in size,and the smallest one was about 2 cm in diameter(Figure 2A).

OUTCOME AND FOLLOW-UP

The postoperative course was uneventful.The patient rejected adjuvant therapy,and chest CT was performed at a 6-mo interval for follow-up.The patient suffered from slight dysphagia again for 24 mo after the operation.Contrast-enhanced CT showed a mass (about 5 cm in diameter) in the posterior-inferior mediastinum-compressed esophagus,and the patient underwent re-operation by video-assisted thoracoscopic surgery.A total of five tumors were resected.Pathological analysis confirmed the diagnosis of dedifferentiated liposarcoma.The patient still rejected postoperative adjuvant chemotherapy or radiotherapy.Unfortunately,the chest CT showed tumor recurrence 15 mo after the re-operation.The condition of the disease was explained to the patient and his family,and the patient rejected repeat surgery and received CTguided radioactive seeds125I implantation in another hospital.After 8 mo,follow-up chest CT showed an enlarged tumor.Finally,the patient rejected any treatment,and died from severe dysphagia and respiratory failure in July 2018.

DISCUSSION

Dedifferentiated liposarcoma is one type of liposarcoma that was first described by Evans in 1979[3].According to the World Health Organization,dedifferentiated liposarcoma is a malignant adipocytic neoplasm showing a transition from atypical lipomatous tumor/well-differentiated liposarcoma to non-lipogenic sarcoma of variable histological grade[1].Dedifferentiated liposarcoma most commonly occurs in the retroperitoneum,followed by extremities,and scrotum/spermatic cord,but its origin in the mediastinum is extremely rare[4].

Figure 1 lmaging findings.

The present study reviewed the English literature in PubMed between 1950 and 2018 using the keywords:Dedifferentiated/de-differentiated,liposarcoma,mediastinum or mediastinal,and identified 39 cases of primary mediastinal dedifferentiated liposarcoma,including this case[2,5-24].In these cases,the tumors all occurred in adults,and the mean patient age was 62.9 years,with an age range of 34 years to 83 years,and a predilection for males (26 males and 13 females).Of the 39 cases,24 were reported in American and European populations,and 15 cases in Asian populations.There were 24 cases describing symptom details:Sixteen with some symptoms and eight without symptoms.The common complaints included dyspnea(nine cases),cough (five cases),and dysphagia (five cases).The other symptoms included weight loss,hoarseness,chest pain and arm weakness.The tumor most frequently occurred in the anterior and posterior mediastinum (15 cases respectively),followed by the middle (three cases),and the anterior-middle mediastinum (one case).The tumor size varied from 6 cm to 61 cm.The mean size of the tumor was 18.5 cm,and only five cases exhibited a tumor of ＜ 10 cm,meanwhile ten cases were ＞ 20 cm in diameter.The mean SUVmax of the tumor was 3.7 in seven cases (range 1.8 to 9.2),and four cases exhibited ＜ 2.5.Only four cases had reported tumor invasion of the surrounding structures,including pleura,pericardium and the phrenic nerve.Distant metastasis only occurred in four cases,and common metastasis occurred in the lung and pleura.

In terms of initial management,30 patients underwent complete surgical resection,three patients received incomplete surgical resection,two patients received chemotherapy,one patient received neoadjuvant chemotherapy and three patients were unknown.Of the 34 surgical cases,three patients received adjuvant therapy after surgery (two for chemotherapy and one for radiotherapy).Unfortunately,the tumor recurred in 13 cases (13/34,38.2%),and nine cases were further treated by repeat surgery,while the other patients received chemotherapy (one case),chemoradiotherapy (one case),and radiotherapy (one case).Six cases of repeat surgical patients were reported with the second relapse (6/9,66.7%).The mean time of recurrence-free survival (RFS) was 24.5 mo for the first relapse (range 5 mo to 50 mo) and was 35.8 mo for the second relapse (range 8 mo to 96 mo).Median RFS was 24 mo for the first relapse and 14.5 mo for the second relapse.Of the 39 total patients,21 cases were alive with no evidence of disease,five cases were alive with the disease,seven cases were dead (five cases dead of disease and two cases dead of other disease)and six cases were lost to follow-up.The longest survival time was 114 mo.

Figure 2 Pathological findings.

Since the first case reported by Evanset al[22]in 1994,surgical resection was usually utilized in the management of mediastial dedifferentiated liposarcoma.Based on previous reports,complete resection is the optimal method to eradicate the tumor[2,5-9,11-21,23,24].Hahnet al[21]reported six cases of mediastinal dedifferentiated liposarcoma treated by complete resection,and three cases of them had a disease-free survival (DFS) of more than 50 mo.Recently,Miuraet al[2]reported five cases of mediastinal dedifferentiated liposarcoma,and reviewed 14 cases in the literature.They performed complete surgical resection in four patients,and claimed that complete surgical resection is the best treatment for mediastinal dedifferentiated liposarcoma.In our report,the patient underwent complete surgical resection and had an RFS of 24 mo.Although mediastinal dedifferentiated liposarcoma usually grows to be very large,the growth pattern tends to be of the expansive type rather than infiltrative type,and metastasis rarely occurs.Of the 39 cases,only one case showed metastasis and four cases had invaded surrounding structures at the time of the first visit.These conditions are conducive to complete surgical resection.However,13 of 32 patients with complete resection developed local recurrence in the mediastinum,and it appeared that the tumor tended to recur after surgery.Although there was loose connective tissue between the tumor and surrounding structure,and the tumor did not invade surrounding organs,it is difficult to completely resect all of the fat tissue in the mediastinum.In addition,atypical cells were found in the peripheral fat tissue[2].These may explain the predisposition for recurrence.Fortunately,according to the literature review,repeat surgery is still valid for patients with recurrence,with a median RFS of 14.5 mo in seven cases of secondary relapse.Thus,despite a high risk of recurrence,we conclude that a complete resection is the best method to cure the tumor,even in patients with local recurrence.

As discussed above,repeat surgery is still valid for patients with recurrent mediastial dedifferentiated liposarcoma,but some patients refused repeat surgery or were unsuitable for repeat surgery.External radiotherapy is an optional strategy used to treat these patients.Miuraet al[2]reported a patient with recurrent mediastial dedifferentiated liposarcoma who was treated by radiotherapy,and the disease was well-controlled.Coulibalyet al[19]reported a case of recurrent dedifferentiated liposarcoma of the mediastinum treated by repeat surgery combined with adjuvant radiotherapy (60 Gy),and the patient had an RFS of 8 years.However,an adequate therapeutic dose of radiotherapy to the mediastinal tumor may damage the important adjacent organs,including lung,esophagus and heart,which are often radiosensitive and have a low radiation tolerance.125I brachytherapy can deliver a large total radiotherapy dose to the target tumor and overcome these problems.Radioactive seeds125I implantation was widely used in advanced hepatic carcinoma and soft tissue sarcoma with good outcomes[25,26].Yanget al[25]reported CT-guided125I seed implantation for inoperable retroperitoneal,including eight cases of liposacoma,and good local control was achieved.We consider125I brachytherapy to be effective because its application to locally recurrent tumors was effective in this case,with a PFS of 8 mo,although its efficacy has not been confirmed in dedifferentiated liposarcoma.To our knowledge,this is the first attempt to treat mediastinal dedifferentiated liposarcoma by CT-guided125I seed implantation.This approach needs to be further explored by large sample studies.

Due to its rarity,with only a few case reports,the long-term prognosis of mediastinal dedifferentiated liposarcoma is not clear.Coulibalyet al[19]reported a patient with mediasinal dedifferentiated liposarcoma,who underwent complete surgery with a DFS of 15 mo.The patient received repeat surgery and adjuvant radiotherapy with a DFS of 96 mo,and died 3 mo later.The survival time of the patient was 114 mo.This is the longest survival time in the literature.Hahnet al[21]studied 24 cases of mediastinal liposarcoma,including eight cases of dedifferentiated liposarcoma.In the last follow-up,four patients were alive with no evidence of disease with a median DFS of 51.5 mo,and one patient died of unrelated disease with a survival time of 5 mo.In this study,of the 39 cases,there were 21 cases alive with no evidence of disease with a mean DFS of 29.8 mo,and five patients died of the disease with a mean survival time of 42.3 mo.However,as mentioned above,local recurrence was common,with 13 (13/39,33.3%) cases developing recurrent tumors after a mean interval of 24.5 mo.The mean tumor size of ten patients with recurrence was 24.5 ±17.3 cm,and that of 16 patients without recurrence was 17.1 ± 9.6 cm.The difference was statistically significant between the two groups.According to our literature review,we speculated tumor size to be one of the risk factors for tumor recurrence,whereas gender,tumor location and symptoms are not.Therefore,we speculate that complete surgical resection and tumor size are associated with recurrence and prognosis,and complete resection should be attempted if possible.

PET/CT and SUVmax were widely used to evaluate the tumor characteristics.In this case,the SUVmax results of the tumor was 1.8 and relatively low.Miuraet al[2]reported two cases of mediastinal dedifferentiated liposarcoma with a low SUVmax result,and three cases with a high SUVmax result.Therefore,it seems that PET/CT cannot reliably identify mediastinal dedifferentiated liposarcoma.Meanwhile,we found the ki-67 index to be 5%,which was relatively low and consistent with the low SUVmax result.Thus,we speculate that SUVmax and Ki-67 may be used as prognostic indicators in mediastinal dedifferentiated liposarcoma.

CONCLUSION

In summary,we described a case of primary multifocal and recurrent mediastinal dedifferentiated liposarcoma treated by combining surgery with125I brachytherapy,as well as a review of the literature.We suggest that surgical resection provides beneficial effects for dedifferentiated liposarcoma in mediastinum,even in cases with local recurrence.125I brachytherapy may be beneficial for recurrent unresectable patients.