Liposarcoma of the retropharyngeal space with rapidly worsening dyspnea: A case report and review of the literature

  • Authors:
    • Jian‑Guo He
    • Hua Jiang
    • Bei‑Bei Yang
    • Peng‑Fang Lin
  • View Affiliations

  • Published online on: April 17, 2013     https://doi.org/10.3892/ol.2013.1310
  • Pages: 1939-1942
Metrics: Total Views: 0 (Spandidos Publications: | PMC Statistics: )
Total PDF Downloads: 0 (Spandidos Publications: | PMC Statistics: )


Abstract

Liposarcomas represent a significant proportion of soft‑tissue sarcomas. However, their occurrence in the head and neck is infrequent and they are exceedingly rare in the retropharyngeal space. The present study reports the case of a 58‑year‑old patient with retropharyngeal liposarcoma. Uniquely, the patient presented with rapidly worsening dyspnea. The diagnosis of liposarcoma was established following retropharyngeal tumor excision, although biopsies were performed twice. Adjuvant radiotherapy was refused by the patient. However, during the post‑operative follow‑up period, no sign of either local tumor recurrence or distant metastasis was observed. Previously reported cases were also reviewed to analyze the diagnosis, treatment and prognosis of this disease.

Introduction

Liposarcoma is the most common type of soft-tissue sarcoma. However, head and neck liposarcomas are unusual, accounting for only 1.8–6.3% of cases (1). Furthermore, cases of liposarcoma in the retropharyngeal space are extremely rare. To the best of our knowledge, only five cases have been reported previously (15). Unlike previous cases, the present study reports a highly unusual case of retropharyngeal liposarcoma with rapidly worsening dyspnea and total dysphagia following an accident and subsequent surgery. Due to the difficulties of biopsy, radiological examination and pathohistological examination, a retropharyngeal well-differentiated liposarcoma may be easily misdiagnosed as a lipoma. The retropharyngeal space is extremely close to vital neurovascular structures and the extent of any surgical excision is restricted to avoid severe complications. These difficulties may affect the prognosis of patients with retropharyngeal liposarcoma. In the present study, the diagnosis, treatment and prognosis of this disease is discussed by analyzing the present case and by reviewing previously reported cases. This study was approved by the ethics committee of the Second Affiliated Hospital, School of Medicine, Zhejiang University. Written informed consent was obtained from the patient.

Case report

A 58-year-old male patient presented with rapidly worsening dyspnea and total dysphagia occurring within several hours. Three years earlier the patient had noted bilateral neck swelling. The swelling grew slowly and one year later the patient developed mild dysphagia. As the patient was unaware of the potential severity of the symptom, a prompt examination and treatment were not provided. This symptom did not markedly progress until the occurrence of a traffic accident. Due to this accident, the patient underwent tibiofibular fracture surgery at a local hospital. Post-operatively, the patient recovered well and ate as usual. However, three days subsequent to the surgery, the patient suddenly developed rapidly worsening dyspnea and total dysphagia. Attempts at intubation failed, so a tracheostomy was performed under local anesthesia. The patient was then referred to the Department of Otolaryngology (Second Affiliated Hospital, Zhejiang University, Hangzhou, China). A physical examination revealed an extremely large, soft, non-tender mass measuring ∼11×10×8 cm, involving the bilateral neck. A laryngoscopy showed a retropharyngeal mass that was reducing the space of the pharynx. A computed tomography (CT) scan of the neck revealed a large, well-circumscribed, fatty, dense mass measuring 11×11×9 cm, which extended from the retropharyngeal space to the sides of the neck and from the level of the hyoid bone to the superior margin of the mediastinum. The mass displaced the trachea and larynx anteriorly and the carotid arteries laterally. The mass was not enhanced following contrast agent administration (Fig. 1A and B). Due to the internal fixation of the leg, magnetic resonance imaging (MRI) was not an option. In addition, a CT scan of the chest and abdomen was performed and no similar mass was observed.

An ultrasound-guided core biopsy of the mass revealed histological components of fibrous, vascular and fatty tissues. An incisional biopsy of the lesion was then performed with the patient under local anesthesia. The histology indicated a vascular fibrous lipoma. Subsequently, a surgical excision of the retropharyngeal mass was performed under general anesthesia using an H-shaped incision. The tumor was well-encapsulated and adhered to the posterior pharyngeal wall. The tumor was subsequently resected completely and measured as weighing 401 g (Fig. 2). The posterior pharyngeal and esophageal walls were completely preserved. Microscopically, the lesion had components of mature adipocytes and lipoblasts with nuclear atypia (Fig. 3). A diagnosis of a well-differentiated liposarcoma was confirmed. The suggested adjuvant radiotherapy was not accepted by the patient.

During the post-operative course, the patient developed vocal hoarseness. A laryngoscopy revealed right-sided vocal fold weakness, which the patient recovered from one month later. The patient was decannulated and the nasogastric tube was removed. Upon follow-up at 20 months, there were no signs of either local tumor recurrence or distant metastasis.

Discussion

The retropharyngeal space is the potential space lying between the prevertebral fascia posteriorly and the buccopharyngeal membrane covering the constrictor muscles anteriorly. It extends from the skull base to the mediastinum. The retropharyngeal space is separated from the parapharyngeal space by a thin fascial layer and closed by the internal jugular vein, common carotid artery and vagus nerve. Liposarcomas usually present as painless enlarging masses and when they arise in the retropharyngeal space they are difficult to detect early and are usually discovered incidentally. Patients with a retropharyngeal mass usually present with dysphagia and foreign body sensation and when these symptoms are not as clear the patients may become habituated to their symptoms. Physical findings include bilateral neck swelling and a reduced anteroposterior diameter of the pharynx, although these do not appear until the tumors have reached a large size (15). In the present case, as in all five previously reported cases, prior to the liposarcoma being identified, it had attained an extremely large size and compressed the pharynx, causing dysphagia and ultimately dyspnea. However, unlike previous cases, the present patient presented rapidly worsening dyspnea and total dysphagia following tibiofibular fracture surgery. This indicates that stresses, including trauma or surgery, may stimulate the growth of the tumor. Similarly, stress and surgical intervention have also been demonstrated to promote tumor development in another study (6). However, the mechanism remains unclear. Natural killer cell activity and β-adrenergic receptors may be involved in this process (6).

Lipocytes of various shapes and sizes with nuclear atypia indicate a diagnosis of liposarcoma. The classification proposed by Enzinger and Weiss is widely accepted and has been adopted by the World Health Organization. This classification identifies four subtypes of liposarcoma: well-differentiated, myxoid, dedifferentiated and pleomorphic (7). The histological appearances of these vary from well-differentiated neoplasms with scattered atypical cells to pleomorphic neoplasms resembling high-grade malignant fibrous histiocytomas (7). CT and MRI scans aid in establishing a diagnosis. Murphey et al indicated that well-differentiated liposarcomas are frequently diagnosed in CT or MRI scans, with a largely lipomatous mass (>75% of the lesion) and non-lipomatous components in thick septa or focal nodules (8). The identification of a nodular dominant focus (>1 cm in size) of non-lipomatous tissue using CT or MRI suggests a dedifferentiated liposarcoma (8,9). Myxoid liposarcomas have a high water content and pleomorphic liposarcomas are high-grade sarcomatous lesions that typically appear as heterogeneous soft-tissue masses (8). However, a well-differentiated liposarcoma is difficult to distinguish from a lipoma by CT or MRI scans and is commonly misdiagnosed, even with a biopsy. Notably, all reported cases, including the present case, were well-differentiated liposarcoma, although 33.3% were misdiagnosed as lipoma pre-operatively (15). In retropharyngeal liposarcomas, due to the deep location and the large tumor, a core biopsy or incisional biopsy usually obtains only a small part of the tumor. This may be one of the reasons behind the frequent misdiagnoses.

The principal management approach for liposarcoma is wide surgical excision. However, in the head and neck, the lesion is usually close to vital neurovascular structures, so the extent of surgical excision is restricted to avoid severe complications and the use of adjuvant radiotherapy is increasing. Certain studies have demonstrated the effect of radiotherapy in reducing the rate of local recurrence of liposarcomas (10). Eeles et al observed that adjuvant radiotherapy significantly decreased the rate of local recurrence of head and neck sarcomas (11). Our previous study also showed that adjuvant radiotherapy is important in the management of sarcomas of the parapharyngeal space (12). However, for well-differentiated liposarcomas of the head and neck, certain authors have suggested that wide surgical resection is sufficient (13). The majority of studies have been confined by the small series of patients used to assess the value of adjuvant radiotherapy in the treatment of head and neck liposarcomas (14,15).

Among the various series of retropharyngeal liposarcomas in the literature, only one patient received adjuvant radiotherapy in the initial treatment and the follow-up revealed no evidence of recurrence (2). Among the other five patients with surgery alone, only one patient developed recurrence within a year and received re-excision with adjuvant radiotherapy (1). Six months after re-excision, there were no signs of recurrence (1). Additionally, from these five patients, the follow-up of the present patient was the longest and there have been no signs of either recurrence or metastasis. Although the reported periods of follow-up were not long enough, with two cases with a follow-up of less than one year (2,3), one case with no follow-up reported (4) and the other three, including the present case, reporting a follow-up of between 18 and 20 months (1,5), no clear benefits of adjuvant radiotherapy were observed.

The major prognostic factor for liposarcoma is the histological subtype. Well-differentiated liposarcoma is the most common subtype of all liposarcomas, recurring locally, but rarely metastasizing (16). Patients with this type of liposarcoma have an improved prognosis compared with those with other subtypes (17). Myxoid tumors, similar to the well-differentiated variety, are unlikely to metastasize and have a favorable five-year survival rate. However, these tumors have high local recurrence rates and are more locally invasive (18). The other two subtypes are significantly more aggressive and have worse prognoses (18).

Although all six reported cases of retropharyngeal liposarcoma were of the well-differentiated subtype, certain characteristics of this unusual tumor may affect the prognosis due to its unique localization. Late detection may provide sufficient time for tumor invasion and metastases to occur. Misdiagnosis may lead to the diagnosis of a benign lesion, which may result in a limitation of the extent of surgical excision. In addition, liposarcomas located in deep anatomical sites, including the retroperitoneum and mediastinum, have a relatively unfavorable prognosis (19). This may be due to the difficulties of using adequate surgical margins. Similarly, in the head and neck, patients with facial, scalp and laryngeal tumors have an improved prognosis compared with those with intraoral, pharyngeal and neck tumors (19). The retropharyngeal space is a deep potential space that is extremely close to vital neurovascular structures, so the extent of excision is restricted to avoid severe complications. The difficulties of surgery may also affect the prognosis of patients with retropharyngeal liposarcoma.

In conclusion, although well-differentiated liposarcoma is the most common subtype of liposarcoma and has an improved prognosis, retropharyngeal liposarcoma has a number of unfavorable prognostic factors due to its unique localization. No adequate evidence has demonstrated the value of adjuvant radiotherapy for treating retropharyngeal liposarcomas. However, for liposarcomas, adjuvant radiotherapy has been shown to decrease the rate of local recurrence in a number of literature studies.

References

1 

Yueh B, Bassewitz HL and Eisele DW: Retropharyngeal liposarcoma. Am J Otolaryngol. 16:331–340. 1995. View Article : Google Scholar : PubMed/NCBI

2 

Gundelach R, Ullah R, Coman S and Campbell K: Liposarcoma of the retropharyngeal space. J Laryngol Otol. 119:651–654. 2005. View Article : Google Scholar : PubMed/NCBI

3 

Menown IB, Liew SH, Napier SS and Primrose WJ: Retro- pharyngeal liposarcoma. J Laryngol Otol. 106:469–471. 1992. View Article : Google Scholar : PubMed/NCBI

4 

Hermans R, Dewitte B, Delaere P, Feenstra L and Baert AL: Retropharyngeal liposarcoma. J Belge Radiol. 76:176–177. 1993.PubMed/NCBI

5 

Prince ME, Nasser JG, Fung BR and Broderick I: Liposarcoma of the retropharyngeal space: review of the literature. J Otolaryngol. 26:139–142. 1997.PubMed/NCBI

6 

Lee LW, Shahzad MM, Lin YG, Armaiz-Pena G, Mangala LS, Han HD, et al: Surgical stress promotes tumor growth in ovarian carcinoma. Clin Cancer Res. 15:2695–2702. 2009. View Article : Google Scholar : PubMed/NCBI

7 

Enzinger FM and Weiss SW: Soft Tissue Tumours. 2nd edition. Mosby; St. Louis, MO: pp. 346–382. 1988

8 

Murphey MD, Arcara LK and Fanburg-Smith J: From the archives of the AFIP: imaging of musculoskeletal liposarcoma with radiologic-pathologic correlation. Radiographics. 25:1371–1395. 2005. View Article : Google Scholar : PubMed/NCBI

9 

Wang Y and Shi H: Dedifferentiated liposarcoma of the neck: CT fingdings. AJNR Am J Neuroradiol. 33:E4–E6. 2012. View Article : Google Scholar : PubMed/NCBI

10 

Suit HD, Russell WO and Martin RG: Sarcoma of soft tissue: clinical and histopathologic parameters and response to treatment. Cancer. 35:1478–1483. 1975. View Article : Google Scholar : PubMed/NCBI

11 

Eeles RA, Fisher C, A’Hern RP, Robinson M, Rhys-Evans P, Henk JM, et al: Head and neck sarcomas: prognostic factors and implications for treatment. Br J Cancer. 68:201–207. 1993. View Article : Google Scholar : PubMed/NCBI

12 

Yang BB, Jiang H and Chang HY: Malignant triton tumour of the parapharyngeal space: a case arising from the cervical sympathetic nerve. J Laryngol Otol. 122:531–534. 2008.PubMed/NCBI

13 

Nouri H, Hassani R, Aderdour L and Raji A: The well-differentiated liposarcoma of the hypopharynx. Eur Ann Otorhinolaryngol Head Neck Dis. 128:143–145. 2011. View Article : Google Scholar : PubMed/NCBI

14 

Rogers J, Patil Y, Strickland-Marmol L and Padhya T: Lipomatous tumors of the parapharyngeal space: case series and literature review. Arch Otolaryngol Head Neck Surg. 136:621–624. 2010. View Article : Google Scholar : PubMed/NCBI

15 

Makeieff M, Pelliccia P, Poizat F, Arnaud S, Rat F, Cupissol D, Guerrier B and Costes V: Laryngeal dedifferentiated liposarcoma. Eur Arch Otorhinolaryngol. 267:991–994. 2010. View Article : Google Scholar : PubMed/NCBI

16 

Enzinger FM and Winslow DJ: Liposarcoma: a study of 103 cases. Virchows Arch Pathol Anat Physiol Klin Med. 335:367–388. 1962. View Article : Google Scholar : PubMed/NCBI

17 

Saunders JR, Jacques DA, Casterline PF, Percarpio B and Goodloe S Jr: Liposarcomas of the head and neck: a review of the literature and addition of four cases. Cancer. 43:162–168. 1979. View Article : Google Scholar : PubMed/NCBI

18 

Golledge J, Fisher C and Rhys-Evans PH: Head and neck liposarcoma. Cancer. 76:1051–1058. 1995. View Article : Google Scholar

19 

Stout AP: Liposarcoma - the malignant tumor of lipoblasts. Ann Surg. 119:86–107. 1944.PubMed/NCBI

Related Articles

Journal Cover

June 2013
Volume 5 Issue 6

Print ISSN: 1792-1074
Online ISSN:1792-1082

Sign up for eToc alerts

Recommend to Library

Copy and paste a formatted citation
x
Spandidos Publications style
He JG, Jiang H, Yang BB and Lin PF: Liposarcoma of the retropharyngeal space with rapidly worsening dyspnea: A case report and review of the literature. Oncol Lett 5: 1939-1942, 2013
APA
He, J., Jiang, H., Yang, B., & Lin, P. (2013). Liposarcoma of the retropharyngeal space with rapidly worsening dyspnea: A case report and review of the literature. Oncology Letters, 5, 1939-1942. https://doi.org/10.3892/ol.2013.1310
MLA
He, J., Jiang, H., Yang, B., Lin, P."Liposarcoma of the retropharyngeal space with rapidly worsening dyspnea: A case report and review of the literature". Oncology Letters 5.6 (2013): 1939-1942.
Chicago
He, J., Jiang, H., Yang, B., Lin, P."Liposarcoma of the retropharyngeal space with rapidly worsening dyspnea: A case report and review of the literature". Oncology Letters 5, no. 6 (2013): 1939-1942. https://doi.org/10.3892/ol.2013.1310