Hoarseness due to lymph node metastasis of hepatocellular carcinoma: A case report

Introduction

Hepatocellular carcinoma (HCC) is one of the most common types of primary cancer worldwide, with an estimated incidence of ~23,000 mortalities from liver or intrahepatic bile duct cancer (1). The primary treatment strategy for HCC is resection or liver transplantation; however, only a minority of patients present with resectable disease. Although advances in the treatment of HCC have resulted in prolonged survival of patients, the incidence of recurrence or extrahepatic metastasis associated with HCC has also risen (2). This aggressive cancer has a high recurrence rate, predominantly in the residual liver following hepatectomy. The recurrence rate following resection is 50% at 2 years and 75% at 5 years (3). The incidence of extrahepatic recurrence of HCC has been reported to be 14.0–25.8% (4). Patients with extrahepatic metastasis have a poor prognosis. Current managements for these patients are oral administration of sorafenib and possibly transarterial chemoembolization for the hepatic tumors if the patient has sufficient remaining liver function (5). The most frequent metastatic sites are the lungs, lymph nodes, bones and adrenal glands (6). Metastases in the mediastinum are rare, particularly under the arch of the aorta. The present study reports the case of a patient presenting with hoarseness caused by lymph node metastasis of HCC under the arch of aorta.

Case report

A 30-year-old male patient who presented with hoarseness and back pain for 2 months was admitted to the Department of Hepatopancreatobiliary Surgery, The Affiliated Tumor Hospital of Xinjiang Medical University (Urumqi, China) in August 2014. The patient had undergone right hepatic lobectomy for HCC 2 years before (in November 2013), and received transarterial lipiodol (lipiodol plus doxorubicin and cisplatin) chemoembolization 4 times one month after the resection in The First Affiliated Hospital of Xinjiang Medical University (Urumqi, China). A medical history revealed that the patient had been diagnosed with hepatitis B 14 years prior to admission, and had been undergoing treatment with entecavir (1 tablet/day) for 2 years (since November 2011) at his local hospital. Physical examination revealed enlarged, bilateral supraclavicular masses. The level of α-fetoprotein in the blood was elevated to 25.75 ng/ml (normal levels, <13.40 ng/ml), serum hepatitis B surface antigen was positive and hepatitis B virus DNA levels were 1,640 copies/ml (normal range, 5×102-5×107 copies/ml) (7). All other laboratory test results were normal. A computed tomography scan of the chest and upper abdomen showed intrahepatic recurrence, and multiple enlarged lymph nodes in the bilateral clavicular regions, mediastinum and peritoneum (Fig. 1). The enlarged lymph node found under the arch of the aorta was considered to have invaded the left recurrent laryngeal nerve, causing the hoarseness (Fig. 1C). Percutaneous aspiration biopsy of the enlarged, right supraclavicular lymph node identified malignant cells consistent with HCC by hematoxylin and eosin staining (Fig. 2). The multiple lymph node metastases complicated with intrahepatic recurrence were unsuitable for resection or radiofrequency ablation, but the patient was administered radiotherapy (20 Gy/10 times) in October 2013); back pain was relieved as a result. However, despite the use of recombinant human interleukin 11, the patient exhibited a decrease in platelet count from 128×109 cells/l to 70×109 cells/l (normal range, 125×109-350×109 cells/l), which indicated radiation intolerance. The patient refused sorafenib treatment on cost grounds and was discharged from the hospital. The patient succumbed to disease 4 months after radiotherapy. Written informed consent was obtained from the patients wife for the publication of the patients information.

Figure 1. Abdominal and chest computed tomography scans showing abnormal masses in the liver, clavicular region, mediastinum and peritoneal lymph nodes. (A) Liver mass (arrow). (B) Multiple enlarged lymph nodes in bilateral clavicular regions (arrows). (C) Enlarged mediastinum lymph nodes (small arrow) and a particularly enlarged lymph node under the arch of the aorta (big arrow). (D) Enlarged peritoneal lymph node (arrow).

Figure 2. Histopathological examination of the enlarged, right supraclavicular lymph node revealed the presence of malignant cells (hematoxylin and eosin stain; magnification, ×400).

Discussion

Lymph node metastasis of HCC is closely associated with poor survival and a high risk of tumor recurrence. Although cases with mediastinal lymph node metastasis of HCC have been reported (8–11), to the best of our knowledge, the present study describes the first case of hoarseness caused by lymph node metastasis. In the present case, a pathological examination of the enlarged, right supraclavicular lymph node identified malignant cells consistent with HCC.

The treatment options for extrahepatic metastases developing after hepatic resection of HCC are limited. Regional lymph node dissection should always be performed to determine the stage of the tumor. Hepatic resection with regional lymphadenectomy is a safe procedure for patients with HCC (12), with a systematic review recommending routine lymph node dissection in patients with HCC at the time of resection (13). Experience suggests that a solitary lymph node metastasis from HCC can be treated surgically if there is no evidence of recurrence in other regions (14). Radiofrequency ablation is also effective and may be safely applied to retroperitoneal metastatic HCC lymph nodes (15). However, the majority of extrahepatic lymph node metastases of HCC are multiple and are not suitable for resection or radiofrequency ablation, as was the case with the present patient.

HCC is known as a radiosensitive tumor, and an increasing number of reports underline the efficacy of radiotherapy in the management of HCC (16–18); however, the application of radiotherapy in patients with HCC is limited due to the poor radiation tolerance of the normal liver to local control doses and the varied locations of the tumors. Recent improvements in radiation therapy delivery techniques have provided novel tools to treat patients with extrahepatic metastasis. Patients with intact liver function and without associated symptoms were found to have the most favorable prognosis out of all patients undergoing radiotherapy for lymph node metastasis from HCC (19). In a previous study, a major response to a radiation dose of ≥45 Gy was observed, with a dose-response relationship determined for local control radiotherapy (20). In the present case, following the administration of 20 Gy radiation, the patient presented with a decrease in platelet count, which indicated radiation intolerance, despite relief of the symptom of pain following treatment. Thus, stereotactic body radiation therapy should be applied under strict conditions with the expertise of radiation oncology departments.

Sorafenib has also been shown to be effective in the treatment of patients with advanced or metastatic HCC (21,22); however, it is only indicated for patients with well-preserved liver function (Child-Pugh A class) and advanced stage tumors (Barcelona Clinic Liver Cancer C) or tumors that progress upon locoregional treatment (23,24). Despite well-preserved liver function, the present patient refused to receive sorafenib therapy on cost grounds.

In conclusion, the treatment options for extrahepatic metastasis of HCC are limited. The provision of careful follow-up and the control of extrahepatic recurrence following treatment are important for improving the quality of life and prognosis of HCC patients with extrahepatic metastases. Further studies are required to develop standard treatments that achieve this, including systemic adjuvant chemotherapy and radiotherapy.

References