Thyroid metastasis in a patient with hepatocellular carcinoma: case report and review of literature
© Liang et al; licensee BioMed Central Ltd. 2007
Received: 18 June 2007
Accepted: 24 December 2007
Published: 24 December 2007
Despite the apparent low incidence of cancer metastatic to the thyroid, autopsy and clinical series suggest it is more common than generally. Although lung, renal, and breast cancer are probably the most common primary sites, a number of cancers have been reported to metastasize to the thyroid synchronously with diagnosis of primary tumor or years after apparently curative treatment.
We report a rare case of a hepatocellular carcinoma metasatic to the thyroid. The patient presented seven months after original diagnosis and treatment with hepatic lobectomy with multiple neck lesions producing a mass effect on the trachea and bilateral lymphadenopathy. Fine-needle aspiration revealed highly anaplastic carcinoma, and immunohistochemistry confirmed hepatocellular carcinoma. The patient received total thyroidectomy as palliative therapy because of the presence of multiple recurrent lesions in the liver.
Clinicians should consider the possibility of metastatic cancer in each patient who presents with a new thyroid mass, especially those with a history of cancer, however remote. In cases where cytology or histology is not diagnostic, immunohistochemistry may be definitive in making the diagnosis.
Although metastatic disease in the thyroid is infrequently seen, both autopsy and clinical series indicate the problem is more common than generally thought. Autopsy series on patients with cancer have yielded incidence rates ranging from 1.25% to as high as 24%, and some authors have suggested that the incidence of metastatic disease in the thyroid may have risen during the twentieth century [1, 2]. Recent reports suggest that the most common primary sites are the kidney, lung, breast, and gastrointestinal tract [1–7]. However, a wide variety of cancers may metastasize to the thyroid, including nasopharyngeal carcinoma, choriocarcinoma, osteosarcoma , leiyomyosarcoma, liposarcoma , melanoma , and tumors of neuroendocrine origin [6, 8].
Our clinical experience with a patient whose hepatocellular carcinoma (HCC) metastasized to the thyroid led to a review of the literature, where three other cases involving HCC were identified [9, 10]. Discussion of these cases highlights possible difficulties in evaluating these patients, ranging from making the diagnosis to evaluating thyroid disease in the context of the patient's condition in order to make treatment decisions and determine prognosis. Our experience in Asia allows us to see differences in the clinical profile of thyroid metastasis compared with that in Western countries; this may be useful to physicians who see patients from various parts of the world.
A 54-year-old man was admitted for weight loss, upper abdominal distension with a palpable mass, and epigastric pain for one month. Dull pain had worsened and the abdominal mass had become increasingly evident for the preceding week. His history was remarkable for Hepatitis B infection for more than 20 years. Physical examination was negative for spider angioma, shifting dullness, jaundice or scleral icterus, hand flapping tremor, or thyroid mass. Laboratory data were normal: serum aspartate aminotransferase, 18 IU/L; alanine aminotransferase, 18 IU/L; creatinine, 0.8 mg/dL. Abdominal ultrasonography revealed a mixed echoic mass at level S3–4 (maximum diameter, 9.8 cm), and the entire liver parenchyma had heterogeneous echogenicity. Computed tomography (CT) of the liver revealed multiple foci of heterogeneously enhanced mass lesions. The largest was roughly 8.9 cm × 6.7 cm. Serum alpha-fetoprotein was elevated with a level of 162.4 ng/mL (normal, < 12 ng/ml).
Left hepatic lobectomy was performed two weeks after initial diagnosis, and histopathologic analysis revealed a moderately to poorly differentiated HCC. The cut surface revealed a well-defined, tan-white, firm tumor measuring 8.4 cm × 6.5 cm × 5.5 cm with obvious necrosis. The tumor directly invaded the liver capsule and was adherent to fat on the anterior superior surface. The surgical margin was 1 cm from the tumor and microscopically negative for tumor cells. Intraoperatively, two well-defined, black spongy tumors measuring up to 2 cm in diameter were noted near the main tumor mass. No liver cirrhosis, cholestasis, or portal vein thrombosis was seen.
Microscopically, the tumor featured cells growing in solid nests and a pseudoglandular, as well as a focal trabecular pattern. Individual cells showed marked nuclear pleomorphism and prominent nucleoli with abundant eosinophilic granular cytoplasm and frequent mitotic figures. There was extensive fibrosis and necrosis. Perineural invasion was found near the hilum, but no invasion of blood or lymphatic vessels was evident. Mucicarmine stain was negative for mucin in the carcinoma. In scattered areas, cells were immunochemically positive for cytokeratin (CK) 7 and negative for CK 20. The two small black and spongy tumors were typical of cavernous hemangioma. No liver cirrhosis was noted. After complete pathologic examination, the patient's pTNM stage according to the AJCC Cancer Staging Manual (6th Edition)  was pT1N0M0 (solitary tumor without vascular invasion).
Metastatic thyroid cancer may be more common than primary thyroid malignancy, especially in patients who have a history of cancer . A variety of presentations, from neck masses felt by the patient to nodular goiters discovered on physical examination have been reported, as have lesions revealed on imaging studies [1, 2, 7, 9, 12]. Our patient's presentation with multiple nodules, bilateral lymphadenopathy, and dysphagia and dyspnea, strongly suggested advanced local or metastatic cancer. In light of the patient's recurrent HCC and results of fine needle aspiration of the thyroid lesion, both the surgeon and pathologist believed it more likely the thyroid mass represented metastatic HCC than a primary neoplasm. Total thyroidectomy with regional lymph node dissection was performed and pathological examination confirmed the diagnosis of metastatic HCC. A previous case report of HCC metastatic to the thyroid indicates that a markedly different clinical picture can develop with the same primary neoplasm. In this case, an elderly man had no history of cancer presented with a single neck mass that moved with swallowing, which could well have been primary thyroid cancer .
Hematogenous and lymphogenous pathways for metastasis to the thyroid have been suggested . Although one would consider hematogenous metastasis via a major vein would be most likely with HCC, it is possible that our patient had lymphogenous metastasis, with disease spreading to one or more nodes before spreading to the thyroid gland itself. Only a series of cases with careful imaging and pathologic evaluation will determine which route of metastasis is more common with HCC.
Fine needle aspiration is often used to obtain tissue for analysis; however, it may be difficult to distinguish primary from metastatic disease in instances when cells are highly anaplastic . In the case reported by Masuda et al , fine needle aspirate cytology was not diagnostic, and a core needle biopsy was obtained. The tissue showed histological architecture resembling a hepatocellular cord and positive immunostaining for alpha-fetoprotein. The primary tumor was discovered on abdominal imaging.
The use of immunohistochemistry has allowed far more undifferentiated cancers to be correctly identified than was possible in 1960, when Elliott and Frantz published their paper on metastatic carcinomas 'masquerading' as primary thyroid cancers . Because only 20% to 30% of anaplastic thyroid carcinomas are positive for thyroid markers such as thyroglobulin, it is important to be aware of any previous malignancies so appropriate marker staining can be done . In our case, the thyroid sample was negative for TTF-1, CK 7, and CK 20, but positive for alpha-fetoprotein, which is relatively specific for HCC, although of low sensitivity . A report on use of immunohistochemistry to differentiate several malignancies, including HCC, that are difficult to distinguish by histology and cytology noted that negative stain results for anaplastic cytology may not be informative in identifying the site of origin, and biopsy should be considered .
We concur with the recommendation made by several previous authors that all patients with a history of cancer, however remote, should be evaluated for possible metastasis when a new thyroid lesion is discovered [2, 7]. In our review of the literature, metastases appeared 15 years [1, 7], 16 years , 24 years , and 42 years  after the diagnosis of the primary cancer (the last two cases were renal cell carcinoma and colorectal carcinoma primaries, respectively). We also agree with Lam and Lo , who compared cases of Chinese and Japanese patients with those from the West and concluded that differences in primary sites between Western and Eastern countries probably reflect incidence rates of cancers in a region rather than different biological behavior.
Knowledge of an individual patient's personal and family history, as well as region of origin, may be very useful in determining what immunostains to perform for patients with unknown primary tumor and highly anaplastic thyroid metastasis. Patients with widely disseminated cancer have poor prognoses, but patients with a single thyroid metastasis may have improved quality of life and longer survival if the correct diagnosis is made and treated accordingly.
thyroid transcription facter-1.
We thank Elizabeth Coolidge-Stolz, MD, for her assistance in finalizing the text of our manuscript, with work done at our expense.
Written informed consent was obtained from the patient for publication of this case report
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