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Colon metastasis from hepatocellular carcinoma: a case report and literature review
World Journal of Surgical Oncology volume 18, Article number: 189 (2020)
Hepatocellular carcinoma (HCC) is a malignant tumor with frequent intrahepatic metastases; extrahepatic metastases are not rare but less frequent compared to intrahepatic ones. The most frequent sites of extrahepatic metastases are the lungs, followed by the lymph nodes, bones, and adrenal glands. Case report covering gastrointestinal (GI) tract involvement from HCC is limited.
A 60-year-old man was referred to us in May 2019 with a diagnosis of sigmoid colon tumor. The patient had a history of HCC and had received two stages of open resections for the primary and the abdominal metastasis successively and many times of transcatheter arterial chemoembolization (TACE). The sigmoid colon tumor received Hartmann procedure after abdominal enhanced computerized tomography (CT) scan and colonoscopy, while postoperative pathology and immunohistochemistry identified it as extrahepatic colonic metastasis from HCC.
The ratio of extrahepatic metastasis to the digestive tract was very low, and the majority was upper gastrointestinal involvement because of direct invasion or intraperitoneal implantation. TACE may be the risk factor of retrograde hematogenous metastasis to the downstream colon.
Hepatocellular carcinoma; Extrahepatic metastases; Colon metastasis; Transcatheter arterial chemoembolization
Hepatocellular carcinoma (HCC) is a highly malignant tumor all over the world and is also a global disease with high mortality. With the largest population of hepatitis B infections, China has the greatest number of primary liver cancer, and the incidence rate is 26.67/100,000; that is over 373,000 new cases per year, of which 80% are HCC . Extrahepatic metastases are less frequent than intrahepatic ones with the incidence reported between 13.5–42% of metastasis cases . The most frequent extrahepatic metastatic sites are the lungs, followed by the lymph nodes, bones, and adrenal glands, while gastrointestinal (GI) tract involvement is rare among these extrahepatic metastases. Case report covering GI involvement from HCC was limited and in lack of comprehensive analysis. We report a rare case of extrahepatic metastasis of the colon from HCC and review the related literature on the disease.
A 60-year-old man, who had hematochezia for 45 days, was referred to our department of colorectal surgery on May 15, 2019. He was diagnosed with sigmoid colon tumor after colonoscopy showed a protuberant mass occupying the lumen with stenosis, 30 cm proximal to the anus. The patient had a history of hepatitis B since 1979 and was treated by Traditional Chinese Medicine (TCM) only. He was first rushed to hospital in emergency in 2009 with the complaint of right upper abdominal pain for 7 h. After a CT scan, he was confirmed to have the rupture and hemorrhage due to liver cancer, as well as cirrhosis and splenomegaly. Right hepatectomy was performed, and postoperative pathology showed a moderately differentiated hepatocellular carcinoma 65 × 31 × 61 mm in size with nodular cirrhosis, but the status of the lymphatic or vascular involvement was not reported by then. After the surgery, entecavir was prescribed by a hepatologist to control the hepatitis B virus (HBV) infection. In October 2010, intrahepatic nodules were found during regular follow-up and treated by interventional therapy. In April 2013, arterial blood supply appeared in two nodules near the diaphragmatic surface of the right lobe of the liver when doing magnetic resonance imaging (MRI) follow-up, and transcatheter arterial chemoembolization (TACE) was used. In August 2013, anti-HBV treatment was restarted when HBV-DNA copy soared to 3.46 × 105 IU/ml. For the coming four and a half years, no signs of recurrence or metastasis was found until February 2018, when the patient felt a growing mass on the left side of the abdomen, and his alpha-fetoprotein (AFP) level went up to as high as 5.00 × 104 ng/ml. CT scans considered the mass in his left middle abdomen to be an intraperitoneal implantation metastasis, 200 × 150 mm in size, and MRI also showed an intrahepatic metastasis in the infero-posterior segment of the right lobe of the liver. TACE was again implemented to treat intrahepatic metastasis followed by abdominal tumor resection. HCC with moderate and low differentiation associated with hemorrhage and necrosis was the pathological diagnosis. Immunohistochemistry revealed positive expression of AFP and hepatocyte, and negative in carcinoembryonic antigen (CEA). In May 2018, 3 months after the surgery, another intrahepatic metastasis was detected by MRI. In order to eliminate the focus and any possible micro-metastasis, radiofrequency ablation and TACE were performed successively in the case of adequate liver function reservation. In November 2018, the patient’s AFP level gradually rose to 2.91 × 103 ng/ml, and MRI showed enhanced blood supply to the subcapsular lesion at the upper posterior segment of the right lobe of the liver, which was considered to be a recurrence. Ultrasound-guided percutaneous radiofrequency ablation (PRFA) was carried out, as well as TACE 3 weeks after that. Recovering from those therapies, the patient began to take Sorafenat (400 mg, twice a day) as targeted therapy for 4 months, and then replaced by regorafenib (160 mg, once a day, last for 3 weeks, every 4 weeks repeat) at the end of March 2019 because of continuously rising AFP level. Programmed cell death protein 1 (PD-1) inhibitor toripalimab injection was added as an immunotherapy in April 2019.
At this admission, abdominal enhanced CT revealed a thickened sigmoid wall with adjacent nodules (Fig. 1), as well as a nodule in the right lobe of the liver. The patient’s AFP level was 2.10 × 104 ng/ml which was extremely high during his whole history. Chest CT scan showed a nodule in the dorsal segment of the lower lobe of the left lung, 13 mm in diameter, which was first considered to be a metastasis. The patient received enterolysis and Hartmann procedure (tumor resection and descending colostomy) on May 17, 2019. During the operation, we found a large endogenic mass of the colon, a relatively smooth serous layer (Fig. 2a, b) and clean intraperitoneal conditions. The operation was successful, and the intraoperative bleeding volume was about 20 ml. The postoperative pathological diagnosis was poorly differentiated adenocarcinoma accumulating in the whole intestinal wall, positive in vascular thrombosis, negative in nerve invasion, and no metastasis was found in 17 peri-intestinal lymph nodes. The distal, proximal, and circumferential cutting edges were all negative, while two cancerous nodules were observed (Figs. 3 and 4). Further immunohistochemical testing clarified the hepatocellular origin from the positive expression of heat shock protein 70 (HSP70), AFP and B-catenin, and negative expression of caudal-related homeobox transcription factor 2 (CDX-2) and eytokertin-20 (CK-20), with antigen Ki67 (Ki-67(+)) 80% (Figs. 5 and 6). The patient had recovered smoothly without any complications and was discharged on May 27. He continued taking toripalimab injection every 3 weeks since June 8, and TACE was performed again on June 12 to cure the nodule in the liver. Entecavir tablets were prescribed to anti-HBV virus by a hepatologist synchronously. Besides monthly blood tests of the tumor marker and HBV-DNA copy, he was also told to have enhanced abdominal CT and liver MRI every 3 months. The recent follow-up in August 2019 showed no signs of recurrence or metastasis in both the abdomen and liver. The AFP level also fell to 1.33 × 103ng/ml from 2.10 × 104ng/ml. Chest CT scan indicated that the pulmonary nodule was smaller than before.
HCC is a highly malignant tumor with a high rate of metastasis. Extrahepatic metastases are less frequent than intrahepatic ones with the incidence reported between 13.5–42% of metastasis cases. Uka et al.  investigated 151 patients with extrahepatic metastases from 995 HCC patients followed up regularly, and found that extrahepatic metastases were most frequently seen in the lungs (47%), lymph nodes (45%), bones (37%), and adrenal glands (12%), and most of them were even asymptomatic, which could only be found by autopsy. The ratio of extrahepatic metastases to the GI tract was extremely low (0.7%), only one case of colon metastasis detected from autopsy. Lin et al.  found 11 GI tract metastases of 2237 HCC patients at their hospital during more than 9 years. Chen et al.  collected 396 patients with HCC between the year 1982 to 1988 in their hospital, and identified 8 cases (2%) with secondary involvement of the GI tract, but no colon metastasis case was included (3 stomach, 4 duodenum, 1 jejunum, and 1 unknown). Terada et al.  found only 1 case of colon involvement as unusual extrahepatic metastatic sites among 52 extrahepatic metastasis cases in both autopsy (n = 31) and surgery (n = 21). Some studies also showed a low rate of GI involvement from HCC of about 4–12%, though not so low as in the previous ones [6, 7]. Case report covering GI involvement from HCC was limited (Table 1). Among all these cases, the most possible metastatic way is direct invasion, so upper GI is its favorite target organ, such as the stomach and duodenum. Chen et al.  also warned the doctors of direct invasion of the GI tract after regional treatment such as transcatheter arterial embolization (TAE) because of inflammatory response and adhesion to the liver or tumor capsule. Tumor thrombi will also result in metastasis to the stomach via the portal system. Upper GI bleeding is the most common symptom, and some massive bleeding may be followed by coma which can be regarded as a terminal episode of the disease . Besides GI bleeding, abdominal pain, intussusception, and intestinal obstruction are also common manifestations in these patients.
Compared to the upper GI tract, the colon and the rectum are much more rare locations for HCC metastases owing to the indirect position to the liver and upper stream of venous backflow. Ou et al.  searched MEDLINE database and listed 8 reports including patients with colonic metastasis from HCC in recent years and revealed that ascending and transverse colons were the most frequent sites in direct invasion as they were more adjacent to the primary region than any other parts of the colon. Intraperitoneal implantation is the most possible way for this kind of metastasis. That means the metastatic tumor will first deposit in the serous membrane surrounding the intestinal wall, and the mucous membrane is the last layer for the tumor to spread. The mass may compress or encase the intestines when it grows. So it is unusual to see the integrity lesion inside the intestinal cavity by colonoscopy. Yoo et al.  once reported such a case, and no tumor could be seen through colonoscopy but a bulging contoured mass. It was different in our case. At first, we did not realize the tumor in the sigmoid colon to be an extrahepatic metastasis from HCC because of the obvious mass growing in the colon wall which could be easily recognized by colonoscopy. During the operation, we still believed it to be a typical colon cancer because of the relatively smooth serous layer and clean intraperitoneal conditions. The tumor grew as large as 90 × 70 × 25 mm, and the way of metastasis remained unknown, neither from direct invasion nor from intraperitoneal implantation. Hematogenous metastasis was the only possible way, which might explain the source of the mass. Hu et al.  studied seven stomach involvement cases of 8267 HCC patients and found that patients with cirrhosis and/or portal vein thrombosis were more vulnerable to hematogenous pathway gastric metastasis when having TAE treatment because of portal hypertension. Kohli et al.  also reported a patient with cryptogenic cirrhosis suffering from splenic flexure metastasis from HCC after liver transplantation due to hematogenous metastasis. Our patient received TACE four times before sigmoid colon tumor resection, so we boldly hypothesized that TACE might increase the portal venous pressure inducing the blood to flow backward to the colon through inferior mesenteric vein, which finally formed that huge metastatic lesion.
HCC patients with advanced primary tumor stage (T3, T4) are at high risk of developing extrahepatic metastases, and on the other hand, most GI metastases are found in patients with advanced stage HCC [2, 9]. Though there is no standard guideline, surgical intervention should be practiced to relieve the symptoms or treat life-threatening GI metastases under the circumstances that the patient has good physical condition and adequate hepatic reserve. According to Fujii et al. , the median survival time of HCC patients with GI tract invasion treated by surgical resection is longer than those who receive nonsurgical and supportive treatment, but this result probably has bias because the latter ones may give up surgery on account of their late disease staging or poor physical condition. Multivariate analysis revealed that younger age, normal alpha fetoprotein, single site of extrahepatic disease, local treatment to the primary tumor, and surgery to the metastatic disease were associated with better overall survival and liver cancer-specific survival . Though surgery, to some extent, can improve the survival of HCC patients with extrahepatic metastases, the prognosis of these patients is still poor. The median survival of HCC patients with colonic metastasis was only 2.5 months , which was even shorter than 8.1 months in patients with other extrahepatic metastasis . GI bleeding is the most common complication, and in some serious cases may lead to death directly. Bowel obstruction is another life-threatening consequence such as the one in our case. For sure, surgery cannot cure the disease, but it may relieve the symptoms and prolong overall survival.
Patients who have had a history of HCC with high AFP level initially diagnosed with colorectal cancer should be considered extrahepatic metastases from HCC as well. Direct invasion, intraperitoneal implantation, and hematogenous metastasis are the most possible ways for the tumor to spread. TACE/TAE will raise the portal venous pressure, which may cause retrograde hematogenous metastases to the downstream colon. Though HCC patients with colon metastasis have very poor prognosis, surgery is an effective way to relieve the symptoms and prolong overall survival.
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All data and material are fully available without restriction.
Magnetic resonance imaging
Transcatheter arterial chemoembolization
Hepatitis B virus
Percutaneous radiofrequency ablation
Transhepatic arterial embolization
WJ Wang, XL Zhang. Cancer in China: the status quo and burden of disease, DRC Research Report, Special Issue, No.26, 2019 (Total 1654) 2019-4-18.
Uka K, Aikata H, Takaki S, Shirakawa H, Jeong SC, Yamashina K, et al. Clinical features and prognosis of patients with extrahepatic metastases from hepatocellular carcinoma. World J Gastroenterol. 2007;13(3):414–20.
Lin CP, Cheng JS, Lai KH, Lo GH, Hsu PI, Chan HH, et al. Gastrointestinal metastasis in hepatocellular carcinoma: radiological and endoscopic studies of 11 cases. J Gastroenterol Hepatol. 2000;15:536–41.
Chen LT, Chen CY, Jan CM, Wang WM, Lan TS, Hsieh MY, et al. Gastrointestinal tract involvement in hepatocellular carcinoma: clinical, radiological and endoscopic studies. Endoscopy. 1990;22(3):118–23.
Terada T, Marou H. Unusual extrahepatic metastatic sites from hepatocellular carcinoma. Int J Clin Exp Pathol. 2013;6(5):816–20.
Nakashima T, Okuda K, Kojiro M, Jimi A, Yamaguchi R, Sakamoto K, et al. Pathology of hepatocellular carcinoma in Japan. 232 consecutive cases autopsied in ten years. Cancer. 1983;51:863–77.
Anthony PP. Primary carcinoma of the liver: a study of 282 cases in Ugandan Africans. J Pathol. 1973;110:37–48.
Zhu XM, Lou Z, He J, Sui JK, Ma J, Gong HF, et al. Hematogenous transverse colon metastasis from primary hepatocellular carcinoma. Int J Colorectal Dis. 2016;31:1241–2.
Yoo DJ, Chung YH, Lee YS, Kim SE, Jin YJ, Lee YM, et al. Sigmoid colon metastasis from hepatocellular carcinoma. The Korean Journal of Hepatology. 2010;16:397–400. https://doi.org/10.3350/kjhep.2010.16.4.397.
Igawa A, Oka S, Tanaka S, Nakano M, Aoyama T, Watari I, et al. Small bowel metastasis of hepatocellular carcinoma detected by capsule endoscopy. Case Rep Gastroenterol. 2013;7:492–7.
SF Huang, JW Chou, HC Lai. A rare cause of bloody stools in a 57-year-old woman with hepatocellular carcinoma. Gastroenterology, 2011;140(2), e5–e6. doi:10.1053.
Nozaki Y, Kobayashi N, Shimamura T, Akiyama T, Inamori M, Iida H, et al. Colonic metastasis from hepatocellular carcinoma: manifested by gastrointestinal bleeding. Dig Dis Sci. 2008;53:3265–6.
Tapuria N, Sinha CK, Michael NG, Fisher PW. Hematogenous metastasis to ascending colon in a patient with hepatocellular carcinoma and autoimmune hepatitis. Eur J Gastroenterol Hepatol. 2007;19:607–9.
Ruhail Kohli, Andrei S. Purysko, Binu V. John. Hematochezia from metastasis of hepatocellular carcinoma to colon in a patient who underwent liver transplantation. Clinical Gastroenterology and Hepatology, 2014;12:xxiii–xxiv.
Ou TM, Tsai WC, Hsieh TY, Shih YL. Hepatocellular carcinoma with colonic metastasis. Singapore Med J. 2014;55(6):e93–5.
Kanazawa M, Sugaya T, Tominaga K, Takahashi F, Takenaka K, Nakano M, et al. Jejunal metastasis from hepatocellular carcinoma. Intern Med. 2018;57:947–50.
Iwaki K, Ohta M, Ishio T, Kai S, IWashita Y, Shibata K, et al. Metastasis of hepatocellular carcinoma to spleen and small intestine. J Hepatobiliary Pancreat Surg. 2008;15:213–9.
Yang PM, Sheu JC, Yang TH, Chen DS, Yu JY, Lee CS, et al. Metastasis of hepatocellular carcinoma to the proximal jejunum manifested by occult gastrointestinal bleeding. Am J Gastroenterol. 1987 Feb;82(2):165–7.
Cosenza CA, Sher LS, Poletti BJ, Tschirhart D, Noguchi H, Hoffman AL, et al. Metastasis of hepatocellular carcinoma to the right colon manifested by gastrointestinal bleeding. Am Surg. 1999 Mar;65(3):218–21.
Kim HS, Shin JW, Kim GY, Kim YM, Cha HJ, Jeong YK, et al. Metastasis of hepatocellular carcinoma to the small bowel manifested by intussusception. World J Gastroenterol. 2006;12(12):1969–71.
Hirashita T, Ohta M, Iwaki K, Kai S, Shibata K, Sasaki A, et al. Direct invasion to the colon by hepatocellular carcinoma: report of two cases. World J Gastroenterol. 2008;14:4583–5.
Sung JL, Wang TH, Yu JY. Clinical study on primary carcinoma of the liver in Taiwan. Am J Dig Dis. 1967;12(10):1036–49.
Hu ML, Tai WC, Chuah SK, Chiu YC, Wu KL, Chou YP, et al. Gastric metastasis of hepatocellular carcinoma via a possible existing retrograde hematogenous pathway. J Gastroenterol Hepatol. 2010;25(2):408–12.
Fujii K, Nagino M, Kamiya J, Uesaka K, Sano T, Yuasa N, et al. Complete resection of hepatocellular carcinoma with direct invasion to the stomach remnant. J Hepatobiliary Pancreat Surg. 2004;11:441–4.
Oweira H, Petrausch U, Helbling D, Schmidt J, Mehrabi A, Schöb O, et al. Prognostic value of site-specific extra-hepatic disease in hepatocellular carcinoma: a SEER database analysis. Expert Rev Gastroenterol Hepatol. 2017;11(7):695–701.
Uchino K, Tateishi R, Shiina S, Kanda M, Masuzaki R, Kondo Y, et al. Hepatocellular carcinoma with extrahepatic metastasis: clinical features and prognostic factors. Cancer. 2011;117:4475–83.
The authors thank Xiao-Han Shen, MD, from Ningbo Pathological Diagnosis Center, for assistance with the pathology images.
Ningbo Natural Science Foundation, China(Grant No.2018A610368).
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The study was approved by the Ethics Committee of HwaMei Hospital, University of Chinese Academy of Sciences.
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Yu, Y., Cao, Y., Wu, Z. et al. Colon metastasis from hepatocellular carcinoma: a case report and literature review. World J Surg Onc 18, 189 (2020). https://doi.org/10.1186/s12957-020-01960-2