Intrabiliary growth type of metastasis from colon cancer, 12 years after curative colectomy: a case report.


Journal

BMC surgery
ISSN: 1471-2482
Titre abrégé: BMC Surg
Pays: England
ID NLM: 100968567

Informations de publication

Date de publication:
18 Jan 2019
Historique:
received: 13 06 2018
accepted: 27 12 2018
entrez: 20 1 2019
pubmed: 20 1 2019
medline: 26 2 2019
Statut: epublish

Résumé

Liver is a common location of colorectal metastasis, but intrabiliary growth of liver metastasis is not well recognized. Furthermore, intrabiliary metastasis that discovered over 10 years after excision has rarely been described. An 80-year-old man was admitted due to the presence of a liver mass in segment 5 (S5) concomitant with elevated carcinoembryonic antigen (CEA), and carbohydrate antigen (CA) 19-9. He underwent right hemicolectomy for colon cancer 12 years prior. Enhanced computed tomography (CT) showed dilated bile ducts with periductal enhancement in S5; hence, cholangiocarcinoma was suspected. Upon anterior segmentectomy, we observed that the cut surface of the specimen exhibited a yellowish-white tumor within the bile ducts. Histologically, the tumor formed within the papillary process, extended along the lumen, and replaced the normal bile duct epithelium. Immunohistochemical studies showed that the liver tumor and primary colon cancer were negative for cytokeratin (CK) 7 and positive for CK20 and Caudal-type homeobox transcription factor 2 (CDX-2). In addition, both tumors showed a same KRAS mutation. We diagnosed the liver tumor as liver metastasis recurrence from colon cancer. Intrabiliary growth type of metastasis (IGM) is difficult to distinguish from cholangiocarcinoma, and sometimes develops long after surgery; thus, careful examination of a patient's history is needed in such cases.

Sections du résumé

BACKGROUND BACKGROUND
Liver is a common location of colorectal metastasis, but intrabiliary growth of liver metastasis is not well recognized. Furthermore, intrabiliary metastasis that discovered over 10 years after excision has rarely been described.
CASE PRESENTATION METHODS
An 80-year-old man was admitted due to the presence of a liver mass in segment 5 (S5) concomitant with elevated carcinoembryonic antigen (CEA), and carbohydrate antigen (CA) 19-9. He underwent right hemicolectomy for colon cancer 12 years prior. Enhanced computed tomography (CT) showed dilated bile ducts with periductal enhancement in S5; hence, cholangiocarcinoma was suspected. Upon anterior segmentectomy, we observed that the cut surface of the specimen exhibited a yellowish-white tumor within the bile ducts. Histologically, the tumor formed within the papillary process, extended along the lumen, and replaced the normal bile duct epithelium. Immunohistochemical studies showed that the liver tumor and primary colon cancer were negative for cytokeratin (CK) 7 and positive for CK20 and Caudal-type homeobox transcription factor 2 (CDX-2). In addition, both tumors showed a same KRAS mutation. We diagnosed the liver tumor as liver metastasis recurrence from colon cancer.
CONCLUSION CONCLUSIONS
Intrabiliary growth type of metastasis (IGM) is difficult to distinguish from cholangiocarcinoma, and sometimes develops long after surgery; thus, careful examination of a patient's history is needed in such cases.

Identifiants

pubmed: 30658608
doi: 10.1186/s12893-018-0466-4
pii: 10.1186/s12893-018-0466-4
pmc: PMC6339384
doi:

Substances chimiques

CDX2 Transcription Factor 0
CDX2 protein, human 0

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

8

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Auteurs

Shin Sasaki (S)

Department of Surgery, Kurume University School of Medicine, 67 Asahi-machi, Kurume, 8300011, Japan. sasaki_shin@med.kurume-u.ac.jp.
Division of Hepatobiliary and Pancreatic Surgery, Department of Surgery, Kurume University School of Medicine, 67 Asahi-machi, Kurume, 8300011, Japan. sasaki_shin@med.kurume-u.ac.jp.

Yoriko Nomura (Y)

Department of Surgery, Kurume University School of Medicine, 67 Asahi-machi, Kurume, 8300011, Japan.

Shogo Fukutomi (S)

Department of Surgery, Kurume University School of Medicine, 67 Asahi-machi, Kurume, 8300011, Japan.

Nobuhisa Shirahama (N)

Department of Surgery, Kurume University School of Medicine, 67 Asahi-machi, Kurume, 8300011, Japan.

Hironori Kusano (H)

Department of Pathology, Kurume University School of Medicine, 67 Asahi-machi, Kurume, 8300011, Japan.

Jun Akiba (J)

Department of Diagnostic Pathology, Kurume University Hospital, 67 Asahi-machi, Kurume, 8300011, Japan.

Hisamune Sakai (H)

Department of Surgery, Kurume University School of Medicine, 67 Asahi-machi, Kurume, 8300011, Japan.

Toru Hisaka (T)

Department of Surgery, Kurume University School of Medicine, 67 Asahi-machi, Kurume, 8300011, Japan.

Osamu Nakashima (O)

Clinical Laboratory, Kurume University Hospital, 67 Asahi-machi, Kurume, 8300011, Japan.

Hirohisa Yano (H)

Department of Pathology, Kurume University School of Medicine, 67 Asahi-machi, Kurume, 8300011, Japan.

Yoshito Akagi (Y)

Department of Surgery, Kurume University School of Medicine, 67 Asahi-machi, Kurume, 8300011, Japan.

Hiroyuki Tanaka (H)

Department of Surgery, Kurume University School of Medicine, 67 Asahi-machi, Kurume, 8300011, Japan.

Koji Okuda (K)

Department of Surgery, Kurume University School of Medicine, 67 Asahi-machi, Kurume, 8300011, Japan.

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Classifications MeSH