Ann Hepatobiliary Pancreat Surg.  2018 May;22(2):164-168. 10.14701/ahbps.2018.22.2.164.

Multidisciplinary approach for treatment of primary hepatic choriocarcinoma in adult male patient

Affiliations
  • 1Department of Hematology-Oncology, Gangneung Asan Hospital, University of Ulsan College of Medicine, Gangneung, Korea.
  • 2Department of Surgery, Gangneung Asan Hospital, University of Ulsan College of Medicine, Gangneung, Korea. pskys74@hanmail.net
  • 3Department of Pathology, Gangneung Asan Hospital, University of Ulsan College of Medicine, Gangneung, Korea.
  • 4Department of Surgery, Division of Hepatobiliary Surgery and Liver Transplantation, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.

Abstract

Choriocarcinoma is a rare malignant germ cell tumor and it usually occurs in the gonads (ovary or testis) and uterus. Primary hepatic choriocarcinoma (PHC) is a variant of choriocarcinoma featuring sole liver presentation without any evidence of gonodal involvements. Adult male patients with PHC carry dismal prognosis and their median survival period was less than 5 months. We herein present a first Korean case of a 54-year-old male patient with adult PHC, who was treated by surgical resection and chemotherapy through a multidisciplinary approach.

Keyword

Liver; Choriocarcinoma; Surgery; Chemotherapy

MeSH Terms

Adult*
Choriocarcinoma*
Drug Therapy
Female
Gonads
Humans
Liver
Male*
Middle Aged
Neoplasms, Germ Cell and Embryonal
Pregnancy
Prognosis
Uterus

Figure

  • Fig. 1 Pre- and postoperative computed tomography (CT) scan findings. Preoperative CT scan showed that the initial tumor diameter was 6.3 cm (A). The size of the main tumor increased to 11 cm after 3 weeks (B), and new nodules (arrow) were found on the right and left lobes in the same CT scan (C and D); CT scan taken 1 week after surgery showed increase in the sizes of the remnant tumors (arrows) to up to 2.5 cm (E and F); Follow-up CT after chemotherapy showed a decrease in the size of the remnant multiple tumors (arrows) to achieve partial response by RECIST (G and H).

  • Fig. 2 Pathological findings. Gross appearance showed the multilobulated hemorrhagic mass with extracapsular mass extension (arrows) (A); Biphasic pleomorphic cells of cytotrophoblasts and syncytiotrophoblasts (arrow), and hemorrhage and necrosis (arrowhead) were observed (H&E stain, ×200) (B); Diffuse expression of β-hCG was identified in immunohistochemistry staining (×200) (C).


Cited by  1 articles

Primary Hepatic Choriocarcinoma with Pregnancy: A Diagnostic and Therapeutic Challenge
Amith Kumar Pakkala, Phani Kumar Nekarakanti, Bheerappa Nagari, Ashish Kumar Bansal, Gourang Shroff, Megha S Uppin
Korean J Gastroenterol. 2023;81(2):91-94.    doi: 10.4166/kjg.2022.116.


Reference

1. Fernández Alonso J, Sáez C, Pérez P, Montaño A, Japón MA. Primary pure choriocarcinoma of the liver. Pathol Res Pract. 1992; 188:375–377. discussion 378–379. PMID: 1626001.
Article
2. Arai M, Oka K, Nihei T, Hirota K, Kawano H, Kawasaki T, et al. Primary hepatic choriocarcinoma: a case report. Hepatogastroenterology. 2001; 48:424–426. PMID: 11379323.
3. Sekine R, Hyodo M, Kojima M, Meguro Y, Suzuki A, Yokoyama T, et al. Primary hepatic choriocarcinoma in a 49-year-old man: report of a case. World J Gastroenterol. 2013; 19:9485–9489. PMID: 24409080.
Article
4. Eisenhauer EA, Therasse P, Bogaerts J, Schwartz LH, Sargent D, Ford R, et al. New response evaluation criteria in solid tumours: revised RECIST guideline (version 1.1). Eur J Cancer. 2009; 45:228–247. PMID: 19097774.
Article
5. Scholz M, Zehender M, Thalmann GN, Borner M, Thoni H, Studer UE. Extragonadal retroperitoneal germ cell tumor: evidence of origin in the testis. Ann Oncol. 2002; 13:121–124. PMID: 11863093.
Article
6. Fine G, Smith RW Jr, Pachter MR. Primary extragenital choriocarcinoma in the male subject. Case report and review of the literature. Am J Med. 1962; 32:776–794. PMID: 13892927.
7. Bakhshi GD, Borisa AD, Bhandarwar AH, Tayade MB, Yadav RB, Jadhav YR. Primary hepatic choriocarcinoma: a rare cause of spontaneous haemoperitoneum in an adult. Clin Pract. 2012; 2:e73. PMID: 24765472.
Article
8. Shi H, Cao D, Wei L, Sun L, Guo A. Primary choriocarcinoma of the liver: a clinicopathological study of five cases in males. Virchows Arch. 2010; 456:65–70. PMID: 20013345.
Article
9. Garcia RL, Ghali VS. Gastric choriocarcinoma and yolk sac tumor in a man: observations about its possible origin. Hum Pathol. 1985; 16:955–958. PMID: 4040885.
Article
10. Waseda Y, Komai Y, Yano A, Fujii Y, Noguchi N, Kihara K. Pathological complete response and two-year disease-free survival in a primary gastric choriocarcinoma patient with advanced liver metastases treated with germ cell tumor-based chemotherapy: a case report. Jpn J Clin Oncol. 2012; 42:1197–1201. PMID: 23071288.
Article
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