Right trisectionectomy for liver metastasis of granulosa cell tumor: a case report and literature review.

Granulosa cell tumor Late recurrence Liver metastasis Right trisectionectomy

Journal

Surgical case reports
ISSN: 2198-7793
Titre abrégé: Surg Case Rep
Pays: Germany
ID NLM: 101662125

Informations de publication

Date de publication:
03 Jun 2020
Historique:
received: 07 04 2020
accepted: 20 05 2020
entrez: 5 6 2020
pubmed: 5 6 2020
medline: 5 6 2020
Statut: epublish

Résumé

Granulosa cell tumor (GCT) is a type of ovarian sex cord-stromal tumor with low-grade malignancy, which can recur long after primary resection. All reports on GCTs in the liver describe cases of metastases, while there are no previous reports of primary GCTs originating from the liver. We report a case of GCT, with recurrence of liver metastasis long after ovariectomy, which was subsequently resected by a right trisectionectomy. A 76-year-old woman presented with a history of surgical resection of an ovarian tumor performed 30 years previously; no details of the tumor were available. When she was 68 years old, an abdominal ultrasound revealed a small liver mass, which was diagnosed as a hepatic hemangioma with slow growth. Outpatient follow-up was discontinued for 5 years, and the patient was not examined again until the age of 76 years. At this point, the tumor had substantially increased in size, and surgical resection was required owing to suspicion of malignancy. The patient was then referred to our hospital. Contrast-enhanced computed tomography (CT) showed a large tumor, approximately 18 cm in size, occupying the right lobe and medial section of the liver. After percutaneous transhepatic portal vein embolization, a right trisectionectomy was performed. The histopathological findings of the resected specimen showed that the tumor cells had "coffee bean-like" nuclear grooves, which are characteristic of a GCT. Acidophilic non-structural Call-Exner bodies were also observed. Inhibin-α, CD99, and CD56 markers of sex cord-stromal tumors were detected on immunohistological examination; all pathology suggested a GCT. We considered the tumor to be a liver metastasis of a previous ovarian GCT that was resected 30 years prior by ovariectomy. There was no recurrence for > 15 months after the hepatectomy. We report a case of a GCT in the liver, which was identified to be a liver metastasis. Right trisectionectomy was subsequently performed for tumor resection. Clinicians should be aware that ovarian GCTs may recur in the liver, and that GCT recurrence may occur long after ovariectomy of the primary ovarian GCT.

Sections du résumé

BACKGROUND BACKGROUND
Granulosa cell tumor (GCT) is a type of ovarian sex cord-stromal tumor with low-grade malignancy, which can recur long after primary resection. All reports on GCTs in the liver describe cases of metastases, while there are no previous reports of primary GCTs originating from the liver. We report a case of GCT, with recurrence of liver metastasis long after ovariectomy, which was subsequently resected by a right trisectionectomy.
CASE PRESENTATION METHODS
A 76-year-old woman presented with a history of surgical resection of an ovarian tumor performed 30 years previously; no details of the tumor were available. When she was 68 years old, an abdominal ultrasound revealed a small liver mass, which was diagnosed as a hepatic hemangioma with slow growth. Outpatient follow-up was discontinued for 5 years, and the patient was not examined again until the age of 76 years. At this point, the tumor had substantially increased in size, and surgical resection was required owing to suspicion of malignancy. The patient was then referred to our hospital. Contrast-enhanced computed tomography (CT) showed a large tumor, approximately 18 cm in size, occupying the right lobe and medial section of the liver. After percutaneous transhepatic portal vein embolization, a right trisectionectomy was performed. The histopathological findings of the resected specimen showed that the tumor cells had "coffee bean-like" nuclear grooves, which are characteristic of a GCT. Acidophilic non-structural Call-Exner bodies were also observed. Inhibin-α, CD99, and CD56 markers of sex cord-stromal tumors were detected on immunohistological examination; all pathology suggested a GCT. We considered the tumor to be a liver metastasis of a previous ovarian GCT that was resected 30 years prior by ovariectomy. There was no recurrence for > 15 months after the hepatectomy.
CONCLUSIONS CONCLUSIONS
We report a case of a GCT in the liver, which was identified to be a liver metastasis. Right trisectionectomy was subsequently performed for tumor resection. Clinicians should be aware that ovarian GCTs may recur in the liver, and that GCT recurrence may occur long after ovariectomy of the primary ovarian GCT.

Identifiants

pubmed: 32494954
doi: 10.1186/s40792-020-00880-3
pii: 10.1186/s40792-020-00880-3
pmc: PMC7270424
doi:

Types de publication

Journal Article

Langues

eng

Pagination

125

Références

Cancer. 2014 Feb 1;120(3):344-51
pubmed: 24166194
Gynecol Oncol. 2001 Nov;83(2):400-4
pubmed: 11606104
Eur J Gynaecol Oncol. 2001;22(3):187-93
pubmed: 11501769
Gynecol Oncol. 2007 Oct;107(1):30-8
pubmed: 17583777
HPB Surg. 1996;10(1):55-7
pubmed: 9187554
Int J Surg Oncol. 2018 Mar 29;2018:4547892
pubmed: 29796312
Surg Gynecol Obstet. 1967 Jan;124(1):65-70
pubmed: 6015796
J Gynecol Oncol. 2011 Sep;22(3):214-7
pubmed: 21998767
Indian J Surg Oncol. 2013 Mar;4(1):37-47
pubmed: 24426698
South Asian J Cancer. 2017 Apr-Jun;6(2):87-88
pubmed: 28702418
Patient Saf Surg. 2018 Jun 4;12:15
pubmed: 29881460
Gynecol Oncol. 2012 Feb;124(2):244-9
pubmed: 22019525
Hum Pathol. 2005 Feb;36(2):195-201
pubmed: 15754297
Eur J Gynaecol Oncol. 2010;31(3):342-4
pubmed: 21077485
J Ovarian Res. 2018 Dec 14;11(1):100
pubmed: 30547828
Int J Surg Case Rep. 2015;12:7-10
pubmed: 25979613
Oncol Lett. 2015 Feb;9(2):816-818
pubmed: 25621056
Gynecol Oncol. 2005 Jan;96(1):235-40
pubmed: 15589608
Surgery. 2012 Jun;151(6):851-9
pubmed: 22306838
J Clin Oncol. 2007 Jul 10;25(20):2944-51
pubmed: 17617526

Auteurs

Itsuki Koganezawa (I)

Department of Digestive and Transplantation Surgery, Tokyo Medical University Hachioji Medical Center, 1163 Tatemachi, Hachiojishi, Tokyo, 193-0998, Japan.

Koichi Tomita (K)

Department of Digestive and Transplantation Surgery, Tokyo Medical University Hachioji Medical Center, 1163 Tatemachi, Hachiojishi, Tokyo, 193-0998, Japan.

Masashi Nakagawa (M)

Department of Digestive and Transplantation Surgery, Tokyo Medical University Hachioji Medical Center, 1163 Tatemachi, Hachiojishi, Tokyo, 193-0998, Japan.

Yosuke Ozawa (Y)

Department of Digestive and Transplantation Surgery, Tokyo Medical University Hachioji Medical Center, 1163 Tatemachi, Hachiojishi, Tokyo, 193-0998, Japan.

Toshimichi Kobayashi (T)

Department of Digestive and Transplantation Surgery, Tokyo Medical University Hachioji Medical Center, 1163 Tatemachi, Hachiojishi, Tokyo, 193-0998, Japan.

Toru Sano (T)

Department of Digestive and Transplantation Surgery, Tokyo Medical University Hachioji Medical Center, 1163 Tatemachi, Hachiojishi, Tokyo, 193-0998, Japan.

Rina Tsutsui (R)

Department of Digestive and Transplantation Surgery, Tokyo Medical University Hachioji Medical Center, 1163 Tatemachi, Hachiojishi, Tokyo, 193-0998, Japan.

Naokazu Chiba (N)

Department of Digestive and Transplantation Surgery, Tokyo Medical University Hachioji Medical Center, 1163 Tatemachi, Hachiojishi, Tokyo, 193-0998, Japan.

Akira Okimura (A)

Department of Diagnostic Pathology, Tokyo Medical University Hachioji Medical Center, 1163 Tatemachi, Hachiojishi, Tokyo, 193-0998, Japan.

Munehide Nakatsugawa (M)

Department of Diagnostic Pathology, Tokyo Medical University Hachioji Medical Center, 1163 Tatemachi, Hachiojishi, Tokyo, 193-0998, Japan.

Hiroshi Hirano (H)

Department of Diagnostic Pathology, Tokyo Medical University Hachioji Medical Center, 1163 Tatemachi, Hachiojishi, Tokyo, 193-0998, Japan.

Shigeyuki Kawachi (S)

Department of Digestive and Transplantation Surgery, Tokyo Medical University Hachioji Medical Center, 1163 Tatemachi, Hachiojishi, Tokyo, 193-0998, Japan. skawachi@tokyo-med.ac.jp.

Classifications MeSH