A rare intrahepatic splenosis mimicking hepatocellular carcinoma: A case report.

intrahepatic splenosis liver tumor splenectomy trauma

Journal

Molecular and clinical oncology
ISSN: 2049-9469
Titre abrégé: Mol Clin Oncol
Pays: England
ID NLM: 101613422

Informations de publication

Date de publication:
Nov 2023
Historique:
received: 02 06 2023
accepted: 11 08 2023
medline: 19 10 2023
pubmed: 19 10 2023
entrez: 19 10 2023
Statut: epublish

Résumé

Intrahepatic splenosis (IHS) is a rare disease that is considered to result from heterotopic autotransplantation or implantation of splenic tissue after splenic trauma or surgery. A 46-year-old man with a treatment history of a left lateral liver segmentectomy and splenectomy for a road traffic injury 30 years earlier presented to Sakai City Medical Center (Sakai, Japan) with acute abdominal pain in November 2019. Physical examination showed no significant signs, and serum data were normal. Computed tomography revealed a hypodense mass measuring 2.5x1.7 cm in segment 7 of the liver. Gadoxetic acid-enhanced magnetic resonance imaging showed early enhancement in the arterial phase and washout in the delayed phase. Therefore, laparoscopic surgery was performed with a preoperative diagnosis of hepatocellular carcinoma. Pathological examination of the tumor showed IHS. The postoperative course was uneventful, and the patient developed no new abnormal region in the liver during 2 years of follow-up. The present study presented a case of IHS assumed to be hepatocellular carcinoma. IHS should be considered as a differential diagnosis of a liver mass detected years after splenic trauma or surgery, even in cases with imaging patterns suggesting malignancy.

Identifiants

pubmed: 37854327
doi: 10.3892/mco.2023.2687
pii: MCO-19-5-02687
pmc: PMC10580247
doi:

Types de publication

Case Reports

Langues

eng

Pagination

91

Informations de copyright

Copyright © 2023, Spandidos Publications.

Déclaration de conflit d'intérêts

The authors declare that they have no competing interests.

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Auteurs

Issei Umeda (I)

Department of Gastroenterological Surgery, Sakai City Medical Center, Sakai, Osaka 593-8304, Japan.
Department of Gastroenterological Surgery, Kindai University Hospital, Osaka-sayama, Osaka 589-8511, Japan.

Hideo Tomihara (H)

Department of Gastroenterological Surgery, Sakai City Medical Center, Sakai, Osaka 593-8304, Japan.

Sakae Maeda (S)

Department of Gastroenterological Surgery, Sakai City Medical Center, Sakai, Osaka 593-8304, Japan.

Akihiro Kitagawa (A)

Department of Gastroenterological Surgery, Sakai City Medical Center, Sakai, Osaka 593-8304, Japan.

Kana Miyamoto (K)

Department of Gastroenterological Surgery, Sakai City Medical Center, Sakai, Osaka 593-8304, Japan.

Ryohei Kawabata (R)

Department of Gastroenterological Surgery, Sakai City Medical Center, Sakai, Osaka 593-8304, Japan.

Kazuhiro Nishikawa (K)

Department of Gastroenterological Surgery, Sakai City Medical Center, Sakai, Osaka 593-8304, Japan.

Shingo Noura (S)

Department of Gastroenterological Surgery, Sakai City Medical Center, Sakai, Osaka 593-8304, Japan.

Yumiko Yasuhara (Y)

Department of Pathology and Laboratory, Sakai City Medical Center, Sakai, Osaka 593-8304, Japan.

Atsushi Miyamoto (A)

Department of Gastroenterological Surgery, Sakai City Medical Center, Sakai, Osaka 593-8304, Japan.

Classifications MeSH