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von Meyenburg complexes are more frequently associated with cholangiocarcinoma.
Jain, Dhanpat; Khandakar, Binny; Ni, Pu; Kenney, Barton; Qin, Lihui; Deshpande, Vikram; Fiel, Maria Isabel.
Afiliação
  • Jain D; Department of Pathology, Yale School of Medicine, New Haven, Connecticut, USA dhanpat.jain@yale.edu.
  • Khandakar B; Department of Pathology and Laboratory Medicine, Donald Barbara Zucker School of Medicine at Hofstra/Northwell, Manhasset, New York, USA.
  • Ni P; Department of Pathology, Molecular and Cell-Based Medicine, Icahn School of Medicine at Mount Sinai, New York City, New York, USA.
  • Kenney B; Department of Pathology, Middlesex Health, Middletown, Connecticut, USA.
  • Qin L; Department of Pathology, Weill Cornell Medical College, New York City, New York, USA.
  • Deshpande V; Department of Pathology, Harvard Medical School, Boston, Massachusetts, USA.
  • Fiel MI; Department of Pathology, Molecular and Cell-Based Medicine, Icahn School of Medicine at Mount Sinai, New York City, New York, USA.
J Clin Pathol ; 2024 May 10.
Article em En | MEDLINE | ID: mdl-38729770
ABSTRACT

AIM:

There is some evidence that von Meyenburg complexes (VMCs) can progress to cholangiocarcinoma (CC). This study aimed to evaluate the prevalence of VMCs in CC cases.

METHODS:

All hepatic resections and explants with intra-hepatic CC (I-CC) and hilar-CC (H-CC) from 1985 to 2020 were studied. Hepatic resections (n=68) for benign lesions or metastatic colonic carcinoma and 15 cases with cirrhosis without any cancer were used as controls.

RESULTS:

A total of 118 cases of CC (88 I-CC, 30 H-CC) were identified. Of these, 61 (52%) patients had no known background liver disease, and 20 (17%) had cirrhosis. Associated liver disorders included metabolic dysfunction-associated steatohepatitis (23), chronic viral hepatitis B or C (13), biliary disease (primary or secondary sclerosing cholangitis) (8), polycystic kidney disease (6), cryptogenic cirrhosis (5) and others miscellaneous disorders (7). VMCs were present in 34 (39%) of 88 I-CC cases and 7 (23%) of 30 H-CC cases. VMCs were present within the tumour (20 cases), outside the cancer (21 cases) or at both locations (10 cases). VMCs with dysplasia/carcinoma in situ were seen in 19 of 41 (46%) cases with CC and VMCs. In addition, bile duct adenomas were identified in 6 (5%) of CC. 7% of controls showed the presence of VMCs compared with 35% of CC cases (p<0.05).

CONCLUSIONS:

VMCs are seen far more frequently in patients with CC than in the control group. The findings support the hypothesis that VMCs could represent a precursor of CC or a marker for a higher risk of developing CC.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article