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Metastatic tumors to the pancreas: Balancing clinical impression with cytology findings.
Abdallah, Mohamed A; Bohy, Kimberlee; Singal, Ashwani; Xie, Chencheng; Patel, Bhaveshkumar; Nelson, Morgan E; Bleeker, Jonathan; Askeland, Ryan; Abdullah, Ammar; Aloreidi, Khalil; Atiq, Muslim.
Afiliação
  • Abdallah MA; Department of Internal Medicine, University of South Dakota Sanford School of Medicine, Sioux Falls, SD, United States.
  • Bohy K; Department of Pathology, University of South Dakota Sanford School of Medicine, Sioux Falls, SD, United State.
  • Singal A; Department of Internal Medicine, University of South Dakota Sanford School of Medicine, Sioux Falls, SD, United States.
  • Xie C; Department of Internal Medicine, University of South Dakota Sanford School of Medicine, Sioux Falls, SD, United States.
  • Patel B; Department of Internal Medicine, University of South Dakota Sanford School of Medicine, Sioux Falls, SD, United States.
  • Nelson ME; Department of Internal Medicine, University of South Dakota Sanford School of Medicine, Sioux Falls, SD, United States.
  • Bleeker J; Department of Internal Medicine, University of South Dakota Sanford School of Medicine, Sioux Falls, SD, United States.
  • Askeland R; Department of Pathology, University of South Dakota Sanford School of Medicine, Sioux Falls, SD, United State.
  • Abdullah A; Department of Internal Medicine, University of South Dakota Sanford School of Medicine, Sioux Falls, SD, United States.
  • Aloreidi K; Department of Internal Medicine, University of South Dakota Sanford School of Medicine, Sioux Falls, SD, United States.
  • Atiq M; Department of Internal Medicine, University of South Dakota Sanford School of Medicine, Sioux Falls, SD, United States.
Ann Hepatobiliary Pancreat Surg ; 26(1): 91-97, 2022 Feb 28.
Article em En | MEDLINE | ID: mdl-35168205
ABSTRACT
BACKGROUNDS/

AIMS:

Metastatic lesions of the pancreas (PMET) account for 1%-5% of all malignant solid pancreatic lesions (SPL). In this study we evaluated the utility of endoscopic ultrasonography with fine needle aspiration (EUS-FNA) in diagnosing PMET.

METHODS:

Patients who underwent EUS-FNA at a community referral center between 2011-2017 for SPL were identified. Clinical, radiologic, and EUS-FNA features of those with PMET were compared to those with primary solid tumors of the pancreas pancreatic adenocarcinoma (PDAC) and neuroendocrine tumors (PNET).

RESULTS:

A total of 191 patients were diagnosed with solid pancreatic malignancy using EUS-FNA 156 PDAC, 27 PNET, and eight (4.2%) had PMET. Patients with PMET were less likely to have abdominal pain (25.0% vs. 76.3% vs. 48.2%; p < 0.01) or obstructive jaundice (37.5% vs. 58.3% vs. 0%; p < 0.01) compared to PDAC and PNET. Those with PMET were more likely to have mass lesions with/without biliary or pancreatic ductal dilatations (100% vs. 86.5% vs. 85.2%; p < 0.01) and lower CA19-9 (82.5 ± 43.21 U/mL vs. 4,639.30 ± 11,489.68 U/mL vs. 10.50 ± 10.89 U/mL; p < 0.01) compared to PDAC and PNET. Endosonographic features were similar among all groups. Seven (87.5%) patients with PMET had a personal history of malignancy prior to PMET diagnosis. The primary malignancy was renal cell carcinoma in five PMET.

CONCLUSIONS:

PMET are exceedingly rare, comprising less than 5% of SLP. Patients with PMET are less likely to present with symptoms and mostly identified by surveillance imaging for the primary malignancy.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article