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Moray micro forceps biopsy improves the diagnosis of specific pancreatic cysts
Author(s) -
Zhang M. Lisa,
Arpin Ronald N.,
Brugge William R.,
Forcione David G.,
Basar Omer,
Pitman Martha B.
Publication year - 2018
Publication title -
cancer cytopathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.29
H-Index - 57
eISSN - 1934-6638
pISSN - 1934-662X
DOI - 10.1002/cncy.21988
Subject(s) - gnas complex locus , medicine , cyst , intraductal papillary mucinous neoplasm , mucinous cystadenoma , serous fluid , serous cystadenoma , biopsy , carcinoembryonic antigen , atypia , pathology , adenocarcinoma , cystadenocarcinoma , cystadenoma , kras , radiology , pancreas , cancer , colorectal cancer , biology , biochemistry , gene
BACKGROUND Making a specific diagnosis of pancreatic cysts preoperatively is difficult. The new disposable Moray micro forceps biopsy (MFB) device allows tissue sampling from the pancreatic cyst wall/septum and aims to improve diagnosis. This study compares the diagnostic performance of the MFB with the current conventional analysis of pancreatic cyst fluid (PCF). METHODS A total of 48 patients sampled with MFB were identified. Cysts were classified as mucinous on PCF based on extracellular mucin/mucinous epithelium, carcinoembryonic antigen (CEA) levels ≥192 ng/mL, or KRAS/GNAS mutation. A diagnosis of intraductal papillary mucinous neoplasm was supported by GNAS mutation; a diagnosis of serous cystadenoma was supported by Von Hippel‐Lindau tumor suppressor ( VHL ) mutation. A diagnosis of mucinous cystic neoplasm required the presence of subepithelial ovarian‐type stroma. A high‐risk cyst was defined as a mucinous cyst with high‐grade dysplasia or an adenocarcinoma. Comparisons in diagnostic performance between PCF and MFB were made. RESULTS The mean age of the patients was 69.6 years (range, 27‐90 years); 25 of 48 patients (52.1%) were female. Cysts were in the pancreatic head (13 patients), neck (2 patients), body (20 patients), and tail (13 patients), averaging 3.1 cm (range, 1.2‐6.0 cm). There was concordance with mucinous versus nonmucinous classification (60.4% for PCF vs 58.3% for MFB; P = .949). Three high‐risk cysts were detected by PCF and 2 were detected by MFB ( P = .670). However, MFB diagnosed significantly more specific cysts compared with PCF (50.0% for MFB vs 18.8% for PCF; P <.001). CONCLUSIONS PCF analysis and MFB have comparable performance in distinguishing between mucinous and nonmucinous cysts and for detecting high‐risk cysts. However, MFB was found to be superior for diagnosing specific cyst subtypes, thus adding significant value to preoperative patient management. Cancer Cytopathol 2018;126:414‐20. © 2018 American Cancer Society .

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