Background: Accurate risk stratification of pancreatic cystic lesions (PCL) is important in determining the risk/benefit of resection, particularly in pts at increased surgical risk due to advanced age and comorbidities. The current approach utilizing multiple diagnostic modalities is limited. Review of surgical specimens from resected pancreatic cystic neoplasms shows characteristic morphology of the interior of these lesions, with “sponge-like” microcystic areas in serous cystadenomas, smooth pale walls with adherent mucin in mucinous lesions and side-branch orifices in side-branch IPMN. We considered the idea that in-vivo examination of the interior of a cyst with a fiberoptic probe could help classify PCLs and possibly detect small neoplastic mural lesions not seen by EUS. Methods: We used a 0.77 mm optical probe (SpyGlass, Boston Scientific) introduced via 19 Ga needle (Echotip, Wilson-Cook). The needle was inserted into the cyst under EUS. The cyst fluid was aspirated completely and the fluid sent for analysis. Saline was infused into the cyst, repeated until the aspirate was clear. The following data were collected: technical success, duration, image quality (poor, adequate, excellent), wall morphology, fluid characteristics, and complications. Results: 5 pts (three men), of median age 78 (77-85) with one pancreatic cyst each were included in the study. Two cysts were in the head, one in the body, and one in the tail of the pancreas. The median diameter of the cysts was 25 mm (17-50). The mean duration of the Spyglass examination was 11 min (6-16). Image quality was poor in 1, adequate in 2 and excellent in 2 examinations. The optical probe detected lesions not seen by EUS in 2 of the 5 pts. In Pt 1 a small yellow nodule was seen on the posterior cyst wall covered with mucin, not visible on CT or previous EUS, on which we performed FNA. Cytology revealed carcinoma, surgical pathology showed IPMN with CIS, with a focus of microinvasion. In Pt 2 the optical probe showed a tan polypoid lesion arising from an otherwise smooth pale wall of the cyst. Cytology revealed reactive epithelial cells staining for CEA. CEA 13,354, amylase 370. In Pts 3 and 4, the optical probe confirmed side-branch IPMN and, in Pt 5, pseudocyst. Conclusion. Our technique allows direct visualization of the interior of pancreatic cysts at the time of EUS/FNA and appears feasible in moderately sized cysts without densely stained fluid, located in the superior head, body and tail. Our results suggest a need to study the utility of this technique in detecting features that may help classify indeterminate cystic lesions and detect small high-grade mural lesions missed by EUS.
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