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review of literature on clinical pancreatology - The Pancreapedia

review of literature on clinical pancreatology - The Pancreapedia

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which is essential in tumor and nodal staging <str<strong>on</strong>g>of</str<strong>on</strong>g> gastrointestinal cancers. In the recentdecade, however, many therapeutic applicati<strong>on</strong>s <str<strong>on</strong>g>of</str<strong>on</strong>g> EUS have become possible. Currently,interventi<strong>on</strong>al EUS endoscopy involves celiac plexus neurolysis, pseudocyst drainage, andintratumoral fine-needle injecti<strong>on</strong> therapy for inoperable pancreatic malignancy. Emergingtechniques include the accurate endoscopic delivery <str<strong>on</strong>g>of</str<strong>on</strong>g> radioactive beads to localize tumortherapy as well as other therapies, such as radi<str<strong>on</strong>g>of</str<strong>on</strong>g>requency ablati<strong>on</strong> or cryotherapy.Diagnostic and therapeutic access to the biliary tree and pancreatic duct is increasingly beingused successfully in failed endoscopic retrograde cholangiopancreatography (ERCP)procedures. A <str<strong>on</strong>g>review</str<strong>on</strong>g> discusses these procedures and several evolving future applicati<strong>on</strong>s,including vascular access and EUS-guided enteral anastomosis [420].<strong>The</strong> role <str<strong>on</strong>g>of</str<strong>on</strong>g> EUS to evaluate subtle radiographic abnormalities <str<strong>on</strong>g>of</str<strong>on</strong>g> the pancreas is not welldefined. To assess the yield <str<strong>on</strong>g>of</str<strong>on</strong>g> EUS + FNA for focal or diffuse pancreaticenlargement/fullness seen <strong>on</strong> abdominal CT scan in the absence <str<strong>on</strong>g>of</str<strong>on</strong>g> discrete mass lesi<strong>on</strong>s aretrospective database <str<strong>on</strong>g>review</str<strong>on</strong>g> <str<strong>on</strong>g>of</str<strong>on</strong>g> 691 pancreatic EUS exams were <str<strong>on</strong>g>review</str<strong>on</strong>g>ed. Sixty-nine metinclusi<strong>on</strong> criteria <str<strong>on</strong>g>of</str<strong>on</strong>g> having been performed for focal enlargement or fullness <str<strong>on</strong>g>of</str<strong>on</strong>g> the pancreas.Known chr<strong>on</strong>ic pancreatitis, pancreatic calcificati<strong>on</strong>s, acute pancreatitis, discrete mass <strong>on</strong>imaging, pancreatic duct dilati<strong>on</strong> (greater than 4 mm) and obstructive jaundice wereexcluded. FNA was performed in 19/69 (28 %) with 4 new diagnoses <str<strong>on</strong>g>of</str<strong>on</strong>g> pancreaticadenocarcinoma, <strong>on</strong>e metastatic renal cell carcinoma, <strong>on</strong>e metastatic col<strong>on</strong> cancer, <strong>on</strong>echr<strong>on</strong>ic pancreatitis and 12 benign results. Eight patients had discrete mass lesi<strong>on</strong>s <strong>on</strong> EUS;two were cystic. All malignant diagnoses had a discrete solid mass <strong>on</strong> EUS. It was c<strong>on</strong>cludedthat pancreatic enlargement/fullness is <str<strong>on</strong>g>of</str<strong>on</strong>g>ten a benign finding related to anatomic variati<strong>on</strong>,but was related to malignancy in 9 percent <str<strong>on</strong>g>of</str<strong>on</strong>g> these patients (6/69). EUS should be str<strong>on</strong>glyc<strong>on</strong>sidered as the next step in the evaluati<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g> patients with focal enlargement <str<strong>on</strong>g>of</str<strong>on</strong>g> thepancreas when <strong>clinical</strong> suspici<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g> malignancy exists [421].Hyperechogenic pancreas suggestive <str<strong>on</strong>g>of</str<strong>on</strong>g> fatty replacement is a comm<strong>on</strong> finding duringendoscopic ultrasound. Recent data have implicated pancreatic steatosis as a risk factor forpancreatitis and pancreatic malignancy. Hepatic steatosis has been linked to obesity,increased age, hypertriglyceridemia, hyperglycemia, and hyperinsulinemia. <strong>The</strong> objective <str<strong>on</strong>g>of</str<strong>on</strong>g><strong>on</strong>e study was to evaluate the effect <str<strong>on</strong>g>of</str<strong>on</strong>g> body mass index (BMI), hepatic steatosis, and othermetabolic risk factors <strong>on</strong> HP seen <strong>on</strong> EUS. Patients with hyperechogenic pancreas wereidentified by a <str<strong>on</strong>g>review</str<strong>on</strong>g> <str<strong>on</strong>g>of</str<strong>on</strong>g> a structured EUS database. <strong>The</strong> degree <str<strong>on</strong>g>of</str<strong>on</strong>g> echogenicity was judgedrelative to the liver (or spleen if the liver is hyperechogenic) at a similar depth. Variousdemographic and metabolic risk factors were assessed. Chr<strong>on</strong>ic pancreatitis was excludedbased <strong>on</strong> normal findings <strong>on</strong> prior imaging studies. Each case was age matched and sexmatched to 1 c<strong>on</strong>trol with a normal pancreas <strong>on</strong> EUS. By multivariate logistic regressi<strong>on</strong>analysis, BMI, hepatic steatosis, and alcohol use in excess <str<strong>on</strong>g>of</str<strong>on</strong>g> 14 g/wk were highly associatedwith the presence <str<strong>on</strong>g>of</str<strong>on</strong>g> hyperechogenic pancreas compared with c<strong>on</strong>trols. Hepatic steatosiswas the str<strong>on</strong>gest predictor with an odds ratio <str<strong>on</strong>g>of</str<strong>on</strong>g> nearly 14-fold [422].Endoscopic ultrasound-guided fine-needle aspirati<strong>on</strong> biopsiEndoscopic ultrasound-guided fine needle aspirati<strong>on</strong> (EUS-FNA) is an effective method forproviding tissue diagnosis, but problems occur when lesi<strong>on</strong>s are small or the cytologicaldiagnosis is indeterminate. To prospectively evaluate the utility <str<strong>on</strong>g>of</str<strong>on</strong>g> EUS-FNA in patients withsmall solid pancreatic lesi<strong>on</strong>s and those with initial indeterminate or negative cytologicaldiagnosis a total <str<strong>on</strong>g>of</str<strong>on</strong>g> 119 EUS-FNA procedures <strong>on</strong> 46 patients (mean age 56 years) for 47small solid pancreatic lesi<strong>on</strong>s (range 7-30 mm, mean 17 mm in diameter) were studied.FNAs were performed in the presence <str<strong>on</strong>g>of</str<strong>on</strong>g> a cytopathologist. If cytological diagnoses wereindeterminate, EUS-FNA was repeated within 3 weeks. Diagnoses were c<strong>on</strong>firmedhistologically or by follow-up (<strong>clinical</strong> and imaging: EUS + FNA and CT). On average, 3.7passes were performed. It was not observed any complicati<strong>on</strong>s. Initial cytological findingswere: malignant 17 (36 %), benign 21 (45 %), and indeterminate 9 (19 %). Eight (78 %) <str<strong>on</strong>g>of</str<strong>on</strong>g>

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