Evidence map›Paper›PMID 39969684›Full record

Observational studyIndian journal of gastroenterology : official journal of the Indian Society of Gastroenterology2025

EUS FNAC without rapid on-site evaluation is comparable to EUS FNB with macroscopic on-site evaluation in evaluation of intra-abdominal masses.

Mohd Rafiq Najar, Monika Jain, Gurwant Singh Lamba, Sawan Bopanna

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Observational study in Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

4 authors.

Mohd Rafiq NajarCentre for Liver and Gastrosciences, Sri Balaji Action Medical Institute, A4 Block, Paschim Vihar, New Delhi, 110 063, India.
Monika JainCentre for Liver and Gastrosciences, Sri Balaji Action Medical Institute, A4 Block, Paschim Vihar, New Delhi, 110 063, India.
Gurwant Singh LambaCentre for Liver and Gastrosciences, Sri Balaji Action Medical Institute, A4 Block, Paschim Vihar, New Delhi, 110 063, India.
Sawan BopannaCentre for Liver and Gastrosciences, Sri Balaji Action Medical Institute, A4 Block, Paschim Vihar, New Delhi, 110 063, India. sawan_bops2001@yahoo.com.ORCID 0009-0009-5342-7212

Funding

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6 · The paper itself

Abstract

introductionEndoscopic ultrasound-guided tissue acquisition (EUS TA) has become the mainstay for tissue diagnosis of abdominal mass lesions. Two widely used and accepted methods for obtaining diagnostic material, namely fine needle aspiration cytology (EUS FNAC) and needle core biopsy (EUS FNB), have distinct advantages and disadvantages. We compared the diagnostic accuracy of EUS FNAC without on-site pathology and EUS FNB taken within the same endoscopic session in evaluation of intra-abdominal masses.

methodsIn this prospective observational study, we included patients undergoing EUS FNAC and EUS FNB for the diagnosis of solid intra-abdominal masses. Sample size was calculated based on the available literature. Location, origin, dimensions of the intra-abdominal masses and number of passes taken were recorded. EUS-guided FNAC followed by EUS-guided FNB was done back-to-back during the same endoscopic session. FNAC smears were prepared and air dried and alcohol-fixed slides were prepared. Adequacy of the FNB specimen was judged visually. The diagnostic accuracy of FNA and FNB specimens was then calculated based on the final diagnosis and compared.

resultsOf the 58 patients included, 50% of patients were females with a mean age of 53.91 ± 17.16 years. Nineteen pancreatic masses (32.7%), three gastric mass lesions (5.1%), one adrenal mass (1.7%), one liver mass (1.7%), three gallbladder masses (5.1%) and 31 lymph nodal masses (53.4%) were sampled. With EUS FNB, malignancy was diagnosed in 38/58 (65.5%), benign diseases in 19/58 (32.7%) and 1/58 (1.7%) was inconclusive. Number of passes was more in the EUS FNAC group compared to EUS FNB, but not statistically significant. Sensitivity and specificity of EUS FNAC without rapid on-site evaluation (ROSE) were found to be 92.4% and 100%, respectively. Diagnostic accuracy of EUS FNAC was 93.1% and when compared with EUS FNB with macroscopic on-site evaluation (MOSE), no statistically significant difference was noted.

conclusionEUS FNAC and EUS FNB are comparable for the diagnosis of intra-abdominal masses in terms of diagnostic accuracy, sample adequacy, number of passes and safety. In resource-constraint settings, either EUS FNAC or EUS FNB alone may be sufficient for diagnosis with EUS FNB being preferred in select cases where maintained tissue architecture is needed.

Indexed as

Abdominal NeoplasmsEndoscopic Ultrasound-Guided Fine Needle AspirationAdultAgedBiopsy, Large-Core NeedleFemaleHumansMaleMiddle AgedProspective StudiesRapid On-site EvaluationSensitivity and SpecificityEndoscopic ultrasoundFine needle aspiration cytologyFine needle biopsyMacroscopic on-site evaluationRapid on-site evaluation

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.