2021
DOI: 10.1111/vcp.13073
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Needle rinse cell blocks as an ancillary technique: Diagnostic and clinical utility in gastrointestinal neoplasia

Abstract: Background Fine‐needle aspirate (FNA) cytology is often the first‐choice method for diagnosing gastrointestinal nodular lesions. The FNA material can be converted to histopathology specimens by a needle rinse cell block (NRCB) technique, allowing ancillary studies to refine the cytologic diagnosis. Despite use in human pathology, NRCB has never been applied to canine or feline gastrointestinal neoplasia. Objective This study described NRCB methodology and its diagnostic utility in specific cases of neoplastic … Show more

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Cited by 7 publications
(12 citation statements)
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“…Other comparative techniques include gel, cell block, and needle rinse cell block. [1][2][3][4] The resultant tissue architecture and arrangement were very similar to full-thickness biopsy and with the presence of osteoid supporting the diagnosis of osteosarcoma. The interpretation of the initial routine cytology was osteosarcoma or less likely plasma cell tumor.…”
mentioning
confidence: 60%
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“…Other comparative techniques include gel, cell block, and needle rinse cell block. [1][2][3][4] The resultant tissue architecture and arrangement were very similar to full-thickness biopsy and with the presence of osteoid supporting the diagnosis of osteosarcoma. The interpretation of the initial routine cytology was osteosarcoma or less likely plasma cell tumor.…”
mentioning
confidence: 60%
“…With direct aspiration and formalin fixation, similar architecture was maintained when compared to histopathology. Other comparative techniques include gel, cell block, and needle rinse cell block 1–4 . The resultant tissue architecture and arrangement were very similar to full‐thickness biopsy and with the presence of osteoid supporting the diagnosis of osteosarcoma.…”
Section: Introductionmentioning
confidence: 84%
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“…The CB was obtained following the cell tube block technique [ 20 , 21 ]. Briefly, capillary tubes were filled with effusion and needle rinse fluids, sealed with clay, and spun in a microhematocrit centrifuge (12,700 g for 5 min).…”
Section: Methodsmentioning
confidence: 99%