Usefulness of EUS-guided fine needle aspiration biopsy in the diagnosis of suspected or recurring lymphoproliferative disorders. (December 2016)

• Record Type: Journal Article
• Authors: Poincloux, Laurent; André, Morgane; Darcha, Claude; Goutte, Marion; Dapoigny, Michel; Bommelaer, Gilles; Abergel, Armand; Tournilhac, Olivier
• Is Part Of: Surgical oncology. Volume 25:Number 4(2016)
• Page Start: 459
• Page End: 465
• Publication Date: 2016-12
• Subjects: EUS-FNAB -- Lymphoma -- Sub-classification -- Immunohistochemistry; Cancer -- Surgery -- Periodicals; Neoplasms -- surgery -- Periodicals; Cancer -- Chirurgie -- Périodiques; Electronic journals; 616.994059
• DOI: 10.1016/j.suronc.2015.08.007
• Languages: English
• ISSNs: 0960-7404

Abstract

Abstract: Background: EUS-guided fine needle aspiration biopsy (EUS-FNAB) of deep-seated lymphadenopathy is proposed to identify lymphoproliferative disorders when no superficial lesion is accessible. Methods: We analyzed prospectively collected data of 115 EUS-FNABs from 73 thoracic or abdomino-pelvic targets in 52 patients with suspected lymphoproliferative disorders (LPDs) between January 2005 and May 2011 from a single institution. Conventional histology and immunohistochemistry procedures were performed on samples. Results: No complications were recorded. An LPD was identified in 29 cases and ruled out in 21 cases. In 2 cases the analysis was negative, but an LPD was identified using a secondary procedure. For the identification of LPDs irrespective of subtype, this procedure has positive and negative predictive values of 100% and 91.3% respectively, with 93.6% sensitivity and 100% specificity. In 31 patients finally diagnosed with LPDs, an accurate diagnosis meeting the 2008 World Health Organization classification criteria was established in 21 (68%) cases, success being significantly associated with target size above 30 mm in multivariate analysis (odds ratio 7.47; p = 0.05). Conclusion: EUS-FNAB of deep-seated lymphadenopathy with conventional morphological assessment appears to have a high diagnostic value for LPD identification and can obviate invasive surgery. A sub-classification was possible in two thirds of the cases. Highlights: EUS-FNAB presents high diagnostic value in LPD identification. Conventional histology and immunophenotyping enabled LPD subclassification in 68%. EUS-FNAB is safe, quick, and can obviate invasive surgery in LPD. EUS-FNAB could be proposed as first-line diagnosis tool in suspected/recurring LPD.