Clin Endosc.  2024 May;57(3):364-374. 10.5946/ce.2023.095.

Comparison of 19-gauge conventional and Franseen needles for the diagnosis of lymphadenopathy and classification of malignant lymphoma using endoscopic ultrasound fine-needle aspiration

Affiliations
  • 1Department of Gastroenterology, Gifu Municipal Hospital, Gifu, Japan
  • 2Department of Gastroenterological Endoscopy, Kanazawa Medical University, Ishikawa, Japan
  • 3Department of Pathology and Translational Research, Gifu University Graduate School of Medicine, Gifu, Japan
  • 4Department of Diagnostic Pathology, Gifu Municipal Hospital, Gifu, Japan
  • 5Department of Hematology, Gifu Municipal Hospital, Gifu, Japan
  • 6First Department of Internal Medicine, Gifu Univeristy Hospital, Gifu, Japan

Abstract

Background/Aims
Endoscopic ultrasound-guided fine-needle aspiration (EUS-FNA) using a 19-gauge needle is an efficient sampling method for the diagnosis of lymphadenopathy. This study compared 19-gauge conventional and Franseen needles for the diagnosis of lymphadenopathy and classification of malignant lymphoma (ML).
Methods
Patient characteristics, number of needle passes, puncture route, sensitivity, specificity, and accuracy of cytology/histology for lymphadenopathy were analyzed in patients diagnosed with lymphadenopathy by EUS-FNA using conventional or Franseen needles.
Results
Between 2012 and 2022, 146 patients met the inclusion criteria (conventional [n=70] and Franseen [n=76]). The median number of needle passes was significantly lower in the conventional group than in the Franseen group (3 [1–6] vs. 4 [1–6], p=0.023). There were no significant differences in cytological/histological diagnoses between the two groups. For ML, the immunohistochemical evaluation rate, sensitivity of flow cytometry, and cytogenetic assessment were not significantly different in either group. Bleeding as adverse events (AEs) were observed in three patients in the Franseen group.
Conclusions
Both the 19-gauge conventional and Franseen needles showed high accuracy in lymphadenopathy and ML classification. Considering sufficient tissue collection and the avoidance of AEs, the use of 19-gauge conventional needles seems to be a good option for the diagnosis of lymphadenopathy.

Keyword

19-gauge; Endoscopic ultrasound-guided fine-needle aspiration; Franseen needle; Lymphadenopathy; Malignant lymphoma

Figure

  • Fig. 1. The process of lymphadenopathy and malignant lymphoma diagnosis using a 19-gauge conventional or Franseen needle. (A) Endoscopic ultrasound (EUS) fine needle aspiration performed under EUS guidance in Doppler mode. (B) Cytology stained with Giemsa shows small, atypical lymphocytes. Scale bar=20 μm. (C) Histopathology shows a lymphoid follicle consisting of small, atypical lymphocytes. Scale bar=50 μm. (D) Immunohistochemical staining is positive in CD20, CD10, Bcl-2, and negative in CD3. (E) The flow cytometry analysis of this case shows the expression of B-cell lineage antigens (CD10, CD19, and CD20) and immunoglobulin light chains (κ). Scale bar=20 μm. (F) A G-banded karyotyping analysis finds t(14;18)(q32;q21) chromosomal translocation (arrows). (G) The fluorescence in situ hybridization assay of this case indicates a green signal for IGH, a red signal for BCL-2, and a yellow signal (arrows) for a fusion of IGH and BCL-2.

  • Fig. 2. Flowchart of patient selection.

  • Fig. 3. A bleeding case in the Franseen needle group. (A) A 20-mm mediastinum lymphadenopathy (arrow) was detected by computed tomography. (B) The lymphadenopathy was punctured via a transesophageal route using a 19-gauge Franseen needle. (C) Mediastinal enlargement with chest pain was observed one day after puncture test. The vessel (arrowheads) was observed in the hematoma around the lymphadenopathy using contrast computed tomography. (D) Embolization of the vessel was required for hemostasis.


Reference

1. Wani S, Muthusamy VR, Komanduri S. EUS-guided tissue acquisition: an evidence-based approach (with videos). Gastrointest Endosc. 2014; 80:939–959.
Article
2. Yasuda I, Goto N, Tsurumi H, et al. Endoscopic ultrasound-guided fine needle aspiration biopsy for diagnosis of lymphoproliferative disorders: feasibility of immunohistological, flow cytometric, and cytogenetic assessments. Am J Gastroenterol. 2012; 107:397–404.
Article
3. Itoi T, Tsuchiya T, Itokawa F, et al. Histological diagnosis by EUS-guided fine-needle aspiration biopsy in pancreatic solid masses without on-site cytopathologist: a single-center experience. Dig Endosc. 2011; 23 Suppl 1:34–38.
Article
4. Bang JY, Hawes R, Varadarajulu S. A meta-analysis comparing ProCore and standard fine-needle aspiration needles for endoscopic ultrasound-guided tissue acquisition. Endoscopy. 2016; 48:339–349.
Article
5. Yasuda I, Tsurumi H, Omar S, et al. Endoscopic ultrasound-guided fine-needle aspiration biopsy for lymphadenopathy of unknown origin. Endoscopy. 2006; 38:919–924.
Article
6. Mukai S, Itoi T, Yamaguchi H, et al. A retrospective histological comparison of EUS-guided fine-needle biopsy using a novel franseen needle and a conventional end-cut type needle. Endosc Ultrasound. 2019; 8:50–57.
Article
7. Sugimoto M, Irie H, Takagi T, et al. Efficacy of EUS-guided FNB using a Franseen needle for tissue acquisition and microsatellite instability evaluation in unresectable pancreatic lesions. BMC Cancer. 2020; 20:1094.
Article
8. de Moura DT, McCarty TR, Jirapinyo P, et al. EUS-guided fine-needle biopsy sampling versus FNA in the diagnosis of subepithelial lesions: a large multicenter study. Gastrointest Endosc. 2020; 92:108–119.
Article
9. Itonaga M, Yasukawa S, Fukutake N, et al. Comparison of 22-gauge standard and Franseen needles in EUS-guided tissue acquisition for diagnosing solid pancreatic lesions: a multicenter randomized controlled trial. Gastrointest Endosc. 2022; 96:57–66.
Article
10. Swerdlow SH, Campo E, Pileri SA, et al. The 2016 revision of the World Health Organization classification of lymphoid neoplasms. Blood. 2016; 127:2375–2390.
Article
11. Facciorusso A, Crinò SF, Muscatiello N, et al. Endoscopic ultrasound fine-needle biopsy versus fine-needle aspiration for tissue sampling of abdominal lymph nodes: a propensity score matched multicenter comparative study. Cancers (Basel). 2021; 13:4298.
Article
12. Hedenström P, Chatzikyriakos V, Shams R, et al. High sensitivity of endoscopic ultrasound-guided fine-needle aspiration and endoscopic ultrasound-guided fine-needle biopsy in lymphadenopathy caused by metastatic disease: a prospective comparative study. Clin Endosc. 2021; 54:722–729.
Article
13. de Moura DT, McCarty TR, Jirapinyo P, et al. Endoscopic ultrasound fine-needle aspiration versus fine-needle biopsy for lymph node diagnosis: a large multicenter comparative analysis. Clin Endosc. 2020; 53:600–610.
Article
14. Farinha P, Gascoyne RD. Molecular pathogenesis of mucosa-associated lymphoid tissue lymphoma. J Clin Oncol. 2005; 23:6370–6378.
Article
15. Nadel B, Marculescu R, Le T, et al. Novel insights into the mechanism of t(14;18)(q32;q21) translocation in follicular lymphoma. Leuk Lymphoma. 2001; 42:1181–1194.
Article
16. Le Gouill S, Talmant P, Touzeau C, et al. The clinical presentation and prognosis of diffuse large B-cell lymphoma with t(14;18) and 8q24/c-MYC rearrangement. Haematologica. 2007; 92:1335–1342.
Article
17. Camacho FI, García JF, Cigudosa JC, et al. Aberrant Bcl6 protein expression in mantle cell lymphoma. Am J Surg Pathol. 2004; 28:1051–1056.
Article
18. Yoshida K, Iwashita T, Uemura S, et al. Efficacy of contrast-enhanced EUS for lymphadenopathy: a prospective multicenter pilot study (with videos). Gastrointest Endosc. 2019; 90:242–250.
Article
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