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Endobronchial ultrasound-guided transbronchial needle aspiration in the diagnosis of lymphoma
  1. M P Kennedy1,
  2. C A Jimenez1,
  3. J F Bruzzi2,
  4. A D Mhatre1,
  5. X Lei3,
  6. F J Giles4,
  7. T Fanning5,
  8. R C Morice1,
  9. G A Eapen1
  1. 1
    Department of Pulmonary Medicine, University of Texas MD Anderson Cancer Center, Houston, Texas, USA
  2. 2
    Department of Radiology, University of Texas MD Anderson Cancer Center, Houston, Texas, USA
  3. 3
    Department of Statistics, University of Texas MD Anderson Cancer Center, Houston, Texas, USA
  4. 4
    Department of Leukemia, University of Texas MD Anderson Cancer Center, Houston, Texas, USA
  5. 5
    Department of Pathology, University of Texas MD Anderson Cancer Center, Houston, Texas, USA
  1. Dr G A Eapen, MD Anderson Cancer Center, Department of Pulmonary Medicine, Unit 403, 1515 Holcombe Boulevard, Houston, Texas 77030, USA; geapen{at}mdanderson.org

Abstract

Background: The diagnostic accuracy of endobronchial ultrasound-guided transbronchial needle aspiration (EBUS-TBNA) for the diagnosis of lymphoma in patients with mediastinal lymphadenopathy is not well defined.

Methods: A retrospective review was performed of all patients with mediastinal lymphadenopathy referred for EBUS-TBNA between August 2005 and December 2006 in whom lymphoma was suspected based on prior history or clinical presentation. Mediastinal biopsy specimens were taken using a linear array ultrasonic bronchoscope (Olympus XBF-UC 160F) and a 22-gauge cytology needle (NA-202C Olympus) with on-site cytopathological support. The EBUS-TBNA result was compared with a reference standard of pathological tissue diagnosis or a composite of ⩾6 months of clinical follow-up with radiographic imaging.

Results: Of 236 patients who underwent EBUS-TBNA, 25 were eligible for inclusion. Indications for EBUS-TBNA were suspected mediastinal recurrence of lymphoma (n = 13) and mediastinal lymphadenopathy of unknown cause (n = 12). Adequate lymph node sampling was accomplished in 24/25 patients (96%); there were no complications. EBUS-TBNA identified lymphoma in 10 patients and benign disease in 14 patients. There was one false negative EBUS-TBNA for lymphoma (lymphoma prevalence 11/25 (44%)). Follow-up over a median of 10.5 months (range 1–19) confirmed stable or regressive lymphadenopathy in all 14 patients without a lymphoma diagnosis, consistent with a benign diagnosis. Overall, EBUS-TBNA had a sensitivity of 90.9%, specificity of 100%, positive predictive value of 100% and negative predictive value of 92.9% for the diagnosis of lymphoma.

Conclusions: EBUS-TBNA is an accurate, safe and useful tool in the investigation of suspected lymphoma with isolated mediastinal adenopathy, and may diminish the need for more invasive procedures such as mediastinoscopy.

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Footnotes

  • Competing interests: None.