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- 2017
Comparison of the yield of 19-G eXcelon core needle to a 21-G EBUS needle during endobronchial ultrasound guided transbronchial needle aspiration of mediastinal lymph nodes for the detection of granulomas in cases of suspected sarcoidosisAbstract: Granulomatous diseases are thought to be the most common cause of mediastinal adenopathy (1). Endobronchial ultrasound aided bronchoscopic transbronchial needle aspiration (EBUS-TBNA) provides us with a mechanism to perform lymph node biopsies under real time ultrasound guidance (1). However, the diagnostic performance of EBUS-TBNA using the traditional 21-G needle is obfuscated to some extent because of the lack of its ability to supply core biopsy from lymph nodes and hence failing to demonstrate granulomas in a significant number of cases (15%) (2). The diagnosis of sarcoidosis requires the clear demonstration of a non-caseating granuloma (3). Some authors have used the presence of epithelioid cells alone from EBUS-TBNA samples for diagnosing sarcoidosis which has resulted in >90% sensitivity for the procedure using the 21-G EBUS needle but further analysis based on presence of granulomas have reduced their yields to <70% (4). The 19-G core needle used for conventional TBNA (c-TBNA) can provide a histological core (5). Although achieving histological cores with a 22-G needle has been previously reported (in 92% cases), the relevance of such “core biopsies” is unclear (6). Cores were reported to be available in 92% of 22-G EBUS-TBNA samples. However, this report goes on to document that histological material leading to diagnosis was available in only 57% of the cases (6). It leads us to question whether such histological cores obtained by the 22-G needle are of the same diagnostic utility as a true core biopsy. Thus, one well-recognized drawback of EBUS-TBNA has been lack of preserved cellular architecture on needle aspirates using the 22-G and 21-G needles. Few studies have addressed the questions whether a 21-G EBUS-TBNA needle has a higher diagnostic yield compared to a 22-G needle. Unfortunately, the verdict is far from being clear (7). Hence, we have used the 19-G conventional TBNA needle to perform a hybrid EBUS TBNA for those patients with an initial negative 21-G EBUS-TBNA biopsy yet have a high possibility of having sarcoidosis. We aim to review our single center experience with the 19-G core needle biopsy used with an EBUS bronchoscope in this paper. This is a hybrid procedure that used a 19-G c-TBNA needle fitted to a regular EBUS bronchoscope in order to provide core samples under direct visualization. The procedure is described in the online supplement. We then systemically evaluated whether performing EBUS with a 19-G core needle resulted in an increased yield of granulomas than regular EBUS TBNA with a 21-G needle alone. A specific 19-G
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