Literature DB >> 35992555

Diffuse large B-cell lymphoma with cardiac invasion diagnosed using transesophageal ultrasound-guided bronchoscopic aspiration.

Daiki Nagayama1,2, Toshiyuki Sumi1,2, Yoshiko Keira3, Yusuke Tanaka2, Haruhiko Michimata1,2, Yuta Koshino1,2, Hiroki Watanabe1, Yuichi Yamada1, Hirofumi Chiba2.   

Abstract

Transesophageal ultrasound-guided bronchoscopic aspiration (EUS-B-FNA) allowed for minimally invasive and simultaneous diagnosis and evaluation of the degree of invasion by echocardiography. EUS-B-FNA may be useful for the evaluation and diagnosis of tumours with cardiac invasion.
© 2022 The Authors. Respirology Case Reports published by John Wiley & Sons Australia, Ltd on behalf of The Asian Pacific Society of Respirology.

Entities:  

Keywords:  DLBCL; EUS‐B‐FNA; cardiac invasion; mediastinal tumour; transesophageal approach

Year:  2022        PMID: 35992555      PMCID: PMC9379347          DOI: 10.1002/rcr2.1022

Source DB:  PubMed          Journal:  Respirol Case Rep        ISSN: 2051-3380


CLINICAL IMAGE

A 34‐year‐old woman presented with dyspnoea and a 1‐month history of coughing. Chest computed tomography showed a mass in the anterior mediastinum with suspected partial cardiac invasion (Figure 1). Transesophageal ultrasound‐guided bronchoscopic aspiration (EUS‐B‐FNA) confirmed tumour invasion of the left atrium (Video 1). Transesophageal needle biopsy of the tumour adjacent to the heart was performed while simultaneously visualizing the cardiac invasion (Figure 2). Diffuse large B‐cell lymphoma (DLBCL) diagnosis was confirmed through immunohistochemical staining (Figure 3). No arrhythmia, bleeding, extravasation, pericardial tamponade or other adverse events occurred. The patient received rituximab, etoposide, prednisolone, vincristine, cyclophosphamide and doxorubicin (R‐EPOCH), and the tumour shrank enough without developing tumour embolism. EUS‐B‐FNA enables safe real‐time sampling of lung tumours and mediastinal lymph nodes adjacent to the oesophagus. While a percutaneous needle biopsy could have been performed to confirm left atrial invasion, EUS‐B‐FNA allowed for minimally invasive and simultaneous diagnosis and evaluation of the degree of invasion by echocardiography, which resulted in prompt initiation of chemotherapy. Thus, EUS‐B‐FNA may be useful for evaluating and diagnosing tumours with cardiac invasion.
FIGURE 1

Enhanced computed tomography findings. Chest CT reveals suspected partial invasion of tumour adjacent to the heart into the left atrium. CT, computed tomography; LA, left atrium; T, tumour; E, oesophagus

VIDEO 1

EUS‐B‐FNA findings. Tumours invading the endocardium of the left atrium can be observed visible and hidden with the heartbeat.

FIGURE 2

EUS‐B‐FNA findings. EUS‐B‐FNA findings show tumour invasion into the left atrium (A) and fine‐needle aspiration (B) of the mediastinal tumour adjacent to the heart. The red circle indicates tumour invasion. EUS‐B‐FNA, transesophageal ultrasound‐guided bronchoscopic aspiration

FIGURE 3

Pathological examination of specimens. H&E staining of specimens and immunohistochemistry for CD20, Ki67, Bcl‐2 and TdT. The tumour cells expressed CD20 and Ki67 (index 90%–100%) but not Bcl‐2 and TdT. The scale bar represents 1000 μm (A), 50 μm (B–F). H&E, haematoxylin and eosin

Enhanced computed tomography findings. Chest CT reveals suspected partial invasion of tumour adjacent to the heart into the left atrium. CT, computed tomography; LA, left atrium; T, tumour; E, oesophagus EUS‐B‐FNA findings. Tumours invading the endocardium of the left atrium can be observed visible and hidden with the heartbeat. EUS‐B‐FNA findings. EUS‐B‐FNA findings show tumour invasion into the left atrium (A) and fine‐needle aspiration (B) of the mediastinal tumour adjacent to the heart. The red circle indicates tumour invasion. EUS‐B‐FNA, transesophageal ultrasound‐guided bronchoscopic aspiration Pathological examination of specimens. H&E staining of specimens and immunohistochemistry for CD20, Ki67, Bcl‐2 and TdT. The tumour cells expressed CD20 and Ki67 (index 90%–100%) but not Bcl‐2 and TdT. The scale bar represents 1000 μm (A), 50 μm (B–F). H&E, haematoxylin and eosin

AUTHOR CONTRIBUTION

Conceptualization: Toshiyuki Sumi. Data curation: Yusuke Tanaka, Haruhiko Michimata and Daiki Nagayama. Formal analysis: Yoshiko Keira and Hiroki Watanabe. Investigation: Yoshiko Keira and Yuichi Yamada. Roles/Writing – original draft: Toshiyuki Sumi. Writing – review & editing: Hirofumi Chiba.

CONFLICT OF INTEREST

None declared.

ETHICS STATEMENT

The authors declare that appropriate written informed consent was obtained for the publication of this manuscript and accompanying images.
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