Open Access
CC BY 4.0 · Endoscopy 2025; 57(S 01): E402-E404
DOI: 10.1055/a-2599-6761
E-Videos

Synchronous multiple primary early stage esophageal cancers diagnosed in a teenager using confocal laser endomicroscopy

Jing Liu
1   Department of Gastroenterology, Zhongnan Hospital of Wuhan University, Wuhan, China (Ringgold ID: RIN89674)
,
Mu Cai
1   Department of Gastroenterology, Zhongnan Hospital of Wuhan University, Wuhan, China (Ringgold ID: RIN89674)
,
Mei Yang
2   Department of Gastroenterology, Ezhou Central Hospital, Ezhou, Hubei, China (Ringgold ID: RIN650074)
,
Jun Luo
3   Department of Pathology, Zhongnan Hospital of Wuhan University, Wuhan, China (Ringgold ID: RIN89674)
,
Qiu Zhao
1   Department of Gastroenterology, Zhongnan Hospital of Wuhan University, Wuhan, China (Ringgold ID: RIN89674)
› Author Affiliations
 

Esophageal cancer predominantly affects the elderly and is often overlooked in the young, resulting in patients presenting at advanced disease stages with poorer survival [1]. Early diagnosis is pivotal. Confocal laser endomicroscopy (CLE) holds significant promise in diagnosing and monitoring early upper gastrointestinal tract cancers. In a previous study, we reported the use of CLE to image a gastric adenocarcinoma, fundic gland type [2], thereby aiding diagnosis.

We now report the case of a 16-year-old boy with a 1-year history of intermittent epigastric pain who underwent an esophagogastroduodenoscopy (EGD) that revealed multiple esophageal lesions. The EGD identified two 0-IIb lesions at 23–25 cm and 30 cm from the incisors, featuring patchy, reddish mucosa with clear borders ([Fig. 1] a, b). Magnification endoscopy with narrow-band imaging (ME-NBI) showed brownish, regularly patterned lesions, classified as B1 according to the Japanese Society of Esophagus criteria ([Fig. 1] c, d). Lugol iodine chromoendoscopy revealed Lugol-voiding lesions, with a pink sign later transitioning to a bright silver sign under NBI ([Fig. 1] e–h). CLE demonstrated white feathery substances, detached cells, the absence of localized squamous epithelium, thickened intrapapillary capillary loops, and normal peristalsis ([Fig. 2]; [Video 1]). The patient underwent complete endoscopic submucosal dissection (ESD) of both lesions ([Fig. 3])

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Fig. 1 Images of an esophageal epidermoid lesion on: a, b white-light endoscopy; c, d narrow-band imaging; e–h Lugol chromoendoscopy.
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Fig. 2 Confocal laser endomicroscopy (CLE) images showing multiple white feathery substances, as well as detached cells, local absence of squamous epithelium, and thickened intrapapillary capillary loops.
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Fig. 3 Images of the two lesions that were managed by endoscopic submucosal dissection (ESD) showing: a, b the macroscopic appearance of the resection specimens; c, d the endoscopic appearance of the post-ESD defect for: a, c the lesion that was 23 cm from the incisors; b, d the lesion that was 30 cm from the incisors.
Confocal laser endomicroscopy is performed on synchronous multiple primary early stage esophageal cancers in a 16-year-old boy.Video 1

Histopathology showed the lesion at 23 cm from the incisors to be a 0.9 × 0.6-cm squamous cell carcinoma, invading the submucosa and affecting submucous glands/ducts (200 μm), with INFb pattern ([Fig. 4] a). The other lesion showed high grade dysplasia ([Fig. 4] b). Immunohistochemical testing showed Ki-67 positivity in the epithelial layer. A diagnosis of synchronous multiple primary early esophageal cancer (T1aN0M0) was made. Multiple esophageal cancers have a poorer prognosis, necessitating surgery, radiotherapy, or chemotherapy [3] [4]. In this case, the patient underwent radiotherapy post-ESD.

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Fig. 4 Histopathological appearance after hematoxylin and eosin (H&E) staining showing: a esophageal squamous cell carcinoma in the lesion that was 23 cm from the incisors; b high grade dysplasia in the lesion that was 30 cm from the incisors.

For patients with esophageal cancer who do not have tobacco and alcohol as risk factors, endoscopists should thoroughly examine the esophageal region for synchronous lesions. The CLE biopsy technique is safe, repeatable, and noninvasive, and demonstrates high sensitivity and specificity for early superficial esophageal squamous cell carcinoma, addressing the limitations of high definition white-light endoscopy and low resolution NBI, and the diagnostic variability of flexible indigo carmine-enhanced chromoendoscopy [5].

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Conflict of Interest

The authors declare that they have no conflict of interest.


Correspondence

Jing Liu, MD
Department of Gastroenterology, Zhongnan Hospital of Wuhan University
169 Donghu Road
Wuhan, Hubei 430071
China   

Publication History

Article published online:
14 May 2025

© 2025. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/).

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Oswald-Hesse-Straße 50, 70469 Stuttgart, Germany


Zoom
Fig. 1 Images of an esophageal epidermoid lesion on: a, b white-light endoscopy; c, d narrow-band imaging; e–h Lugol chromoendoscopy.
Zoom
Fig. 2 Confocal laser endomicroscopy (CLE) images showing multiple white feathery substances, as well as detached cells, local absence of squamous epithelium, and thickened intrapapillary capillary loops.
Zoom
Fig. 3 Images of the two lesions that were managed by endoscopic submucosal dissection (ESD) showing: a, b the macroscopic appearance of the resection specimens; c, d the endoscopic appearance of the post-ESD defect for: a, c the lesion that was 23 cm from the incisors; b, d the lesion that was 30 cm from the incisors.
Zoom
Fig. 4 Histopathological appearance after hematoxylin and eosin (H&E) staining showing: a esophageal squamous cell carcinoma in the lesion that was 23 cm from the incisors; b high grade dysplasia in the lesion that was 30 cm from the incisors.