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GE-Portuguese Journal of Gastroenterology

Print version ISSN 2341-4545On-line version ISSN 2387-1954

GE Port J Gastroenterol vol.28 no.4 Lisboa Aug. 2021  Epub Feb 28, 2022

https://doi.org/10.1159/000511533 

Endoscopic Snapshot

Leiomyoma-Like Mesenchymal Proliferation Arising in a Device-Assisted Full-Thickness Resection Site

Proliferação mesenquimatosa do tipo leimioma no local de ressecção endoscópica transmural prévia

Vincent Zimmera  b 

Kai Emrichc 

aDepartment of Medicine, Marienhausklinik St. Josef Kohlhof, Neunkirchen, Germany

bDepartment of Medicine II, Saarland University Medical Center, Saarland University, Homburg, Germany

cInstitute of Pathology Saarbrücken-Rastpfuhl, Saarbrücken, Germany


Keywords Colonoscopy; Full-thickness resection device; Endoscopic resection; Polyp

Palavras Chave Colonoscopia; Ressecção endoscópica; Ressecção endoscópica transmural; Pólipo

A 67-year-old female patient presented for sigmoidoscopy 12 months after complex endoscopic resection in the rectum. This included piecemeal endoscopic mucosal resection (peripheral parts) coupled with central device-assisted endoscopic full-thickness resection (EFTR; Full-Thickness Resection Device; Ovesco, Tübingen, Germany) for a large supra-anal EMR recurrence with marked fibrosis. Pathology confirmed low-grade adenoma at the time. At the recent endoscopy, an estimated 10-mm, nodular lesion emerged within the otherwise unremarkable resection site with exuberant fibrosis (Fig. 1a). Consistent with the initial endoscopic impression, further assessment using linked color imaging (Fig. 1b) and blue laser imaging did not suggest neoplastic surface and/or irregular vessel pattern (Fig. 1c). With an aim to achieve a distinct tissue diagnosis of this presumed clip artifact, the lesion was resected en bloc by conventional mucosectomy. Pathology indicated presence of a nodular proliferation of eosinophilic spindle-shaped cells devoid of nuclear atypia (Fig. 1d: HE. ×1.6; Fig. 1e: HE. ×5). Ancillary immunohistochemistry including CD34, CD117, DOG-1 (discovered in gastrointestinal stromal tumor-1), and smooth muscle actin (SMA) confirmed SMA to be exclusively expressed within this leiomyoma-like mesenchymal proliferative lesion (Fig. 1f: SMA, ×5).

Fig. 1: a An estimated 10-mm, nodular lesion within the otherwise unremarkable resection site with exuberant tissue fibrosis. b, c Image-enhanced endoscopy using linked color imaging and blue laser imaging without evidence of neoplastic surface and/or vessel pattern alterations. d, e Pathology indicates a nodular proliferation of eosinophilic spindle-shaped cells without nuclear atypia (HE, ×1.6 and ×5, respectively). f Immunohistochemistry staining for SMA indicates high lesional expression, while immunohistochemistry for CD34, CD117, DOG-1 (discovered in gastrointestinal stromal tumor-1) proved unremarkable (SMA, ×5). 

Device-assisted EFTR has gained much momentum in recent years for the endoscopic resection of selected colorectal lesions [1]. However, the full spectrum of EFTR-related, novel clip artifacts, reflective of transmural tissue capture, is still unfolding, with which endoscopists should become acquainted to avoid undue procedures such as re-do EFTR and/or surgery [2-4].

References

1 Mão de-Ferro S, Castela J, Pereira D, Chaves P, Dias Pereira A. Endoscopic Full-Thickness Resection of Colorectal Lesions with the New FTRD System: Single-Center Experience. GE Port J Gastroenterol. 2019 Jul;26(4):235-41. [ Links ]

2 Currais P, Roseira J, Castela J, Mão-de-Ferro S, Pereira AD. Heterogeneity of endoscopic full-thickness resection scars. Gastrointest Endosc. 2020 Aug;92(2):433-4. [ Links ]

3 Zimmer V, Eltze E. Granulation polyp arising in a former device-assisted full-thickness resection site: another kind of clip artifact? Gastrointest Endosc. 2019 Apr;89(4):893-4. [ Links ]

4 Al-Taee A, Dinarvand P, Carpenter D, AlKaade S. Benign polypoid growth after endoscopic full-thickness resection. Gastrointest Endosc. 2020 Aug;92(2):432-3. [ Links ]

Statement of Ethics The patient has given written informed consent for publication (including publication of images)

Funding Sources The authors did not receive any funding

Received: July 28, 2020; Accepted: August 24, 2020

Corresponding author Vincent Zimmer Department of Medicine Marienhausklinik St. Josef Kohlhof Klinikweg 1-5, DE-66539 Neunkirchen (Germany) vincent.zimmer@gmx.de

Conflict of Interest Statement

The authors have no conflicts of interest to declare

Author Contributions

V.Z.: clinical care, drafting, and finalization of the manuscript. K.E.: pathology, revision, and final approval of the manuscript

Creative Commons License This is an open-access article distributed under the terms of the Creative Commons Attribution License