Open Access
CC BY 4.0 · Endoscopy 2026; 58(S 01): E139-E140
DOI: 10.1055/a-2772-6004
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Novel application of metal-clip traction-assisted endoscopic intermuscular dissection for a rare calcifying fibrous tumor

Authors

  • Suhuan Liao

    1   Department of Gastroenterology, South China Hospital, Medical School, Shenzhen University, Shenzhen, China
  • Silin Huang

    1   Department of Gastroenterology, South China Hospital, Medical School, Shenzhen University, Shenzhen, China
  • Qi Sun

    2   Department of Pathology, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China
  • Miao He

    1   Department of Gastroenterology, South China Hospital, Medical School, Shenzhen University, Shenzhen, China
  • Yin Xiao

    1   Department of Gastroenterology, South China Hospital, Medical School, Shenzhen University, Shenzhen, China
 

A 34-year-old man was admitted for endoscopic resection of a 12-mm rectal subepithelial lesion (SEL; [Fig. 1] a). Preoperative abdominal magnetic resonance imaging showed no evidence of lymphadenopathy or distant metastasis. Endoscopic ultrasonography (EUS) revealed a tumor that was predominantly located in the submucosa and was closely related to the muscularis propria, exhibiting homogeneous hypoechoic ([Fig. 1] b). In order to ensure the complete removal of the lesion, endoscopic intermuscular dissection (EID) was performed ([Video 1]). We used a EG-601WR gastroscope (Fujifilm, Tokyo, Japan) and resected the tumor using a dual knife. The primary challenge in EID involves the dissection of the intermuscular plane. To enhance visualization of the surgical field, we employed an ST hood and a metal-clip traction technique, with the intermuscular dissection being carried out in the Endocut I mode (effect 2, duration 3, and interval 3) of the VIO200-D electrosurgical system. The procedure was continued under this approach until complete tumor resection was achieved ([Fig. 2] a–f). The total procedure time was 50 minutes. Histopathological examination showed a hypocellular tumor composed of collagenous fibrous tissue with scattered inflammatory infiltrates. Uniform spindle-shaped tumor cells were dispersed among dense collagen bundles. Immunohistochemistry was positive for SDHB, with a Ki67 index of 3%, and negative for CD117, CD34, DOG-1, and S-100, consistent with a calcifying fibrous tumor (CFT; [Fig. 3] a–f).

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Fig. 1 a Colonoscopy revealed a rectal subepithelial lesion measuring approximately 12 mm in diameter. b Endoscopic ultrasonography revealed a hypoechoic lesion originating from the submucosa and was closely related to the muscularis propria, exhibiting homogeneous echotexture.
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Fig. 2 a The muscularis propria was exposed by mucosal incision and submucosal dissection. b A metal-clip traction was used. c With traction, the intermuscular space was adequately exposed. d Postoperative trauma. e Suture the defection with metal clips. f Resected tumor.
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Fig. 3 Histological findings. a Low-power field, HE staining: the submucosal tumor was directly adjacent to the muscularis propria, with the circular muscle layer visible beneath it. b, c High-power field, HE staining: a hypocellular tumor composed of collagenous fibrous tissue with scattered inflammatory cell infiltrates. d High-power field, positive with SDHB. e, f High-power field, negative for DOG-1 and CD-117.
Resection of a rare calcifying fibrous tumor using endoscopic intermuscular dissection and metal-clip traction.Video 1

The CFT is a rare benign soft tissue lesion of unknown etiology and exceedingly rare in the rectum, with only isolated cases reported in the literature [1] [2]. Definitive diagnosis depends critically on postoperative histopathological assessment and exclusion of other entities via immunohistochemical studies. EID has been primarily reported for the treatment of rectal neuroendocrine tumors and deeply invasive rectal cancers [3] [4] [5]. EID can also be a treatment option for diagnostically challenging rectal SELs, particularly when EUS suggests the lesion located in the deep submucosal layer, closely associated with the muscularis propria.

Endoscopy_UCTN_Code_TTT_1AQ_2AD_3AD


Contributorsʼ Statement

Suhuan Liao: Data curation, Resources, Supervision, Writing – original draft, Writing – review & editing. Silin Huang: Investigation, Methodology, Resources, Writing – review & editing. Qi Sun: Methodology, Resources. Miao He: Investigation, Methodology. Yin Xiao: Software.

Conflict of Interest

The authors declare that they have no conflict of interest.


Correspondence

Silin Huang, MD
Department of Gastroenterology, South China Hospital, Medical School, Shenzhen University
No. 1, Fuxin Road
Longgang District, Shenzhen
China   

Publication History

Article published online:
29 January 2026

© 2026. 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/).

Georg Thieme Verlag KG
Oswald-Hesse-Straße 50, 70469 Stuttgart, Germany


Zoom
Fig. 1 a Colonoscopy revealed a rectal subepithelial lesion measuring approximately 12 mm in diameter. b Endoscopic ultrasonography revealed a hypoechoic lesion originating from the submucosa and was closely related to the muscularis propria, exhibiting homogeneous echotexture.
Zoom
Fig. 2 a The muscularis propria was exposed by mucosal incision and submucosal dissection. b A metal-clip traction was used. c With traction, the intermuscular space was adequately exposed. d Postoperative trauma. e Suture the defection with metal clips. f Resected tumor.
Zoom
Fig. 3 Histological findings. a Low-power field, HE staining: the submucosal tumor was directly adjacent to the muscularis propria, with the circular muscle layer visible beneath it. b, c High-power field, HE staining: a hypocellular tumor composed of collagenous fibrous tissue with scattered inflammatory cell infiltrates. d High-power field, positive with SDHB. e, f High-power field, negative for DOG-1 and CD-117.