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DOI: 10.1055/a-0978-6734
Endoscopic resection of early-stage SMAD4 juvenile polyposis does not prevent disease spreading in the stomach
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Publication History
Publication Date:
09 August 2019 (online)
To the best our knowledge, juvenile polyposis with a SMAD4 germline mutation is a rare disease [1] [2], and its precise endoscopic aspect has been described in the colon [3] but not in the stomach. The natural history of this particular polyposis has not been well described.
We report a case of early-stage SMAD4 polyposis in a 25-year-old woman who was also receiving treatment for Rendu–Osler disease. It was an early-stage SMAD4 polyposis with a single large lesion ([Fig. 1]) surrounding the cardia. According to the endoscopic aspect in white-light imaging, the lesion was nodular (Paris classification Is). Using narrow-band imaging (Olympus, Tokyo, Japan), dual focus, and acetic acid dyeing, the mucosal pattern appeared regular with large pits consistent with hyperplasia. As the lesion had been detected at an early stage, we decided to attempt endoscopic submucosal dissection (ESD) to remove all of the polyp with margins in order to stop the evolution of the disease ([Video 1]). En bloc resection was achieved and appeared to be endoscopically complete; the resected specimen measured 8 × 3 cm. Histology confirmed the hyperplastic nature of the polyp with free margins (focal contact in few points).
Video 1 SMAD4 juvenile polyposis aspect before and after endoscopic submucosal dissection of the main initial lesion.
Quality:
During the follow-up period, the dissected area had a depressed aspect without recurrence at the scar site. However, the hyperplastic polyp recurred all around the previous resection site and spread all around the cardia ([Fig. 2]).
In parallel, a second small juvenile polyp was present in the fundus and was described with blue-laser imaging and linked-color imaging. The lesion was small (< 5 mm) and presented the same regular mucosal pattern with hyperplastic features ([Fig. 3], [Fig. 4]).
SMAD4 polyposis at an early stage seems to begin around the cardia but endoscopic resection, even when complete, does not prevent the lesion from spreading all around the cardia.
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Competing interests
None
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References
- 1 Chung AD, Mortelé KJ. Combined juvenile polyposis syndrome and hereditary hemorrhagic telangiectasia (JPS/HHT) with MRI and endoscopic correlation. Clin Imaging 2018; 54: 37-39
- 2 Iyer NK, Burke CA, Leach BH. et al. SMAD4 mutation and the combined syndrome of juvenile polyposis syndrome and hereditary haemorrhagic telangiectasia. Thorax 2010; 65: 745-746
- 3 Takeda K, Kudo S-E, Mori Y. et al. Magnifying chromoendoscopic and endocytoscopic findings of juvenile polyps in the colon and rectum. Oncol Lett 2016; 11: 237-242
Corresponding author
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References
- 1 Chung AD, Mortelé KJ. Combined juvenile polyposis syndrome and hereditary hemorrhagic telangiectasia (JPS/HHT) with MRI and endoscopic correlation. Clin Imaging 2018; 54: 37-39
- 2 Iyer NK, Burke CA, Leach BH. et al. SMAD4 mutation and the combined syndrome of juvenile polyposis syndrome and hereditary haemorrhagic telangiectasia. Thorax 2010; 65: 745-746
- 3 Takeda K, Kudo S-E, Mori Y. et al. Magnifying chromoendoscopic and endocytoscopic findings of juvenile polyps in the colon and rectum. Oncol Lett 2016; 11: 237-242