ArticleFrontiers in oncology2022
Clinicopathological characteristics of gastrointestinal schwannomas: A retrospective analysis of 78 cases.
Article in Frontiers in oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.
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Who cites it
17 citing papers in PubMed, 15 citations in OpenAlex.
- Management of Gastrointestinal Schwannomas: A State-of-the-Art Review.Journal of gastrointestinal cancer · 2026Review
- Gastric schwannoma: diagnostic challenges, pathological features, and surgical management : a narrative review.World journal of surgical oncology · 2026Review
- Analysis of clinical-imaging-pathological features and preoperative misdiagnosis status of 47 cases of gastric schwannomas: a single-center retrospective study over 13 years.World journal of surgical oncology · 2026Article
- Malignant peripheral nerve sheath tumor of the ileocecal region: a case report.Frontiers in oncology · 2026Article
- Case Report: Benign colonic schwannoma with restricted diffusion mimicking malignancy.Frontiers in oncology · 2026Article
- Successful Sphincter-Preserving Resection of a Giant Rectal Schwannoma Using Transanal Total Mesorectal Excision: A Case Report.Surgical case reports · 2026Article
- Gastrointestinal schwannomas: A case series of 9 patients and literature review.Turkish journal of surgery · 2025Article
- Careful Interpretation of Positron Emission Tomography Findings in Gastric Schwannomas: A Case Report.Cureus · 2025Article
- Unveiling the Rare: A Case Report of Rectal Schwannoma in a Neurofibromatosis Type 1 Patient.Cureus · 2025Article
- Clinicopathological features and treatment of gastrointestinal schwannomas.World journal of gastroenterology · 2025Article
- Gastric schwannoma with atypical manifestations in an adult patient: case report and literature review.Ecancermedicalscience · 2025Article
- Incidental Finding of an Asymptomatic Jejunal Schwannoma: A Rare Case Report and Review of Literature.The American journal of case reports · 2024Review
- Article
- A huge benign gastric schwannomas presented with upper and lower gastrointestinal bleeding: a case report and literature review.Journal of surgical case reports · 2024Article
- Preoperative differentiation of gastric schwannomas and gastrointestinal stromal tumors based on computed tomography: a retrospective multicenter observational study.Frontiers in oncology · 2024Article
- Gastric schwannoma: Two case reports and review of the literature.Radiology case reports · 2023Article
- Differentiating gastric schwannoma from gastric stromal tumor (≤5 cm) by histogram analysis based on iodine-based material decomposition images: a preliminary study.Frontiers in oncology · 2023Article
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Authors and funding
7 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Introduction: Schwannomas are tumors arising from Schwan cells of the neural sheath, which rarely occur in the gastrointestinal tract. The aim of the present study was to analyze the clinicopathological features and treatment outcomes of gastrointestinal schwannomas (GISs). Methods: Patients who were diagnosed with GISs in our hospital from January 2010 to December 2021 were selected. Data about demographic characteristics, clinical symptoms, treatment methods and outcomes, pathological results, and follow-up results were retrospectively collected and analyzed. Results: A total of 78 patients with 79 GISs were included, the female-to-male ratio was 55:23, and the average age was 52.12 ± 12.26 years. One-third (26/78) of the patients were asymptomatic. A total of 79 GISs were removed, and the average size was 3.63 ± 2.03 cm (range, 0.3-10 cm). As for tumor location, 54 GISs were located in the stomach, 14 in the esophagus, 2 in the duodenum, 6 in the colorectum (4 in the colon and 2 in the rectum), and the other 3 in the small intestine. A total of 23 and 55 patients underwent endoscopic and surgical resections, respectively. Compared with surgical resection, endoscopic resection is associated with a smaller diameter, lower cost, and shorter hospital stay. Pathological results revealed that S100 was positive in all the GISs. No recurrence was noticed during a median follow-up of 45 months (range, 6-148 months). Conclusion: GISs are rare gastrointestinal tumors with favorable prognoses, which are most commonly seen in the stomach and diagnosed by pathological findings with immunohistochemical staining. Surgical resection remains the standard method for removing GISs, while endoscopic resection may serve as an alternative method for selected patients with GISs and may be attempted in GISs with a diameter of <3 cm and no signs of malignancy.
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