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Li Y, Beizai P, Russell JW, Westbrook L, Nowain A, Wang HL. ‘Mucosal Schwann cell hamartoma of the gastroesophageal junction: A series of 6 cases and comparison with colorectal counterpart.’ Annals of diagnostic pathology. 2020, 47: 151531.

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Article

Colorectal Mucosal Schwann-cell Hamartoma: A Case Report and Review of the Literature

1Department of Pathology, SUNY Downstate Health Science University, Brooklyn, NY, USA


American Journal of Medical Case Reports. 2024, Vol. 12 No. 3, 49-55
DOI: 10.12691/ajmcr-12-3-6
Copyright © 2024 Science and Education Publishing

Cite this paper:
Kristina Loukeris, Elmira Mostafidi. Colorectal Mucosal Schwann-cell Hamartoma: A Case Report and Review of the Literature. American Journal of Medical Case Reports. 2024; 12(3):49-55. doi: 10.12691/ajmcr-12-3-6.

Correspondence to: Elmira  Mostafidi, Department of Pathology, SUNY Downstate Health Science University, Brooklyn, NY, USA. Email: Elmira.mostafidi@downstate.edu

Abstract

Background: Here, we report a sigmoid mucosal Schwann cell hamartoma as an uncommon entity. Though unexpected, the pathologist should consider this among differential diagnoses and be able to distinguish the microscopic features when examining colorectal biopsies. Finally, we have reviewed the literature for similar cases reported over the past two decades. Case presentation: A 55-year-old woman was found to have a 5 mm sessile polyp during her screening colonoscopy. The microscopic study revealed colonic mucosa with ill-defined proliferation of uniform spindle-shaped cells arranged in a haphazard pattern within the lamina propria. All cells had elongated bland nuclei with eosinophilic cytoplasm and unclear cell borders. Edema and mild lymphoplasmacytic infiltration were noticed in the lamina propria. No nuclear atypia, necrosis, or mitosis was identified. On immunohistochemistry, Schwann cells showed diffuse and strong nuclear and cytoplasmic positivity for S-100 protein. CD117 (C-kit) and desmin were negative. Conclusion: Colorectal MSCH has a benign nature, and the lack of axons and strong immunoreactivity for S-100 protein can help distinguish MSCH from most similar entities.

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