A Case of Brunner's Gland Hyperplasia Accompanied by an Increase in Endocrine Cells and Endocrine Cell Micronests.

brunner's gland hyperplasia endocrine cell micronests hypergastrinemia myofibroblasts smooth muscle cells

Journal

Cureus
ISSN: 2168-8184
Titre abrégé: Cureus
Pays: United States
ID NLM: 101596737

Informations de publication

Date de publication:
Sep 2024
Historique:
accepted: 03 09 2024
medline: 9 9 2024
pubmed: 9 9 2024
entrez: 9 9 2024
Statut: epublish

Résumé

Endocrine cell micronests (ECMs) are aggregates of endocrine cells known as enterochromaffin-like cells, typically measuring approximately 50 μm and usually observed in the mucosal layer of atrophic gastric fundic glands associated with hypergastrinemia. Although there are numerous reports on gastric ECMs, reports on duodenal ECMs are exceedingly rare. We report a rare case of Brunner's gland hyperplasia with increased endocrine cells and ECMs. An approximately 40 mm polyp was found in the duodenal bulb of a 57-year-old Japanese male patient during an upper gastrointestinal endoscopy, and a polypectomy was performed. Microscopic examination revealed hyperplasia of Brunner's glands in the duodenal polyp. Compared to normal Brunner's glands, hyperplastic Brunner's glands exhibited more endocrine cells. Additionally, many ECMs were observed in the fibromuscular connective tissue, comprising smooth muscle cells and myofibroblasts, adjacent to the hyperplastic Brunner's glands. The patient presented with hypergastrinemia (2,500 pg/mL; normal range: 30-140 pg/mL), and the ECMs were considered related to this condition. This case represents the first instance of a benign duodenal lesion with an increase in endocrine cells and the presence of ECMs.

Identifiants

pubmed: 39246633
doi: 10.7759/cureus.68688
pmc: PMC11378870
doi:

Types de publication

Case Reports Journal Article

Langues

eng

Pagination

e68688

Informations de copyright

Copyright © 2024, Meguro et al.

Déclaration de conflit d'intérêts

Human subjects: Consent was obtained or waived by all participants in this study. The Ethics Committee at the Affiliated Hospital of Hamamatsu University School of Medicine issued approval 81-004. Conflicts of interest: In compliance with the ICMJE uniform disclosure form, all authors declare the following: Payment/services info: All authors have declared that no financial support was received from any organization for the submitted work. Financial relationships: All authors have declared that they have no financial relationships at present or within the previous three years with any organizations that might have an interest in the submitted work. Other relationships: All authors have declared that there are no other relationships or activities that could appear to have influenced the submitted work.

Auteurs

Shiori Meguro (S)

Department of Regenerative and Infectious Pathology, Hamamatsu University School of Medicine, Hamamatsu, JPN.

Hideya Kawasaki (H)

Department of Preeminent Bioimaging Research, Hamamatsu University School of Medicine, Hamamatsu, JPN.

Isao Kosugi (I)

Department of Regenerative and Infectious Pathology, Hamamatsu University School of Medicine, Hamamatsu, JPN.

Yasunori Enomoto (Y)

Department of Regenerative and Infectious Pathology, Hamamatsu University School of Medicine, Hamamatsu, JPN.

Satoshi Osawa (S)

Department of Endoscopic and Photodynamic Medicine, Hamamatsu University Hospital, Hamamatsu, JPN.

Ken Sugimoto (K)

First Department of Medicine, Hamamatsu University School of Medicine, Hamamatsu, JPN.

Satoshi Baba (S)

Department of Diagnostic Pathology, Hamamatsu University Hospital, Hamamatsu, JPN.

Toshihide Iwashita (T)

Department of Regenerative and Infectious Pathology, Hamamatsu University School of Medicine, Hamamatsu, JPN.

Classifications MeSH