| Literature DB >> 31464953 |
Chun-Hui Shou1, Zhi-Jian Li, Wei-Li Yang, Welda E H Tjhoi, Zhi-Cheng Zhao, Ji-Ren Yu.
Abstract
RATIONALE: Adenoid cystic carcinoma (ACC) rarely occurs in the digestive tract, particularly in the gastroesophageal junction. PATIENT CONCERNS: A 44-year-old male vomiting blood was admitted to our hospital. Endoscopic ultrasound showed a 2.2 × 3.0 cm submucosal tumor in the gastroesophageal junction. DIAGNOSIS: According to the histopathological examination, the tumor was composed predominantly of ductal epithelial and myoepithelial cells. Immunohistochemical staining revealed that the tumor expressed cytokeratin, cluster of differentiation 117, p63, and calponin. Based on these findings, ACC was diagnosed.Entities:
Mesh:
Year: 2019 PMID: 31464953 PMCID: PMC6736487 DOI: 10.1097/MD.0000000000016999
Source DB: PubMed Journal: Medicine (Baltimore) ISSN: 0025-7974 Impact factor: 1.817
Figure 1The preoperative (A, B) and intraoperative (C, D) endoscopy showing the tumor. (A)+(B): Endoscopic ultrasound showing a hypoechoic tumor located in the gastroesophageal junction with the size of 22.4 mm × 30.4 mm; (C): Intraoperative normal white light of the tumor (D): The Resected surface after excision.
Figure 2Histology and immunohistochemistry of the tumor. (A): Micrograph of the resected specimen showing mostly in tubular patterns and partly cribriform pattern (hematoxylin and eosin staining; magnification, x100). (B): Cytokeratin staining (magnification, x200); (C): Cluster of differentiation 117 staining (magnification, x200); (D): P63 staining (magnification, x200).
The clinical data of the present and reported cases of esophageal adenoid cystic carcinoma.