A small adenocarcinoma in the cervical esophagus

Tanaka, Kyosuke; Yamada, Reiko; Tsuboi, Junya; Kuroda, Naoki; Hamada, Yasuhiko

doi:10.1016/j.vgie.2018.12.003

Cited by 2 publications

(2 citation statements)

References 10 publications

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“…Developing high-resolution endoscopy and image-enhanced endoscopy is expected to contribute to the early detection of EAC. Table 1 shows a review of previous reports on early EAC derived from EGM treated with endoscopic resection (5,(13)(14)(15)(16)(17)(18)(19)(20)(21)(22)(23)(24)(25)(26). Seventeen cases, including our two cases, were identified between 2001 and 2021.…”

Section: Discussionmentioning

confidence: 99%

Early Esophageal Adenocarcinoma with Non-Barrett's Columnar Epithelium Origin: Two Case Reports and a Literature Review

et al. 2023

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We herein report two cases of early esophageal adenocarcinoma derived from non-Barrett's columnar epithelium. Both patients, a 65-year-old woman and 60-year-old man, had elevated lesions on white-light imaging. Magnifying endoscopy revealed slightly irregular surface and vessel patterns, and both patients were successfully treated with endoscopic submucosal dissection. Histopathologically, both lesions comprised of welldifferentiated gastric mucin phenotype adenocarcinoma. One lesion was accompanied by ectopic gastric mucosa, but the other was speculated to be ectopic gastric mucosa according to the tumor locus at the upper thoracic esophagus. Despite its rarity, endoscopists should consider the existence of adenocarcinoma derived from non-Barrett's columnar epithelium.

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Section: Discussionmentioning

confidence: 99%

Early Esophageal Adenocarcinoma with Non-Barrett's Columnar Epithelium Origin: Two Case Reports and a Literature Review

et al. 2023

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“…The literature review may help determine a treatment strategy (4,(6)(7)(8)(9)(10)(11)(12)(13)(14)(15)(16)(17)(18)(19)(20)(21)(22)(23)(24)(25). Most of the reported patients with stage 0 and I adenocarcinomas underwent endoscopic treatment or surgery and had considerably good results without any recurrences (4,8,11,12,14,(20)(21)(22)(23)(24)(25). For patients with stage II, surgery alone without adjuvant treatment was adequate (9,18,22).…”

Section: Figure 1 Preliminary Evaluations Esophagoscopy Shows a Half-circumferential Tumour At The Left Wall Of The Cervical Oesophagus 1mentioning

confidence: 99%

Human Epidermal Growth Factor Receptor 2-positive Primary Adenocarcinoma in the Cervical Oesophagus: A Case Report

Horinouchi

Yoshida

Matsumoto

et al. 2021

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Background/Aim: Cervical oesophageal adenocarcinoma (COA) is extremely rare. We present a case of human epidermal growth factor receptor 2 (HER2)-positive COA that showed repeated recurrences despite multidisciplinary treatments. Case Report: A 49-year-old male was diagnosed with clinical stage IVA COA that originated from ectopic gastric mucosa. He initially underwent definitive chemoradiotherapy (CRT) (60.0 Gy/30 fractions, 5fluorouracil, and cisplatin). Two months after CRT, the right supraclavicular lymph node (LN) reenlarged and salvage lymphadenectomy was performed. Immunohistochemical staining revealed a HER2-positive adenocarcinoma. Four months after lymphadenectomy, multiple metastases in the mediastinal LNs and lungs were detected, and S-1, oxaliplatin and trastuzumab were administered. Four months after chemotherapy, the patient presented with new liver metastasis. Further metastasis was prevented by Nivolumab treatment for four months. Conclusion: HER2-positive COA may be more aggressive and may require further intensive treatments. This literature review may be helpful in determining treatment strategies for COA.

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A small adenocarcinoma in the cervical esophagus

Cited by 2 publications

References 10 publications

Early Esophageal Adenocarcinoma with Non-Barrett's Columnar Epithelium Origin: Two Case Reports and a Literature Review

Early Esophageal Adenocarcinoma with Non-Barrett's Columnar Epithelium Origin: Two Case Reports and a Literature Review

Human Epidermal Growth Factor Receptor 2-positive Primary Adenocarcinoma in the Cervical Oesophagus: A Case Report

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