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伴有食管蹼形成的普卢默-文森综合征,并获取了详细的内镜图像。

Plummer-Vinson Syndrome with Esophageal Web Formation in which Detailed Endoscopic Images Were Obtained.

作者信息

Hirose Takashi, Funasaka Kohei, Furukawa Kazuhiro, Yamamura Takeshi, Ishikawa Takuya, Ohno Eizaburo, Nakamura Masanao, Kawashima Hiroki, Miyahara Ryoji, Hirooka Yoshiki

机构信息

Department of Gastroenterology and Hepatology, Nagoya University Graduate School of Medicine, Japan.

Department of Endoscopy, Nagoya University Hospital, Japan.

出版信息

Intern Med. 2019 Mar 15;58(6):785-789. doi: 10.2169/internalmedicine.1628-18. Epub 2018 Nov 19.

DOI:10.2169/internalmedicine.1628-18
PMID:30449792
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6465006/
Abstract

Plummer-Vinson syndrome is a rare entity, characterized by dysphagia, esophageal web formation, and iron deficiency anemia. The patient was a 63-year-old woman with a clinical history of iron deficiency anemia and glossitis in her 20s to 40s and who had experienced swallowing difficulties for the past 20 years. A membranous stricture was found in the cervical esophagus during a fluoroscopic examination. An endoscopic examination conducted under general anesthesia revealed an oblique linear scar on the proximal surface of the stricture. Sequential balloon dilation was performed successfully. We suggest that the esophageal web formation might have been related to the healing of an esophageal ulcer.

摘要

普卢默-文森综合征是一种罕见病症,其特征为吞咽困难、食管蹼形成和缺铁性贫血。该患者为一名63岁女性,有缺铁性贫血和20多岁至40多岁时患舌炎的临床病史,且在过去20年中一直有吞咽困难。在荧光镜检查中发现颈段食管有膜状狭窄。全身麻醉下进行的内镜检查显示狭窄近端表面有一条斜行线性瘢痕。成功进行了序贯球囊扩张。我们认为食管蹼形成可能与食管溃疡的愈合有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcf3/6465006/6bfcefb1c715/1349-7235-58-0785-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcf3/6465006/f7bfba2be9d5/1349-7235-58-0785-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcf3/6465006/595478b3dfad/1349-7235-58-0785-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcf3/6465006/4712245405b3/1349-7235-58-0785-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcf3/6465006/6bfcefb1c715/1349-7235-58-0785-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcf3/6465006/f7bfba2be9d5/1349-7235-58-0785-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcf3/6465006/595478b3dfad/1349-7235-58-0785-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcf3/6465006/4712245405b3/1349-7235-58-0785-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcf3/6465006/6bfcefb1c715/1349-7235-58-0785-g004.jpg

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Plummer-Vinson Syndrome with Esophageal Web Formation in which Detailed Endoscopic Images Were Obtained.伴有食管蹼形成的普卢默-文森综合征,并获取了详细的内镜图像。
Intern Med. 2019 Mar 15;58(6):785-789. doi: 10.2169/internalmedicine.1628-18. Epub 2018 Nov 19.
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A Rare Case of Plummer-Vinson Syndrome.一例罕见的普卢默-文森综合征病例。
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本文引用的文献

1
Iron deficiency anemia and Plummer-Vinson syndrome: current insights.缺铁性贫血与普卢默-文森综合征:当前见解
J Blood Med. 2017 Oct 19;8:175-184. doi: 10.2147/JBM.S127801. eCollection 2017.
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Revisiting plummer vinson syndrome.再探普卢默-文森综合征。
Ann Med Health Sci Res. 2013 Jan;3(1):119-21. doi: 10.4103/2141-9248.109476.
3
Esophageal web resolved by endoscopic incision in a patient with Plummer-Vinson syndrome.一名患有普卢默-文森综合征的患者,其食管蹼经内镜下切开术得以解决。
Gastrointest Endosc. 2011 Nov;74(5):1142-3. doi: 10.1016/j.gie.2011.06.037. Epub 2011 Aug 6.
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Plummer-Vinson syndrome in a 15-year-old boy.一名15岁男孩患普卢默-文森综合征。
Turk J Pediatr. 2009 Jul-Aug;51(4):384-6.
5
Plummer-Vinson syndrome successfully treated by endoscopic dilatation.经内镜扩张成功治疗普卢默-文森综合征。
J Gastroenterol Hepatol. 2007 Dec;22(12):2348-51. doi: 10.1111/j.1440-1746.2006.03430.x.
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Plummer-Vinson syndrome.普卢默-文森综合征
Orphanet J Rare Dis. 2006 Sep 15;1:36. doi: 10.1186/1750-1172-1-36.
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Squamous cell cancer of the oesophagus.食管鳞状细胞癌
Best Pract Res Clin Gastroenterol. 2001 Apr;15(2):249-65. doi: 10.1053/bega.2000.0172.
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Dilation therapy of upper esophageal webs in two cases of Plummer-Vinson syndrome.两例普卢默-文森综合征患者上食管蹼的扩张治疗
Endoscopy. 1996 Feb;28(2):266-7. doi: 10.1055/s-2007-1005446.
9
Plummer-Vinson syndrome. A case report and literature review.普卢默-文森综合征。病例报告及文献综述。
Arch Intern Med. 1995 Oct 9;155(18):2008-11. doi: 10.1001/archinte.155.18.2008.
10
Tissue changes in iron deficiency.缺铁时的组织变化。
Br J Haematol. 1969 Jan-Feb;16(1):1-4. doi: 10.1111/j.1365-2141.1969.tb00372.x.