Surgery for Killian-Jamieson diverticulum: a report of two cases

Abstract Background Killian-Jamieson diverticulum (KJD) is a rare diverticulum arising from a muscular gap in the anterolateral wall of the proximal cervical esophagus. The first choice of treatment for KJD remains controversial due to its rare incidence. Here, we report two cases of KJD for which w...

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Main Authors: Kohei Saisho, Satoru Matono, Toshiaki Tanaka, Naoki Mori, Haruhiro Hino, Masahiro Fujisaki, Masashi Nakagawa, Fumihiko Fujita, Yoshito Akagi
Format: Article
Language:English
Published: Japan Surgical Society 2020-01-01
Series:Surgical Case Reports
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Online Access:https://doi.org/10.1186/s40792-020-0789-0
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author Kohei Saisho
Satoru Matono
Toshiaki Tanaka
Naoki Mori
Haruhiro Hino
Masahiro Fujisaki
Masashi Nakagawa
Fumihiko Fujita
Yoshito Akagi
author_facet Kohei Saisho
Satoru Matono
Toshiaki Tanaka
Naoki Mori
Haruhiro Hino
Masahiro Fujisaki
Masashi Nakagawa
Fumihiko Fujita
Yoshito Akagi
author_sort Kohei Saisho
collection DOAJ
description Abstract Background Killian-Jamieson diverticulum (KJD) is a rare diverticulum arising from a muscular gap in the anterolateral wall of the proximal cervical esophagus. The first choice of treatment for KJD remains controversial due to its rare incidence. Here, we report two cases of KJD for which we performed different surgery: diverticulectomy in one case and diverticulopexy in the other. Case presentation Case 1 involved a 58-year-old woman presenting progressive pharyngeal discomfort for the past year. She was diagnosed as KJD using endoscopic and radiographic findings. She underwent diverticulectomy with cricopharyngeal and proximal esophageal myotomy. Staple line leakage developed at 1 month after surgery and was successfully treated conservatively. At 5 months after surgery, she was asymptomatic. Case 2 involved a 77-year-old woman presenting dysphagia for the past 2 years. She had a history of bilateral breast cancer and had hypertension, asthma, and osteoporosis. Taking her age and medical history into account, we selected diverticulopexy with cricopharyngeal and proximal esophageal myotomy. The postoperative course was uneventful. At 2 years after surgery, she remained free of dysphagia. Conclusion The first choice of surgery for KJD is diverticulectomy. In a high-risk patient, diverticulopexy is a reasonable treatment. We recommend the addition of myotomy as a part of any surgical treatment.
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spelling doaj-art-db4df45e94bf40b395141e952ca96d352025-08-20T03:58:53ZengJapan Surgical SocietySurgical Case Reports2198-77932020-01-01611610.1186/s40792-020-0789-0Surgery for Killian-Jamieson diverticulum: a report of two casesKohei Saisho0Satoru Matono1Toshiaki Tanaka2Naoki Mori3Haruhiro Hino4Masahiro Fujisaki5Masashi Nakagawa6Fumihiko Fujita7Yoshito Akagi8Department of Surgery, Kurume University School of MedicineDepartment of Surgery, Kurume University School of MedicineDepartment of Surgery, Kurume University School of MedicineDepartment of Surgery, Kurume University School of MedicineDepartment of Surgery, Kurume University School of MedicineDepartment of Surgery, Kurume University School of MedicineDepartment of Surgery, Kurume University School of MedicineDepartment of Surgery, Kurume University School of MedicineDepartment of Surgery, Kurume University School of MedicineAbstract Background Killian-Jamieson diverticulum (KJD) is a rare diverticulum arising from a muscular gap in the anterolateral wall of the proximal cervical esophagus. The first choice of treatment for KJD remains controversial due to its rare incidence. Here, we report two cases of KJD for which we performed different surgery: diverticulectomy in one case and diverticulopexy in the other. Case presentation Case 1 involved a 58-year-old woman presenting progressive pharyngeal discomfort for the past year. She was diagnosed as KJD using endoscopic and radiographic findings. She underwent diverticulectomy with cricopharyngeal and proximal esophageal myotomy. Staple line leakage developed at 1 month after surgery and was successfully treated conservatively. At 5 months after surgery, she was asymptomatic. Case 2 involved a 77-year-old woman presenting dysphagia for the past 2 years. She had a history of bilateral breast cancer and had hypertension, asthma, and osteoporosis. Taking her age and medical history into account, we selected diverticulopexy with cricopharyngeal and proximal esophageal myotomy. The postoperative course was uneventful. At 2 years after surgery, she remained free of dysphagia. Conclusion The first choice of surgery for KJD is diverticulectomy. In a high-risk patient, diverticulopexy is a reasonable treatment. We recommend the addition of myotomy as a part of any surgical treatment.https://doi.org/10.1186/s40792-020-0789-0Killian-Jamieson diverticulumPharyngoesophageal diverticulumDiverticulectomyDiverticulopexy
spellingShingle Kohei Saisho
Satoru Matono
Toshiaki Tanaka
Naoki Mori
Haruhiro Hino
Masahiro Fujisaki
Masashi Nakagawa
Fumihiko Fujita
Yoshito Akagi
Surgery for Killian-Jamieson diverticulum: a report of two cases
Surgical Case Reports
Killian-Jamieson diverticulum
Pharyngoesophageal diverticulum
Diverticulectomy
Diverticulopexy
title Surgery for Killian-Jamieson diverticulum: a report of two cases
title_full Surgery for Killian-Jamieson diverticulum: a report of two cases
title_fullStr Surgery for Killian-Jamieson diverticulum: a report of two cases
title_full_unstemmed Surgery for Killian-Jamieson diverticulum: a report of two cases
title_short Surgery for Killian-Jamieson diverticulum: a report of two cases
title_sort surgery for killian jamieson diverticulum a report of two cases
topic Killian-Jamieson diverticulum
Pharyngoesophageal diverticulum
Diverticulectomy
Diverticulopexy
url https://doi.org/10.1186/s40792-020-0789-0
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