Surgical Case Reports最新文献

筛选
英文 中文
Intraoperative severe gastric venous congestion during total pancreatectomy with replaced common hepatic artery: a case report. 用肝总动脉替代全胰腺切除术时术中严重胃静脉充血:病例报告。
IF 0.7
Surgical Case Reports Pub Date : 2024-08-08 DOI: 10.1186/s40792-024-01983-x
Takahiro Yamanaka, Kenichiro Araki, Hideki Suzuki, Hidenobu Osawa, Ken Shirabe
{"title":"Intraoperative severe gastric venous congestion during total pancreatectomy with replaced common hepatic artery: a case report.","authors":"Takahiro Yamanaka, Kenichiro Araki, Hideki Suzuki, Hidenobu Osawa, Ken Shirabe","doi":"10.1186/s40792-024-01983-x","DOIUrl":"10.1186/s40792-024-01983-x","url":null,"abstract":"<p><strong>Background: </strong>Gastric venous congestion (GVC) is one of the complications of total pancreatectomy (TP). Here, we report a case of intraoperative severe GVC during TP with a replaced common hepatic artery (RCHA).</p><p><strong>Case presentation: </strong>A 65-year-old female patient was diagnosed with intraductal papillary mucinous carcinoma. Her CHA branched from the superior mesenteric artery as RCHA. She underwent subtotal stomach preserving TP. The tumor was resected with splenic artery (SpA) and total gastric vein transections. Severe GVC and bleeding from the stomach tube occurred intraoperatively. A strong pulsation was observed in the left gastric artery (LGA), and we suspected an increased blood flow from the celiac artery (CeA) to the LGA after SpA resection. Total gastrectomy (TG) was then performed to control the severe GVC-related bleeding. The patient was discharged without complications 19 days postoperatively.</p><p><strong>Conclusion: </strong>TP with RCHA may increase the risk of severe GVC due to increased blood flow from CeA to LGA.</p>","PeriodicalId":22096,"journal":{"name":"Surgical Case Reports","volume":null,"pages":null},"PeriodicalIF":0.7,"publicationDate":"2024-08-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11306704/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141903014","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Appendiceal goblet cell adenocarcinoma with perineural invasion extending into the ileocecal lesion. 阑尾鹅口疮细胞腺癌,有神经周围侵犯并延伸到回盲部病灶。
IF 0.7
Surgical Case Reports Pub Date : 2024-08-07 DOI: 10.1186/s40792-024-01984-w
Yuka Hosokawa, Sunao Fujiyoshi, Ken Imaizumi, Kengo Shibata, Nobuki Ichikawa, Tadashi Yoshida, Shigenori Homma, Takeaki Kudo, Nanase Okazaki, Utano Tomaru, Akinobu Taketomi
{"title":"Appendiceal goblet cell adenocarcinoma with perineural invasion extending into the ileocecal lesion.","authors":"Yuka Hosokawa, Sunao Fujiyoshi, Ken Imaizumi, Kengo Shibata, Nobuki Ichikawa, Tadashi Yoshida, Shigenori Homma, Takeaki Kudo, Nanase Okazaki, Utano Tomaru, Akinobu Taketomi","doi":"10.1186/s40792-024-01984-w","DOIUrl":"10.1186/s40792-024-01984-w","url":null,"abstract":"<p><strong>Background: </strong>Appendiceal goblet cell adenocarcinoma (GCA) is a rare subtype of primary appendiceal adenocarcinoma with an incidence of 1-5 per 10,000,000 people per year. Appendiceal tumors are often diagnosed after appendectomy for acute appendicitis. Notably, however, there is currently no standard treatment strategy for GCA, including additional resection. We report a case of appendiceal GCA with perineural extension into the cecum, in which ileal resection was considered effective.</p><p><strong>Case presentation: </strong>A 41-year-old man was diagnosed with acute appendicitis and underwent appendectomy. Histopathological findings revealed GCA (T3, Pn1). He was referred to our hospital for additional resection. Preoperative examination indicated a diagnosis of GCA cT3N0M0. Laparoscopic ileocecal resection and D3 lymph node dissection were performed 2 months after initial appendectomy. The patient had a good postoperative course and was discharged 8 days after surgery. Histopathological findings showed a GCA invading the cecum, despite an intact appendiceal stump, no lymph node metastasis, no vascular invasion, and no horizontal extension into the submucosa. Direct invasion of the tumor through the serosa was not observed, but perineural extension was conspicuous in the cecum, suggesting that the GCA extended into the cecum via perineural invasion. The resection margins were negative. The patient has survived free of recurrence for a year after ileocecal resection.</p><p><strong>Conclusions: </strong>The current patient was diagnosed with appendiceal GCA following appendectomy for acute appendicitis. Despite intact of appendiceal stump and no evidence of lymph node or distant metastasis, he underwent laparoscopic ileocecal resection and D3 lymph node dissection 2 months after initial appendectomy, with a favorable outcome. Despite the detection of perineural invasion, the patient declined adjuvant therapy. This case suggests that extensive resection may be required in patients with appendiceal GCA, but the role of adjuvant therapy remains unclear.</p>","PeriodicalId":22096,"journal":{"name":"Surgical Case Reports","volume":null,"pages":null},"PeriodicalIF":0.7,"publicationDate":"2024-08-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11303649/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141898298","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Successful thoracoscopic enucleation of a calcifying fibrous tumor of the lower mediastinum in a young woman. 成功为一名年轻女性实施胸腔镜下纵隔钙化纤维瘤去核手术。
IF 0.7
Surgical Case Reports Pub Date : 2024-08-01 DOI: 10.1186/s40792-024-01981-z
Ryo Yokota, Takeshi Matsutani, Keisuke Mishima, Ryo Yamagiwa, Hirotoshi Kubokura, Norio Motoda, Nobuhiko Taniai, Hiroshi Yoshida
{"title":"Successful thoracoscopic enucleation of a calcifying fibrous tumor of the lower mediastinum in a young woman.","authors":"Ryo Yokota, Takeshi Matsutani, Keisuke Mishima, Ryo Yamagiwa, Hirotoshi Kubokura, Norio Motoda, Nobuhiko Taniai, Hiroshi Yoshida","doi":"10.1186/s40792-024-01981-z","DOIUrl":"10.1186/s40792-024-01981-z","url":null,"abstract":"<p><strong>Background: </strong>Calcifying fibrous tumor (CFT) arising from the pleura is a relatively rare benign lesion in young and middle-aged adults. We report a 31-year-old woman with pleural CFT who underwent successful complete thoracoscopic enucleation.</p><p><strong>Case presentation: </strong>An asymptomatic woman presented with a mass in the right lower lung field that was incidentally detected on a chest X-ray during a routine medical checkup. Chest computed tomography showed a well-defined mass in the lower mediastinum, with a maximum diameter of approximately 5.5 cm. Esophagogastroduodenoscopy showed no abnormal findings in the esophagus. An endoscopic ultrasonography (EUS) revealed a well-defined tumor with no internal blood flow. EUS-fine needle aspiration failed to establish a definitive diagnosis. Therefore, thoracoscopic tumor enucleation was performed for diagnostic and therapeutic purposes. Based on the histopathological findings of the resected specimen, the presence of a tumor with a high fibrous component in a young woman, and the identification of granulomatous calcifications, a diagnosis of CFT was established.</p><p><strong>Conclusions: </strong>Complete thoracoscopic tumor enucleation was successfully performed for CFT arising from the pleura in a young adult woman.</p>","PeriodicalId":22096,"journal":{"name":"Surgical Case Reports","volume":null,"pages":null},"PeriodicalIF":0.7,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11294290/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141861022","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Robotic hemi-colectomy for ascending colon cancer in a patient with situs inversus totalis. 机器人半结肠切除术治疗全坐位不全患者的升结肠癌。
IF 0.7
Surgical Case Reports Pub Date : 2024-08-01 DOI: 10.1186/s40792-024-01982-y
Junki Kato, Takahisa Hirokawa, Kenji Kobayashi, Moritsugu Tanaka, Masahiro Kimura
{"title":"Robotic hemi-colectomy for ascending colon cancer in a patient with situs inversus totalis.","authors":"Junki Kato, Takahisa Hirokawa, Kenji Kobayashi, Moritsugu Tanaka, Masahiro Kimura","doi":"10.1186/s40792-024-01982-y","DOIUrl":"10.1186/s40792-024-01982-y","url":null,"abstract":"<p><strong>Background: </strong>Situs inversus totalis (SIT) is a rare congenital anomaly in which the thoracic and abdominal cavity structures are completely opposite to normal. Performing robot-assisted surgery in these patients is difficult because of these anomalies. A few reports have described robot-assisted surgery for rectal cancer in patients with SIT, but no reports to date have described robot-assisted surgery for colon cancer.</p><p><strong>Case presentation: </strong>A 74-year-old female presented with abdominal pain and was diagnosed with ascending colon cancer and SIT. We carefully planned the surgical procedure and performed robot-assisted hemi-colectomy. Although we used unusual port placement, the operation was performed safely. The patient was discharged without any complications.</p><p><strong>Conclusions: </strong>Robot-assisted surgery is safe and efficient for patients with anatomical anomalies.</p>","PeriodicalId":22096,"journal":{"name":"Surgical Case Reports","volume":null,"pages":null},"PeriodicalIF":0.7,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11291778/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141861021","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Posttraumatic aortic regurgitation and root pseudoaneurysm following blunt chest trauma: a case report. 胸部钝挫伤后主动脉瓣反流和根部假性动脉瘤:病例报告。
IF 0.7
Surgical Case Reports Pub Date : 2024-07-31 DOI: 10.1186/s40792-024-01963-1
Hiroaki Aizawa, Haruo Yamauchi, Masahiko Ando, Minoru Ono
{"title":"Posttraumatic aortic regurgitation and root pseudoaneurysm following blunt chest trauma: a case report.","authors":"Hiroaki Aizawa, Haruo Yamauchi, Masahiko Ando, Minoru Ono","doi":"10.1186/s40792-024-01963-1","DOIUrl":"10.1186/s40792-024-01963-1","url":null,"abstract":"<p><strong>Background: </strong>The simultaneous diagnosis of severe aortic regurgitation and aortic root pseudoaneurysm resulting from traffic injury is extremely rare. This report presents the case of a patient with Marfan syndrome who experienced aortic root pseudoaneurysm and subacute severe aortic regurgitation following a traffic accident.</p><p><strong>Case presentation: </strong>A 64-year-old woman was diagnosed with Marfan syndrome 16 years ago and is undergoing ongoing follow-up at an outpatient clinic. Eight years previously, the patient underwent total arch replacement combined with J-graft open stent graft<sup>®</sup> (JGOS; Japan Lifeline Co., Tokyo, Japan) deployment for acute type A dissection. Five months before presentation, the patient suffered a left rib fracture in a traffic accident and received conservative management at a local hospital. The patient presented to the emergency room with worsening shortness of breath and orthopnea. Echocardiography revealed severe aortic regurgitation and moderate tricuspid regurgitation. Computed tomography revealed new-onset pseudoaneurysm at the aortic root. Surgical repair was successfully performed using a modified Bentall procedure with a bioprosthetic valve and tricuspid annuloplasty. Intraoperative findings revealed pseudoaneurysm with perforation of the right sinus of Valsalva. Although the left and right aortic valve leaflets were normal, the noncoronary leaflet exhibited a ruptured fibrous strand of a cusp fenestration, resulting in acute aortic regurgitation.</p><p><strong>Conclusions: </strong>This case report highlights the rare occurrence of aortic root pseudoaneurysm and subacute aortic regurgitation following a traffic accident. In cases of blunt chest trauma, particularly in patients with Marfan syndrome, frequent examination is crucial to assess the possibility of posttraumatic aortic regurgitation and aortic injury.</p>","PeriodicalId":22096,"journal":{"name":"Surgical Case Reports","volume":null,"pages":null},"PeriodicalIF":0.7,"publicationDate":"2024-07-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11291823/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141856600","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A case of late-presenting congenital diaphragmatic hernia diagnosed at 5 years with acute abdomen. 一例晚期先天性膈疝患者,5 岁时被诊断为急腹症。
IF 0.7
Surgical Case Reports Pub Date : 2024-07-30 DOI: 10.1186/s40792-024-01980-0
Ryuta Masuya, Kazuhiko Nakame, Shun Munakata, Shinsuke Takeno, Atsushi Nanashima, Satoshi Ieiri
{"title":"A case of late-presenting congenital diaphragmatic hernia diagnosed at 5 years with acute abdomen.","authors":"Ryuta Masuya, Kazuhiko Nakame, Shun Munakata, Shinsuke Takeno, Atsushi Nanashima, Satoshi Ieiri","doi":"10.1186/s40792-024-01980-0","DOIUrl":"10.1186/s40792-024-01980-0","url":null,"abstract":"<p><strong>Background: </strong>Some congenital diaphragmatic hernias are diagnosed beyond 1 month. A late-presenting congenital diaphragmatic hernia shows a variety of clinical manifestations, and the preoperative clinical course is variable. We herein report a pediatric case of late-presenting congenital diaphragmatic hernia diagnosed as acute abdomen.</p><p><strong>Case presentation: </strong>A 5-year-old boy was brought to our hospital because of herniation of the intestine into the left thoracic cavity, which was observed on radiography performed for abdominal pain. Enhanced computed tomography showed herniation of the small intestine and colon into the left thoracic cavity. Emergency laparoscopic surgery was performed based on the diagnosis of left diaphragmatic hernia. The entire small intestine and part of the colon herniated from the posterolateral defect of the diaphragm. We were able to retract the herniated intestine back into the abdomen but confirmed that the diaphragmatic defect and closure of the defect seemed to be technically challenging via laparoscopy; therefore, we converted the procedure to open laparotomy. The diaphragmatic defect was directly closed with interrupted sutures, and the thoracic cavity was degassed. Postoperatively, the left lung was found to be poorly expanded, but pulmonary hypoplasia was not evident in this case.</p><p><strong>Conclusions: </strong>We herein report a pediatric case of late-presenting congenital diaphragmatic hernia diagnosed as abdominal pain. Late-presenting congenital diaphragmatic hernias present with a wide variety of symptoms; therefore, it is important to be reminded of these conditions and check chest radiographs in children presenting with acute or chronic respiratory or gastrointestinal symptoms of unknown etiology.</p>","PeriodicalId":22096,"journal":{"name":"Surgical Case Reports","volume":null,"pages":null},"PeriodicalIF":0.7,"publicationDate":"2024-07-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11289203/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141793568","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Utilizing a sutureless valve for prosthetic valve endocarditis after aortic root replacement. 利用无缝合瓣膜治疗主动脉根部置换术后的人工瓣膜心内膜炎。
IF 0.7
Surgical Case Reports Pub Date : 2024-07-30 DOI: 10.1186/s40792-024-01977-9
Yukihiro Hayatsu, Masaaki Naganuma, Hayate Nomura, Kazuhiro Yamaya, Masaki Hata
{"title":"Utilizing a sutureless valve for prosthetic valve endocarditis after aortic root replacement.","authors":"Yukihiro Hayatsu, Masaaki Naganuma, Hayate Nomura, Kazuhiro Yamaya, Masaki Hata","doi":"10.1186/s40792-024-01977-9","DOIUrl":"10.1186/s40792-024-01977-9","url":null,"abstract":"<p><strong>Background: </strong>Reoperation following aortic root replacement is associated with significantly high operative mortality. Etiologies related to infection are known to increase the operative mortality rate more than other etiologies. In such a clinical setting, a sutureless valve could lower the operative mortality by shortening the cardiac arrest and the operative time.</p><p><strong>Case presentation: </strong>A 61-year-old male underwent emergent aortic root and total arch replacement with an open stent graft for acute type-A aortic dissection. A bioprosthetic valve was employed for aortic root replacement using the double-sewing ring technique. A fungal infection by Candida parapsilosis was postoperatively detected and improved with intravenous antifungal drug administration. However, he developed congestive heart failure one year later, and the blood cultures turned positive repeatedly for Candida parapsilosis. The prosthetic valve infection was suspected upon identifying vegetation on the bioprosthetic valve through transthoracic echocardiography. The computed tomography scan and operative findings confirmed that the infection was localized on the prosthetic valve. Consequently, the infected valve was removed without a vascular conduit, and a sutureless valve was implanted. The postoperative course was uneventful, without any evidence of recurrent fungal infection, and the patient was discharged on postoperative day 28.</p><p><strong>Conclusions: </strong>Deploying a sutureless valve can facilitate a more straightforward and minimally invasive redo procedure. Preoperative computed tomography can predict the valve size, which is the key to implanting a sutureless valve successfully after the modified Bentall procedure.</p>","PeriodicalId":22096,"journal":{"name":"Surgical Case Reports","volume":null,"pages":null},"PeriodicalIF":0.7,"publicationDate":"2024-07-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11289299/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141793570","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Conversion surgery for BRCA-mutated pancreatic ductal adenocarcinoma with liver metastasis treated with platinum-based chemotherapy followed by olaparib. BRCA 基因突变的胰腺导管腺癌伴肝脏转移,在接受铂类化疗和奥拉帕利(olaparib)治疗后转为手术治疗。
IF 0.7
Surgical Case Reports Pub Date : 2024-07-30 DOI: 10.1186/s40792-024-01975-x
Takumi Funo, Daisuke Hashimoto, So Yamaki, Kazuki Matsumura, Hidetaka Miyazaki, Yuki Matsui, Denys Tsybulskyi, Nguyen Thanh Sang, Xu Yaolin, Sohei Satoi
{"title":"Conversion surgery for BRCA-mutated pancreatic ductal adenocarcinoma with liver metastasis treated with platinum-based chemotherapy followed by olaparib.","authors":"Takumi Funo, Daisuke Hashimoto, So Yamaki, Kazuki Matsumura, Hidetaka Miyazaki, Yuki Matsui, Denys Tsybulskyi, Nguyen Thanh Sang, Xu Yaolin, Sohei Satoi","doi":"10.1186/s40792-024-01975-x","DOIUrl":"10.1186/s40792-024-01975-x","url":null,"abstract":"<p><strong>Background: </strong>With recent dramatic developments in chemotherapy, attempts to incorporate surgery into the multidisciplinary treatment of unresectable pancreatic ductal adenocarcinoma with metastasis (UR-M PDAC) have emerged. Maintenance therapy with olaparib after chemotherapy including a platinum-based regimen, which inhibits the poly ADP-ribose polymerase (PARP) involved in DNA repair, was approved for UR-M PDAC with positive BRCA mutations.</p><p><strong>Case presentation: </strong>A 47-year-old male patient with a high carbohydrate antigen 19-9 (CA19-9) level was diagnosed with PDAC in the pancreatic tail. Staging laparoscopy revealed occult liver metastasis. Because BRCA2 mutation was confirmed, triple combination chemotherapy with SOXIRI (S-1/oxaliplatin/irinotecan) was introduced and continued for 16 weeks, followed by 14 weeks of olaparib. After that, CA19-9 was normalized, and no obvious liver metastases of any size could be seen on imaging studies during chemotherapy. Since staging laparoscopy after chemotherapy proved that the liver metastasis had disappeared, laparoscopic distal pancreatectomy was performed, and curative resection was completed. After adjuvant chemotherapy with olaparib for 12 months, the patient is alive 36 months from his initial diagnosis and 27 months postoperatively without recurrence.</p><p><strong>Conclusion: </strong>We report a case of PDAC with liver metastasis and BRCA mutation-positivity who underwent conversion surgery and achieved long-term survival after irinotecan-based chemotherapy followed by maintenance therapy with olaparib.</p>","PeriodicalId":22096,"journal":{"name":"Surgical Case Reports","volume":null,"pages":null},"PeriodicalIF":0.7,"publicationDate":"2024-07-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11289193/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141793569","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Pancreaticoduodenectomy after postoperative gastric tube reconstruction for esophageal cancer with median arcuate ligament syndrome: a case report. 食管癌术后胃管重建术后胰十二指肠切除术并发正中弓形韧带综合征:病例报告。
IF 0.7
Surgical Case Reports Pub Date : 2024-07-29 DOI: 10.1186/s40792-024-01974-y
Hideki Izumi, Hisamichi Yoshii, Rika Fujino, Shigeya Takeo, Yukiko Kojima, Junichi Kaneko, Masaya Mukai, Osamu Chino, Hiroyasu Makuuchi
{"title":"Pancreaticoduodenectomy after postoperative gastric tube reconstruction for esophageal cancer with median arcuate ligament syndrome: a case report.","authors":"Hideki Izumi, Hisamichi Yoshii, Rika Fujino, Shigeya Takeo, Yukiko Kojima, Junichi Kaneko, Masaya Mukai, Osamu Chino, Hiroyasu Makuuchi","doi":"10.1186/s40792-024-01974-y","DOIUrl":"10.1186/s40792-024-01974-y","url":null,"abstract":"<p><strong>Background: </strong>Pancreaticoduodenectomy (PD) is considered a challenging surgery for resecting the gastroduodenal artery (GDA), right gastric artery (RGA), and lymph node tumors. In cases of pancreatic head cancer surgery, vascular anastomosis or right gastroepiploic artery (RGEA)/GDA preservation is necessary after postoperative gastric tube reconstruction for esophageal cancer. Therefore, we report for the first time an extremely rare case of PD in a patient with pancreatic head cancer and median arcuate ligament syndrome (MALS) after gastric tube reconstruction following esophageal cancer surgery, in which the entire pancreatic head arcade was preserved.</p><p><strong>Case presentation: </strong>The patient was a 76-year-old man who had undergone esophageal cancer surgery after sternal gastric tube reconstruction 7 years ago. He was referred to our hospital because of the suspicion of intraductal papillary mucinous carcinoma (IPMC) owing to an enlarged cystic lesion and a substantial component in the uncinate process of the pancreas. Preoperative three-dimensional computed (3D-CT) tomography angiography showed celiac axis stenosis and pancreatic head arcade dilation. The diagnosis was IPMC without evidence of invasion; therefore, gastric tube blood flow was maintained by preserving the GDA and RGEA. Due to MALS, the GDA blood flow was supplied through the pancreatic head arcade, necessitating its preservation. The GDA-RGEA, right gastroepiploic vein, and anterior superior pancreaticoduodenal artery were taped over the entire pancreatic head for preservation. The inferior pancreaticoduodenal artery (IPDA) was also taped on the dorsal pancreas and the posterior or anterior IPDA, which further bifurcates were taped to preserve them. Subsequently, PD was performed.</p><p><strong>Conclusion: </strong>We report a case of PD after gastric tube reconstruction for esophageal cancer with MALS, in which the pancreatic head arcade vessels were successfully preserved using 3D-CT to confirm the operation of the vessels.</p>","PeriodicalId":22096,"journal":{"name":"Surgical Case Reports","volume":null,"pages":null},"PeriodicalIF":0.7,"publicationDate":"2024-07-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11286890/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141789088","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Minimally invasive pancreaticoduodenectomy for circumportal pancreas: literature review and report of two type IIIA cases. 环主动脉胰腺的微创胰十二指肠切除术:文献综述和两例 IIIA 型病例的报告。
IF 0.7
Surgical Case Reports Pub Date : 2024-07-29 DOI: 10.1186/s40792-024-01979-7
Hajime Imamura, Tomohiko Adachi, Mampei Yamashita, Ayaka Kinoshita, Takashi Hamada, Hajime Matsushima, Takanobu Hara, Akihiko Soyama, Kazuma Kobayashi, Kengo Kanetaka, Susumu Eguchi
{"title":"Minimally invasive pancreaticoduodenectomy for circumportal pancreas: literature review and report of two type IIIA cases.","authors":"Hajime Imamura, Tomohiko Adachi, Mampei Yamashita, Ayaka Kinoshita, Takashi Hamada, Hajime Matsushima, Takanobu Hara, Akihiko Soyama, Kazuma Kobayashi, Kengo Kanetaka, Susumu Eguchi","doi":"10.1186/s40792-024-01979-7","DOIUrl":"10.1186/s40792-024-01979-7","url":null,"abstract":"<p><strong>Background: </strong>Circumportal pancreas is a rare morphological variant with clinical significance due to the high risk of postoperative pancreatic fistula in patients undergoing pancreaticoduodenectomy. Type IIIA (suprasplenic anteportal) is the most common type of circumportal pancreas. We present two cases of type IIIA treated with minimally invasive pancreaticoduodenectomy, and review the literature on patients with circumportal pancreas who underwent pancreatic surgery.</p><p><strong>Case presentation: </strong>Case 1: Laparoscopic Pancreaticoduodenectomy for Non-functioning Pancreatic Neuroendocrine Neoplasm with Circumportal Pancreas. A 69-year-old female with no prior medical history presented with a pancreatic head mass detected during routine ultrasound. CT revealed a 20 mm hypervascular tumor in pancreas head and a suprasplenic circumportal pancreas with an anteportal duct. The main pancreatic duct (MPD) was not in the parenchyma on the dorsal side of the portal vein (PV). Laparoscopic pancreaticoduodenectomy was performed. The anteportal side was resected with an ultrasonic device, and the retroportal side with a mesh-reinforced stapler. Pancreaticojejunostomy was performed without complications. Case 2: Robot-assisted Pancreaticoduodenectomy for Pancreatic Head Cancer and Non-functioning Pancreatic Neuroendocrine Neoplasm in the pancreatic tail with Circumportal Pancreas. A 72-year-old male with no prior medical history presented with a dilated main pancreatic duct on ultrasound. Diagnosed with pancreatic head cancer (Stage IIA), he underwent neoadjuvant chemotherapy. Contrast-enhanced CT revealed pancreatic cancer in the head and a tumor in the tail with unknown pathology. Robot-assisted pancreaticoduodenectomy was performed, and pancreatectomy on the left side of the tail tumor was planned. Intraoperative findings revealed a circumportal pancreas with the MPD not running through the dorsal parenchyma. After resected the parenchyma on the left side of the tail tumor, parenchyma on the dorsal side of the PV was dissected using SynchroSeal®. Pancreaticojejunostomy was performed without complications. The postoperative course was uneventful.</p><p><strong>Conclusions: </strong>The optimal location and method of pancreatic resection should be selected according to the type of circumportal pancreas and the location of the lesion to be resected to minimize the risk of pancreatic fistula. Minimally invasive surgery for circumportal pancreas remains challenging even for surgical teams with sufficient experience and skills, and careful consideration are necessary for its application.</p>","PeriodicalId":22096,"journal":{"name":"Surgical Case Reports","volume":null,"pages":null},"PeriodicalIF":0.7,"publicationDate":"2024-07-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11286910/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141789087","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
相关产品
×
本文献相关产品
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信