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Total venous coronary artery bypass grafting for acute myocardial infarction with Leriche syndrome and porcelain aorta: a case report. 全静脉冠状动脉旁路移植术治疗急性心肌梗死合并Leriche综合征和瓷主动脉1例。
IF 0.5 Q4 SURGERY Pub Date : 2026-01-20 eCollection Date: 2026-01-01 DOI: 10.1093/jscr/rjaf1102
Hideki Isa, Kentaro Shirakura, Tasuku Kawarabayashi, Hidenobu Akamatsu, Koji Kagawa, Kazuki Miyatani, Nobuhiro Mochizuki, Fumitaka Suzuki, Ryohei Ushioda, Ryo Okubo, Aina Hirofuji, Shingo Kunioka, Masahiro Tsutsui, Hiroyuki Kamiya

Leriche syndrome is an occlusive disease involving the abdominal aorta and iliac arteries that is frequently associated with ischemic heart disease (IHD). The internal thoracic arteries in patients with Leriche syndrome often serve as important collateral pathways to the lower extremities. Therefore, graft selection for coronary artery bypass grafting (CABG) requires special consideration. We performed on-pump total venous CABG in a patient with acute heart failure secondary to IHD complicated by Leriche syndrome who required emergent coronary revascularization. This strategy was chosen to preserve lower limb perfusion. When coronary revascularization is a priority for patients with IHD complicated by Leriche syndrome, on-pump total venous CABG is a reasonable option because of the need to preserve lower limb perfusion and difficulty of using mechanical circulatory support devices for occlusive disease.

Leriche综合征是一种累及腹主动脉和髂动脉的闭塞性疾病,常与缺血性心脏病(IHD)相关。Leriche综合征患者的胸内动脉常作为通往下肢的重要侧支通路。因此,冠状动脉旁路移植术(CABG)的移植物选择需要特别考虑。我们对一例继发于IHD并发Leriche综合征的急性心力衰竭患者进行了无泵全静脉冠脉搭桥治疗,该患者需要紧急冠脉重建术。选择这种策略是为了保持下肢灌注。当合并Leriche综合征的IHD患者优先考虑冠状动脉血运重建时,无泵全静脉冠脉搭桥是一个合理的选择,因为需要保持下肢灌注,并且闭塞性疾病难以使用机械循环支持装置。
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引用次数: 0
Small bowel ischemia caused by wrapping of the appendix around the small bowel after adhering to eroded mesh following elective laparoscopic TAPP repair. 选择性腹腔镜TAPP修复后,粘连侵蚀网片后阑尾包裹小肠引起的小肠缺血。
IF 0.5 Q4 SURGERY Pub Date : 2026-01-20 eCollection Date: 2026-01-01 DOI: 10.1093/jscr/rjaf1096
Abdulrahman Ghoneim, Mohamed Issa, Marvi Shams, Mohamed Awad

Laparoscopic transabdominal preperitoneal (TAPP) repair is the gold standard for treatment of inguinal hernia. Its complications are well known; however, its rare complications, such as mesh erosion and migration are commonly overlooked. There is established evidence about mesh complications; however, we have not found a similar case to what we encountered. We present a case of an elderly male who presented with a closed-loop bowel obstruction following a TAPP repair. Intraoperatively, the appendix tip was adherent to the eroded mesh through a defect in the peritoneal flap. The appendix formed a constricting wrap around the terminal ileum with a resultant ischemia of the bowel in the presence of a competent ileocecal valve. Reasons accounting to mesh erosion can be divided into primary and secondary causes. Complications from mesh erosion vary from fistulation up to bowel ischemia. Failure to recognize these complications can lead to considerable morbidity.

腹腔镜经腹腹膜前修补术(TAPP)是治疗腹股沟疝的金标准。它的复杂性是众所周知的;然而,其罕见的并发症,如网片侵蚀和迁移通常被忽视。有关于补片并发症的确凿证据;然而,我们没有发现与我们遇到的类似的情况。我们提出一个老年男性的情况下,谁提出了闭合性肠梗阻后,TAPP修复。术中,阑尾尖端通过腹膜瓣的缺损附着在侵蚀的补片上。阑尾在回肠末端形成一个狭窄的包裹,导致肠缺血,存在一个有效的回盲瓣。核算网孔侵蚀的原因可分为主要原因和次要原因。网状物侵蚀的并发症从瘘到肠缺血不等。未能认识到这些并发症可导致相当大的发病率。
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引用次数: 0
Post-lobectomy lung abscess. 肺叶切除术后肺脓肿。
IF 0.5 Q4 SURGERY Pub Date : 2026-01-20 eCollection Date: 2026-01-01 DOI: 10.1093/jscr/rjaf1087
Sarah E Kim, Daniel Steeno, Hassan A Qureshi, Alexander P Lynch, Francis J Podbielski

A residual lung parenchyma abscess following pulmonary resection for lung cancer is a rare and potentially serious condition. We present a case of successful nonoperative management of a lung abscess that developed after a right upper lobectomy for adenocarcinoma in a 76-year-old man who experienced systemic symptoms 6 weeks after his initial surgery. Imaging revealed an abscess in the previous surgical cavity. We discuss management strategies and challenges associated with this uncommon condition.

摘要肺癌肺切除术后残留的肺实质脓肿是一种罕见且潜在严重的疾病。我们报告一例成功的非手术治疗的肺脓肿后发展的右上肺叶腺癌在76岁的男子谁经历了全身症状6周后,他的初次手术。影像学显示先前手术腔内有脓肿。我们将讨论与这种罕见疾病相关的管理策略和挑战。
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引用次数: 0
Complex case of congenital pulmonary sequestration with successful "EXIT" procedure. 先天性肺隔离的复杂病例成功的“EXIT”手术。
IF 0.5 Q4 SURGERY Pub Date : 2026-01-20 eCollection Date: 2026-01-01 DOI: 10.1093/jscr/rjaf1066
Rūta Bernatavičienė, Gabija Pikturnaitė, Gilvydas Verkauskas, Arūnas Strumila

The ex-utero intrapartum treatment (EXIT) procedure preserves fetal oxygenation via the umbilical cord in urgent respiratory distress. We report a rare case of congenital extralobar pulmonary sequestration with pedicle torsion. A 22-year-old primigravida at 29 + 4 weeks presented with a fetal supradiaphragmatic mass, hydrothorax, and cardiac displacement; fetal magnetic resonance imaging (MRI) confirmed pulmonary sequestration. Rapid fetal deterioration led to the termination of the pregnancy and the application of ex-utero intrapartum treatment procedure during Cesarean section. Before cord clamping, intubation along with thoracocentesis enabled neonatal breathing. The 2140 g newborn required intensive care for respiratory distress, heart failure, and pulmonary hypertension and was discharged stable after 3 weeks. Elective thoracoscopy at the age of 6 months removed the sequestration, confirming pedicle torsion; recovery was uneventful. This case highlights the importance of early diagnosis, multidisciplinary collaboration, and timely use of ex-utero intrapartum treatment to manage life-threatening fetal lung anomalies.

在紧急呼吸窘迫的情况下,子宫外产时治疗(EXIT)程序可通过脐带保留胎儿氧合。我们报告一例罕见的先天性叶外肺隔离伴椎弓根扭转。一例22岁的初产妇29 + 4周时出现胎儿膈上肿块、胸水和心脏移位;胎儿核磁共振成像(MRI)证实肺隔离。在剖宫产术中,胎儿迅速恶化导致终止妊娠和应用宫外产内处理程序。在脐带夹紧之前,插管和胸腔穿刺使新生儿能够呼吸。这名2140克的新生儿因呼吸窘迫、心力衰竭和肺动脉高压需要重症监护,3周后出院,病情稳定。6个月时择期胸腔镜取出隔离物,确认椎弓根扭转;恢复过程平淡无奇。该病例强调了早期诊断、多学科合作和及时使用子宫外产时治疗对处理危及生命的胎儿肺异常的重要性。
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引用次数: 0
Collision thyroid tumors: a case report of coexisting papillary and follicular carcinoma. 碰撞性甲状腺肿瘤:乳头状癌和滤泡癌共存1例。
IF 0.5 Q4 SURGERY Pub Date : 2026-01-20 eCollection Date: 2026-01-01 DOI: 10.1093/jscr/rjaf1106
Danilo Estuardo Torselli-Valladares, Víctor Argueta, Carlos Rene Cordón, Marco Antonio Peñalonzo

Collision tumors of the thyroid gland are defined by the coexistence of two or more histologically and morphologically distinct neoplasms, separated by normal thyroid tissue. This phenomenon is rare, with the most frequently reported combination being the coexistence of medullary carcinoma and papillary carcinoma. This case reports a 73-year-old female patient with an asymptomatic thyroid nodule. Ultrasonographic examination revealed a solid, isoechoic, well-defined nodule with a halo and peripheral vascularization, measuring 4.3 × 2.5 cm in the left lobe. Fine-needle aspiration cytology classified the nodule as Bethesda IV (follicular tumor). Following total thyroidectomy, histopathological analysis identified papillary carcinoma in the isthmus and minimally invasive follicular carcinoma in the left lobe.

甲状腺碰撞瘤的定义是两个或两个以上组织学和形态学上不同的肿瘤共存,被正常甲状腺组织分开。这种现象是罕见的,最常见的合并报道是髓样癌和乳头状癌共存。本病例报告一位73岁女性患者无症状甲状腺结节。超声检查显示左肺叶一实性、等回声、界限分明的结节,有晕,周围有血管形成,尺寸为4.3 × 2.5 cm。细针穿刺细胞学诊断结节为Bethesda IV(滤泡性肿瘤)。甲状腺全切除术后,组织病理学分析发现峡部乳头状癌和左叶微创滤泡癌。
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引用次数: 0
Right renal autotransplantation as a kidney-sparing strategy in complex symptomatic angiomyolipoma. 右肾自体移植作为复杂症状血管平滑肌脂肪瘤的保肾策略。
IF 0.5 Q4 SURGERY Pub Date : 2026-01-20 eCollection Date: 2026-01-01 DOI: 10.1093/jscr/rjaf1110
Christian Gordon, Francisco Javier Cornejo, Frans Ivan Serpa, Ligia M Redroban, Camila Domenica Valenzuela Molineros, Santiago Muñoz-Palomeque

We present the case of a 34-year-old male with right flank pain. Computed tomography revealed at least six cortical, expansible, fat-density lesions in the right kidney and two similar lesions in the left kidney, consistent with angiomyolipomas. Surgical management consisted of radical right nephrectomy with immediate renal autotransplantation. Ex vivo tumour excision was performed under ultrasound guidance and hydrodissection, followed by cortical reconstruction and reimplantation into the ipsilateral iliac fossa. Vascular anastomoses were fashioned end-to-side to the external iliac vessels, and ureteral reimplantation was achieved using the Taguchi technique with double-J stent placement. The postoperative course was uneventful, with preserved renal function. This case highlights the value of multidisciplinary assessment, individualized planning, and meticulous surgical technique to avoid unnecessary radical nephrectomy, particularly in patients with bilateral renal tumors.

我们提出的情况下,34岁的男性右侧疼痛。计算机断层扫描显示右肾至少6个皮质性、可扩张性、脂肪密度病变,左肾2个类似病变,符合血管平滑肌脂肪瘤。手术治疗包括根治性右肾切除术和立即自体肾移植。在超声引导和水解剖下进行离体肿瘤切除,随后进行皮质重建并重新植入同侧髂窝。血管吻合端侧与髂外血管吻合,输尿管再植采用田口技术,双j型支架置入。术后过程平稳,肾功能得以保留。本病例强调了多学科评估、个体化规划和细致的手术技术的价值,以避免不必要的根治性肾切除术,特别是双侧肾肿瘤患者。
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引用次数: 0
Young patient with aortoduodenal fistula post-tumour resection and aortic graft reconstruction in childhood: a case report. 儿童肿瘤切除及主动脉移植重建术后并发十二指肠瘘的年轻患者1例。
IF 0.5 Q4 SURGERY Pub Date : 2026-01-20 eCollection Date: 2026-01-01 DOI: 10.1093/jscr/rjaf1091
Inez Ohashi Torres, Jesus Sebastian Luna Medrano, Samuel Pugliero, Gisela Serra Rodrigues Costa, Erasmo Simão da Silva, Nelson De Luccia
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引用次数: 0
Spontaneous splenic rupture: a sporadic presentation of tuberculosis-a case report. 自发性脾破裂:散发性肺结核一例报告。
IF 0.5 Q4 SURGERY Pub Date : 2026-01-20 eCollection Date: 2026-01-01 DOI: 10.1093/jscr/rjaf1103
Zeru A Sambi, Mehari A Tsegay

Atraumatic or spontaneous splenic rupture is a rare but life-threatening emergency. Common causes include hematologic malignancies and infections, but tuberculous involvement of the spleen is exceedingly uncommon. To our knowledge, this represents the third reported case of spontaneous rupture of a tuberculous spleen. We report a 50-year-old human immunodeficiency virus (HIV) -positive woman who presented with cough, fever, and abdominal distension, with abdominal examination suggesting peritoneal irritation and laboratory tests showing severe anemia. Emergency laparotomy revealed a ruptured spleen with 500 ml of hemolyzed blood, and splenectomy was performed. Histopathology confirmed splenic tuberculosis. The postoperative course was uneventful. Splenic tuberculosis typically occurs in disseminated disease among immunocompromised individuals. Fever of unknown origin is the commonest presentation; spontaneous rupture is exceptionally rare and difficult to diagnose. Although antitubercular therapy is the mainstay of treatment, hemodynamically unstable patients require surgery. Spontaneous splenic rupture should be considered in immunocompromised patients with an acute abdomen, as early recognition is lifesaving.

非外伤性或自发性脾破裂是一种罕见但危及生命的紧急情况。常见的原因包括血液恶性肿瘤和感染,但结核累及脾脏是非常罕见的。据我们所知,这是第三例报告的自发性结核性脾破裂病例。我们报告一位50岁的人类免疫缺陷病毒(HIV)阳性妇女,她表现为咳嗽、发烧和腹胀,腹部检查提示腹膜刺激,实验室检查显示严重贫血。急诊剖腹探查发现脾脏破裂伴500毫升溶血,并行脾切除术。组织病理学证实为脾结核。术后过程平淡无奇。脾结核通常发生在免疫功能低下个体的弥散性疾病中。病因不明的发热是最常见的表现;自发性破裂极为罕见且难以诊断。虽然抗结核治疗是主要的治疗方法,但血流动力学不稳定的患者需要手术治疗。免疫功能低下的急腹症患者应考虑自发性脾破裂,因为早期识别是挽救生命的。
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引用次数: 0
A rare surgical emergency during pregnancy: a case report. 妊娠期罕见的外科急诊1例报告。
IF 0.5 Q4 SURGERY Pub Date : 2026-01-19 eCollection Date: 2026-01-01 DOI: 10.1093/jscr/rjaf1080
Zouhry Ibrahim, Guetmy Zakaria, Alaoui Babana Amina, Mohammed Boufeloussen, Khedid Yahia, Alami Faricha Hassan

Acute pelvic pain during pregnancy often presents a diagnostic challenge. We report a case of adnexal torsion occurring in the third trimester of pregnancy in order to highlight this diagnosis, for which only early management can prevent irreversible ischemic damage that may compromise future fertility. The patient was a nulliparous woman at 30 weeks of amenorrhea who initially presented with symptoms suggestive of appendicitis. Through a McBurney incision, surgical exploration revealed a necrotic right ovary associated with reactive appendicitis. An oophorectomy and appendectomy were performed. The postoperative course was uneventful.

妊娠期急性盆腔疼痛通常是一个诊断难题。我们报告了一个发生在妊娠晚期的附件扭转的病例,以强调这种诊断,只有早期处理才能防止不可逆的缺血性损伤,这可能会损害未来的生育能力。患者为闭经30周未生育妇女,最初表现为阑尾炎症状。通过McBurney切口,手术探查发现坏死的右卵巢伴反应性阑尾炎。行卵巢切除术和阑尾切除术。术后过程平淡无奇。
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引用次数: 0
An unexpected finding of large bowel obstruction from colonic diaphragm disease following prolonged use of indomethacin. 长期使用吲哚美辛后意外发现结肠隔膜疾病引起的大肠梗阻。
IF 0.5 Q4 SURGERY Pub Date : 2026-01-19 eCollection Date: 2026-01-01 DOI: 10.1093/jscr/rjaf1074
Isabella Zappala, Joseph Do Woong Choi, Evangeline Woodford, Raymond Kwok, Peter Dutton

Colonic stricture leading to large bowel obstruction is an uncommon presentation to the emergency department. Strictures are commonly established secondary to diverticular disease, inflammatory bowel disease, malignancy or ischaemic/infective colitis. The formation of a colonic stricture secondary to the chronic use of non-steroidal anti-inflammatory drugs (NSAIDs) is an unusual finding. We present a case of a 48-year-old lady who presented with a large bowel obstruction secondary to NSAID-induced right colonic stricture in a patient who was initially thought to have an index presentation of colonic Crohn's disease.

结肠狭窄导致大肠梗阻是一个罕见的表现,以急诊科。狭窄通常继发于憩室病、炎症性肠病、恶性肿瘤或缺血性/感染性结肠炎。慢性使用非甾体抗炎药(NSAIDs)后继发结肠狭窄是一种罕见的发现。我们报告了一例48岁的女性,她最初被认为是结肠克罗恩病的指数表现,但因非甾体抗炎药引起的右结肠狭窄而继发大肠梗阻。
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引用次数: 0
期刊
Journal of Surgical Case Reports
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