Pub Date : 2024-11-16eCollection Date: 2024-01-01DOI: 10.1155/2024/5764491
Diego Salcedo Miranda, Jorge Roberto Galvis O, Luis Gerardo García-Herreros, David Torres Cortes, Oscar Rivero Rapalino
Paraganglioma of the middle mediastinum has a prevalence of 1%-2% of paragangliomas and less than 1% of mediastinal masses. It is generally asymptomatic and can easily be confused with other pathologies. The following is the case of a 50-year-old patient who, as an incidental finding, documented an injury between the aorta and the pulmonary artery, hypervascularized, which was embolized prior to surgery, which facilitated the complete resection of the lesion by sternotomy. With favorable evolution of the patient and discharge on the fourth postoperative day. A thorough review of the literature on the diagnostic and treatment approach to this pathology has been also carried out.
{"title":"Bronchial Artery Embolization for a Mediastinal Aortopulmonary Paraganglioma Safe Resection: A Case Report.","authors":"Diego Salcedo Miranda, Jorge Roberto Galvis O, Luis Gerardo García-Herreros, David Torres Cortes, Oscar Rivero Rapalino","doi":"10.1155/2024/5764491","DOIUrl":"10.1155/2024/5764491","url":null,"abstract":"<p><p>Paraganglioma of the middle mediastinum has a prevalence of 1%-2% of paragangliomas and less than 1% of mediastinal masses. It is generally asymptomatic and can easily be confused with other pathologies. The following is the case of a 50-year-old patient who, as an incidental finding, documented an injury between the aorta and the pulmonary artery, hypervascularized, which was embolized prior to surgery, which facilitated the complete resection of the lesion by sternotomy. With favorable evolution of the patient and discharge on the fourth postoperative day. A thorough review of the literature on the diagnostic and treatment approach to this pathology has been also carried out.</p>","PeriodicalId":9600,"journal":{"name":"Case Reports in Surgery","volume":"2024 ","pages":"5764491"},"PeriodicalIF":0.6,"publicationDate":"2024-11-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11585371/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142709271","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}
Pub Date : 2024-11-14eCollection Date: 2024-01-01DOI: 10.1155/2024/4475216
Christina S Boutros, Alexander W Loftus, Aria Bassiri, Laura E Davis, Randy Vince, Jillian Sinopoli, Leonidas Tapias, Philip A Linden, Christopher W Towe, Boxiang Jiang
Staghorn calculi pose challenges in urology, often necessitating more invasive procedures such as percutaneous nephrolithotomy (PCNL) to clear a large stone burden with fewer procedures. Here we present a case of a 76-year-old female with chronic kidney disease and a malrotated right pelvic kidney who underwent PCNL for a 3.5 cm staghorn calculus. Postoperatively, she developed a rare complication of ascending colon perforation, requiring emergent surgical intervention including exploratory laparotomy and right hemicolectomy. Colon perforation during PCNL is rare (0.3%-0.8%). Preoperative imaging, namely computed tomography (CT) of the abdomen and pelvis, is crucial to identify anatomical variations and mitigate the risk of injury. Conservative management strategies have demonstrated success in similar cases, emphasizing the importance of prompt recognition and multidisciplinary management. This case contributes to the paucity of literature regarding this rare complication underscoring the necessity for detailed preoperative planning to avoid complications in PCNL, especially in patients with complex renal anatomy. Future research should focus on developing tailored guidelines for PCNL in patients with anatomical abnormalities to enhance procedural safety and optimize outcomes.
{"title":"A Rare Cause of Colon Perforation After Percutaneous Nephrolithotomy-A Case Report and Review of the Literature.","authors":"Christina S Boutros, Alexander W Loftus, Aria Bassiri, Laura E Davis, Randy Vince, Jillian Sinopoli, Leonidas Tapias, Philip A Linden, Christopher W Towe, Boxiang Jiang","doi":"10.1155/2024/4475216","DOIUrl":"10.1155/2024/4475216","url":null,"abstract":"<p><p>Staghorn calculi pose challenges in urology, often necessitating more invasive procedures such as percutaneous nephrolithotomy (PCNL) to clear a large stone burden with fewer procedures. Here we present a case of a 76-year-old female with chronic kidney disease and a malrotated right pelvic kidney who underwent PCNL for a 3.5 cm staghorn calculus. Postoperatively, she developed a rare complication of ascending colon perforation, requiring emergent surgical intervention including exploratory laparotomy and right hemicolectomy. Colon perforation during PCNL is rare (0.3%-0.8%). Preoperative imaging, namely computed tomography (CT) of the abdomen and pelvis, is crucial to identify anatomical variations and mitigate the risk of injury. Conservative management strategies have demonstrated success in similar cases, emphasizing the importance of prompt recognition and multidisciplinary management. This case contributes to the paucity of literature regarding this rare complication underscoring the necessity for detailed preoperative planning to avoid complications in PCNL, especially in patients with complex renal anatomy. Future research should focus on developing tailored guidelines for PCNL in patients with anatomical abnormalities to enhance procedural safety and optimize outcomes.</p>","PeriodicalId":9600,"journal":{"name":"Case Reports in Surgery","volume":"2024 ","pages":"4475216"},"PeriodicalIF":0.6,"publicationDate":"2024-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11581789/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142686233","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}
Pub Date : 2024-11-06eCollection Date: 2024-01-01DOI: 10.1155/2024/7782678
Stephanie Washburn, Raj Jessica Thomas, Douglas Grider
Inflammatory myofibroblastic tumor (IMT) is a rare mesenchymal tumors of unknown etiology composed of myofibroblastic cells admixed with inflammatory cells. Presented is a 72-year-old male hospitalized for severe abdominal pain and hematochezia with onset of associated symptoms of fever and sweats a few hours prior to abdominal pain. A computed tomography (CT) demonstrated left colonic thickening interpreted as partial obstruction, gross adhesions, and ischemia. At surgery, marked bowel ischemia from the distal transverse to proximal sigmoid colon was seen with extensive gross adhesions. Histopathology revealed a mesenteric mass chiefly composed of stellate-to-spindled myofibroblastic cells and fibrous adhesions, intermixed with lymphocytes, histiocytes, and plasma cells. The tumor was positive for desmin, smooth muscle actin, and keratin; tumor staging, grade, and postsurgical follow-up were not completed as the patient expired postoperatively. Illustrated is a rare pathologic mimic of ischemic colitis with fibrous adhesions, IMT. Thus, it should not be assumed that fibrous adhesions are always the etiology of obstruction when "adhesions" between sections of bowel are noted radiologically or surgically.
{"title":"A Rare Case of Inflammatory Myofibroblastic Tumor Mimicking Fibrous Adhesions Resulting in Bowel Obstruction.","authors":"Stephanie Washburn, Raj Jessica Thomas, Douglas Grider","doi":"10.1155/2024/7782678","DOIUrl":"10.1155/2024/7782678","url":null,"abstract":"<p><p>Inflammatory myofibroblastic tumor (IMT) is a rare mesenchymal tumors of unknown etiology composed of myofibroblastic cells admixed with inflammatory cells. Presented is a 72-year-old male hospitalized for severe abdominal pain and hematochezia with onset of associated symptoms of fever and sweats a few hours prior to abdominal pain. A computed tomography (CT) demonstrated left colonic thickening interpreted as partial obstruction, gross adhesions, and ischemia. At surgery, marked bowel ischemia from the distal transverse to proximal sigmoid colon was seen with extensive gross adhesions. Histopathology revealed a mesenteric mass chiefly composed of stellate-to-spindled myofibroblastic cells and fibrous adhesions, intermixed with lymphocytes, histiocytes, and plasma cells. The tumor was positive for desmin, smooth muscle actin, and keratin; tumor staging, grade, and postsurgical follow-up were not completed as the patient expired postoperatively. Illustrated is a rare pathologic mimic of ischemic colitis with fibrous adhesions, IMT. Thus, it should not be assumed that fibrous adhesions are always the etiology of obstruction when \"adhesions\" between sections of bowel are noted radiologically or surgically.</p>","PeriodicalId":9600,"journal":{"name":"Case Reports in Surgery","volume":"2024 ","pages":"7782678"},"PeriodicalIF":0.6,"publicationDate":"2024-11-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11561171/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142615428","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}
Pub Date : 2024-10-30eCollection Date: 2024-01-01DOI: 10.1155/2024/4874411
Antonio Faita, Giulia Montagner, Diletta Trojan, Valerio Maria Di Pasquale Fiasca
Mastoid obliteration can be performed after canal wall down (CWD) mastoidectomy with various materials. Homologous bone tissue harvested from cadaver donor represents a feasible option with advantages. The purpose of the study is to describe the case of a patient diagnosed with middle ear cholesteatoma treated with mastoidectomy of the CWD and mastoid obliteration with homologous freeze-dried corticocancellous bone particulate in the Cittadella Hospital Ear, Nose, Throat (ENT) unit. The preoperative characteristics of the patients, the procurement and processing of bone allografts, the surgical technique, and postsurgical outcomes are described. No perioperative and postoperative complications were observed, and no rejection or foreign body reactions occurred. The patient then underwent a seriated follow-up. Audiometric tests showed an improvement in hearing levels. The volume of the neoexternal ear canal was 2.01 cm3. The case demonstrated clinical stability, substantial hearing recovery, and no need for specialist cleaning of the reformed external ear canal (EEC). The freeze-dried bone tissue allograft, in the technical way we used, appears to be a viable option in mastoid obliteration because homologous bone is not affected by material shortage, has fast assimilation, and ensures a useful radiological examination scan, at a low cost.
{"title":"Mastoid Obliteration With Freeze-Dried Bone Allograft in Canal Wall Down Tympanoplasty: Description of a Novel Technique and Case Report.","authors":"Antonio Faita, Giulia Montagner, Diletta Trojan, Valerio Maria Di Pasquale Fiasca","doi":"10.1155/2024/4874411","DOIUrl":"https://doi.org/10.1155/2024/4874411","url":null,"abstract":"<p><p>Mastoid obliteration can be performed after canal wall down (CWD) mastoidectomy with various materials. Homologous bone tissue harvested from cadaver donor represents a feasible option with advantages. The purpose of the study is to describe the case of a patient diagnosed with middle ear cholesteatoma treated with mastoidectomy of the CWD and mastoid obliteration with homologous freeze-dried corticocancellous bone particulate in the Cittadella Hospital Ear, Nose, Throat (ENT) unit. The preoperative characteristics of the patients, the procurement and processing of bone allografts, the surgical technique, and postsurgical outcomes are described. No perioperative and postoperative complications were observed, and no rejection or foreign body reactions occurred. The patient then underwent a seriated follow-up. Audiometric tests showed an improvement in hearing levels. The volume of the neoexternal ear canal was 2.01 cm<sup>3</sup>. The case demonstrated clinical stability, substantial hearing recovery, and no need for specialist cleaning of the reformed external ear canal (EEC). The freeze-dried bone tissue allograft, in the technical way we used, appears to be a viable option in mastoid obliteration because homologous bone is not affected by material shortage, has fast assimilation, and ensures a useful radiological examination scan, at a low cost.</p>","PeriodicalId":9600,"journal":{"name":"Case Reports in Surgery","volume":"2024 ","pages":"4874411"},"PeriodicalIF":0.6,"publicationDate":"2024-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11540884/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142603404","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}
Background: Odontoid fracture (OF) is one of the most common spinal fractures. Type II in D'Alonzo's classification is still the most common and should be considered unstable unless proven otherwise. Thus, surgical stabilization has received significant attention. Although posterior displacement is common in type II OF, complete displacement is extremely rare, and very few reports are available in the literature. Case Presentation: We report the case of a 60-year-old man with acute type II OF with complete posterior displacement and myelopathy. The patient was managed utilizing a posterior-only single approach for reduction and stabilization. Conclusion: Posterior displacement of type II OF has been traditionally managed with close reduction and anterior or posterior stabilization. Closed reduction in cases of complete posterior displacement carries a significant risk of neurologic deterioration. Anterior, combined, and posterior approaches have been taken for this condition. The posterior-only approach in experienced hands has the least mortality and morbidity with at least the same neurologic and fusion outcomes.
背景:舌骨骨折(OF)是最常见的脊柱骨折之一。达朗佐分类法中的 II 型仍是最常见的类型,除非证据确凿,否则应视为不稳定型。因此,手术稳定受到了广泛关注。虽然后方移位在 II 型 OF 中很常见,但完全移位却极为罕见,文献中也鲜有报道。病例介绍:我们报告了一名 60 岁男性的病例,他患有急性 II 型 OF,并伴有完全后方移位和脊髓病。我们采用后方单一入路对患者进行了截骨和稳定治疗。结论:II 型 OF 后方移位的传统治疗方法是闭合复位和前方或后方稳定。在完全后方移位的病例中,闭合复位术有很大的神经功能恶化风险。对这种情况的处理方法有前路、联合和后路。在经验丰富的医生手中,单纯后路手术的死亡率和发病率最低,神经功能和融合效果至少相同。
{"title":"Posterior-Only Approach for Management of Complete Posterior Displaced Type II Odontoid Fracture.","authors":"Seyed Reza Mousavi, Majid Reza Farrokhi, Hamid Jangiaghdam, Mohammadhadi Amir Shahpari Motlagh","doi":"10.1155/2024/8473999","DOIUrl":"10.1155/2024/8473999","url":null,"abstract":"<p><p><b>Background:</b> Odontoid fracture (OF) is one of the most common spinal fractures. Type II in D'Alonzo's classification is still the most common and should be considered unstable unless proven otherwise. Thus, surgical stabilization has received significant attention. Although posterior displacement is common in type II OF, complete displacement is extremely rare, and very few reports are available in the literature. <b>Case Presentation:</b> We report the case of a 60-year-old man with acute type II OF with complete posterior displacement and myelopathy. The patient was managed utilizing a posterior-only single approach for reduction and stabilization. <b>Conclusion:</b> Posterior displacement of type II OF has been traditionally managed with close reduction and anterior or posterior stabilization. Closed reduction in cases of complete posterior displacement carries a significant risk of neurologic deterioration. Anterior, combined, and posterior approaches have been taken for this condition. The posterior-only approach in experienced hands has the least mortality and morbidity with at least the same neurologic and fusion outcomes.</p>","PeriodicalId":9600,"journal":{"name":"Case Reports in Surgery","volume":"2024 ","pages":"8473999"},"PeriodicalIF":0.6,"publicationDate":"2024-10-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11527521/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142557256","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}
Pub Date : 2024-10-23eCollection Date: 2024-01-01DOI: 10.1155/2024/6188288
Boubker Idrissi Kaitouni, Hamza Ouzzaouit, Talha Laalou, Hamza Sekkat, Mohamed Mahi, Ittimade Nassar, Omar El Aoufir, Youness Bakkali, Mouna Mhamdi Alaoui, Farid Sabbah, Mohammed Raiss, Abdelmalek Hrora
Iatrogenic aneurysms of the splenic artery constitute a rare yet potentially severe complication arising from diverse medical or surgical interventions. The clinical complexity and challenging management strategies associated with these aneurysms pose significant difficulties for clinicians. This circumstance is exemplified in our case report, detailing an iatrogenic aneurysm of the splenic artery that emerged secondary to a pancreatic fistula following a median pancreatectomy performed for a Frantz tumor. The intricate clinical presentation of this case underscores the considerable management challenges posed by such iatrogenic complications.
{"title":"Median Pancreatectomy for Frantz Tumor: Management of a Splenic Artery Aneurysm by Radiological Embolization.","authors":"Boubker Idrissi Kaitouni, Hamza Ouzzaouit, Talha Laalou, Hamza Sekkat, Mohamed Mahi, Ittimade Nassar, Omar El Aoufir, Youness Bakkali, Mouna Mhamdi Alaoui, Farid Sabbah, Mohammed Raiss, Abdelmalek Hrora","doi":"10.1155/2024/6188288","DOIUrl":"10.1155/2024/6188288","url":null,"abstract":"<p><p>Iatrogenic aneurysms of the splenic artery constitute a rare yet potentially severe complication arising from diverse medical or surgical interventions. The clinical complexity and challenging management strategies associated with these aneurysms pose significant difficulties for clinicians. This circumstance is exemplified in our case report, detailing an iatrogenic aneurysm of the splenic artery that emerged secondary to a pancreatic fistula following a median pancreatectomy performed for a Frantz tumor. The intricate clinical presentation of this case underscores the considerable management challenges posed by such iatrogenic complications.</p>","PeriodicalId":9600,"journal":{"name":"Case Reports in Surgery","volume":"2024 ","pages":"6188288"},"PeriodicalIF":0.6,"publicationDate":"2024-10-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11524693/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142543890","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}
Pub Date : 2024-10-16eCollection Date: 2024-01-01DOI: 10.1155/2024/6230715
Ali Alkhaibary, Norah Mohammad Alotaibi, Ghaida Abdullah Albattah, Rahaf Alotaibi, Fahd AlSufiani, Ahmed Aloraidi
Background: Schwannomas are well-encapsulated, solitary tumors that grow slowly from the nerve sheath. Sellar schwannomas tend to be mistaken for other sellar/parasellar lesions due to similar clinical and radiological findings. The present article describes the clinical presentation, radiological findings, histopathological features, and outcome of a patient with sellar schwannoma. Case Description: A 23-year-old female, known to have hypothyroidism secondary to Hashimoto's thyroiditis, presented with multiple episodes of galactorrhea, weight gain, and irregular menstrual cycle for 8 months. It was associated with decreased visual acuity and episodic headaches. Neurological examination revealed no focal deficits. Brain magnetic resonance imaging (MRI) showed a well-defined lobulated lesion in the sellar region, compressing the right optic nerve and optic chiasm. The patient underwent craniotomy and tumor resection. The histopathological sections were diagnostic of schwannoma. Postoperatively, the patient noted a subjective improvement in her visual acuity. She was discharged in stable condition with regular follow-ups at neurosurgery, endocrine, and ophthalmology clinics. Conclusion: Schwannoma of the sellar region is rare and can be misdiagnosed as pituitary adenomas. Preoperative hormonal profile and meticulous neuroradiological assessment narrow down the differential diagnosis for patients with sellar lesions. The diagnosis of sellar schwannomas is established with histopathology and immunohistochemistry results.
{"title":"Sellar Schwannoma Masquerading as Giant Pituitary Adenoma: A Diagnostic Challenge.","authors":"Ali Alkhaibary, Norah Mohammad Alotaibi, Ghaida Abdullah Albattah, Rahaf Alotaibi, Fahd AlSufiani, Ahmed Aloraidi","doi":"10.1155/2024/6230715","DOIUrl":"https://doi.org/10.1155/2024/6230715","url":null,"abstract":"<p><p><b>Background:</b> Schwannomas are well-encapsulated, solitary tumors that grow slowly from the nerve sheath. Sellar schwannomas tend to be mistaken for other sellar/parasellar lesions due to similar clinical and radiological findings. The present article describes the clinical presentation, radiological findings, histopathological features, and outcome of a patient with sellar schwannoma. <b>Case Description:</b> A 23-year-old female, known to have hypothyroidism secondary to Hashimoto's thyroiditis, presented with multiple episodes of galactorrhea, weight gain, and irregular menstrual cycle for 8 months. It was associated with decreased visual acuity and episodic headaches. Neurological examination revealed no focal deficits. Brain magnetic resonance imaging (MRI) showed a well-defined lobulated lesion in the sellar region, compressing the right optic nerve and optic chiasm. The patient underwent craniotomy and tumor resection. The histopathological sections were diagnostic of schwannoma. Postoperatively, the patient noted a subjective improvement in her visual acuity. She was discharged in stable condition with regular follow-ups at neurosurgery, endocrine, and ophthalmology clinics. <b>Conclusion:</b> Schwannoma of the sellar region is rare and can be misdiagnosed as pituitary adenomas. Preoperative hormonal profile and meticulous neuroradiological assessment narrow down the differential diagnosis for patients with sellar lesions. The diagnosis of sellar schwannomas is established with histopathology and immunohistochemistry results.</p>","PeriodicalId":9600,"journal":{"name":"Case Reports in Surgery","volume":"2024 ","pages":"6230715"},"PeriodicalIF":0.6,"publicationDate":"2024-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11498973/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142495730","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}
Pub Date : 2024-10-16eCollection Date: 2024-01-01DOI: 10.1155/2024/9455342
Salvatore Nicolardi, Gabriele De Masi De Luca, Federica Mangia, Cosimo Angelo Greco, Salvatore Zaccaria
Aortic valve replacement (AVR) in a patient with a bio-Bentall conduit can be very challenging, especially if there was a previous endocarditis process for significant morbidity and mortality. We report a case of sutureless AVR in an old patient with a bio-Bentall conduit (Carpentier-Edwards Perimount Magna Ease 25 aortic valve and Hemashield 30 aortic conduit), who developed an endocarditis on aortic prosthesis valve. We believe that sutureless AVR is the best option for redo-operation in older patients with a high surgical risk because it allows for easy rapid deployment implantation, avoids anchoring sutures on a fragile aortic anulus, and reduces cardiopulmonary and aortic cross-clamp times. In this setting, it should be considered as a safe and valid alternative not only to traditional prosthesis but also in selected cases to transcatheter valve-in-valve solutions.
对使用生物本托尔导管的患者进行主动脉瓣置换术(AVR)是一项非常具有挑战性的工作,尤其是如果之前曾发生过心内膜炎,则会导致严重的发病率和死亡率。我们报告了一例使用生物本托尔导管(Carpentier-Edwards Perimount Magna Ease 25 主动脉瓣和 Hemashield 30 主动脉导管)的高龄患者的无缝合自体瓣膜置换术,该患者的主动脉假体瓣膜发生了心内膜炎。我们认为,对于手术风险较高的老年患者来说,无缝线主动脉瓣置换术是重新手术的最佳选择,因为它可以轻松快速地部署植入物,避免在脆弱的主动脉瓣环上锚定缝线,并缩短心肺和主动脉交叉钳夹时间。在这种情况下,不仅应将其视为传统人工瓣膜的一种安全有效的替代方法,而且在某些情况下还应将其视为经导管瓣中瓣解决方案的一种安全有效的替代方法。
{"title":"Sutureless and Rapid Deployment Prosthesis in Redo-Bentall Endocarditis.","authors":"Salvatore Nicolardi, Gabriele De Masi De Luca, Federica Mangia, Cosimo Angelo Greco, Salvatore Zaccaria","doi":"10.1155/2024/9455342","DOIUrl":"https://doi.org/10.1155/2024/9455342","url":null,"abstract":"<p><p>Aortic valve replacement (AVR) in a patient with a bio-Bentall conduit can be very challenging, especially if there was a previous endocarditis process for significant morbidity and mortality. We report a case of sutureless AVR in an old patient with a bio-Bentall conduit (Carpentier-Edwards Perimount Magna Ease 25 aortic valve and Hemashield 30 aortic conduit), who developed an endocarditis on aortic prosthesis valve. We believe that sutureless AVR is the best option for redo-operation in older patients with a high surgical risk because it allows for easy rapid deployment implantation, avoids anchoring sutures on a fragile aortic anulus, and reduces cardiopulmonary and aortic cross-clamp times. In this setting, it should be considered as a safe and valid alternative not only to traditional prosthesis but also in selected cases to transcatheter valve-in-valve solutions.</p>","PeriodicalId":9600,"journal":{"name":"Case Reports in Surgery","volume":"2024 ","pages":"9455342"},"PeriodicalIF":0.6,"publicationDate":"2024-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11498972/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142495731","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}
Pub Date : 2024-10-15eCollection Date: 2024-01-01DOI: 10.1155/2024/7806541
Mehta Razzaghi, Hosna Rezaei, Farshid Mohammadi, Amir Mohammad Salehi
Enterobius vermicularis is a common parasitic infection worldwide. Acute appendicitis (AA) is a frequently encountered condition in general surgery; however, its association with E. vermicularis remains controversial. AA caused by E. vermicularis is a relatively uncommon infection that primarily affects children. We reported a 21-year-old female who was admitted to our hospital due to right lower quadrant abdominal tenderness. Laboratory tests and imaging were not consistent with AA. She underwent a diagnostic laparoscopy and appendectomy. Histopathological examinations revealed the presence of E. vermicularis in the lumen of the appendix, which caused its obstruction without evidence of inflammatory cell infiltration or lymphoid hyperplasia.
蠕虫肠杆菌是一种全球常见的寄生虫感染。急性阑尾炎(AA)是普外科经常遇到的一种疾病,但其与蚯蚓虫的关系仍存在争议。由蠕虫引起的急性阑尾炎是一种相对少见的感染,主要影响儿童。我们报告了一名因右下腹压痛而入院的 21 岁女性患者。实验室检查和影像学检查均与 AA 不相符。她接受了诊断性腹腔镜检查和阑尾切除术。组织病理学检查显示,阑尾腔内存在蚓部包虫,导致阑尾阻塞,但无炎症细胞浸润或淋巴细胞增生的迹象。
{"title":"<i>Enterobius vermicularis</i> in the Appendiceal Lumen: A Case Report.","authors":"Mehta Razzaghi, Hosna Rezaei, Farshid Mohammadi, Amir Mohammad Salehi","doi":"10.1155/2024/7806541","DOIUrl":"https://doi.org/10.1155/2024/7806541","url":null,"abstract":"<p><p><i>Enterobius vermicularis</i> is a common parasitic infection worldwide. Acute appendicitis (AA) is a frequently encountered condition in general surgery; however, its association with <i>E. vermicularis</i> remains controversial. AA caused by <i>E. vermicularis</i> is a relatively uncommon infection that primarily affects children. We reported a 21-year-old female who was admitted to our hospital due to right lower quadrant abdominal tenderness. Laboratory tests and imaging were not consistent with AA. She underwent a diagnostic laparoscopy and appendectomy. Histopathological examinations revealed the presence of <i>E. vermicularis</i> in the lumen of the appendix, which caused its obstruction without evidence of inflammatory cell infiltration or lymphoid hyperplasia.</p>","PeriodicalId":9600,"journal":{"name":"Case Reports in Surgery","volume":"2024 ","pages":"7806541"},"PeriodicalIF":0.6,"publicationDate":"2024-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11496576/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142516302","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}
Pub Date : 2024-10-08eCollection Date: 2024-01-01DOI: 10.1155/2024/6019946
Punchoor Ramesh Bhat, Vipin T A
Anorectal diseases are a major health threat in the field of health sciences. Fistula-in-ano is one of the treatable complex benign lesions of the rectum and anal canal. Complex high anal fistulas can reoccur even after surgical treatment. Establishing a cure for cryptoglandular fistula-in-ano is problematic, as a significant percentage of these diseases persist or recur if the internal opening of the anal fistula is left untreated. Here, we report a case of complex left anterolateral supralevator anal fistula with communication to the prostate gland that forms a prostatic abscess, as it is very rare. After following Ksharasutra (Ayurvedic medicated seton) treatment with regular wound care, significant regression in the condition was observed. A follow-up scan showed no evidence of fistula-in-ano. A 50-year-old businessman presented with complaints of discomfort deep inside the rectum and perineum associated with pain at the base of the scrotum and pus discharge from the perianal region for 1 year. He was diagnosed to have a complex left anterolateral supralevator anal fistula with communication to the prostate substance after a thorough clinical examination and transrectal ultrasonography. After undergoing Ksharasutra treatment for 4 months, pus discharge completely stopped, and sonofistulogram report showed no evidence of fistula-in-ano. Images of the sonofistulogram report were documented before and after the treatment. This article highlights the unique feature of Ksharasutra therapy where the fistula extending to the prostate was treated with no loss of function of the anal sphincter.
{"title":"Complex Anterior Supralevator Anal Fistula With Prostatic Abscess Treated With Ksharasutra: A Case Report.","authors":"Punchoor Ramesh Bhat, Vipin T A","doi":"10.1155/2024/6019946","DOIUrl":"https://doi.org/10.1155/2024/6019946","url":null,"abstract":"<p><p>Anorectal diseases are a major health threat in the field of health sciences. Fistula-in-ano is one of the treatable complex benign lesions of the rectum and anal canal. Complex high anal fistulas can reoccur even after surgical treatment. Establishing a cure for cryptoglandular fistula-in-ano is problematic, as a significant percentage of these diseases persist or recur if the internal opening of the anal fistula is left untreated. Here, we report a case of complex left anterolateral supralevator anal fistula with communication to the prostate gland that forms a prostatic abscess, as it is very rare. After following <i>Ksharasutra</i> (Ayurvedic medicated seton) treatment with regular wound care, significant regression in the condition was observed. A follow-up scan showed no evidence of fistula-in-ano. A 50-year-old businessman presented with complaints of discomfort deep inside the rectum and perineum associated with pain at the base of the scrotum and pus discharge from the perianal region for 1 year. He was diagnosed to have a complex left anterolateral supralevator anal fistula with communication to the prostate substance after a thorough clinical examination and transrectal ultrasonography. After undergoing Ksharasutra treatment for 4 months, pus discharge completely stopped, and sonofistulogram report showed no evidence of fistula-in-ano. Images of the sonofistulogram report were documented before and after the treatment. This article highlights the unique feature of Ksharasutra therapy where the fistula extending to the prostate was treated with no loss of function of the anal sphincter.</p>","PeriodicalId":9600,"journal":{"name":"Case Reports in Surgery","volume":"2024 ","pages":"6019946"},"PeriodicalIF":0.6,"publicationDate":"2024-10-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11479797/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142458742","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}