Introduction: Bladder injuries that occur during laparoscopic surgery are rare but a serious complication. In particular, patients with urachal remnants have a high risk for bladder injuries during suprapubic port insertion. We report the case of a bladder injury caused by a urachal remnant during laparoscopic ileocecal resection for cecal cancer.
Case presentation: A 46-year-old man diagnosed with cT2, N0, M0, stage I cecal cancer underwent laparoscopic ileocecal resection. A suprapubic port was inserted under direct vision. After ileocecal resection, a bladder injury was discovered after the removal of the suprapubic port. The suprapubic port wound was extended to reveal the bladder wall around the injury, and the injury was sutured. During surgery, preoperative computed tomography (CT) results were reviewed, and sagittal CT revealed a urachal remnant. The postoperative course was uneventful, and the patient was discharged 10 days after surgery.
Discussion: Urachal remnants are rare in adults. This case emphasizes that although it is difficult to diagnose asymptomatic urachal remnants preoperatively, sagittal CT scans may aid in the diagnosis. Careful consideration of port placement and preoperative urethral catheter insertion is important to prevent bladder injuries in cases of urachal remnants.
Conclusion: Sagittal CT scans are considered effective in detecting diverticulum-type urachal remnants. Port placement without the need for a suprapubic trocar should be considered in cases with urachal remnants.
{"title":"Bladder injury caused by a urachal remnant during laparoscopic ileocecal resection: A case report.","authors":"Takenori Segawa, Mizunori Yaegashi, Yuichiro Hirata, Noriyuki Sasaki, Akira Sasaki","doi":"10.1016/j.ijscr.2024.110597","DOIUrl":"https://doi.org/10.1016/j.ijscr.2024.110597","url":null,"abstract":"<p><strong>Introduction: </strong>Bladder injuries that occur during laparoscopic surgery are rare but a serious complication. In particular, patients with urachal remnants have a high risk for bladder injuries during suprapubic port insertion. We report the case of a bladder injury caused by a urachal remnant during laparoscopic ileocecal resection for cecal cancer.</p><p><strong>Case presentation: </strong>A 46-year-old man diagnosed with cT2, N0, M0, stage I cecal cancer underwent laparoscopic ileocecal resection. A suprapubic port was inserted under direct vision. After ileocecal resection, a bladder injury was discovered after the removal of the suprapubic port. The suprapubic port wound was extended to reveal the bladder wall around the injury, and the injury was sutured. During surgery, preoperative computed tomography (CT) results were reviewed, and sagittal CT revealed a urachal remnant. The postoperative course was uneventful, and the patient was discharged 10 days after surgery.</p><p><strong>Discussion: </strong>Urachal remnants are rare in adults. This case emphasizes that although it is difficult to diagnose asymptomatic urachal remnants preoperatively, sagittal CT scans may aid in the diagnosis. Careful consideration of port placement and preoperative urethral catheter insertion is important to prevent bladder injuries in cases of urachal remnants.</p><p><strong>Conclusion: </strong>Sagittal CT scans are considered effective in detecting diverticulum-type urachal remnants. Port placement without the need for a suprapubic trocar should be considered in cases with urachal remnants.</p>","PeriodicalId":48113,"journal":{"name":"International Journal of Surgery Case Reports","volume":"125 ","pages":"110597"},"PeriodicalIF":0.6,"publicationDate":"2024-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142682778","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-11-12DOI: 10.1016/j.ijscr.2024.110596
Smoter Šimon, Slyško Roman
Introduction
Phlegmasia cerulea dolens (PCD) is a rare, life- and limb-threatening condition of acute massive deep vein thrombosis (DVT) that requires emergent therapeutic intervention. While endovascular therapy is the preferred treatment approach, we describe a case where surgical embolectomy is an alternative approach in specific scenarios. In our case, we presented a patient with simultaneous PCD and acute limb ischemia (ALI).
Case report
A patient presented with haematuria, abdominal pain, cyanotic changes in the limb, and sensory/motor deficits in the right lower limb. Imaging tests revealed thromboembolic occlusion of both the arterial and venous systems and a bleeding tumour in the pelvic region. Due to the rapid progression of symptoms, macroscopic haematuria with anaemia, renal failure, and the necessity for intervention in both the arterial and venous systems, we performed a successful simultaneous surgical embolectomy of the arterial and venous systems right lower limb, resulting in prompt symptom resolution.
Discussion
Phlegmasia cerulea dolens is a rare manifestation of massive iliofemoral deep vein thrombosis. Its pathophysiology can indirectly compromise arterial patency. Treatment options include endovascular therapy - catheter-directed thrombolysis (CDT), percutaneous mechanical thrombectomy (PMT) or surgical intervention. These options carry risks, including damage to the venous endothelium or periprocedural pulmonary embolism. This case report demonstrates a situation where surgical intervention was a viable option. We presented a more endothelium-sparing surgical approach using a sterile compression bandage during embolectomy.
In conclusion
To date, there are no established guidelines from professional societies regarding the treatment of PCD. The authors emphasize the need for an individualized approach to patients with PCD. They also highlight the importance of access to comprehensive treatment, including both endovascular and surgical methods.
Methods
work has been reported in line with SCARE criteria.
{"title":"Case report of simultaneous phlegmasia cerulea dolens and acute limb ischemia","authors":"Smoter Šimon, Slyško Roman","doi":"10.1016/j.ijscr.2024.110596","DOIUrl":"10.1016/j.ijscr.2024.110596","url":null,"abstract":"<div><h3>Introduction</h3><div><em>Phlegmasia cerulea dolens</em> (PCD) is a rare, life- and limb-threatening condition of acute massive deep vein thrombosis (DVT) that requires emergent therapeutic intervention. While endovascular therapy is the preferred treatment approach, we describe a case where surgical embolectomy is an alternative approach in specific scenarios. In our case, we presented a patient with simultaneous PCD and acute limb ischemia (ALI).</div></div><div><h3>Case report</h3><div>A patient presented with haematuria, abdominal pain, cyanotic changes in the limb, and sensory/motor deficits in the right lower limb. Imaging tests revealed thromboembolic occlusion of both the arterial and venous systems and a bleeding tumour in the pelvic region. Due to the rapid progression of symptoms, macroscopic haematuria with anaemia, renal failure, and the necessity for intervention in both the arterial and venous systems, we performed a successful simultaneous surgical embolectomy of the arterial and venous systems right lower limb, resulting in prompt symptom resolution.</div></div><div><h3>Discussion</h3><div><em>Phlegmasia cerulea dolens</em> is a rare manifestation of massive iliofemoral deep vein thrombosis. Its pathophysiology can indirectly compromise arterial patency. Treatment options include endovascular therapy - catheter-directed thrombolysis (CDT), percutaneous mechanical thrombectomy (PMT) or surgical intervention. These options carry risks, including damage to the venous endothelium or periprocedural pulmonary embolism. This case report demonstrates a situation where surgical intervention was a viable option. We presented a more endothelium-sparing surgical approach using a sterile compression bandage during embolectomy.</div></div><div><h3>In conclusion</h3><div>To date, there are no established guidelines from professional societies regarding the treatment of PCD. The authors emphasize the need for an individualized approach to patients with PCD. They also highlight the importance of access to comprehensive treatment, including both endovascular and surgical methods.</div></div><div><h3>Methods</h3><div>work has been reported in line with SCARE criteria.</div></div>","PeriodicalId":48113,"journal":{"name":"International Journal of Surgery Case Reports","volume":"125 ","pages":"Article 110596"},"PeriodicalIF":0.6,"publicationDate":"2024-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142644980","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 : 2024-11-12DOI: 10.1016/j.ijscr.2024.110587
Jesús Eduardo Prior-Rosas, Brenda Mejía-Ruíz, Brenda Areli Magdaleno-Becerra, Chantal Guadalupe Nava-Tenorio, Sheila Marilyn Alonso-Domínguez, Gabriela Eugenia Botello-Ortiz
Introduction and importance: Mesenteric cysts are a rare group of intra-abdominal tumors located in the mesentery or omentum, most of this lesion are asymptomatically but occasionally presents with non-specific symptoms, which makes diagnosis difficult.
Case presentation: We present two cases of giant mesenteric cyst in our Institution, the first case is a women of 23 years with previous gynecologic surgery with chronic abdominal pain and large abdominal mass CT showed a giant intraabdominal 30 × 25 × 15 cm, the patient went to laparotomy and a large mesenteric tumor found. The Histopathology reported a Benign cyst mesothelioma (BCM). The second case is a 47 year male with intermittent abdominal pain and abdominal CT shows a 20x21x15 cm tumor. Laparotomy was performed. Histopathology reported a large lymphangioma.
Clinical discussion: BCM tumors are rare intrabdominal lesions often diagnosed in premenopausal women. Its etiopathogenesis is still unclear, associated risk factors are endometriosis, pelvic inflammatory disease and previous pelvic surgery. Lymphangiomas are an infrequent cyst tumors. It results from a failure in the evolutionary development of the lymphatic system, often localized in the head and neck and its localization in the abdomen is even rare. The definitive diagnosis is made by histopathology.
Conclusion: Mesenteric cysts diagnosis if often challenge due to nonspecific symptoms and significant overlap in imaging appearance between the different entities, its diagnosis should be in mind when encounter a cystic abdominal tumor, surgical complete removal of this tumors is the optimal treatment to prevent recurrence and complications.
{"title":"Giant benign mesenteric cysts (mesothelioma and lymphangioma): A report of two cases.","authors":"Jesús Eduardo Prior-Rosas, Brenda Mejía-Ruíz, Brenda Areli Magdaleno-Becerra, Chantal Guadalupe Nava-Tenorio, Sheila Marilyn Alonso-Domínguez, Gabriela Eugenia Botello-Ortiz","doi":"10.1016/j.ijscr.2024.110587","DOIUrl":"https://doi.org/10.1016/j.ijscr.2024.110587","url":null,"abstract":"<p><strong>Introduction and importance: </strong>Mesenteric cysts are a rare group of intra-abdominal tumors located in the mesentery or omentum, most of this lesion are asymptomatically but occasionally presents with non-specific symptoms, which makes diagnosis difficult.</p><p><strong>Case presentation: </strong>We present two cases of giant mesenteric cyst in our Institution, the first case is a women of 23 years with previous gynecologic surgery with chronic abdominal pain and large abdominal mass CT showed a giant intraabdominal 30 × 25 × 15 cm, the patient went to laparotomy and a large mesenteric tumor found. The Histopathology reported a Benign cyst mesothelioma (BCM). The second case is a 47 year male with intermittent abdominal pain and abdominal CT shows a 20x21x15 cm tumor. Laparotomy was performed. Histopathology reported a large lymphangioma.</p><p><strong>Clinical discussion: </strong>BCM tumors are rare intrabdominal lesions often diagnosed in premenopausal women. Its etiopathogenesis is still unclear, associated risk factors are endometriosis, pelvic inflammatory disease and previous pelvic surgery. Lymphangiomas are an infrequent cyst tumors. It results from a failure in the evolutionary development of the lymphatic system, often localized in the head and neck and its localization in the abdomen is even rare. The definitive diagnosis is made by histopathology.</p><p><strong>Conclusion: </strong>Mesenteric cysts diagnosis if often challenge due to nonspecific symptoms and significant overlap in imaging appearance between the different entities, its diagnosis should be in mind when encounter a cystic abdominal tumor, surgical complete removal of this tumors is the optimal treatment to prevent recurrence and complications.</p>","PeriodicalId":48113,"journal":{"name":"International Journal of Surgery Case Reports","volume":"125 ","pages":"110587"},"PeriodicalIF":0.6,"publicationDate":"2024-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142644987","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-11-12DOI: 10.1016/j.ijscr.2024.110589
Jihène Houas, Monia Ghammam, Heyfa BelHadj-Miled, Amal Kedissa, Mouna Bellakhdher, Mohamed Abdelkefi
Introduction and importance: Rosai-Dorfman disease (RDD) is a rare benign histiocytic proliferative disorder characterized by painless lymph node enlargement and extranodal involvement. This disease often presents diagnostic challenges due to its variable clinical manifestations and the need for histologic confirmation.
Case series presentation: This case series examines five patients diagnosed with Rosai-Dorfman disease who presented with a variety of clinical manifestations. Patients ranged in age from 21 to 72 years and presented with a variety of symptoms including cervical lymphadenopathy, mediastinal adenopathies, thyroid nodules, and nasal obstruction. Diagnoses were confirmed by histologic examination and immunostaining, primarily with anti-PS100 antibody. Treatments included surgery, corticosteroids, and laser resection, with most cases showing favorable outcomes and no recurrence at follow-ups ranging from one to five years.
Clinical discussion: The diverse presentations of RDD in this case series underscore the importance of considering this entity in the differential diagnosis of lymphadenopathy and other mass lesions. Histologic examination and immunostaining are critical for accurate diagnosis.
Conclusion: This case series aims to highlight the diverse presentations, diagnostic approaches, and treatment outcomes of patients with Rosai-Dorfman disease and to contribute to a better understanding of this rare condition.
{"title":"Destombes-Rosai-Dorfman disease: A case series of nodular and extra nodular involvement.","authors":"Jihène Houas, Monia Ghammam, Heyfa BelHadj-Miled, Amal Kedissa, Mouna Bellakhdher, Mohamed Abdelkefi","doi":"10.1016/j.ijscr.2024.110589","DOIUrl":"https://doi.org/10.1016/j.ijscr.2024.110589","url":null,"abstract":"<p><strong>Introduction and importance: </strong>Rosai-Dorfman disease (RDD) is a rare benign histiocytic proliferative disorder characterized by painless lymph node enlargement and extranodal involvement. This disease often presents diagnostic challenges due to its variable clinical manifestations and the need for histologic confirmation.</p><p><strong>Case series presentation: </strong>This case series examines five patients diagnosed with Rosai-Dorfman disease who presented with a variety of clinical manifestations. Patients ranged in age from 21 to 72 years and presented with a variety of symptoms including cervical lymphadenopathy, mediastinal adenopathies, thyroid nodules, and nasal obstruction. Diagnoses were confirmed by histologic examination and immunostaining, primarily with anti-PS100 antibody. Treatments included surgery, corticosteroids, and laser resection, with most cases showing favorable outcomes and no recurrence at follow-ups ranging from one to five years.</p><p><strong>Clinical discussion: </strong>The diverse presentations of RDD in this case series underscore the importance of considering this entity in the differential diagnosis of lymphadenopathy and other mass lesions. Histologic examination and immunostaining are critical for accurate diagnosis.</p><p><strong>Conclusion: </strong>This case series aims to highlight the diverse presentations, diagnostic approaches, and treatment outcomes of patients with Rosai-Dorfman disease and to contribute to a better understanding of this rare condition.</p>","PeriodicalId":48113,"journal":{"name":"International Journal of Surgery Case Reports","volume":"125 ","pages":"110589"},"PeriodicalIF":0.6,"publicationDate":"2024-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142630345","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-11-11DOI: 10.1016/j.ijscr.2024.110565
Ahmad Alkheder, Ibrahim Fathallah, Abd Alrhman Alajrd, Ahmed Al-Talep, Zeina Alsodi, Saleh Takkem
{"title":"Corrigendum to \"A rare case of teratoma in the right atrium: A case report study\" [Int. J. Surg. Case Rep. 124 (2024) 110448].","authors":"Ahmad Alkheder, Ibrahim Fathallah, Abd Alrhman Alajrd, Ahmed Al-Talep, Zeina Alsodi, Saleh Takkem","doi":"10.1016/j.ijscr.2024.110565","DOIUrl":"https://doi.org/10.1016/j.ijscr.2024.110565","url":null,"abstract":"","PeriodicalId":48113,"journal":{"name":"International Journal of Surgery Case Reports","volume":" ","pages":"110565"},"PeriodicalIF":0.6,"publicationDate":"2024-11-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142630321","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Mediastinal liposarcoma is an extremely rare malignant tumor of adipocytic differentiation, comprising less than 1 % of all liposarcomas. The majority occur in the lower extremities, with approximately 75 % of cases. Myxoid liposarcoma of the anterior mediastinum can present similarly to other thoracic pathologies.
Case presentation
We present the case of a 36-year-old female who presented with a 14-day history of worsening dyspnea at rest, along with swelling of the upper extremities and face. On examination, distended neck and anterior chest veins were observed. Imaging studies revealed a large anterior mediastinal mass causing extrinsic compression of adjacent structures and a mediastinal shift to the right. Following stabilization, the patient underwent successful surgical resection of the mass.
Discussion
Myxomatous liposarcoma is a very rare tumor located in the mediastinum that presents with symptoms resembling other lung diseases. Common complaints include chest pain, shortness of breath, and difficulty swallowing. Diagnosis is largely based on radiological imaging or histological examination after surgery. The primary treatment involves surgery and occasionally chemotherapy. Prompt diagnosis and timely treatment enhance the likelihood of positive outcomes for those affected.
Conclusion
This case underscores the importance of considering mediastinal liposarcoma in the differential diagnosis of patients presenting with chronic cough and unquantified weight loss, especially when symptoms escalate into conditions such as superior vena cava syndrome. Early detection and timely treatment are crucial for improving outcomes. This case contributes valuable insight, particularly relevant to managing complex tumors in resource-limited settings.
{"title":"Resection of a large anterior mediastinum myxoid liposarcoma via clamshell thoracotomy in a resource-limited setting: A rare case report and literature review","authors":"Mekonnen Feyissa Senbu , Hiwot Tedessa Habtamu , Tekaleg Lemessa Kebede , Samson Bitew Wordofa , Lalisa Bedasa Ayana","doi":"10.1016/j.ijscr.2024.110582","DOIUrl":"10.1016/j.ijscr.2024.110582","url":null,"abstract":"<div><h3>Background</h3><div>Mediastinal liposarcoma is an extremely rare malignant tumor of adipocytic differentiation, comprising less than 1 % of all liposarcomas. The majority occur in the lower extremities, with approximately 75 % of cases. Myxoid liposarcoma of the anterior mediastinum can present similarly to other thoracic pathologies.</div></div><div><h3>Case presentation</h3><div>We present the case of a 36-year-old female who presented with a 14-day history of worsening dyspnea at rest, along with swelling of the upper extremities and face. On examination, distended neck and anterior chest veins were observed. Imaging studies revealed a large anterior mediastinal mass causing extrinsic compression of adjacent structures and a mediastinal shift to the right. Following stabilization, the patient underwent successful surgical resection of the mass.</div></div><div><h3>Discussion</h3><div>Myxomatous liposarcoma is a very rare tumor located in the mediastinum that presents with symptoms resembling other lung diseases. Common complaints include chest pain, shortness of breath, and difficulty swallowing. Diagnosis is largely based on radiological imaging or histological examination after surgery. The primary treatment involves surgery and occasionally chemotherapy. Prompt diagnosis and timely treatment enhance the likelihood of positive outcomes for those affected.</div></div><div><h3>Conclusion</h3><div>This case underscores the importance of considering mediastinal liposarcoma in the differential diagnosis of patients presenting with chronic cough and unquantified weight loss, especially when symptoms escalate into conditions such as superior vena cava syndrome. Early detection and timely treatment are crucial for improving outcomes. This case contributes valuable insight, particularly relevant to managing complex tumors in resource-limited settings.</div></div>","PeriodicalId":48113,"journal":{"name":"International Journal of Surgery Case Reports","volume":"125 ","pages":"Article 110582"},"PeriodicalIF":0.6,"publicationDate":"2024-11-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142630595","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}
hydatid disease, caused by Echinococcus granulosus, primarily affects the liver and lungs, with splenic involvement being exceedingly rare, occurring in only 0.5 % of cases. This case report highlights a 17-year-old male presenting with a complicated hydatid cyst in the lung, along with an incidental splenic cyst, emphasizing the importance of single-stage surgery in treating multi-organ hydatid disease.
Case presentation
a 17-year-old male presented with a three-month history of left-sided chest pain and a dry cough. Imaging revealed a complicated hydatid cyst in the left lung and an incidental splenic cyst. Serological tests confirmed the presence of anti-hydatid antibodies. A single-stage surgical approach was performed via a transthoracic route, involving cystectomy and pericystectomy for the pulmonary cyst, followed by removal of the splenic cyst. The postoperative recovery was uneventful, and the patient was discharged on the fifth day with a six-month course of oral albendazole.
Discussion
hydatid disease is a significant public health issue, with simultaneous pulmonary and splenic involvement being rare. Surgical intervention remains the cornerstone of treatment for pulmonary hydatid disease, with medical therapy used as an adjunct. In this case, a single-stage surgery was chosen due to its advantages, such as reduced anesthesia, shorter hospital stays, and faster recovery.
Conclusion
single-stage surgery provides an effective and efficient option for managing multi-organ hydatid disease. This case highlights its feasibility and benefits, particularly in young patients from endemic regions.
{"title":"Single-stage surgical management of simultaneous pulmonary and splenic hydatidosis: A rare case report","authors":"Houssem Messaoudi , Habib Bessrour , Mokhles Lajmi , Wafa Ragmoun , Islam Mejri , Saber Hachicha","doi":"10.1016/j.ijscr.2024.110580","DOIUrl":"10.1016/j.ijscr.2024.110580","url":null,"abstract":"<div><h3>Introduction</h3><div>hydatid disease, caused by <em>Echinococcus granulosus</em>, primarily affects the liver and lungs, with splenic involvement being exceedingly rare, occurring in only 0.5 % of cases. This case report highlights a 17-year-old male presenting with a complicated hydatid cyst in the lung, along with an incidental splenic cyst, emphasizing the importance of single-stage surgery in treating multi-organ hydatid disease.</div></div><div><h3>Case presentation</h3><div>a 17-year-old male presented with a three-month history of left-sided chest pain and a dry cough. Imaging revealed a complicated hydatid cyst in the left lung and an incidental splenic cyst. Serological tests confirmed the presence of anti-hydatid antibodies. A single-stage surgical approach was performed via a transthoracic route, involving cystectomy and pericystectomy for the pulmonary cyst, followed by removal of the splenic cyst. The postoperative recovery was uneventful, and the patient was discharged on the fifth day with a six-month course of oral albendazole.</div></div><div><h3>Discussion</h3><div>hydatid disease is a significant public health issue, with simultaneous pulmonary and splenic involvement being rare. Surgical intervention remains the cornerstone of treatment for pulmonary hydatid disease, with medical therapy used as an adjunct. In this case, a single-stage surgery was chosen due to its advantages, such as reduced anesthesia, shorter hospital stays, and faster recovery.</div></div><div><h3>Conclusion</h3><div>single-stage surgery provides an effective and efficient option for managing multi-organ hydatid disease. This case highlights its feasibility and benefits, particularly in young patients from endemic regions.</div></div>","PeriodicalId":48113,"journal":{"name":"International Journal of Surgery Case Reports","volume":"125 ","pages":"Article 110580"},"PeriodicalIF":0.6,"publicationDate":"2024-11-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142639807","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 : 2024-11-10DOI: 10.1016/j.ijscr.2024.110578
Ali Kada, Hamza Sekkat, Mahdi Bahij, Mohammed Raiss, Farid Sabbah, Abdelmalek Hrora
Introduction and importance: Intestinal intussusception is rare in adults and often associated with underlying malignancies. In this case, a colo-colic intussusception involving the descending colon caused acute obstruction, ischemic pain, and carried a high risk for peritonitis, necessitating urgent surgical intervention to prevent severe complications.
Case presentation: We report the case of a 50-year-old male who presented with acute abdominal obtruction and a three-day history of fecal vomiting, left-sided abdominal pain, and recent rectal bleeding. Imaging revealed colo-colic intussusception of the descending colon due to a colonic tumor. Immediate surgical intervention was performed with an oncologic resection of the invaginated segment, including a left hemicolectomy with lymph node dissection. A diversionary left iliac colostomy was conducted, ensuring clear resection margins and reducing the risk of postoperative complications.
Clinical discussion: Intussusception in adults, while rare, frequently indicates a malignant etiology, and prompt diagnosis and management are essential. In this case, rapid surgical intervention allowed successful removal of the tumor with favorable oncologic outcomes and no recurrence at two-year follow-up. This case highlights the complexity of diagnosing intussusception in adults, where symptoms may mimic other gastrointestinal conditions and are often nonspecific.
Conclusion: This case underscores the critical importance of early detection and intervention for intussusception in adults. Awareness among physicians should be heightened to consider intussusception in adult patients presenting with symptoms such as ischemic pain or a palpable mass with associated pain, as timely intervention can lead to improved outcomes and reduce morbidity.
{"title":"The management of colo-colic intussusception on left colon tumor in an adult: Case presentation and review of the literature.","authors":"Ali Kada, Hamza Sekkat, Mahdi Bahij, Mohammed Raiss, Farid Sabbah, Abdelmalek Hrora","doi":"10.1016/j.ijscr.2024.110578","DOIUrl":"https://doi.org/10.1016/j.ijscr.2024.110578","url":null,"abstract":"<p><strong>Introduction and importance: </strong>Intestinal intussusception is rare in adults and often associated with underlying malignancies. In this case, a colo-colic intussusception involving the descending colon caused acute obstruction, ischemic pain, and carried a high risk for peritonitis, necessitating urgent surgical intervention to prevent severe complications.</p><p><strong>Case presentation: </strong>We report the case of a 50-year-old male who presented with acute abdominal obtruction and a three-day history of fecal vomiting, left-sided abdominal pain, and recent rectal bleeding. Imaging revealed colo-colic intussusception of the descending colon due to a colonic tumor. Immediate surgical intervention was performed with an oncologic resection of the invaginated segment, including a left hemicolectomy with lymph node dissection. A diversionary left iliac colostomy was conducted, ensuring clear resection margins and reducing the risk of postoperative complications.</p><p><strong>Clinical discussion: </strong>Intussusception in adults, while rare, frequently indicates a malignant etiology, and prompt diagnosis and management are essential. In this case, rapid surgical intervention allowed successful removal of the tumor with favorable oncologic outcomes and no recurrence at two-year follow-up. This case highlights the complexity of diagnosing intussusception in adults, where symptoms may mimic other gastrointestinal conditions and are often nonspecific.</p><p><strong>Conclusion: </strong>This case underscores the critical importance of early detection and intervention for intussusception in adults. Awareness among physicians should be heightened to consider intussusception in adult patients presenting with symptoms such as ischemic pain or a palpable mass with associated pain, as timely intervention can lead to improved outcomes and reduce morbidity.</p>","PeriodicalId":48113,"journal":{"name":"International Journal of Surgery Case Reports","volume":"125 ","pages":"110578"},"PeriodicalIF":0.6,"publicationDate":"2024-11-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142682900","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Rathke's cleft cyst (RCC) are non-malignant lesions arising from remnants of Rathke's pouch in the pituitary gland. Apoplexy is seen commonly in pituitary macroadenomas but very rarely in RCCs.
Case presentation
A 30-year-old male presented with a severe headache and vomiting. Imaging revealed an enlarged pituitary gland with possible hemorrhage in a RCC. The cyst was evacuated with endonasal transsphenoidal surgery, and histology confirmed RCC. Follow-up imaging showed complete cyst resolution, although he required levothyroxine for hypothyroidism.
Clinical discussion
The occurrence of hemorrhage within RCCs, although rare, mimics pituitary tumor apoplexy often complicating the diagnosis. The management is similar to pituitary tumor apoplexy, primarily involving surgical intervention. Postoperative care may require long-term hormonal replacement therapy in a significant number of patients.
Conclusion
This report underscores the importance of considering RCC in the differential diagnoses of pituitary lesions with hemorrhage with promising surgical outcome.
{"title":"Rathke's cleft cyst apoplexy presented as pituitary apoplexy: A case report","authors":"Soumya Pahari , Yugant Khand , Stuti Yadav , Paawan Bahadur Bhandari , Purushottam Baniya , Nishan Bhandari","doi":"10.1016/j.ijscr.2024.110571","DOIUrl":"10.1016/j.ijscr.2024.110571","url":null,"abstract":"<div><h3>Introduction and importance</h3><div>Rathke's cleft cyst (RCC) are non-malignant lesions arising from remnants of Rathke's pouch in the pituitary gland. Apoplexy is seen commonly in pituitary macroadenomas but very rarely in RCCs.</div></div><div><h3>Case presentation</h3><div>A 30-year-old male presented with a severe headache and vomiting. Imaging revealed an enlarged pituitary gland with possible hemorrhage in a RCC. The cyst was evacuated with endonasal transsphenoidal surgery, and histology confirmed RCC. Follow-up imaging showed complete cyst resolution, although he required levothyroxine for hypothyroidism.</div></div><div><h3>Clinical discussion</h3><div>The occurrence of hemorrhage within RCCs, although rare, mimics pituitary tumor apoplexy often complicating the diagnosis. The management is similar to pituitary tumor apoplexy, primarily involving surgical intervention. Postoperative care may require long-term hormonal replacement therapy in a significant number of patients.</div></div><div><h3>Conclusion</h3><div>This report underscores the importance of considering RCC in the differential diagnoses of pituitary lesions with hemorrhage with promising surgical outcome.</div></div>","PeriodicalId":48113,"journal":{"name":"International Journal of Surgery Case Reports","volume":"125 ","pages":"Article 110571"},"PeriodicalIF":0.6,"publicationDate":"2024-11-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142644990","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 : 2024-11-09DOI: 10.1016/j.ijscr.2024.110573
Noureen Kanwal , Jahanzaib Haider , Siraj Haider , Mohammad Iqbal , Kiran Amir , Faisal Saud Dar
Introduction and importance
The curative options for locally advanced hepatocellular carcinomas involving the vessels are very limited. Ex vivo liver resection and auto transplantation (ERAT) is a novel surgical method, which has been used in the management of such complex liver space occupying lesions, which are rendered conventionally unresectable. This technique involves a complete hepatectomy, extracorporeal hepatic resection on the backbench, and then reimplantation of the remnant hepatic parenchyma. George et al. (2019) [1] In literature, Ex vivo liver resection and auto transplantation (ERAT) has been utilized in the management of both benign and malignant liver lesions, including hepatocellular carcinoma (HCC), cholangiocarcinoma, hepatic metastases, hepatic alveolar echinococcosis, focal nodular hyperplasia and hemangioma. Zawistowski et al. (2020) [2].
Case presentation
We report this case of a 28 years old male with a giant hepatocellular carcinoma, that deemed unresectable as it was closely abutting all three hepatic veins. After appropriate preoperative surgical planning, he underwent ex vivo liver resection and autotransplantation (ERAT). Patient had gradual uneventful recovery and he was discharged home on 12th postoperative day.
Clinical discussion
A radical (R0) resection is the main goal of the ex vivo liver resection and autotransplantation (ERAT) procedure, which can be used for curative intent in patients with liver lesions that are conventionally inoperable. It allows for precise extracorporeal resection, maximizes the residual liver volume and increases the likelihood of obtaining negative margins. Furthermore, the bench surgery in ice bath makes it easier to reconstruct the vasculature without the pressure of time constraints in situ, unlike conventional surgery, which can take a long time when done in a bleeding operative field. Zawistowski et al. (2020) [2].
Conclusion
For patients with complex liver lesions believed to be incurable with conventional surgical methods, ex vivo liver resection and autotransplantation (ERAT) provides an alternative.
{"title":"EX vivo liver resection and auto transplantation for a giant hepatocellular carcinoma: A case report","authors":"Noureen Kanwal , Jahanzaib Haider , Siraj Haider , Mohammad Iqbal , Kiran Amir , Faisal Saud Dar","doi":"10.1016/j.ijscr.2024.110573","DOIUrl":"10.1016/j.ijscr.2024.110573","url":null,"abstract":"<div><h3>Introduction and importance</h3><div>The curative options for locally advanced hepatocellular carcinomas involving the vessels are very limited. Ex vivo liver resection and auto transplantation (ERAT) is a novel surgical method, which has been used in the management of such complex liver space occupying lesions, which are rendered conventionally unresectable. This technique involves a complete hepatectomy, extracorporeal hepatic resection on the backbench, and then reimplantation of the remnant hepatic parenchyma. George et al. (2019) [<span><span>1</span></span>] In literature, Ex vivo liver resection and auto transplantation (ERAT) has been utilized in the management of both benign and malignant liver lesions, including hepatocellular carcinoma (HCC), cholangiocarcinoma, hepatic metastases, hepatic alveolar echinococcosis, focal nodular hyperplasia and hemangioma. Zawistowski et al. (2020) [<span><span>2</span></span>].</div></div><div><h3>Case presentation</h3><div>We report this case of a 28 years old male with a giant hepatocellular carcinoma, that deemed unresectable as it was closely abutting all three hepatic veins. After appropriate preoperative surgical planning, he underwent ex vivo liver resection and autotransplantation (ERAT). Patient had gradual uneventful recovery and he was discharged home on 12th postoperative day.</div></div><div><h3>Clinical discussion</h3><div>A radical (R0) resection is the main goal of the ex vivo liver resection and autotransplantation (ERAT) procedure, which can be used for curative intent in patients with liver lesions that are conventionally inoperable. It allows for precise extracorporeal resection, maximizes the residual liver volume and increases the likelihood of obtaining negative margins. Furthermore, the bench surgery in ice bath makes it easier to reconstruct the vasculature without the pressure of time constraints in situ, unlike conventional surgery, which can take a long time when done in a bleeding operative field. Zawistowski et al. (2020) [<span><span>2</span></span>].</div></div><div><h3>Conclusion</h3><div>For patients with complex liver lesions believed to be incurable with conventional surgical methods, ex vivo liver resection and autotransplantation (ERAT) provides an alternative.</div></div>","PeriodicalId":48113,"journal":{"name":"International Journal of Surgery Case Reports","volume":"125 ","pages":"Article 110573"},"PeriodicalIF":0.6,"publicationDate":"2024-11-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142630352","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}