Case Reports in Surgery最新文献_第7页

Ileal Schwannoma: A Rare Cause of Pelvic Mass 回肠许旺瘤：盆腔肿块的罕见病因

IF 0.6

Case Reports in Surgery Pub Date : 2024-02-14 DOI: 10.1155/2024/5572087

M. Jezovit, Hasan Bakirli, I. Bakirov, K. Hureibi, G. Bakirova, Roman Okolicany, Pavol Janac, I. Mečiarová, Nasser Alhwaymel, Ilkin Bakirli, Augustin Prochotsky

{"title":"Ileal Schwannoma: A Rare Cause of Pelvic Mass","authors":"M. Jezovit, Hasan Bakirli, I. Bakirov, K. Hureibi, G. Bakirova, Roman Okolicany, Pavol Janac, I. Mečiarová, Nasser Alhwaymel, Ilkin Bakirli, Augustin Prochotsky","doi":"10.1155/2024/5572087","DOIUrl":"https://doi.org/10.1155/2024/5572087","url":null,"abstract":"The incidence of small bowel schwannomas is extremely low. In the current literature, we found just a few reported small intestine schwannomas that were located in the duodenum, jejunum, or ileum. This study reports a surprising finding of a relatively large size ileal schwannoma in a patient whose preoperative magnetic resonance imaging described a tumour in the lesser pelvis probably derived from the right adnexa. Pfannenstiel incision was made by the gynaecology team, which found a large mass lesion arising from the small intestine and occupying nearly the entire lesser pelvis. The general surgeon was invited, and pathology was successfully managed by segmental resection of the small bowel with primary end-to-end anastomosis. The histopathology study reported a submucosal tumour composed of S-100 protein-positive spindle cells, and the diagnosis of ileal schwannoma was made. The possibility of intestinal neoplasms, including schwannomas, might be contemplated in the differential diagnosis of any pelvic mass lesions. A detailed histology study and immunohistochemical stain are required for the final diagnosis of intestinal schwannomas and to rule out malignant changes, which are extremely important for the further management of patients. To the best knowledge, our case is one of the biggest intestinal schwannomas reported in the current literature.","PeriodicalId":9600,"journal":{"name":"Case Reports in Surgery","volume":"543 3","pages":""},"PeriodicalIF":0.6,"publicationDate":"2024-02-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139838927","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}

引用次数: 0

Conservative Treatment of an Unusual Presentation of Iliopsoas Phlegmon Related to Infected Intrauterine Contraceptive Device. 宫内避孕器感染引起的髂腰肌痰症的保守治疗。

IF 0.6

Case Reports in Surgery Pub Date : 2024-02-06 eCollection Date: 2024-01-01 DOI: 10.1155/2024/9916070

Giuleta Jamsari, Joseph Do Woong Choi, Benedict Kakala, Hillary Hu, Gideon Sandler

引用次数: 0

Chronic Isolated Fallopian Tube Torsion in a Sexually Inactive Adolescent Female Diagnosed Peroperatively. 一名性生活不活跃的青春期女性经手术确诊的慢性孤立性输卵管扭转。

IF 0.6

Case Reports in Surgery Pub Date : 2024-01-22 eCollection Date: 2024-01-01 DOI: 10.1155/2024/2581337

Yuhya Hirahara, Koichi Nagai, Kazunori Mukaida

{"title":"Chronic Isolated Fallopian Tube Torsion in a Sexually Inactive Adolescent Female Diagnosed Peroperatively.","authors":"Yuhya Hirahara, Koichi Nagai, Kazunori Mukaida","doi":"10.1155/2024/2581337","DOIUrl":"10.1155/2024/2581337","url":null,"abstract":"Introduction: Isolated fallopian tube torsion (IFTT) has rarely been confirmed in sexually inactive adolescents, and preoperative diagnosis of IFTT is difficult because of the absence of specific symptoms. Therefore, pediatric patients with IFTT tend to be misdiagnosed before the surgery.Case: A 15-year-old female patient with no history of abdominal surgery or sexual intercourse presented with acute left lower abdominal pain and purpura. MRI revealed hydrosalpinx in the left adnexal region. Her abdominal pain had completely resolved at our examination; she was followed up as an outpatient. One month after the initial presentation, she experienced a large volume of watery discharge. Magnetic resonance imaging, which was performed every three months, showed a gradual decrease in the size of the hydrosalpinx; however, it persisted in the left adnexal region. She was counseled to receive laparoscopy to treat the hydrosalpinx, which was the most likely cause of the watery discharge. IFTT was detected during the laparoscopy, and left salpingectomy was performed for pathological evaluation of the persistent hydrosalpinx. Following laparoscopy, the patient's watery discharge was resolved. Pathological findings confirmed no signs of malignancy.Conclusion: Our current report highlighted watery discharge as an indicative symptom of IFTT. It is unclear whether IFTT induced the hydrosalpinx or vice versa. We presumed that the patient's hydrosalpinx occurred due to IFTT, because the patient complained watery discharge one month after the initial appearance, and noncongenital hydrosalpinx in adolescents, especially without a history of sexual intercourse, is a rare event. Clinicians should consider IFTT in patients presenting with unremitting watery discharge and hydrosalpinx, because IFTT may persist even after the pain disappears.","PeriodicalId":9600,"journal":{"name":"Case Reports in Surgery","volume":"2024 ","pages":"2581337"},"PeriodicalIF":0.6,"publicationDate":"2024-01-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10824574/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139575201","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

Anterolateral Thigh Flap Reconstruction of Full Thickness Lateral Abdominal Wall Defect from Desmoid Tumour 大腿前外侧皮瓣重建蝶形瘤导致的全厚腹壁外侧缺损

IF 0.6

Case Reports in Surgery Pub Date : 2024-01-16 DOI: 10.1155/2024/1908212

Melissa Yeo

引用次数: 0

Chronic Appendicitis: Possible Differential Diagnosis in Patients with Chronic Abdominal Pain 慢性阑尾炎：慢性腹痛患者的可能鉴别诊断

IF 0.6

Case Reports in Surgery Pub Date : 2024-01-09 DOI: 10.1155/2024/6032042

Iva Ljubas, Ivana Jurca, Dora Grgić

{"title":"Chronic Appendicitis: Possible Differential Diagnosis in Patients with Chronic Abdominal Pain","authors":"Iva Ljubas, Ivana Jurca, Dora Grgić","doi":"10.1155/2024/6032042","DOIUrl":"https://doi.org/10.1155/2024/6032042","url":null,"abstract":"In the emergency department, patients frequently present with abdominal pain, with a variety of different causes ranging from intra-abdominal to extra-abdominal and retroperitoneal pathologies which can affect all age groups. Chronic appendicitis is a rare medical condition characterized by less severe and continuous abdominal pain and a clinical picture lasting longer than 1-2 days and extending over months, even years, and it is not always possible to consider it as a preliminary diagnosis. We represent a case report of chronic appendicitis where the patient’s clinical picture led the diagnostics and treatment in different directions and delayed the diagnosis. Namely, our patient was radiologically diagnosed with a collection of denser content retroperitoneally in the right lower quadrant of the abdomen, which in the first place was not related to possible appendicitis, regarding complaints. The existence of chronic appendicitis is a diagnosis unfamiliar to many clinicians and has no official diagnostic criteria. After diagnosis, treatment usually begins with antibiotics, and the next most common step is surgery. The optimal treatment for this condition is unknown. With this case report, we wish to draw attention to chronic appendicitis as a possible differential diagnosis in patients with chronic abdominal pain.","PeriodicalId":9600,"journal":{"name":"Case Reports in Surgery","volume":"110 1","pages":""},"PeriodicalIF":0.6,"publicationDate":"2024-01-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139444559","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}

引用次数: 0

Colon Lipoma Causing Colo-Colic Intussusception in an Adult: A Case Report from Tanzania 结肠脂肪瘤导致成人结肠-结肠肠套叠：坦桑尼亚的病例报告

IF 0.6

Case Reports in Surgery Pub Date : 2024-01-06 DOI: 10.1155/2024/7777258

Jamil M. Suleiman, Mujaheed Suleman, Alex Mremi, Adnan Sadiq, Abbas Mohamedali, Dennis Machaku, J. Lodhia

引用次数: 0

Sclerosing Encapsulating Peritonitis: Solving the Diagnosis Challenge of a Rare Entity. 硬化性包裹性腹膜炎：破解罕见病例的诊断难题

IF 0.6

Case Reports in Surgery Pub Date : 2023-12-27 eCollection Date: 2023-01-01 DOI: 10.1155/2023/4022487

Anwar Rahali, El Mehdi Aboulfath, Noureddine Njoumi, Mohammed Rebbani, Yasser El Brahmi, Mohammed Elfahssi, Abderrahman Elhjouji, Aziz Zentar, Abdelmounaim Ait Ali

{"title":"Sclerosing Encapsulating Peritonitis: Solving the Diagnosis Challenge of a Rare Entity.","authors":"Anwar Rahali, El Mehdi Aboulfath, Noureddine Njoumi, Mohammed Rebbani, Yasser El Brahmi, Mohammed Elfahssi, Abderrahman Elhjouji, Aziz Zentar, Abdelmounaim Ait Ali","doi":"10.1155/2023/4022487","DOIUrl":"10.1155/2023/4022487","url":null,"abstract":"Sclerosing encapsulating peritonitis (SEP) is an unusual fibroinflammatory disease of the peritoneum marked by the development of a fibrous membrane enveloping generally the small intestines. The knowledge around this subject is not completely understood. And the etiology can be either idiopathic or secondary to several diseases, treatments, and/or medications. We present a case of a 52-year-old man suffering from atypical clinical symptoms including recurrent abdominal ascites and intestinal obstruction. An abdominal computed tomography showed findings typical of SEP. Therefore, the patient benefited from exploratory laparotomy, which confirmed the diagnosis of idiopathic SEP. Postoperatively, he again had an episode of bowel obstruction, but this was controlled with steroids. Diagnosis of SEP is a real challenge to surgeons, gastroenterologists, and radiologists. And imagery is very helpful to make the diagnosis. Consequently, it is imperative that all hospital practitioners should distinguish between this lesion and other etiology of acute peritonitis.","PeriodicalId":9600,"journal":{"name":"Case Reports in Surgery","volume":"2023 ","pages":"4022487"},"PeriodicalIF":0.6,"publicationDate":"2023-12-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10764648/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139097396","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

Incidental Discovery of Hepatocellular Carcinoma on 18F-PSMA PET CT Performed for Prostate Cancer Reassessment. 为前列腺癌复查而进行的 18F-PSMA PET CT 意外发现肝细胞癌。

IF 0.6

Case Reports in Surgery Pub Date : 2023-12-13 eCollection Date: 2023-01-01 DOI: 10.1155/2023/1458175

Lauren Hekman, Eva Napierkowski, Natalie C Hartman, Jeffrey L Ellis, Robert H Wagner, Davide Bova, Maria M Picken, Robert C Flanigan

引用次数: 0

Schistosomiasis Involving the Central Nervous System: Case Report of a Rare Complication. 血吸虫病累及中枢神经系统：罕见并发症的病例报告。

IF 0.6

Case Reports in Surgery Pub Date : 2023-12-12 eCollection Date: 2023-01-01 DOI: 10.1155/2023/9968155

Rahaf F Alanazi, Maryam Al Karawi, Abdulrahman Almalki, Fahd Sufiani, Sarmad Al Karawi

引用次数: 0

Neonatal Testicular Torsion with Hydrocele: A Case Report Underscoring the Need for Early Recognition and Management. 新生儿睾丸扭转伴鞘膜积液：一例强调早期识别和处理必要性的病例报告。

IF 0.6

Case Reports in Surgery Pub Date : 2023-12-11 eCollection Date: 2023-01-01 DOI: 10.1155/2023/9979543

Kareem Omran, Sameh Ali Ali, Ehsan Ahmad, Hilal Matta, Wissam Jamal Al Tamr

{"title":"Neonatal Testicular Torsion with Hydrocele: A Case Report Underscoring the Need for Early Recognition and Management.","authors":"Kareem Omran, Sameh Ali Ali, Ehsan Ahmad, Hilal Matta, Wissam Jamal Al Tamr","doi":"10.1155/2023/9979543","DOIUrl":"10.1155/2023/9979543","url":null,"abstract":"Neonatal testicular torsion (NTT) is a rare but significant condition occurring within the first 30-day postbirth, leading to vascular compromise and potential testicular loss. This paper presents a case of NTT detected incidentally in a neonate with bilateral hydrocele, emphasizing the challenge of early diagnosis and management complexities. The infant underwent surgical intervention involving detorsion and bilateral orchiopexy but eventually required right orchiectomy due to necrosis. The paper highlights the prevalence of NTT in conjunction with hydrocele and stresses the importance of parent education and vigilant follow-up. Various diagnostic methods, primarily ultrasonography, and a range of management strategies are discussed, considering factors such as salvage potential, risk to the contralateral testicle, and surgical intervention's risks and benefits. The paper argues for individualized management, taking into account specific neonate conditions and parental preferences, underlining the essential role of informed and empathetic consultation. The case reinforces the urgent need for increased awareness, early detection, and carefully considered therapeutic approaches to prevent devastating outcomes like infertility and the necessity for lifelong hormone supplementation.","PeriodicalId":9600,"journal":{"name":"Case Reports in Surgery","volume":"2023 ","pages":"9979543"},"PeriodicalIF":0.6,"publicationDate":"2023-12-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10728354/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138798029","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