BJR Case Reports最新文献_第5页

A case of congenital fibular hemimelia associated with skeletal and non-skeletal malformations. 先天性腓骨偏瘫伴骨骼及非骨骼畸形1例。

IF 0.5

BJR Case Reports Pub Date : 2025-02-18 eCollection Date: 2025-03-01 DOI: 10.1093/bjrcr/uaaf008

Mahmoud R Manasra, Rahaf E Farah, Roua E Farah, Sama S Yassin, Shadi A Abuisneina

{"title":"A case of congenital fibular hemimelia associated with skeletal and non-skeletal malformations.","authors":"Mahmoud R Manasra, Rahaf E Farah, Roua E Farah, Sama S Yassin, Shadi A Abuisneina","doi":"10.1093/bjrcr/uaaf008","DOIUrl":"10.1093/bjrcr/uaaf008","url":null,"abstract":"Fibular hemimelia (FH) is a rare congenital abnormality where the fibula is either totally or partially absent. It can occur alone or alongside other skeletal malformations, and in very few cases, it may occur along with non-skeletal anomalies. A 4-year-old female was diagnosed with unilateral right-sided FH, accompanied by limb shortening, a right-side ankle deformity, valgus foot, and 3 lateral rays that had been totally absent since the first week of birth. And she was incidentally diagnosed with spina bifida occulta at a 3-year-old age. FH is most commonly unilateral and mostly affects the right side, leads to a limb-length discrepancy, and maybe comes as a symptom of a syndrome such as Foetus-Fibula-Ulna syndrome and so on. Risk factors include prenatal history, drugs, and no supplementation intake. Together, these elements could be a contributing factor to our condition. The congenital limb abnormalities may be discovered during pregnancy by sonography. If present, other investigations need to be done to differentiate the diagnosis. Treatment according to degree: mild, moderate, and severe cases. In our case, the type 2 FH characteristic was shown by sonography, accompanied by limb shortening, lateral rays absent, and a non-skeletal anomaly (spina bifida). These anomalies very rarely come with each other at the same time. To the best of our knowledge, this case is exceptional in that FH is present at birth alongside spina bifida.","PeriodicalId":45216,"journal":{"name":"BJR Case Reports","volume":"11 2","pages":"uaaf008"},"PeriodicalIF":0.5,"publicationDate":"2025-02-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11879310/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143568477","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

Ruptured ovarian dermoid causing chemical peritonitis: a case report. 卵巢皮样破裂致化学性腹膜炎1例。

IF 0.5

BJR Case Reports Pub Date : 2025-02-10 eCollection Date: 2025-01-01 DOI: 10.1093/bjrcr/uaaf004

Vrinda Chandar, Joel Kevin Raj Samuel, Ajay Kumar Singh

引用次数: 0

Giant cell tumour of the larynx-a diagnostic challenge. 喉部巨细胞瘤——诊断上的挑战。

IF 0.5

BJR Case Reports Pub Date : 2025-02-10 eCollection Date: 2025-01-01 DOI: 10.1093/bjrcr/uaaf006

Vitor H Fraga de Abreu, Ricardo Pacheco, Fernando Cunha, Alexandra Borges

引用次数: 0

Endovascular treatment of a giant arteria lusoria aneurysm in a young female with Marfan syndrome. 年轻女性马凡氏综合征巨大阔动脉动脉瘤的血管内治疗。

IF 0.5

BJR Case Reports Pub Date : 2025-02-07 eCollection Date: 2025-03-01 DOI: 10.1093/bjrcr/uaaf005

Sandra Fraund-Cremer, Rene Rusch, Anselm Uebing, Inga Voges, Philipp Schäfer

{"title":"Endovascular treatment of a giant arteria lusoria aneurysm in a young female with Marfan syndrome.","authors":"Sandra Fraund-Cremer, Rene Rusch, Anselm Uebing, Inga Voges, Philipp Schäfer","doi":"10.1093/bjrcr/uaaf005","DOIUrl":"10.1093/bjrcr/uaaf005","url":null,"abstract":"Aneurysms of an aberrant right subclavian artery (ARSA) are rare but constitute a potentially lethal condition, especially with concomitant Marfan syndrome (MFS). A 27-year-old female with confirmed MFS presented with a relevant progression of a known aneurysm of an ARSA in MRI. The patient had undergone valve-sparing aortic root replacement (David procedure) 4 months prior. After interdisciplinary discussion, she underwent endovascular exclusion of the aneurysm using a combination of established vascular plugs and novel shape memory polymer embolization plugs to fill the large ARSA aneurysm volume. The shape memory polymer embolization plugs expand in the vessel to a porous scaffold, designed to support thrombus formation throughout its structure. The polymer is also radiolucent, which minimizes artefact and facilitates follow-up imaging. Development of a strategy for the treatment of ARSA aneurysms is challenging and different surgical, endovascular, and combined approaches have been published. Interdisciplinary discussion is crucial to minimize the overall risk and trauma. In our case of a young female and new mother, an endovascular approach was successfully and safely performed. The future need for surgery due to concomitant MFS is expected.","PeriodicalId":45216,"journal":{"name":"BJR Case Reports","volume":"11 2","pages":"uaaf005"},"PeriodicalIF":0.5,"publicationDate":"2025-02-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11879303/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143568480","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Successful resolution of gastric pneumatosis due to a strangulated hiatus hernia and malrotation through non-surgical management: a case report. 通过非手术治疗成功解决绞窄性裂孔疝和旋转不良引起的胃肺病1例报告。

IF 0.5

BJR Case Reports Pub Date : 2025-02-05 eCollection Date: 2025-01-01 DOI: 10.1093/bjrcr/uaaf007

Shiv Hadani, Dhaara Bhatt, Ashish Bhagat, Vivek Malhotra

引用次数: 0

Cranio-cervical hyperpneumatization: a case report. 颅颈过度通气1例。

IF 0.5

BJR Case Reports Pub Date : 2025-01-23 eCollection Date: 2025-01-01 DOI: 10.1093/bjrcr/uaaf003

Matthew Kueh, Ramnik Behar

引用次数: 0

Rare complications of ERCP-pancreatitis, panniculitis, and polyarthritis syndromeand multifocal osteomyelitis. ercp的罕见并发症-胰腺炎、睫状体炎、多发性关节炎综合征和多灶性骨髓炎。

IF 0.5

BJR Case Reports Pub Date : 2025-01-17 eCollection Date: 2025-01-01 DOI: 10.1093/bjrcr/uaaf002

Ratna Koyyalamudi, Dominic Ku, Kirk Brown, Morgan Schulze

{"title":"Rare complications of ERCP-pancreatitis, panniculitis, and polyarthritis syndromeand multifocal osteomyelitis.","authors":"Ratna Koyyalamudi, Dominic Ku, Kirk Brown, Morgan Schulze","doi":"10.1093/bjrcr/uaaf002","DOIUrl":"10.1093/bjrcr/uaaf002","url":null,"abstract":"Severe pancreatitis following retrograde cholangiopancreatography (ERCP) is an infrequent occurrence. Even rarer are the additional non-pancreatic symptoms that can emerge after ERCP-induced pancreatitis, such as panniculitis and polyarthritis. This combination of symptoms is recognized as the pancreatitis, panniculitis, and polyarthritis syndrome (PPPS). PPPS typically manifests as reddish subcutaneous nodules, primarily in the lower extremities. In some cases, the condition may progress into the bones, causing intramedullary fat necrosis/bone infarcts. Joint complications involve polyarthritis and affect both small and large joints. PPPS tends to develop 3-6 weeks after the peak of clinical pancreatitis. In this report, we present a case of PPPS that occurred as a complication following ERCP. This particular case became further complicated by the presence of bacteraemia and fungaemia, leading to the subsequent development of multi-focal osteomyelitis. The medical imaging included in this report provides a comprehensive overview of the entire clinical course, starting from the initial post-procedural complication and pancreatitis, followed by multi-modal imaging depicting panniculitis using ultrasound and MRI, and finally illustrating the development of multi-focal osteomyelitis. This case serves as an opportunity to explore and understand 2 rare complications associated with pancreatitis: PPPS and multi-focal osteomyelitis.","PeriodicalId":45216,"journal":{"name":"BJR Case Reports","volume":"11 1","pages":"uaaf002"},"PeriodicalIF":0.5,"publicationDate":"2025-01-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11785366/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143080774","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

Unusual presentation of Ascaris lumbricoides in the urinary tract: a case report. 蛔虫在泌尿道中的异常表现：病例报告。

IF 0.5

BJR Case Reports Pub Date : 2025-01-16 eCollection Date: 2025-01-01 DOI: 10.1093/bjrcr/uaaf001

Zaid A Sowaity, Ammar A Zamareh, Tayseer N Sabooh, Amjed T Sowaity, Yazan F Khdour, Mutaz A A Atmeza

{"title":"Unusual presentation of Ascaris lumbricoides in the urinary tract: a case report.","authors":"Zaid A Sowaity, Ammar A Zamareh, Tayseer N Sabooh, Amjed T Sowaity, Yazan F Khdour, Mutaz A A Atmeza","doi":"10.1093/bjrcr/uaaf001","DOIUrl":"10.1093/bjrcr/uaaf001","url":null,"abstract":"Ascaris lumbricoides is one of the most well-known helminthic parasites affecting humans. Ascariasis is prevalent in developing countries where inadequate water, sanitation, and hygiene facilitate human-to-human transmission. In this report, we present a case of a 20-year-old male who arrived at the emergency room with severe right flank pain, high-grade fever, and recurrent vomiting. Diagnostic evaluations were conducted, including a complete blood count test, urinalysis, stool analysis, abdominal ultrasound, and CT scan. The final diagnosis was A lumbricoides found in the distal part of the ureter. A ureteroscopy procedure confirmed the diagnosis and extracted the worm, which measured 6 cm in length, had a brown colour, and exhibited a tight elastic consistency. While Ascaris is commonly found in the gastrointestinal tract, its occurrence in the urinary tract is an extremely rare phenomenon. In our case, the most likely explanation is that the Ascaris accessed the distal ureter through retrograde migration, wherein the worm traverses from the bladder into the ureter.","PeriodicalId":45216,"journal":{"name":"BJR Case Reports","volume":"11 1","pages":"uaaf001"},"PeriodicalIF":0.5,"publicationDate":"2025-01-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11849953/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143494088","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

Right coronary ostial atresia as a cause of arrhythmia and cardiogenic shock in a young woman: a case report. 年轻女性右冠状动脉口闭锁致心律失常和心源性休克1例报告。

IF 0.5

BJR Case Reports Pub Date : 2025-01-10 eCollection Date: 2025-01-01 DOI: 10.1093/bjrcr/uaae049

Velio Ascenti, Silvia Tresoldi, Caterina B Monti, Stefano Lucreziotti, Simone Soldi, Maurizio Cariati, Gianpaolo Carrafiello

引用次数: 0

Desmoid fibromatosis post-cervical spine surgical intervention. 颈椎手术干预后硬纤维瘤病。

IF 0.5

BJR Case Reports Pub Date : 2024-12-17 eCollection Date: 2025-01-01 DOI: 10.1093/bjrcr/uaae050

Dana AlNuaimi, Shareefa Abdulghaffar, Reem AlKetbi, Badreya Khadim, Khalid Ibrahim

{"title":"Desmoid fibromatosis post-cervical spine surgical intervention.","authors":"Dana AlNuaimi, Shareefa Abdulghaffar, Reem AlKetbi, Badreya Khadim, Khalid Ibrahim","doi":"10.1093/bjrcr/uaae050","DOIUrl":"https://doi.org/10.1093/bjrcr/uaae050","url":null,"abstract":"Desmoid tumours are rare benign tumours that show locally aggressive and invasive features leading to potential complications. They can be quite challenging for the treating surgeon if they occur adjacent to neurovascular structures. The aetiology of these tumours is still unclear, but the incidence is higher in females and in patients with a history of trauma or surgical procedures, raising the possibility of genetic and hormonal factors as well as post-traumatic or post-operative inflammatory changes promoting the formation of desmoid fibromatosis. We report a case of a 34-year-old Asian female who presented to our hospital with a history of difficulty in swallowing due to an enlarging lump on the left side of her neck. Patient had a past medical history of previous cervical spinal disc surgery due to a herniated disc. Diagnostic imaging showed a large soft tissue mass centred between the left common carotid artery and the cervical vertebrae displacing the trachea and oesophagus to the right side. A biopsy was obtained, and histopathological examination was suggestive of a desmoid tumour. The patient underwent surgical resection of the tumour but returned later with recurrence and had to undergo the surgery again to achieve full cure.","PeriodicalId":45216,"journal":{"name":"BJR Case Reports","volume":"11 1","pages":"uaae050"},"PeriodicalIF":0.5,"publicationDate":"2024-12-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11697182/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142933078","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