Sharon L. Hsieh MD, MPH , Nathaniel Grabill MD , Mena Louis DO , Bradley Kuhn MD
{"title":"Complicated diverticulitis: Diagnostic precision and surgical solutions in a patient with chronic kidney disease","authors":"Sharon L. Hsieh MD, MPH , Nathaniel Grabill MD , Mena Louis DO , Bradley Kuhn MD","doi":"10.1016/j.radcr.2024.10.039","DOIUrl":"10.1016/j.radcr.2024.10.039","url":null,"abstract":"<div><div>Diverticulitis, an inflammation of diverticula in the colon, can lead to severe complications such as perforation and abscess formation. A 42-year-old female with polycystic kidney disease and chronic kidney disease stage III presented with severe abdominal pain, fever, and inability to tolerate oral intake. The patient was a previous smoker who smoked 0.5 packs per day for 25 years. Initial evaluation revealed leukocytosis and elevated creatinine. A CT scan identified pneumoperitoneum and mild sigmoid diverticulitis, suggesting a perforated viscus. She underwent urgent exploratory laparotomy, which confirmed the CT findings and resulted in an appendectomy, sigmoid colon resection, and ostomy creation. Postoperatively, the patient faced complications, including recurrent pneumoperitoneum and subcutaneous emphysema, detected through follow-up CT scans, leading to further surgical interventions. CT imaging was pivotal in diagnosing, monitoring, and guiding treatment, with noncontrast CT being beneficial given her renal impairment. Early diagnosis and CT imaging are crucial in managing complicated diverticulitis. Postoperative monitoring with CT scans is essential for detecting complications. Follow-up care should include regular colonoscopies to assess diverticular disease and dietary modifications to prevent recurrence. Combining clinical, surgical, and radiologic data ensures effective management and improves patient outcomes.</div></div>","PeriodicalId":53472,"journal":{"name":"Radiology Case Reports","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142553979","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}
Harry Galuh Nugraha , Maria Agustina , Heda Melinda Nataprawira
{"title":"Diagnostic challenges of hiatal hernia Type IV: An imaging perspective","authors":"Harry Galuh Nugraha , Maria Agustina , Heda Melinda Nataprawira","doi":"10.1016/j.radcr.2024.09.147","DOIUrl":"10.1016/j.radcr.2024.09.147","url":null,"abstract":"<div><div>Type IV hiatal hernia is a mixed type of hiatal hernia characterized by the herniation of visceral organs other than the stomach into the mediastinum. It is the least common type of hiatal hernia. We report a case of a 4-month-old male infant who presented with shortness of breath and persistent vomiting. Initial chest X-ray suggested a mediastinal mass, but further evaluation with chest computed tomography (CT) scan revealed herniation of the stomach and duodenum through the hiatal oesophagus into the thoracic cavity. Radiological imaging was crucial in confirming the diagnosis of hiatal hernia.</div></div>","PeriodicalId":53472,"journal":{"name":"Radiology Case Reports","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142553974","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}
Bereket Girum Beyene MD , Michael Teklehaimanot Abera MD , Tesfaye Abebe Zeleka MD , Abdi Alemayehu Dhuguma MD
{"title":"Armored brain as a late complication of CSF overshunting: A rare case report","authors":"Bereket Girum Beyene MD , Michael Teklehaimanot Abera MD , Tesfaye Abebe Zeleka MD , Abdi Alemayehu Dhuguma MD","doi":"10.1016/j.radcr.2024.10.020","DOIUrl":"10.1016/j.radcr.2024.10.020","url":null,"abstract":"<div><div>We hereby present a case of an 18-year-old patient who, following initial cerebrospinal fluid overshunting to relieve a congenital hydrocephalus for Dandy-Walker malformation, developed chronic calcified subdural hematoma or an armored brain as a late complication. Chronic calcified subdural hematoma or armored brain is generally rare, and it is even rarer after overshunting. In this report, we present a rare case of bilateral chronic subdural hematoma, also known as “armored brain”, 18 years after a ventriculoperitoneal shunt was placed during infancy. We emphasize the appearance of the lesion on a noncontrast brain computed tomography.</div></div>","PeriodicalId":53472,"journal":{"name":"Radiology Case Reports","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142553847","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}
{"title":"Cerebral adrenoleukodystrophy presenting as status epilepticus: Unveiling the neurological maze","authors":"Saket Satyasham Toshniwal MD , S. Jiwan Kinkar DNB, MD , Sunil Kumar PhD, MD , Sourya Acharya PhD, DNB","doi":"10.1016/j.radcr.2024.10.018","DOIUrl":"10.1016/j.radcr.2024.10.018","url":null,"abstract":"<div><div>We describe the case of a 7-year-old boy who had repeated episodes of prolonged seizures without recovery of consciousness when he arrived at a rural tertiary care teaching institute hospital in Wardha, India. Detailed history of the patient revealed that the child's symptoms began with left exotropia and visual acuity changes, progressing over 6 months to cognitive decline, hearing impairment, pseudobulbar affect, and motor issues, eventually leading to school dropout. Social isolation and difficulty walking also developed as the disease advanced. MRI brain revealed diffuse white matter lesions bilaterally with raised serum ACTH levels of 5 times the normal range associated with raised levels of tetracosanoic acid (C24) and hexacosanoic acid (C26), along with elevated C24/C22 and C26/C22 ratios. The patient was provisionally diagnosed as X linked cerebral adrenoleukodystrophy. Post treatment and stabilization, the patient was seizure-free on antiepileptic medications, however, patient developed blindness, lost mobility, became bedridden, and progressed to a vegetative state within 6 months. Adrenoleukodystrophy (ALD) is a rare X-linked genetic disorder that primarily affects men. It is caused by mutations in the ABCD 1 gene and is characterized by an abnormal build-up of very long-chain fatty acids (VLCFA) in various body tissues, which affect the spinal cord, white matter, and adrenal glands, causing progressive damage and dysfunction at each location. This case highlights the importance of early diagnosis and intervention to slow down disease progression in order to improve outcome. Also, increased awareness among healthcare professionals to help early detect the signs of this disease is of great importance.</div></div>","PeriodicalId":53472,"journal":{"name":"Radiology Case Reports","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142553850","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}
Sajjad Haider MD , Fawaz Mohammed MBBS , Ayesha Mahnoor Arab BS , Sameer Saleem MD , Jacqueline Dawson Dowe MD , Akhtar Amin MD , Aniruddha Singh MD , Muhammad Shoaib Akbar MD , Mohammed Kazimuddin MD , Mohammed Abdul-Waheed MD
{"title":"Survival case of cardiac strangulation from epicardial pacemaker leads in an adult: A case report","authors":"Sajjad Haider MD , Fawaz Mohammed MBBS , Ayesha Mahnoor Arab BS , Sameer Saleem MD , Jacqueline Dawson Dowe MD , Akhtar Amin MD , Aniruddha Singh MD , Muhammad Shoaib Akbar MD , Mohammed Kazimuddin MD , Mohammed Abdul-Waheed MD","doi":"10.1016/j.radcr.2024.10.019","DOIUrl":"10.1016/j.radcr.2024.10.019","url":null,"abstract":"<div><div>Cardiac strangulation from leads of an epicardial pacemaker is a rarely reported life-threatening complication. We report the case of a 72-year-old female with history of supraventricular tachycardia status post sino-atrial node ablation with epicardial pacemaker placement who presented to the outpatient setting with shortness of breath. Heart catheterization was performed which showed elevated right and left heart pressures. Compression involving the mid left anterior descending artery and left circumflex artery was noted from an epicardial lead on coronary angiography consistent with cardiac strangulation. The patient was then referred to cardiothoracic surgery for epicardial pacemaker lead removal. The literature has only reported one other survival case of cardiac strangulation in an adult.</div></div>","PeriodicalId":53472,"journal":{"name":"Radiology Case Reports","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142553906","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}
{"title":"Swallowed drug-filled packet impaction and appendiceal neoplasm: Two rare causes of bowel obstruction detected in the same patient","authors":"Eduard Sanchis-Querol MD , Ana-Liz Briceño-Andino MD , Teresa Álvarez-Petraglia MD , Alejandro Grinfeld MD , Samanta Landini MD , Gustavo Maida MD , Diana Velásquez MD","doi":"10.1016/j.radcr.2024.09.146","DOIUrl":"10.1016/j.radcr.2024.09.146","url":null,"abstract":"<div><div>Bowel obstruction, perforation and acute drug overdose due to packet rupture are known complication of “body-packing”. We present the case of a 47-year-old man, who ingested drug-filled packets with acute bowel obstruction. A CT scan revealed multiple hyperdense ovoid bodies along distended and fluid-filled small bowel loops and an infiltrating appendiceal tumor with proximal packet retention. Peritoneal carcinomatosis was also observed. Urgent laparotomy confirmed the radiological findings. This study aims to highlight the coincidence of 2 exceedingly rare causes of bowel obstruction in a single patient and emphasize the need for meticulous finding evaluation in acutely ill patients to avoid the perceptual errors associated with “satisfaction of search” bias.</div></div>","PeriodicalId":53472,"journal":{"name":"Radiology Case Reports","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142553977","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}
Brandon Thinh Duc Dang MD, Alan Victor Krauthamer MD
{"title":"Vascular lesions: Hemangioma or venous malformation?","authors":"Brandon Thinh Duc Dang MD, Alan Victor Krauthamer MD","doi":"10.1016/j.radcr.2024.10.069","DOIUrl":"10.1016/j.radcr.2024.10.069","url":null,"abstract":"<div><div>We present a case of a 62-year-old female who was incidentally found to have a venous malformation. Venous malformations are part of a larger category of slow flow vascular malformations and are associated with various familial syndromes and localized intravascular coagulation. Venous malformations were often misdiagnosed as hemangiomas; however, the treatment modalities of vascular malformations and hemangiomas vary significantly. Here we elucidate the imaging findings of venous malformations from various vascular tumors and other malformations.</div></div>","PeriodicalId":53472,"journal":{"name":"Radiology Case Reports","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142553904","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}
{"title":"One artery to rule them all: A case of single coronary artery arising from the right sinus of Valsalva","authors":"Nikolaos S. Ioakeimidis MD, MSc , Panagiotis Pepis MD, MSc , Konstantina Mitrousi MD , Dimitrios Valasiadis MD","doi":"10.1016/j.radcr.2024.10.005","DOIUrl":"10.1016/j.radcr.2024.10.005","url":null,"abstract":"<div><div>A single coronary artery (SCA) is a rare congenital anomaly with an incidence of 0.024 - 0.066% in angiographies and potential implications for adverse events depending on the course of the anomalous artery. We present a unique case of a single coronary artery arising from the right sinus of Valsalva. A 77-year-old female presented to the emergency department with an ongoing 3-hour episode of palpitations and intermittent atypical chest pain over 1 week. Her medical history included hypertension and dyslipidemia. Electrocardiography revealed atrial fibrillation with rapid ventricular response, which was successfully managed with intravenous amiodarone and the diagnostic workup ruled out life threatening thoracic pathology including cardiac ischemia. A CT coronary angiography was performed due to the moderate pretest probability of coronary artery disease. The scan identified a single coronary artery with a common origin of the left main coronary artery (LMCA) and the right coronary artery (RCA), from the right sinus of Valsalva, classified as Lipton Type RII-A which is a benign variant. This case highlights the importance of identifying CAAs, which are often incidental but may have clinical relevance depending on the anatomical course and associated risk factors. Early and accurate diagnosis through advanced imaging techniques is crucial to guide appropriate management and ensure optimal outcomes for the patient.</div></div>","PeriodicalId":53472,"journal":{"name":"Radiology Case Reports","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142553905","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}
{"title":"A rare case: Transcatheter coil embolization in a patient with cystic duct stump injury following cholecystectomy","authors":"Furkan Özdem MD","doi":"10.1016/j.radcr.2024.10.024","DOIUrl":"10.1016/j.radcr.2024.10.024","url":null,"abstract":"<div><div>Acute cholecystitis is a common inflammatory condition of the gallbladder, primarily associated with gallstones. Complications such as bile duct injury and bile leakage can occur following cholecystectomy, significantly impacting morbidity and mortality. Early diagnosis and intervention are essential to improve patient outcomes, with treatment options including endoscopic sphincterotomy and stenting. However, percutaneous coil embolization has emerged as a critical intervention due to the anatomical complexity of the region.</div></div>","PeriodicalId":53472,"journal":{"name":"Radiology Case Reports","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142553986","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}
{"title":"Haemangioma of the breast: The added value of contrast enhanced ultra-sound (CEUS) in the vascularity assessment of a rare mesenchymal lesion","authors":"Cristiana Boldrini MD , Valerio Di Paola MD , Simone Palma MD , Valentina Longo MD , Silvia Amodeo MD , Micol Bottalico , Roberta Dattoli MD , Angelica Marra MD , Vincenza Pignatelli","doi":"10.1016/j.radcr.2024.10.013","DOIUrl":"10.1016/j.radcr.2024.10.013","url":null,"abstract":"<div><div>Haemangiomas have been described in many anatomic locations, but occur quite rarely in the breast; although unfrequent, they are the most common benign vascular tumors of the breast. They are comprised in the cathegory of mesenchymal lesions, a spectrum of lesions that arise in the stroma of the breast as defined by WHO.</div><div>Here we present the case of a breast haemangioma in a 40-years-old woman, with history of a palpable lump in the left breast slowly increasing in size over time. The lesion first underwent diagnostic biopsy in 2018; after a 5-years follow-up with conventional ultrasound, it was studied in 2023 by our group using Contrast Enhanced Ultra-Sound (CEUS) in order to evaluate its vascularization. Basing on our experience, we conclude that in carefully selected cases of histologically proven breast haemangioma, a conservative management with follow-up imaging is safe; CEUS represents a noninvasive method for studying haemangiomas, superior than traditional US thanks to its ability to provide information about vascularity. In those cases with atypical imaging or clinical pathological suspicious characteristics, a complete surgical resection of the vascular tumor is mandatory–in order to exclude the possibility of an underlying angiosarcoma, especially when the lesion measures more than 2 cm.</div></div>","PeriodicalId":53472,"journal":{"name":"Radiology Case Reports","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142553903","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}