Radiology Case Reports最新文献_第2页

Retroperitoneal ganglioneuroma simulating lymphoma: An unusual case presentation

Radiology Case Reports Pub Date : 2025-02-01 DOI: 10.1016/j.radcr.2025.01.061

Charles K. Crawford BS, Mohammad Yasrab MD, Linda C. Chu MD, Elliot K. Fishman MD

引用次数: 0

Multidisciplinary approach in the management of simultaneous stroke and acute arterial ischemia of the arteries of the upper extremity: A case report 多学科方法在同时卒中和上肢动脉急性动脉缺血治疗中的应用：1例报告。

Radiology Case Reports Pub Date : 2025-02-01 DOI: 10.1016/j.radcr.2024.11.008

M.A. Sedgaryan MD, PhD , A.V. Kudrinskiy MD, PhD , A.V. Snitsar MD , M.V. Patlachuk MD , P.A. Talyzin MD , V.A. Shibitov MD, DMSc , I.S. Ishutkin MD

引用次数: 0

Pilomatrixoma of the parotid region: A benign tumor mimicking metastatic cutaneous squamous cell carcinoma

Radiology Case Reports Pub Date : 2025-02-01 DOI: 10.1016/j.radcr.2025.01.065

Nikita Grieder MD , Marcella Pucci MD , Claudio De Vito MD, PhD , Yan Monnier MD, PhD , Nicolas Dulguerov MD , Maxime Mermod MD, PhD

引用次数: 0

Finding of a mass on the mitral valve in a patient on chronic dialysis

Radiology Case Reports Pub Date : 2025-02-01 DOI: 10.1016/j.radcr.2025.01.020

Vasil Papestiev MD, PhD , Marjan Shokarovski MD , Nikola Lazovski MD , Nadica Mehmedovic MD , Valentina Andova MD, PhD , Gordana Petrushevska MD, PhD , Ljubica Georgievska-Ismail MD, PhD

{"title":"Finding of a mass on the mitral valve in a patient on chronic dialysis","authors":"Vasil Papestiev MD, PhD , Marjan Shokarovski MD , Nikola Lazovski MD , Nadica Mehmedovic MD , Valentina Andova MD, PhD , Gordana Petrushevska MD, PhD , Ljubica Georgievska-Ismail MD, PhD","doi":"10.1016/j.radcr.2025.01.020","DOIUrl":"10.1016/j.radcr.2025.01.020","url":null,"abstract":"<div><div>Myxomas are cardiac neoplasms that are most commonly located in the left atrium, usually arising from the vicinity of the fossa ovalis. However, there have been cases, although very rarely, of valvular myxoma. A cardiac mass found incidentally on echocardiography can present a challenge in particular if asymptomatic or found in an unusual location. We present the case of a 58-year-old male with kidney disease treated with chronic dialysis, referred to the cardiology clinic because of an incidental finding of a mitral valvular mass on routine transthoracic echocardiography. Although this lesion was initially misdiagnosed as native valvular endocarditis with vegetation, a series of clinical and radiological investigations led to the preoperative diagnosis of possible papillary fibroelastoma or calcified thrombotic mass. Given the increased risk of embolization due to the mass being mobile and greater than 1 cm in size, the patient was referred to cardiac surgery. Excision of the mass without mitral valve replacement was performed. Histopathological findings of the mass revealed the existence of a cardiac myxoma. In such cases of a mitral valve mass, multimodality imaging should have of high priority to achieve an accurate diagnosis. Although a definitive diagnosis can only be established after surgical excision of the mass and histopathological confirmation, it is very important to consider a differential diagnosis of mitral valve myxoma in any patient with an unexplained mitral valve mass.</div></div>","PeriodicalId":53472,"journal":{"name":"Radiology Case Reports","volume":"20 4","pages":"Pages 2075-2079"},"PeriodicalIF":0.0,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143133611","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

Pilocytic astrocytoma: A rare case report

Radiology Case Reports Pub Date : 2025-02-01 DOI: 10.1016/j.radcr.2025.01.025

Harry Galuh Nugraha PhD , Elsa Yoasta MD , Mirna Sobana MD , Hermin Aminah Usman MD

引用次数: 0

Anomalous origin of the right coronary artery from the opposite sinus with interarterial course: A case report 右冠状动脉异常起源于对侧窦伴动脉间程1例。

Radiology Case Reports Pub Date : 2025-02-01 DOI: 10.1016/j.radcr.2024.07.153

Wassim Beladel MD , Wafa Id El Mouden MD , Mehdi Abdelali MD , Oussama Cheikhna MD , Karim Hasni MD , Mohamed EL Minaoui MD

{"title":"Anomalous origin of the right coronary artery from the opposite sinus with interarterial course: A case report","authors":"Wassim Beladel MD , Wafa Id El Mouden MD , Mehdi Abdelali MD , Oussama Cheikhna MD , Karim Hasni MD , Mohamed EL Minaoui MD","doi":"10.1016/j.radcr.2024.07.153","DOIUrl":"10.1016/j.radcr.2024.07.153","url":null,"abstract":"<div><div>An anomalous origin of the right coronary artery from the opposite sinus (R- ACAOS) with interarterial course is a very rare congenital anomaly with an increased risk of sudden cardiac death. A 29-year-old woman was admitted for exertional angina pectoris. A coronary computed tomography angiography with 3D multiplanar reconstruction revealed an R-ACAOS running between the aorta and pulmonary artery with high anatomical features and no ischemia-induced at the stress test. The heart team staff decided to manage the patient surgically. Coronary arteries are characterized by their origin, course, and boundaries with intracardiac structures and large vessels. Computed tomography angiography is the gold standard exam to confirm the diagnosis and identify high-risk anatomic features that guide the management. It is important to consider treatment options for these patients whether by medical treatment, coronary angioplasty, or surgical repair, because of the increased risk of SCD. We hereby present an R-ACAOS with interarterial course and high anatomic features, which is an uncommon finding and can be fatal if it remains undiscovered.</div></div>","PeriodicalId":53472,"journal":{"name":"Radiology Case Reports","volume":"20 2","pages":"Pages 1263-1267"},"PeriodicalIF":0.0,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11665310/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142883567","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

Osseous sarcoidosis presenting as lytic and blastic bone lesions: A rare diagnostic challenge 骨结节病表现为溶解性和成骨病变：罕见的诊断挑战。

Radiology Case Reports Pub Date : 2025-02-01 DOI: 10.1016/j.radcr.2024.11.010

J. Bastidas , L. López-Nuñez , R. Faré , Javier G. Moríñigo , I. Ros , A. Juan Mas

{"title":"Osseous sarcoidosis presenting as lytic and blastic bone lesions: A rare diagnostic challenge","authors":"J. Bastidas , L. López-Nuñez , R. Faré , Javier G. Moríñigo , I. Ros , A. Juan Mas","doi":"10.1016/j.radcr.2024.11.010","DOIUrl":"10.1016/j.radcr.2024.11.010","url":null,"abstract":"<div><div>Osseous sarcoidosis is a rare manifestation of sarcoidosis, often mimicking other conditions like metastatic disease. Skeletal involvement occurs in only 3%-13% of cases (1), making diagnosis challenging. We present the case of a 63-year-old female with a 1-month history of inflammatory bone pain and multiple lytic and blastic lesions.</div><div>A 63-year-old female presented with a 1-month history of inflammatory pain in the left hip and lumbar spine. Radiological studies, including magnetic resonance imaging (MRI) and computed tomography (CT), revealed multiple bone lesions throughout the lumbar spine, sacrum and iliac bones, raising suspicion of metastatic disease a bone biopsy confirmed a diagnosis of sarcoidosis.</div><div>MRI and CT showed lytic and blastic lesions in the axial skeleton, with FDG-PET indicating diffuse uptake in the iliac bone and mediastinal adenopathy. Imaging was crucial in ruling out metastases and guiding the biopsy, which confirmed the diagnosis.</div><div>Osseous sarcoidosis is a rare entity that poses a significant diagnostic challenge, often resembling metastatic disease. Imaging techniques such as MRI and CT, combined with biopsy, are effective, noninvasive methods for evaluation and diagnosis. The patient was treated with corticosteroids in high doses and systemic methotrexate, showing improvement in inflammatory pain and stabilization of the bone lesions.</div></div>","PeriodicalId":53472,"journal":{"name":"Radiology Case Reports","volume":"20 2","pages":"Pages 1247-1251"},"PeriodicalIF":0.0,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11665402/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142883618","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

Osteoid osteoma of the distal phalanx of the finger: Case report and review of literature 手指远端指骨骨样骨瘤：1例报告及文献复习。

Radiology Case Reports Pub Date : 2025-02-01 DOI: 10.1016/j.radcr.2024.11.034

Ashima Kundu BS, Liana Ysabel Almendras Bautista BS, Haley Clark BS, Usman Beg DO, Amirmasoud Negarestani MD, Emad Allam MD

引用次数: 0

Macrodystrophia lipomatosa: Clinical and radiological insights into localized gigantism 巨大营养不良性脂肪瘤：局部巨人症的临床和放射学观察。

Radiology Case Reports Pub Date : 2025-02-01 DOI: 10.1016/j.radcr.2024.11.029

Nishtha Manuja MBBS , Sandip Mohale MBBS, DNB Medicine , Shreya Khandelwal MBBS , Anshul Sood MBBS

{"title":"Macrodystrophia lipomatosa: Clinical and radiological insights into localized gigantism","authors":"Nishtha Manuja MBBS , Sandip Mohale MBBS, DNB Medicine , Shreya Khandelwal MBBS , Anshul Sood MBBS","doi":"10.1016/j.radcr.2024.11.029","DOIUrl":"10.1016/j.radcr.2024.11.029","url":null,"abstract":"<div><div>A rare type of localized gigantism known as macrodystrophia lipomatosa is characterized by a disproportionate increase in fibroadipose tissues and a gradual overgrowth of all mesenchymal elements. The distribution in the lower extremities’ plantar nerves and the upper extremity's median nerve is most commonly observed. This abnormality is congenital and typically manifests at birth or during the neonatal stage. This deformity begins to mechanically impair joint function, blood supply, and innervation as age advances. The findings from radiography include lucencies in the soft tissues and expansion of the digit's phalanges and soft tissue components, with predominantly distal component involvement. Herein, we present a case of a 20-year-old male from rural India who came to us with the complaint of abnormal asymmetrical swelling of bilateral hand fingers, which has been progressing since birth. Physical examination revealed a soft, non-fluctuant, non-pulsatile swelling with no associated trauma or injury. The clinical picture revealed disproportionate enlargement of phalanges in both hands.</div></div>","PeriodicalId":53472,"journal":{"name":"Radiology Case Reports","volume":"20 2","pages":"Pages 1280-1283"},"PeriodicalIF":0.0,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11666888/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142886281","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

Supracardiac type of total anomalous pulmonary venous connection: Diagnosis and demonstration by multidetector CT angiography 心上型全异常肺静脉连接：多探头CT血管造影的诊断和表现。

Radiology Case Reports Pub Date : 2025-02-01 DOI: 10.1016/j.radcr.2024.11.018

Neha Singh MD , Guriya Kumari MD , Deepak Kumar Singh MCh

引用次数: 0