Radiology Case Reports最新文献_第2页

Multiloculated cystic pelvic mass in a post-menopausal woman: A case of ovarian hydatid cyst mimicking malignancy 绝经后妇女多房囊性盆腔肿块：一例卵巢包虫囊肿模拟恶性肿瘤

Radiology Case Reports Pub Date : 2025-10-04 DOI: 10.1016/j.radcr.2025.09.027

Anamika Jha MD , Abhikanta Khatiwada MD , Sharada Kc MD , Shivali Rao MD

引用次数: 0

A rare ovarian tumor in childhood: Juvenile granulosa cell tumor revealed by pelvic pain and ovarian torsion 一例罕见的儿童期卵巢肿瘤：以骨盆疼痛和卵巢扭转为表现的幼年颗粒细胞瘤

Radiology Case Reports Pub Date : 2025-10-04 DOI: 10.1016/j.radcr.2025.08.014

Karim Haddar MD, Hicham Benramdane MD, Leila Haddar MD, Hamid Ziani MD, Siham Nasri MD, PhD, Imane Kamaoui MD, PhD, Imane Skiker MD, PhD

{"title":"A rare ovarian tumor in childhood: Juvenile granulosa cell tumor revealed by pelvic pain and ovarian torsion","authors":"Karim Haddar MD, Hicham Benramdane MD, Leila Haddar MD, Hamid Ziani MD, Siham Nasri MD, PhD, Imane Kamaoui MD, PhD, Imane Skiker MD, PhD","doi":"10.1016/j.radcr.2025.08.014","DOIUrl":"10.1016/j.radcr.2025.08.014","url":null,"abstract":"<div><div>We report the case of a 5-year-old girl admitted with a one-month history of pelvic heaviness and acute pelvic pain. Imaging revealed a large heterogeneous pelvic mass involving the genital compartment, with features suggestive of a malignant ovarian tumor. MRI demonstrated a 41 × 57 × 48 mm solid mass with heterogeneous enhancement, restricted diffusion, and areas of necrosis, infiltrating the recto-sigmoid junction. Tumor markers including AFP and beta-hCG were negative, while LDH was mildly elevated. Surgical exploration revealed an encapsulated left ovarian mass with 2 twists of the adnexa, prompting detorsion and partial oophorectomy. Histopathology confirmed a juvenile granulosa cell tumor. Postoperative recovery was uneventful. This case highlights the importance of considering JGCT in the differential diagnosis of ovarian masses in prepubertal girls, the value of advanced imaging for characterization and surgical planning, and the excellent prognosis associated with early surgical management.</div></div>","PeriodicalId":53472,"journal":{"name":"Radiology Case Reports","volume":"21 1","pages":"Pages 49-53"},"PeriodicalIF":0.0,"publicationDate":"2025-10-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145223564","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

Endovascular treatment of a deltoid arteriovenous fistula using a combined approach of endovascular intervention and percutaneous embolization 血管内介入联合经皮栓塞治疗三角肌动静脉瘘

Radiology Case Reports Pub Date : 2025-10-04 DOI: 10.1016/j.radcr.2025.09.020

Le Thanh Dung , Vu Tien The , Truong Ngoc Son , Vu Van Tuyen , Nguyen Ngoc Son , Le Dinh Minh , Tran Van Ngoc , Le Tuan Vu , To Tuan Linh , Tran Quang Loc MD

引用次数: 0

Imaging-guided diagnosis and treatment of severe deep thigh infection: Key considerations for limb-salvage over disarticulation 影像引导下的严重大腿深部感染的诊断和治疗：残肢而非断关节的关键考虑因素

Radiology Case Reports Pub Date : 2025-10-04 DOI: 10.1016/j.radcr.2025.09.011

Amine El Farhaoui MD , Ouissal Lekehal MD , Yassine Batou MD , Najib abdeljaouad MD , Hicham Yacoubi MD

引用次数: 0

Two congenital intestinal bands, a rare cause of intestinal obstruction in a young adult, a case report 两个先天性肠带，一种罕见的原因肠梗阻在一个年轻的成年人，一个病例报告

Radiology Case Reports Pub Date : 2025-09-30 DOI: 10.1016/j.radcr.2025.08.096

Suleyman Fantahun Endris MD , Bereket Girum Beyene MD , Desalegn Fekadu Wadaja MD , Michael Teklehaimanot Abera MD

引用次数: 0

Management of a huge ovarian cyst in a first trimester pregnant woman: A case report 孕早期妇女巨大卵巢囊肿的处理：1例报告

Radiology Case Reports Pub Date : 2025-09-30 DOI: 10.1016/j.radcr.2025.09.015

Ibrahim Salum MD , Idd J. Kenedy MD , Michael J. Ephraem MD , Ashley Rafael MD , Glory Mangi MD , Eusebius Maro MD , Godwin Mselle MD , Stephen Gondwe MD , Alex Mremi MD

{"title":"Management of a huge ovarian cyst in a first trimester pregnant woman: A case report","authors":"Ibrahim Salum MD , Idd J. Kenedy MD , Michael J. Ephraem MD , Ashley Rafael MD , Glory Mangi MD , Eusebius Maro MD , Godwin Mselle MD , Stephen Gondwe MD , Alex Mremi MD","doi":"10.1016/j.radcr.2025.09.015","DOIUrl":"10.1016/j.radcr.2025.09.015","url":null,"abstract":"<div><div>Massively huge ovarian cysts during pregnancy are relatively uncommon, and the occurrence of a large ovarian cyst in the first trimester presents diagnostic and therapeutic challenges. Herein, we report a rare case of a huge ovarian cyst identified during the first trimester of pregnancy in a 26-year-old primigravida at 13 weeks of gestation who presented to the antenatal clinic with complaints of abdominal bloating and intermittent lower abdominal pain. Obstetric history was unremarkable. On examination, abdominal distension was noted. A transabdominal ultrasound revealed a large unilocular cystic mass measuring approximately 27 cm × 14 cm, separate from the gestational sac, suggestive of an ovarian origin. The fetus appeared viable with appropriate growth for gestational age. An MRI confirmed a large right ovarian cyst with no solid components or papillary projections, consistent with a benign etiology. Due to increasing abdominal discomfort and risk of torsion, the patient was planned for surgical management. Laparotomy was performed at 13 weeks gestation under general anesthesia. The huge right ovarian cyst was excised. The contralateral ovary was preserved. Histopathological examination confirmed a diagnosis of benign follicular cyst. Postoperative recovery was uneventful. The pregnancy progressed normally. This case highlights the importance of early detection, careful monitoring, and individualized management of large adnexal masses during pregnancy.</div></div>","PeriodicalId":53472,"journal":{"name":"Radiology Case Reports","volume":"20 12","pages":"Pages 6294-6298"},"PeriodicalIF":0.0,"publicationDate":"2025-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145221058","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

Unilateral absent pulmonary artery (UAPA) with patent ductus arteriosus (PDA) in a young woman with repeated respiratory infection: A case report 年轻女性反复呼吸道感染单侧肺动脉缺失伴动脉导管未闭1例

Radiology Case Reports Pub Date : 2025-09-30 DOI: 10.1016/j.radcr.2025.08.095

Abdi Alemayehu Dhuguma MD, Suleyman Fantahun MD, Eyerusalem Getachew MD, Fami Zekeriya MD, Demisu Alemu MPH

{"title":"Unilateral absent pulmonary artery (UAPA) with patent ductus arteriosus (PDA) in a young woman with repeated respiratory infection: A case report","authors":"Abdi Alemayehu Dhuguma MD, Suleyman Fantahun MD, Eyerusalem Getachew MD, Fami Zekeriya MD, Demisu Alemu MPH","doi":"10.1016/j.radcr.2025.08.095","DOIUrl":"10.1016/j.radcr.2025.08.095","url":null,"abstract":"<div><div>Unilateral absent pulmonary artery (UAPA) first introduced in literatures by Oscar Fraentzel in 1898 is a rare vascular anomaly where the main pulmonary artery, rather than bifurcating, gives a solitary pulmonary artery branch to one of the lungs. The other lung, on the affected side, gets blood supply through collateral circulations, frequently through enlarged bronchial arteries. It is seen in 1 in 200,000 live births. It occurs due to the involution of the proximal sixth aortic arch on one side resulting in a unilateral absent pulmonary artery. The diagnosis can be made using contrast-enhanced CT and MRI images. Cases of UAPA can be seen in infants presenting with congestive cardiac failure and pulmonary arterial hypertension (PAH). Undiagnosed cases can result in repeated respiratory infections, complicating with bronchiectasis, pulmonary hypertension, and fibrosis gradually reducing the patient’s quality of life. In adults, the diagnosis is sometimes made with cross-sectional studies when investigating causes of repeated respiratory infection or hemoptysis. We report a case of right-side UAPA with patent ductus arteriosus (PDA) and early signs of PAH in a 24-year-old female patient with a previous history of repeated respiratory infection uncovered during contrast-enhanced chest CT imaging.</div></div>","PeriodicalId":53472,"journal":{"name":"Radiology Case Reports","volume":"20 12","pages":"Pages 6285-6289"},"PeriodicalIF":0.0,"publicationDate":"2025-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145221055","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

Unmasking an idiopathic reno-caval fistula: A rare etiology of right-sided high-output heart failure 揭露特发性肾腔瘘管：右侧高输出量心力衰竭的罕见病因

Radiology Case Reports Pub Date : 2025-09-30 DOI: 10.1016/j.radcr.2025.09.017

Wissarut Sakulpaptong MD , Choutchung Tinakorn Na Ayudhya MD , Luxica Jarutasnangkul MD , Sittinop Titichoatrattana MD , Suphot Srimahachota MD , Pairoj Chattranukulchai MD

{"title":"Unmasking an idiopathic reno-caval fistula: A rare etiology of right-sided high-output heart failure","authors":"Wissarut Sakulpaptong MD , Choutchung Tinakorn Na Ayudhya MD , Luxica Jarutasnangkul MD , Sittinop Titichoatrattana MD , Suphot Srimahachota MD , Pairoj Chattranukulchai MD","doi":"10.1016/j.radcr.2025.09.017","DOIUrl":"10.1016/j.radcr.2025.09.017","url":null,"abstract":"<div><div>An aortocaval fistula is a rare vascular connection between the aorta and inferior vena cava, often caused by abdominal aortic aneurysm, trauma, or infection. It can result in high-output heart failure due to increased venous return and reduced systemic vascular resistance, typically presenting with right-sided symptoms. Renal arteriovenous and reno-caval fistulas are even rarer, with no prior reports of spontaneous idiopathic reno-caval fistulas. A 67-year-old man with hypertension and paroxysmal atrial fibrillation presented with 10 months of generalized edema and exertional dyspnea. He had no history of abdominal trauma or surgery. Examination revealed signs of congestive heart failure and a central abdominal bruit. Echocardiography showed chamber dilation and pulmonary hypertension. Computed tomographic angiography identified a right reno-caval fistula between the right renal artery and inferior vena cava, with associated right renal infarction. The patient underwent successful endovascular embolization using a vascular plug, with gradual resolution of symptoms and improved echocardiographic findings. In cases of high-output heart failure with right-sided symptoms, arteriovenous fistula should be considered, as specific interventions can be highly effective. This rare case underscores the value of a multimodal diagnostic approach combining clinical evaluation and imaging to ensure accurate diagnosis and successful treatment.</div></div>","PeriodicalId":53472,"journal":{"name":"Radiology Case Reports","volume":"20 12","pages":"Pages 6299-6304"},"PeriodicalIF":0.0,"publicationDate":"2025-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145221054","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

Solid pseudopapillary epithelial neoplasm of the pancreatic head: A case report of an atypical site for a rare tumor 胰头实性假乳头状上皮肿瘤：罕见肿瘤非典型部位1例报告

Radiology Case Reports Pub Date : 2025-09-29 DOI: 10.1016/j.radcr.2025.08.091

Samiksha Lamichhane MD , Suraj KC MS , Shritik Devkota MD , Bed Prakash Sah MS , Suresh Prasad Sah MS

引用次数: 0

Sigmoid sinus dural arteriovenous fistula presenting with pulsatile tinnitus in the postpartum period: A case report 乙状窦硬脑膜动静脉瘘表现为产后搏动性耳鸣1例

Radiology Case Reports Pub Date : 2025-09-29 DOI: 10.1016/j.radcr.2025.08.052

Yoshinobu Kamio MD, PhD, Hiroaki Neki MD, PhD, Tomohiro Yamasaki MD, PhD, Tomoya Oishi MD, PhD, Yudai Yamashiro MD, Shinnosuke Fukami MD, Sayaka Ito MD, Kazuhiko Kurozumi MD, PhD

{"title":"Sigmoid sinus dural arteriovenous fistula presenting with pulsatile tinnitus in the postpartum period: A case report","authors":"Yoshinobu Kamio MD, PhD, Hiroaki Neki MD, PhD, Tomohiro Yamasaki MD, PhD, Tomoya Oishi MD, PhD, Yudai Yamashiro MD, Shinnosuke Fukami MD, Sayaka Ito MD, Kazuhiko Kurozumi MD, PhD","doi":"10.1016/j.radcr.2025.08.052","DOIUrl":"10.1016/j.radcr.2025.08.052","url":null,"abstract":"<div><div>Pregnancy and the postpartum period are acknowledged as potential risk factors for cerebrovascular disease. Nonetheless, dural arteriovenous fistulas (DAVFs) identified during the postpartum period have been infrequently documented. A 31-year-old woman with no prior medical history experienced sudden-onset pulsatile tinnitus in the left ear immediately following childbirth. Time-of-flight magnetic resonance angiography revealed a high-signal intensity lesion surrounding the left sigmoid sinus. Subsequent cerebral angiography demonstrated a left-sided sigmoid sinus dural arteriovenous fistula draining into the left sigmoid sinus, with antegrade venous flow and retrograde reflux into the contralateral transverse sinus, but without cortical venous reflux. Transarterial embolization was successfully performed, resulting in complete resolution of the tinnitus. We propose that hormonal fluctuations and hemodynamic changes, including elevated venous pressure associated with pregnancy and the postpartum period, may contribute to the development of DAVFs.</div></div>","PeriodicalId":53472,"journal":{"name":"Radiology Case Reports","volume":"20 12","pages":"Pages 6257-6261"},"PeriodicalIF":0.0,"publicationDate":"2025-09-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145221015","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