Radiology Case Reports最新文献_第7页

Ovarian fibrothecoma in a 15-year-old girl: A rare case report 15岁女孩卵巢纤维鞘瘤：罕见病例报告

Radiology Case Reports Pub Date : 2025-05-05 DOI: 10.1016/j.radcr.2025.04.011

Abourak Chaimae , El Haddad Siham , Bouljrouf Jaoud , Kisra Mounir , Oukassem Siham , Guennouni Asmae , Bahha Soukaina , Belkouchi Lina , Allali Nazik , Chat Latifa

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Bilateral superior cerebellar artery pure arterial malformation masquerading as aneurysms 双侧小脑上动脉单纯动脉畸形伪装成动脉瘤

Radiology Case Reports Pub Date : 2025-05-05 DOI: 10.1016/j.radcr.2025.04.021

Hazem Shoirah MD , Rafique Haynes MD , Gesille Fiallo PA

引用次数: 0

Successful embolization of mesenteric hematoma following blunt trauma: A case report 钝性创伤后肠系膜血肿成功栓塞1例

Radiology Case Reports Pub Date : 2025-05-03 DOI: 10.1016/j.radcr.2025.04.015

Rika Yoshida , Hisatoshi Araki , Yuki Komatsubara , Yuka Ishikura , Mitsunari Maruyama , Shinji Ando , Megumi Nakamura , Takeshi Yoshizako , Akihiko Kidani , Yasushi Kaji

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Adrenal hydatid cyst communicating with a ruptured renal hydatid cyst in the excretory cavities: A rare clinical case 肾上腺包虫囊肿与破裂的肾包虫囊肿在排泄腔内相通：一例罕见的临床病例

Radiology Case Reports Pub Date : 2025-05-03 DOI: 10.1016/j.radcr.2025.03.088

Nadia El Mahi, Amal Mojahid, Siham Bhalil, Hamid Ziani, Siham Nasri, Imane Kamaoui, Imane Skiker

{"title":"Adrenal hydatid cyst communicating with a ruptured renal hydatid cyst in the excretory cavities: A rare clinical case","authors":"Nadia El Mahi, Amal Mojahid, Siham Bhalil, Hamid Ziani, Siham Nasri, Imane Kamaoui, Imane Skiker","doi":"10.1016/j.radcr.2025.03.088","DOIUrl":"10.1016/j.radcr.2025.03.088","url":null,"abstract":"<div><div>Simultaneous involvement of the kidney and adrenal gland by a hydatid cyst is an extremely rare condition. This pathology, caused by <em>Echinococcus granulosus</em>, can lead to severe complications, particularly when the cyst ruptures into the excretory cavities (renal pelvis and ureter). Cyst rupture allows the dissemination of parasitic elements into the urinary tract, resulting in symptoms such as low back pain and urinary disturbances. Diagnosis relies on a combination of imaging (ultrasound, CT scan) and serological tests. Treatment is primarily surgical, involving nephrectomy and adrenalectomy when the structures are severely affected, along with postoperative antiparasitic therapy to prevent recurrence. Although rare, this dual involvement of the kidney and adrenal gland presents a significant diagnostic and therapeutic challenge. We present a rare case of simultaneous involvement of the adrenal gland and kidney, complicated by rupture into the excretory cavities, in a 45-year-old man complaining of low back pain.</div></div>","PeriodicalId":53472,"journal":{"name":"Radiology Case Reports","volume":"20 7","pages":"Pages 3547-3549"},"PeriodicalIF":0.0,"publicationDate":"2025-05-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143902545","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

Diffuse glioma with FGFR3::TACC3 gene fusion and prominent calcification: A case report 弥漫性胶质瘤伴FGFR3::TACC3基因融合并显著钙化1例

Radiology Case Reports Pub Date : 2025-05-03 DOI: 10.1016/j.radcr.2025.04.034

Masaoki Kusunoki , Osamu Togao , Koji Yamashita , Kazufumi Kikuchi , Daisuke Kuga , Yutaka Fujioka , Shun Akamine , Kousei Ishigami

{"title":"Diffuse glioma with FGFR3::TACC3 gene fusion and prominent calcification: A case report","authors":"Masaoki Kusunoki , Osamu Togao , Koji Yamashita , Kazufumi Kikuchi , Daisuke Kuga , Yutaka Fujioka , Shun Akamine , Kousei Ishigami","doi":"10.1016/j.radcr.2025.04.034","DOIUrl":"10.1016/j.radcr.2025.04.034","url":null,"abstract":"<div><div>Diffuse gliomas with fibroblast growth factor receptor 3 (<em>FGFR3</em>) and transforming acidic coiled-coil containing protein 3 (<em>TACC3</em>) gene fusion represent a distinct molecular subtype of isocitrate dehydrogenase (IDH)-wildtype gliomas characterized by unique histopathological features. Although microcalcifications have frequently been reported in histopathological studies, their prevalence and diagnostic significance on radiological imaging remain unclear. We report a case of a 67-year-old woman who presented with a 1-year history of weakness in the left lower limb. Head CT revealed coarse and irregular calcifications in the deep white matter of the right frontal and parietal lobes. At the same time, MRI demonstrated a diffuse gliomatosis cerebri-like growth pattern with infiltration across the corpus callosum and contrast enhancement in distant areas. Histopathological examination confirmed glioblastoma, IDH-wildtype, and subsequent genetic testing revealed <em>FGFR3</em>::<em>TACC3</em> fusion and amplification of <em>FGFR3</em> gene. This case highlights the potential radiological characteristics of diffuse gliomas with <em>FGFR3</em>::<em>TACC3</em> fusion, particularly the presence of coarse calcifications, that may serve as notable imaging features of this tumor. Further research is required to determine whether calcification is a characteristic of this glioma subtype.</div></div>","PeriodicalId":53472,"journal":{"name":"Radiology Case Reports","volume":"20 7","pages":"Pages 3540-3546"},"PeriodicalIF":0.0,"publicationDate":"2025-05-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143902546","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

Early encrustation of a ureteric metallic stent managed by robotic assisted extraction and pyeloplasty 机器人辅助取出和肾盂成形术治疗输尿管金属支架早期结壳

Radiology Case Reports Pub Date : 2025-05-03 DOI: 10.1016/j.radcr.2025.04.017

Ahmed B. Altyeb , Ibrahim A. Khalil , Hosam Tawfik , Nushdan Okasha , Omar Abomarzouk , Abdullah Al Ansari

{"title":"Early encrustation of a ureteric metallic stent managed by robotic assisted extraction and pyeloplasty","authors":"Ahmed B. Altyeb , Ibrahim A. Khalil , Hosam Tawfik , Nushdan Okasha , Omar Abomarzouk , Abdullah Al Ansari","doi":"10.1016/j.radcr.2025.04.017","DOIUrl":"10.1016/j.radcr.2025.04.017","url":null,"abstract":"<div><div>Ureteral obstruction is a commonly encountered condition during daily practice. The mainstay of treatment for ureteral obstruction is drainage and relief of the obstruction, regardless of the etiology. Drainage using the traditional ureteral Double J stent has been recently challenged with new ureteric stent that proposed to have better durability and patient quality of life, particularly in cases that require prolonged insertion. One of these options are the ureteric metallic stents, such as Memokath, although uncommon, encrustation of Memkath can occur, leading to early removal. Here we present a case of 28-year-old gentleman with recurrent right pelviureteric junction obstruction, who had undergone pyeloplasty in childhood, The patient was hesitant to undergo redo pyeloplasty and opted for balloon dilatation with Memokath insertion. however early encrustation occurred leading to worsening of the condition and pain, and he was subsequently managed with robotic assisted laparoscopic Memokath extraction and dismembered pyeloplasty.</div></div>","PeriodicalId":53472,"journal":{"name":"Radiology Case Reports","volume":"20 7","pages":"Pages 3531-3535"},"PeriodicalIF":0.0,"publicationDate":"2025-05-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143898422","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

A journey with Maffucci syndrome: From skull base chondrosarcoma to multiorgan management: A case report and literature review 马夫奇综合征之旅：从颅底软骨肉瘤到多器官治疗：1例报告及文献复习

Radiology Case Reports Pub Date : 2025-05-02 DOI: 10.1016/j.radcr.2025.04.027

Jana Dibas , Aseel Eid , Somaya Al Kiswani , Zaid Sawaftah , Nader Sarhan , Abdullah Nofal , Omar Sawafta , Jehad Khamaysa

引用次数: 0

Pulmonary lymphangioleiomyomatosis (LAM) having no extra-pulmonary manifestations with chemical and mechanical pleurodesis: A case report and review of literature 无肺外表现的肺淋巴管平滑肌瘤病伴化学性和机械性胸膜萎缩1例报告及文献复习

Radiology Case Reports Pub Date : 2025-05-02 DOI: 10.1016/j.radcr.2025.02.103

Mustafa Shehzad MD , Beenish Sabir MBBS , Dawood Shehzad MD , Haris Mumtaz Malik MBBS , Anurag Jha MBBS , Muhammad Nabeel Saddique MBBS , Javed Iqbal RN, Ph.D

{"title":"Pulmonary lymphangioleiomyomatosis (LAM) having no extra-pulmonary manifestations with chemical and mechanical pleurodesis: A case report and review of literature","authors":"Mustafa Shehzad MD , Beenish Sabir MBBS , Dawood Shehzad MD , Haris Mumtaz Malik MBBS , Anurag Jha MBBS , Muhammad Nabeel Saddique MBBS , Javed Iqbal RN, Ph.D","doi":"10.1016/j.radcr.2025.02.103","DOIUrl":"10.1016/j.radcr.2025.02.103","url":null,"abstract":"<div><div>Lymphangioleiomyomatosis (LAM) is a rare, progressive lung disease characterized by abnormal smooth muscle proliferation, leading to cystic destruction of the lung parenchyma. We present the case of a female in her early 40s who presented with intermittent chest pain for 1 month. Imaging revealed left hydropneumothorax with multiple bilateral pulmonary parenchymal cysts, and a subsequent lung biopsy confirmed the diagnosis of pulmonary LAM. The patient underwent video-assisted thoracoscopic surgery (VATS) with mechanical and chemical pleurodesis. Given her stable condition, no immediate sirolimus therapy was initiated, and close follow-up with serial imaging was planned. This case highlights the diagnostic challenges of LAM, especially with low VEGF-D levels, and underscores the role of pleurodesis as a management option in select patients. Early recognition and tailored management are essential to optimize patient outcomes.</div></div>","PeriodicalId":53472,"journal":{"name":"Radiology Case Reports","volume":"20 7","pages":"Pages 3510-3514"},"PeriodicalIF":0.0,"publicationDate":"2025-05-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143898421","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

A typical case of ovarian fibrothecoma in a paucisymptomatic postmenopausal woman 无症状绝经后妇女卵巢纤维鞘瘤的典型病例

Radiology Case Reports Pub Date : 2025-05-02 DOI: 10.1016/j.radcr.2025.03.086

Eric Michel Charlemagne Kessi Junior , Kaoutar Maslouhi , Gray Delors Tsioukaka , Papys Mendes , Lina Belkouchi , Nazik Allali , Latifa Chat , Siham El Haddad

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Syphilis and HIV co-infection presenting with a pituitary abscess: A rare case presentation 梅毒和HIV合并感染表现为垂体脓肿：罕见病例

Radiology Case Reports Pub Date : 2025-05-02 DOI: 10.1016/j.radcr.2025.04.026

Mark A. Colantonio MD, Katherine Shepherd MD, Brooke Shannon DO

引用次数: 0