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New daily persistent headache with May-Thurner physiology and spinal epidural venous congestion: treatment with ascending lumbar vein embolization. 新的每日持续性头痛与梅-瑟纳生理和脊髓硬膜外静脉充血:治疗上升腰静脉栓塞。
IF 0.5 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2025-09-09 eCollection Date: 2025-09-01 DOI: 10.1093/bjrcr/uaaf045
Samuel B Ogunlade, Todd D Rozen, Andrew R Lewis, Beau B Toskich, Zlatko Devcic

May-Thurner physiology (MTP) can lead to various congestion syndromes due to compression of the left common iliac vein (LCIV) by the right common iliac artery (RCIA). This compression may result in venous reflux through the lumbar vein, leading to congestion of the spinal epidural venous plexus (EVP), which could contribute to refractory headaches. This case report details the clinical course of a patient with severe refractory new daily persistent headache associated with MTP who underwent ascending lumbar vein (ALV) embolization. The patient is a 59-year-old female with a 3-year history of daily persistent headache which failed multiple migraine prevention therapies and minimally invasive procedures. Imaging studies revealed significant LCIV compression by the RCIA, retrograde ALV flow, and EVP congestion. The patient underwent ALV embolization, resulting in significant symptomatic relief. At the 22-month follow-up, headache severity reduced by 80%, with the patient no longer requiring routine headache medications. Additionally, treatment of associated pelvic congestion syndrome through gonadal vein embolization resolved longstanding associated pelvic pain and pressure. This case highlights the role of venous congestion in refractory headache syndromes and underscores the potential of targeted venous interventions, such as embolization, in their management. The findings expand on emerging evidence linking venous compression syndromes to headache pathophysiology and support exploring interventional strategies as viable treatment options for selected patients. Further research is needed to validate these findings and establish evidence-based guidelines for clinical practice.

May-Thurner生理(MTP)可导致各种充血综合征,由于右髂总动脉(RCIA)压迫左髂总静脉(LCIV)。这种压迫可能导致通过腰静脉的静脉回流,导致脊髓硬膜外静脉丛(EVP)充血,这可能导致顽固性头痛。本病例报告详细介绍了一例伴有MTP的严重难治性新发持续性头痛患者的临床过程,该患者接受了腰升静脉(ALV)栓塞术。患者为59岁女性,每日持续性头痛3年,多次偏头痛预防治疗和微创手术均无效。影像学研究显示RCIA对LCIV有明显压迫,ALV血流逆行,EVP充血。患者接受了ALV栓塞治疗,症状明显缓解。在22个月的随访中,头痛严重程度降低了80%,患者不再需要常规的头痛药物。此外,通过性腺静脉栓塞治疗相关盆腔充血综合征解决了长期相关的盆腔疼痛和压力。本病例强调了静脉充血在难治性头痛综合征中的作用,并强调了靶向静脉干预的潜力,如栓塞,在其管理中。研究结果扩展了将静脉压迫综合征与头痛病理生理联系起来的新证据,并支持探索干预策略作为选定患者的可行治疗选择。需要进一步的研究来验证这些发现,并为临床实践建立循证指南。
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引用次数: 0
Secondary aneurysmal bone cyst arising from polyostotic craniofacial fibrous dysplasia. 颅面纤维发育不良引起的继发性动脉瘤性骨囊肿。
IF 0.5 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2025-09-09 eCollection Date: 2025-09-01 DOI: 10.1093/bjrcr/uaaf047
Niket Patel, Kiran Kumar Sailagundla, Essaki Rajulu, Shanmuga Jayanthan, Ganesh Rajagopal, Harpreet Singh Grewal

Fibrous dysplasia (FD) is a benign condition affecting osteoblasts, which fail to undergo proper differentiation and maturation, resulting in the replacement of normal osteoid matrix with ground glass fibrous tissue. Aneurysmal bone cyst (ABC) is a benign, expansile, lytic lesion characterized by multiple blood-filled cystic cavities containing haemorrhagic products at varying stages. Secondary ABC arising from craniofacial FD is extremely rare. To date, only 10 cases have been reported in the literature. This report highlights the clinical presentation, imaging findings, and histopathological confirmation of a secondary ABC in a patient with polyostotic craniofacial FD.

纤维发育不良(FD)是一种影响成骨细胞的良性疾病,成骨细胞不能进行适当的分化和成熟,导致正常的类骨基质被磨砂玻璃纤维组织所取代。动脉瘤性骨囊肿(ABC)是一种良性、扩张、溶解性病变,其特征是多个充血的囊腔,在不同阶段含有出血产物。由颅面FD引起的继发性ABC极为罕见。迄今为止,文献中仅报告了10例病例。本报告强调了一例颅面多骨裂FD患者继发性ABC的临床表现、影像学表现和组织病理学证实。
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引用次数: 0
Spot the new lesion: a case report of intra-MRI cerebral haemorrhage with discussion of previous literature. 发现新病灶:mri内脑出血1例并结合文献讨论。
IF 0.5 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2025-09-09 eCollection Date: 2025-09-01 DOI: 10.1093/bjrcr/uaaf046
Ali Mokhtari, Valeria Onofrj, Carine Neugroschl

The appearance of intracranial haemorrhage on magnetic resonance imaging (MRI) is complex and depends on its evolution over time. The ability of the MRI to detect hyperacute haemorrhage has been debated as it seems to depend on several factors (ie, delay of imaging, MRI field strength, imaging technique). We present the first case of intracranial haemorrhage occurring during MRI acquisition in a 61-year-old female suffering a severe hypoxic-ischaemic encephalopathy from a suicide attempt by hanging. The imaging characteristics of the haematoma differ from what has been described in the past, as it lacks the typical peripheral T2 and T2* hypointensity usually seen in hyperacute haematomas. We discuss previous literature in order to explain these peculiar imaging features.

颅内出血在磁共振成像(MRI)上的表现是复杂的,取决于其随时间的演变。MRI检测超急性出血的能力一直存在争议,因为它似乎取决于几个因素(即成像延迟,MRI场强,成像技术)。我们提出的第一例颅内出血发生在MRI采集期间,在一个61岁的女性患有严重缺氧缺血性脑病从自杀企图上吊。血肿的影像学特征不同于以往的描述,因为它缺乏典型的周围T2和T2*低密度,通常见于超急性血肿。我们讨论以前的文献,以解释这些特殊的成像特征。
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引用次数: 0
Idiopathic isolated bilaterally symmetrical brachymetacarpia of the fifth metacarpal in a woman with rheumatoid arthritis. 特发性孤立的双侧对称的第五掌骨短促与类风湿性关节炎的妇女。
IF 0.5 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2025-08-22 eCollection Date: 2026-01-01 DOI: 10.1093/bjrcr/uaaf043
Mohamed Tazi, Fatima Zahrae Taik, Youssef El Hassnaoui, Anass Adnine, Nihad Takrifa, Fatima Ezzahra Abourazzak

We report a rare case of idiopathic, isolated, and bilaterally symmetrical brachymetacarpia of the fifth metacarpal bones in a 60-year-old woman followed for seropositive rheumatoid arthritis. Despite the radiographic anomaly, the patient remained asymptomatic and had normal hand function. Extensive investigations ruled out syndromic or metabolic causes. This case emphasizes the importance of recognizing rare skeletal variants in rheumatologic evaluations.

我们报告一例罕见的特发性,孤立的,双侧对称的第5掌骨近端掌骨在60岁的妇女血清阳性类风湿关节炎跟随。尽管有影像学异常,患者仍无症状,手功能正常。广泛的调查排除了综合征或代谢原因。这个病例强调了在风湿病评估中识别罕见骨骼变异的重要性。
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引用次数: 0
An unusual renal colic during trans-arterial embolization after trauma and its multidisciplinary management. 创伤后经动脉栓塞术中不寻常的肾绞痛及其多学科处理。
IF 0.5 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2025-07-31 eCollection Date: 2025-07-01 DOI: 10.1093/bjrcr/uaaf039
Pierpaolo Biondetti, Anna Maria Ierardi, Elisa De Lorenzis, Jacopo Tintori, Emanuele Montanari, Gianpaolo Carrafiello

Selective embolization is the treatment of choice for traumatic renal pseudoaneurysm (PSA) in stable patients. N-Butyl-2-cyanoacrilate (NBCA) is an embolic agent frequently used to embolize peripheral lesions. N-Butyl-2-cyanoacrilate is one of the most widely used embolic materials because it is easy to prepare, it acts quickly and is highly cost-effective. Its use, however, requires a learning curve before becoming confident and being able to handle it safely. We describe a case of embolization of a renal traumatic PSA without clear pre-procedural CT-evidence of artero-calyx fistula in which the migration of NBCA in the renal pelvis occurred during the procedure. We report the successful multidisciplinary management of this complication.

选择性栓塞是稳定患者外伤性肾假性动脉瘤(PSA)的首选治疗方法。n -丁基-2-氰基丙烯酸酯(NBCA)是一种常用的栓塞剂,用于栓塞周围病变。正丁基-2-氰基丙烯酸酯是应用最广泛的栓子材料之一,因为它易于制备,作用迅速,成本效益高。然而,在变得自信并能够安全地使用它之前,它的使用需要一个学习曲线。我们描述了一个病例的肾创伤性PSA栓塞没有明确的术前ct证据动脉-盏瘘,其中NBCA在肾盂的迁移发生在手术过程中。我们报告成功的多学科管理的并发症。
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引用次数: 0
Aneurysmal bone cyst of the talus: a case report of local recurrence treated with adjuvant therapy. 距骨动脉瘤性骨囊肿:辅助治疗局部复发1例。
IF 0.5 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2025-07-28 eCollection Date: 2025-09-01 DOI: 10.1093/bjrcr/uaaf041
Yasutaka Takagi, Hiroshi Yamada, Hidehumi Ebara, Hiroyuki Hayashi, Hiroyuki Inatani, Yuta Nakamura, Koichiro Ae, Aki Nakanami, Tetsutaro Yahata, Hiroyuki Tsuchiya

Aneurysmal bone cyst (ABC) is a locally destructive benign tumour-like condition of the bones with blood-filled cystic cavities. The talus is an extremely rare site for an ABC, with <20 reported cases till 2012 based on a PubMed database search. Aneurysmal bone cyst recurrence in the talus after curettage and bone grafting is extremely rare. To the best of our knowledge, no detailed reports of resection and adjuvant therapy with artificial bone packing of recurrent ABC of the talus have been published. We report a case of ABC in the talus of a 9-year-old boy. As the initial surgery consisted of only lesion resection and artificial bone (beta-tricalcium phosphate [TCP]) packing, local recurrence was diagnosed. Reoperation was performed 5 months after the initial surgery. The recurrent lesion was resected using a curette, and the bone cavity septum was shaved with a high-speed burr. Phenol-ethanol ablation was used as an adjuvant with artificial bone (beta-TCP) packing to prevent recurrence. No local recurrence was observed 36 months after the reoperation. This extremely rare case of resection and adjuvant therapy with artificial bone packing of recurrent ABC of the talus highlights the need for careful observation to assess the progression of ankle joint osteoarthrosis.

动脉瘤性骨囊肿(ABC)是一种局部破坏性的良性肿瘤样骨骼疾病,伴有充满血液的囊性腔。距骨是ABC极为罕见的部位
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引用次数: 0
Heterotopic pregnancy: a case report about triplets. 异位妊娠:三胞胎一例报告。
IF 0.5 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2025-07-28 eCollection Date: 2025-09-01 DOI: 10.1093/bjrcr/uaaf040
Sara Cherkaoui, Lina Belkouchi, Badra Idrissi, Siham El Haddad, Nazik Allali, Latifa Chat

Heterotopic pregnancy refers to the concomitant presence of an intrauterine pregnancy and an ectopic pregnancy (EP). It is rare and more frequently found in women who have undergone medically assisted procreation. An abdominal location of the ectopic gestational sac is even less common, accounting for 1.4% of all ectopic pregnancies, conferring a high risk of morbidity and mortality. Diagnosis can sometimes be difficult, and pelvic ultrasound alone may not be sufficient. Additional pelvic MRI may be useful to confirm the diagnosis with certainty. Heterotopic pregnancy requires urgent management and is mainly treated surgically, although there are certain situations where medical treatment may be indicated. We report the case of a 29-year-old patient admitted with pelvic pain and mild metrorrhagia, with an elevated beta-hCG level suggesting the diagnosis of an EP, which was confirmed by ultrasound and MRI, revealing the presence of 3 foetuses: 1 was developing in the abdominal cavity while the other 2 were normally present in the uterine cavity.

异位妊娠是指同时存在宫内妊娠和异位妊娠(EP)。这是罕见的,在接受医疗辅助生育的妇女中更常见。异位妊娠囊位于腹部更不常见,占所有异位妊娠的1.4%,具有很高的发病率和死亡率。诊断有时是困难的,单独的盆腔超声可能是不够的。额外的骨盆MRI可能有助于确定诊断。异位妊娠需要紧急处理,主要是手术治疗,尽管在某些情况下可能需要药物治疗。我们报告一例29岁的患者,因盆腔疼痛和轻微的子宫出血而入院,经超声和MRI证实,β - hcg水平升高提示EP的诊断,显示有3个胎儿:1个在腹腔内发育,另外2个在子宫内正常存在。
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引用次数: 0
CT imaging of third inflow cases: a hidden cause of surgical complications and liver pseudolesions. 第三次流入病例的CT表现:手术并发症及肝脏假性脓肿的隐藏原因。
IF 0.5 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2025-07-26 eCollection Date: 2025-07-01 DOI: 10.1093/bjrcr/uaaf042
Gizem Cural Kula, Afak Durur Karakaya

Third inflow refers to the additional blood supply to the liver from a third source, apart from its dual blood supply. Aberrant right and left gastric veins, Sappey and Barlow veins, and the parabiliary venous system are considered the most significant examples of third inflow. Clinically, the third inflow is important due to its association with hepatic pseudolesions and its role in increasing surgical complication risks in hepatobiliary and gastric procedures. Our case series includes 8 cases of aberrant left gastric vein (ALGV) and 1 case of a Sappey vein. In addition to presenting examples of ALGV and Suppey vein, we also highlight ischemic complications of the liver observed in a liver transplant donor and a gastric cancer case. Our aim is to emphasize ALGV-related surgical risks and the importance of assessing vascular variations in preoperative imaging.

第三流是指肝脏在双重血供之外,从第三个来源增加的血供。异常的左右胃静脉、Sappey静脉和Barlow静脉以及旁静脉系统被认为是第三流最重要的例子。临床上,第三流很重要,因为它与肝脏假性脓肿有关,并在肝胆和胃手术中增加手术并发症的风险。我们的病例系列包括8例异常胃左静脉(ALGV)和1例Sappey静脉。除了介绍ALGV和供应静脉的例子外,我们还重点介绍了在肝移植供体和胃癌病例中观察到的肝脏缺血性并发症。我们的目的是强调与algv相关的手术风险和术前影像学评估血管变异的重要性。
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引用次数: 0
Atypical manifestations of Dengue fever: case series in tertiary care hospital in Nepal. 登革热的非典型表现:尼泊尔三级保健医院的病例系列。
IF 0.5 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2025-07-18 eCollection Date: 2025-07-01 DOI: 10.1093/bjrcr/uaaf038
Sudeep Kc, Himani Poudyal

Dengue fever is common in Southeast Asia, including Nepal, caused by the Flavi virus transmitted through mosquito bites of Aedes aegypti species. Symptoms include high-grade fever, skin rash, headache and arthralgia, with a low case fatality rate of less than 1%. Severe forms are characterized by low platelet count, vascular leakage, and low blood pressure, often leading to life-threatening complications. Common imaging findings include gall bladder wall thickening, hepatosplenomegaly, ascites, pericardial effusion, and pleural effusion. Dengue was initially considered non-neurotropic, but recent studies suggest that the virus can invade the central nervous system, indicating its neurotropic potential presenting with encephalitis and meningitis. In this case series, we have described atypical imaging findings of 7 patients in patients with laboratory confirmed dengue fever, which revealed imaging features of psoas hematoma in 1 case, diffuse pulmonary haemorrhage in 1 case, multifocal pneumonia in 1 case, hemorrhagic stroke with venous thrombosis in 1 case, dengue meningoencephalitis in 2 cases and dengue encephalitis with Cytotoxic lesion of the corpus callosum in 1 case. This case series emphasizes the important role of imaging findings in severe dengue patients with suspicion of unusual complications as early detection and prompt treatment are crucial for recovery and to prevent fatal complications.

登革热在包括尼泊尔在内的东南亚很常见,是由通过埃及伊蚊叮咬传播的黄病毒引起的。症状包括高热、皮疹、头痛和关节痛,病死率低于1%。严重的形式以血小板计数低、血管渗漏和低血压为特征,常常导致危及生命的并发症。常见的影像学表现包括胆囊壁增厚、肝脾肿大、腹水、心包积液和胸腔积液。登革热最初被认为是非嗜神经性的,但最近的研究表明,该病毒可侵入中枢神经系统,表明其嗜神经性的潜在表现为脑炎和脑膜炎。在本病例系列中,我们描述了7例实验室确诊的登革热患者的非典型影像学表现,其影像学表现为腰大肌血肿1例,弥漫性肺出血1例,多灶性肺炎1例,出血性卒中伴静脉血栓形成1例,登革脑膜脑炎2例,登革脑炎伴胼胝体细胞毒性病变1例。这一系列病例强调了在怀疑有异常并发症的重症登革热患者中影像学检查的重要作用,因为早期发现和及时治疗对于康复和预防致命并发症至关重要。
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引用次数: 0
Bronchial artery embolization for haemoptysis in patients with lymphoma and leukaemia. 支气管动脉栓塞治疗淋巴瘤、白血病患者咯血。
IF 0.5 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2025-07-17 eCollection Date: 2025-07-01 DOI: 10.1093/bjrcr/uaaf036
Ruben Geevarghese, Elena N Petre, Etay Ziv, Ernesto Santos, Lee Rodriguez, Vlasios S Sotirchos, Ken Zhao, Stephen B Solomon, Erica S Alexander

Haemoptysis in patients with lymphoma and leukaemia can present a therapeutic challenge, given that it is often associated with underlying impairments of haemostasis and immunosuppression. Bronchial artery embolization (BAE) is a mainstay in the treatment of haemoptysis, typically in those requiring emergent management. In this case series, the role of BAE in patients with lymphoma and leukaemia was evaluated. A total of 5 patients were identified between August 2010 and August 2022. Three patients were diagnosed with lymphoma (classical Hodgkin's lymphoma, diffuse large B-cell lymphoma and extra-nodal marginal zone lymphoma) and 2 patients were diagnosed with leukaemia (1 patient with acute myeloid leukaemia and the other with chronic lymphocytic leukaemia). All patients were thrombocytopenic [77.6 ± 28.5 × 109/L (mean ± SD)], at presentation. Three patients had concurrent lung infection at the time of their presentation. Technical success was achieved in 4/5 patients (80%). Clinical success was obtained in 4/5 patients (80%). Recurrence following embolization was seen in 2 patients. Three patients died within 30 days following embolization (from deteriorating respiratory function). Bronchial artery embolization for haemoptysis in patients with lymphoma and leukaemia is safe and feasible. Concurrent lung infection is potentially of significance with regard to initial presentation and overall outcomes following embolization. In select patients, BAE may provide a therapeutic option, though further investigation is required.

淋巴瘤和白血病患者的咯血可能是一个治疗挑战,因为它通常与止血和免疫抑制的潜在损害有关。支气管动脉栓塞(BAE)是治疗咯血的主要方法,特别是在那些需要紧急处理的患者中。在这个病例系列中,BAE在淋巴瘤和白血病患者中的作用被评估。2010年8月至2022年8月共发现5例患者。3例患者诊断为淋巴瘤(经典霍奇金淋巴瘤、弥漫性大b细胞淋巴瘤和结外边缘区淋巴瘤),2例患者诊断为白血病(1例为急性髓性白血病,1例为慢性淋巴细胞白血病)。所有患者就诊时血小板减少[77.6±28.5 × 109/L(平均±SD)]。3例患者在发病时并发肺部感染。4/5(80%)患者技术成功。4/5(80%)患者临床成功。栓塞后复发2例。3例患者栓塞后30天内死亡(呼吸功能恶化)。支气管动脉栓塞治疗淋巴瘤和白血病患者咯血是安全可行的。并发肺部感染对于栓塞后的初始表现和总体结果具有潜在的重要意义。在特定的患者中,BAE可能提供一种治疗选择,尽管需要进一步的研究。
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引用次数: 0
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