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A Case Report of Uterine Torsion in a Postmenopausal Female with a Large Leiomyoma. 绝经后患巨大子宫肌瘤的女性发生子宫扭转的病例报告。
IF 0.6 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2024-06-01 eCollection Date: 2024-01-01 DOI: 10.3941/jrcr.v18i1.5035
Jennifer Qin, Isabelle Wijangco, Marley Rashad, Mark Sugi, Stacy Young

This case report discusses a diagnosis of uterine torsion in an 84-year-old woman who presented with five days of right lower quadrant abdominal pain, nausea, vomiting, constipation, and poor intake. Computed tomography (CT) imaging demonstrated a whorled configuration at the junction of the cervix and lower uterine segment, with the left gonadal vein crossing midline, and two previously known right leiomyomas now appearing on the left. These findings were consistent with the diagnosis of uterine torsion. She then underwent an urgent exploratory laparotomy, and the uterus was found to be dextroverted 270 degrees, with dark mottled purple tissue and engorged vessels. A supracervical hysterectomy and bilateral salpingo-oopherectomy were performed. Final pathology demonstrated extensive necrosis. This case reviews the classic presentation and imaging findings for the rare diagnosis of uterine torsion and options for management of both non-gravid and gravid patients.

本病例报告讨论了一名 84 岁妇女的子宫扭转诊断,该妇女因右下腹疼痛、恶心、呕吐、便秘和食欲不振五天就诊。计算机断层扫描(CT)成像显示,宫颈和子宫下段交界处出现轮状结构,左侧性腺静脉横贯中线,两个先前已知的右侧子宫纵隔肌瘤现在出现在左侧。这些结果与子宫扭转的诊断一致。随后,她接受了紧急的探查性开腹手术,发现子宫向外倾倒 270 度,有深色斑驳的紫色组织和充血的血管。患者接受了宫颈上位切除术和双侧输卵管切除术。最后的病理结果显示该组织广泛坏死。本病例回顾了子宫扭转这一罕见诊断的经典表现和影像学检查结果,以及非妊娠和妊娠患者的治疗方案。
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引用次数: 0
The Value of 3D SPACE MRI in Differentiating between Sequestrated Lumbar Disc Herniation and Tumors: Two Cases and Literature. 3D SPACE MRI 在区分腰椎间盘突出症和肿瘤方面的价值:两例病例和文献。
IF 0.6 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2024-06-01 eCollection Date: 2024-01-01 DOI: 10.3941/jrcr.v18i1.5195
Hissein M Fadoul, Nadeer M Gharaibeh, Gang Wu, Xiaoming Li

Background: Intervertebral disc herniation, defined as the protrusion or extrusion of the disc mass outside the disc space, is common and easy to diagnose on conventional Magnetic Resonance imaging (MRI) or Computed Tomography (CT) scans. However, the sequestrated disc fragments are challenging to detect, and intervertebral disc mass displacement into the dural sac, which can lead to serious neurological problems such as Cauda equina syndrome (CES). The sequestrated disc fragments do not have specific clinical or radiological characteristics that can differentiate an atypical disc mass from a tumor, making the diagnosis difficult preoperatively. Herein, we describe the use of Sampling Perfection with Application Optimized Contrast using different flip angle Evolution in Magnetic Resonance Imaging (3D SPACE MRI) in the diagnosis of the intervertebral disc fragment that mimicked a tumor.

Case presentation: In this study, we report two cases of sequestered lumbar disc herniation. The first case was a 37-year-old patient with a 2-year history of intermittent left lower limb pain that aggravates with exercise and is relieved at rest, while the second case was a 42-year-old patient with a history of 40 days of numbness and pain in the left lower limb.

Conclusion: 3D SPACE MRI is a beneficial diagnostic imaging tool for discriminating between disc mass that mimics a tumor and a tumor before surgery. If the disc fragment mimicking a tumor can be identified before the operation, open surgical treatment won't be necessary for all patients.

背景:椎间盘突出症是指椎间盘肿块突出或挤压到椎间盘间隙外,在传统的磁共振成像(MRI)或计算机断层扫描(CT)中很常见,也很容易诊断。然而,椎间盘碎片嵌顿却很难发现,椎间盘肿块移位到硬膜囊内,可能导致严重的神经系统问题,如马尾综合征(CES)。固着的椎间盘碎片没有特定的临床或放射学特征,无法将非典型椎间盘肿块与肿瘤区分开来,因此术前诊断非常困难。在此,我们介绍了在磁共振成像(3D SPACE MRI)中使用不同翻转角度的完美取样与应用优化对比度(Sampling Perfection with Application Optimized Contrast Using different flip angle Evolution in Magnetic Resonance Imaging)来诊断模仿肿瘤的椎间盘碎片:在本研究中,我们报告了两例腰椎间盘突出症嵌顿病例。第一个病例是一名 37 岁的患者,有 2 年的左下肢间歇性疼痛病史,运动时疼痛加剧,休息时疼痛缓解;第二个病例是一名 42 岁的患者,有 40 天的左下肢麻木和疼痛病史。如果能在手术前识别出模仿肿瘤的椎间盘碎片,那么并非所有患者都需要进行开放手术治疗。
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引用次数: 0
Unusual Unique Renal Metastasis of Rectal Carcinoma. 不寻常的直肠癌肾转移
IF 0.6 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2024-06-01 eCollection Date: 2024-01-01 DOI: 10.3941/jrcr.v18i1.5233
Sidki Kenza, Hatim Essaber, Sara Habib Chorfa, Omor Youssef, Latib Rachida

Rectal cancer Is a Common malignant pathology; its usual spread in volves the liver and lungs. The occurrence of renal metastases is exceptional. CT scanning aims to evaluate extension and may incidentally reveal a renal mass, which can be better characterized through MRI and ultrasound. We describe a case of a solitary renal metastasis from rectal cancer and underscore the significant role of imaging in positively diagnosing this uncommon pathology.

直肠癌是一种常见的恶性病变,通常会扩散到肝脏和肺部。发生肾转移的情况比较少见。CT 扫描的目的是评估转移范围,可能会偶然发现肾脏肿块,而核磁共振成像和超声检查可以更好地确定肾脏肿块的特征。我们描述了一例直肠癌单发肾转移病例,并强调了影像学在积极诊断这种不常见病症方面的重要作用。
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引用次数: 0
Isolated Abducens Nerve Palsy: A Rare Manifestation of Recurrent Extramedullary Myeloma. 孤立性弓状神经麻痹:复发性髓外骨髓瘤的罕见表现
IF 0.6 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2024-06-01 eCollection Date: 2024-01-01 DOI: 10.3941/jrcr.v18i1.5240
Neal Joshi, Joy Li, Ajit Karambelkar, Payton Boere

Multiple myeloma is a plasma cell neoplasm, which may present as a solitary plasmacytoma and, uncommonly, as an extramedullary plasmacytoma. Intracranial plasmacytomas may manifest in central nervous system involvement as cranial nerve palsies. Cranial nerve six palsy is the most common in cases of malignancy. However, isolated abducens palsy presenting as multiple myeloma recurrence is very uncommon. Here, we detail two cases in which intracranial plasmacytoma lesions were present within the region of the Dorello canal, resulting in acute isolated unilateral diplopia from disease recurrence in the absence of systemic marrow involvement.

多发性骨髓瘤是一种浆细胞肿瘤,可表现为单发浆细胞瘤,髓外浆细胞瘤也不常见。颅内浆细胞瘤可累及中枢神经系统,表现为颅神经麻痹。颅神经六麻痹在恶性肿瘤病例中最为常见。然而,以多发性骨髓瘤复发为表现的孤立性外展神经麻痹并不常见。在这里,我们详细介绍了两例颅内浆细胞瘤病变出现在多雷洛管区域,在没有全身骨髓受累的情况下,因疾病复发而导致急性孤立性单侧复视的病例。
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引用次数: 0
Placement of Endovascular Stent for Reperfusion of Cerebral Infarct After Pediatric Traumatic Internal Carotid Artery Dissection. 为小儿外伤性颈内动脉夹层后的脑梗塞再灌注植入血管内支架
IF 0.6 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2024-06-01 eCollection Date: 2024-01-01 DOI: 10.3941/jrcr.v18i1.5217
Arthur Rezayev, William S Coggins, Adewumi Amole, Mudassar Kamran, Tomoko Tanaka

Background: Traumatic intracranial ICA dissections are not commonly seen in children. Dissection resulting in perfusion deficit warrants intervention. Here we encountered a patient who experienced traumatic ICA dissection, treated by endovascular stenting.

Methods: A 10-year-old female presented with aphasia and right sided weakness following trauma. Imaging showed deficit in the left MCA territory without core. Further imaging showed dissection of the left supraclinoid ICA, confirmed by digital subtraction angiography.

Results: A Neuroform Atlas stent was placed without complication. All dysarthria and weakness had resolved on follow-up 5 months post-stenting.

Conclusions: Acute stroke symptoms in children can result in lasting deficits if not treated quickly. Medical management is regarded to be first line, depending on presentation. Endovascular stenting may provide a promising means to treat pediatric ICA dissections involving perfusion deficits and mitigate permanent ischemic changes.

背景:外伤性颅内 ICA 夹层在儿童中并不常见。夹层导致灌注不足,需要进行干预。在这里,我们遇到了一位经历了外伤性 ICA 夹层的患者,她接受了血管内支架治疗:一名 10 岁女性患者在外伤后出现失语和右侧肢体无力。影像学检查显示左侧 MCA 区无核心缺损。进一步造影显示左侧锁骨上ICA夹层,数字减影血管造影证实了这一结果:结果:放置了Neuroform Atlas支架,无并发症。支架植入后 5 个月随访,所有构音障碍和乏力症状均已缓解:结论:儿童急性脑卒中症状如不尽快治疗,可导致持久的功能障碍。结论:儿童急性脑卒中症状如不尽快治疗,可导致持久的功能障碍。血管内支架置入术可能是治疗涉及灌注障碍的小儿主动脉夹层并减轻永久性缺血性改变的有效方法。
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引用次数: 0
Imaging findings of arterial calcification due to deficiency of CD73: A case study CD73 缺乏导致动脉钙化的影像学发现:病例研究
IF 1 Q3 Medicine Pub Date : 2024-02-09 DOI: 10.3941/jrcr.v17i12.5175
Aniruddh Mandalapu, Kathryn J Stevens
A 52-year-old male developed right knee pain after hiking in Guatemala. On his return he underwent a knee MRI for an indication of medial knee pain, which demonstrated a medial meniscal tear. However, the MRI demonstrated marked tortuosity and dense calcification of the popliteal artery, confirmed on subsequent radiographs. Review of previous CT studies of the abdomen and lower extremities showed severe ectasia and arterial calcification in the femoral and popliteal arteries bilaterally, but no calcifications in the aorta and common iliac arteries. Dual energy CT studies of the extremities demonstrated extensive periarticular soft tissue calcification throughout the wrists, hands, ankle and feet without evidence of uric acid. Review of the electronic medical records revealed a diagnosis of Arterial Calcification due to Deficiency of CD73 (ACDC), a rare genetic disorder presenting with debilitating pain in the wrists and hands, claudication of the calves, thighs and buttocks, progressing to chronic ischemia of the feet which may be limb-threatening. The patient was enrolled in an NIH trial of bisphosphonates and dual-antiplatelet therapy with stabilization of symptoms. This case discusses the imaging findings of this rare condition, differential diagnosis to consider, and current management.
一名 52 岁的男性在危地马拉徒步旅行后出现右膝疼痛。回国后,他因膝关节内侧疼痛接受了膝关节核磁共振成像检查,结果显示为内侧半月板撕裂。然而,核磁共振成像显示腘动脉有明显的迂曲和密集钙化,这在随后的X光片上得到了证实。之前的腹部和下肢 CT 检查显示,双侧股动脉和腘动脉存在严重的异位和动脉钙化,但主动脉和髂总动脉没有钙化。四肢的双能 CT 检查显示,腕部、手部、踝关节和足部均有广泛的关节周围软组织钙化,但无尿酸证据。查看电子病历后发现,该患者被诊断为 CD73 缺乏引起的动脉钙化(ACDC),这是一种罕见的遗传性疾病,表现为手腕和手部疼痛,小腿、大腿和臀部跛行,进而发展为慢性足部缺血,可能危及肢体。患者参加了美国国立卫生研究院的双磷酸盐和双抗血小板治疗试验,症状有所稳定。本病例讨论了这种罕见疾病的影像学检查结果、需要考虑的鉴别诊断以及目前的治疗方法。
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引用次数: 0
Myopericytoma. A rare case of parapharyngeal localization. 肌细胞瘤。咽旁定位的罕见病例。
IF 1 Q3 Medicine Pub Date : 2024-02-09 DOI: 10.3941/jrcr.v17i12.5186
Vincenzo Dolcetti, Sergio Ruggiero, R. Pellini, Anastasia Mercurio, A. Vidiri
This case study presents a 66-year-old man referred to the Otolaryngology and Head and Neck Surgery department due to a one-history of persistent pain in the left posterior cervical region. No abnormalities were detected in the oral and pharyngeal regions during clinical and endoscopic examinations. Subsequently, a magnetic resonance imaging revealed a lesion (14 x 12 x 14 mm) into the left parapharyngeal space, with high signal intensity on T2-weighted images, enhancement after contrast medium, restricted signal on diffusion weighted imaging and high vascularization on perfusion MRI. The histological examination of the lesion led to a diagnosis of myopericitoma. Post-surgery, no adjuvant therapy was administered. Myopericytomas are rare soft-tissue benign neoplasms, predominantly reported in extremities, with a limited number of cases in the head and neck region and almost never described in the literature with elective localization in the parapharyngeal space.
本病例研究介绍了一名因左颈椎后部持续疼痛而转诊至耳鼻咽喉头颈外科的 66 岁男性。临床和内窥镜检查均未发现口腔和咽部异常。随后,磁共振成像显示左侧咽旁间隙有一病灶(14 x 12 x 14 毫米),T2 加权成像呈高信号强度,造影剂后增强,弥散加权成像呈局限性信号,灌注磁共振成像呈高血管化。病变组织学检查诊断为肌瘤。手术后未进行辅助治疗。肌细胞瘤是一种罕见的软组织良性肿瘤,据报道主要发生在四肢,头颈部的病例数量有限,文献中几乎从未描述过选择性定位在咽旁间隙的病例。
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引用次数: 0
Myopericytoma. A rare case of parapharyngeal localization. 肌细胞瘤。咽旁定位的罕见病例。
IF 1 Q3 Medicine Pub Date : 2024-02-09 DOI: 10.3941/jrcr.v17i12.5186
Vincenzo Dolcetti, Sergio Ruggiero, R. Pellini, Anastasia Mercurio, A. Vidiri
This case study presents a 66-year-old man referred to the Otolaryngology and Head and Neck Surgery department due to a one-history of persistent pain in the left posterior cervical region. No abnormalities were detected in the oral and pharyngeal regions during clinical and endoscopic examinations. Subsequently, a magnetic resonance imaging revealed a lesion (14 x 12 x 14 mm) into the left parapharyngeal space, with high signal intensity on T2-weighted images, enhancement after contrast medium, restricted signal on diffusion weighted imaging and high vascularization on perfusion MRI. The histological examination of the lesion led to a diagnosis of myopericitoma. Post-surgery, no adjuvant therapy was administered. Myopericytomas are rare soft-tissue benign neoplasms, predominantly reported in extremities, with a limited number of cases in the head and neck region and almost never described in the literature with elective localization in the parapharyngeal space.
本病例研究介绍了一名因左颈椎后部持续疼痛而转诊至耳鼻咽喉头颈外科的 66 岁男性。临床和内窥镜检查均未发现口腔和咽部异常。随后,磁共振成像显示左侧咽旁间隙有一病灶(14 x 12 x 14 毫米),T2 加权成像呈高信号强度,造影剂后增强,弥散加权成像呈局限性信号,灌注磁共振成像呈高血管化。病变组织学检查诊断为肌瘤。手术后未进行辅助治疗。肌细胞瘤是一种罕见的软组织良性肿瘤,据报道主要发生在四肢,头颈部的病例数量有限,文献中几乎从未描述过选择性定位在咽旁间隙的病例。
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引用次数: 0
Blastomycosis of the Central Nervous System 中枢神经系统布氏杆菌病
IF 1 Q3 Medicine Pub Date : 2024-02-09 DOI: 10.3941/jrcr.v17i12.5167
Alexander Kazmer, Rami El-Baba, Andreas Kontosis, Ewa Borys, Mariah Siddiqui
The reported incidence of blastomycosis is increasing in certain regions of the United States. The diagnosis is primarily made via urine antigen testing, culture, or cytology smear. The differential diagnosis for blastomycosis includes pneumonia, tuberculosis, and non-infectious pulmonary disease. Clinical context and epidemiologic exposure play a crucial role in diagnosis. However, the differential can expand significantly if there is disseminated central nervous system involvement, especially if pulmonary manifestations are not seen. Imaging begins to play a vital role when differentiating disseminated blastomycosis from other etiologies such as malignancy. Herein we present a case of a 58-year-old male who presented with seizures and right sided gaze preference found to have disseminated central nervous system blastomycosis. In this article, we will discuss symptoms and imaging findings of disseminated blastomycosis to help guide diagnosis and management.
据报道,美国某些地区的囊霉病发病率正在上升。诊断主要通过尿液抗原检测、培养或细胞学涂片。囊霉菌病的鉴别诊断包括肺炎、肺结核和非传染性肺部疾病。临床背景和流行病学接触在诊断中起着至关重要的作用。然而,如果中枢神经系统受累,尤其是肺部表现不明显时,鉴别范围会大大增加。在将播散性囊霉菌病与其他病因(如恶性肿瘤)进行鉴别时,影像学检查开始发挥重要作用。本文中我们介绍了一例 58 岁男性患者的病例,该患者因癫痫发作和右侧凝视偏好而被发现患有播散性中枢神经系统囊霉菌病。本文将讨论播散性囊霉菌病的症状和影像学检查结果,以帮助指导诊断和治疗。
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引用次数: 0
Blastomycosis of the Central Nervous System 中枢神经系统布氏杆菌病
IF 1 Q3 Medicine Pub Date : 2024-02-09 DOI: 10.3941/jrcr.v17i12.5167
Alexander Kazmer, Rami El-Baba, Andreas Kontosis, Ewa Borys, Mariah Siddiqui
The reported incidence of blastomycosis is increasing in certain regions of the United States. The diagnosis is primarily made via urine antigen testing, culture, or cytology smear. The differential diagnosis for blastomycosis includes pneumonia, tuberculosis, and non-infectious pulmonary disease. Clinical context and epidemiologic exposure play a crucial role in diagnosis. However, the differential can expand significantly if there is disseminated central nervous system involvement, especially if pulmonary manifestations are not seen. Imaging begins to play a vital role when differentiating disseminated blastomycosis from other etiologies such as malignancy. Herein we present a case of a 58-year-old male who presented with seizures and right sided gaze preference found to have disseminated central nervous system blastomycosis. In this article, we will discuss symptoms and imaging findings of disseminated blastomycosis to help guide diagnosis and management.
据报道,美国某些地区的囊霉病发病率正在上升。诊断主要通过尿液抗原检测、培养或细胞学涂片。囊霉菌病的鉴别诊断包括肺炎、肺结核和非传染性肺部疾病。临床背景和流行病学接触在诊断中起着至关重要的作用。然而,如果中枢神经系统受累,尤其是肺部表现不明显时,鉴别范围会大大增加。在将播散性囊霉菌病与其他病因(如恶性肿瘤)进行鉴别时,影像学检查开始发挥重要作用。本文中我们介绍了一例 58 岁男性患者的病例,该患者因癫痫发作和右侧凝视偏好而被发现患有播散性中枢神经系统囊霉菌病。本文将讨论播散性囊霉菌病的症状和影像学检查结果,以帮助指导诊断和治疗。
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引用次数: 0
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Journal of Radiology Case Reports
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