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Upper Limb Meromelia with Oligodactyly and Brachymesophalangy of the Foot: An Unusual Association 上肢缺趾畸形伴足少趾和足短管畸形:一种不寻常的关联
Pub Date : 2019-06-24 DOI: 10.1155/2019/3419383
M. Özdemir, R. Kavak, Ö. Eraslan
Meromelia is a rare skeletal abnormality characterized by the partial absence of at least one limb. Several mechanisms have been postulated to explain the etiopathogenesis of the disorder. Most of the cases of meromelia are reported to be sporadic. It can occur either in isolation or with other congenital malformations. VACTERL association, gastroschisis, atrial septal defect, proximal femoral focal deficiency, and fibular hemimelia are the congenital abnormalities reported to be in association with meromelia. However, no other congenital abnormalities in association with meromelia have been recorded to date. We herein present an unusual case of bilateral upper limb meromelia accompanied by unilateral oligodactyly and brachymesophalangy of the foot.
缺肢畸形是一种罕见的骨骼异常,其特征是至少有一个肢体部分缺失。已经假设了几种机制来解释这种疾病的发病机制。据报道,大多数小粒贫血病例是散发的。它既可以单独发生,也可以与其他先天性畸形一起发生。VACTERL关联、胃裂、房间隔缺损、股近端局灶性缺陷和腓骨半贫血是报道的先天性异常,与半贫血有关。然而,到目前为止,还没有其他先天性异常与粟粒贫血有关的记录。我们在此提出一个不寻常的情况下,双侧上肢缺趾伴单侧缺趾和足短管畸形。
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引用次数: 2
Microgallbladder: Self-Remitting Acute Cholecystitis-Like Condition Unique to Patients with Cystic Fibrosis 微胆囊:囊性纤维化患者特有的自缓解急性胆囊炎样疾病
Pub Date : 2019-06-19 DOI: 10.1155/2019/6737428
Mina S Mousa, J. Feldman, Paresh Mahajan
Microgallbladder is a nonsurgical medical condition characterized by chronic inflammation and atrophy of the gallbladder, which is considered a highly specific imaging finding unique to patients with cystic fibrosis (CF), and has been incidentally reported on abdominal imaging in up to 45% of cases with CF. The impairment of exocrine water efflux in CF leads to the production of hyperviscous biliary secretions, cholestasis, and transient cystic duct obstruction of the microgallbladder causing microcholecystitis—interestingly a self-remitting acute cholecystitis-like condition without surgical intervention. We present a case report of a 22-year-old male patient with history of CF with multiple hospital admissions for unexplained chronic abdominal pain found to be caused by microgallbladder, which was managed conservatively.
微胆囊是一种以胆囊慢性炎症和萎缩为特征的非手术内科疾病,被认为是囊性纤维化(CF)患者特有的高度特异性影像学发现,高达45%的CF患者在腹部影像学上也有报道。CF患者外分泌水排出障碍导致胆道分泌物高粘稠、胆汁淤积、而微胆囊的短暂性囊管阻塞引起微胆囊炎——有趣的是,一种无需手术干预即可自行缓解的急性胆囊炎样疾病。我们报告一例22岁男性CF病史患者,多次住院,原因不明的慢性腹痛,发现是由微胆囊引起的,这是保守处理。
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引用次数: 3
Two Cases of Primary Testicular Lymphoma Presenting with Direct Spread along the Spermatic Cord and Gonadal Vessels 原发性睾丸淋巴瘤沿精索及性腺血管直接扩散2例
Pub Date : 2019-06-18 DOI: 10.1155/2019/5953618
M. Ellatif, Raekha Kumar, A. Weller, D. Katz, E. Vrentzou
Primary testicular lymphoma is a rare testicular neoplasm that mainly affects elderly patients, with Human Immunodeficiency Virus (HIV) being a known risk factor in the younger population. Approximately 20% of patients will have disseminated disease with extra-nodal involvement at clinical presentation. Rarely, direct spread along the spermatic cord and gonadal vessels can occur and has been described in the literature. We present two cases of this phenomenon where the primary testicular tumour has spread along the gonadal vein to its origin at the inferior vena cava.
原发性睾丸淋巴瘤是一种罕见的睾丸肿瘤,主要影响老年患者,人类免疫缺陷病毒(HIV)是年轻人群中已知的危险因素。约20%的患者临床表现为弥散性疾病伴淋巴结外受累。很少,沿着精索和性腺血管的直接扩散可以发生,并已在文献中描述。我们提出两个病例的这种现象,原发睾丸肿瘤已沿生殖腺静脉扩散到它的起源在下腔静脉。
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引用次数: 7
Cholecystohepatic Duct: A Biliary Duct Variant Resulting in Postcholecystectomy Bile Leak—Case Report and Review of Normal and Common Variant Biliary Anatomy 胆囊-肝管:胆囊切除术后胆漏的一种胆管变异——正常和常见变异胆道解剖的病例报告和回顾
Pub Date : 2019-06-17 DOI: 10.1155/2019/6812793
Nathan Meyer, S. Al-katib, Farnoosh Sokhandon
Although relatively infrequent, bile duct leaks are among the primary complications of hepatobiliary surgery and cholecystectomy given the large number of these operations performed annually around the world. Variant biliary anatomy increases the risk of surgical complications, especially if unrecognized on preoperative imaging or intraoperatively. Presented here is a case of a patient with an unrecognized cholecystohepatic duct at the time of surgery leading to bile leak after cholecystectomy. Numerous factors made for a technically difficult surgery with obscuration of the true anatomy, ultimately resulting in transection of the cholecystohepatic duct. Understanding normal and variant biliary anatomy will help prevent avoidable complications of hepatobiliary surgery.
尽管相对不常见,但胆管泄漏是肝胆手术和胆囊切除术的主要并发症之一,因为全世界每年都有大量胆管手术和胆囊切除术。胆道解剖结构的变异增加了手术并发症的风险,尤其是术前或术中未被识别的胆道解剖。本文报告一例胆囊切除术后患者在手术时出现未被识别的胆囊肝管,导致胆漏。许多因素造成技术上困难的手术,掩盖了真实的解剖结构,最终导致胆囊肝管横断。了解正常和变异的胆道解剖结构将有助于预防可避免的肝胆手术并发症。
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引用次数: 4
Dural and Leptomeningeal Spine Metastases of Breast Cancer. 乳腺癌的硬脊膜和脊膜脊柱转移。
Pub Date : 2019-05-29 eCollection Date: 2019-01-01 DOI: 10.1155/2019/4289362
Fernando Matos, Luís Cerqueira

We present a case of a 57-year-old female diagnosed with invasive ductal breast cancer, which was treated and in remission for 12 years. In 2018 she presented a progressive dorsal back pain, which prevented her from performing basic tasks. An MR study was performed and revealed the presence of an extramedullary metastatic sleeve located in the thoracic intradural space. Concomitant multiple small nodular foci were adhering diffusely to the spinal cord, compatible with leptomeningeal metastatic disease. The occurrence of both forms of spread in the spine is uncommon, and its distinction on imaging is of particular importance taking into account the differences in treatment approach and prognosis.

我们提出一个57岁的女性诊断为浸润性导管乳腺癌,这是治疗和缓解了12年。2018年,她出现了渐进式背部疼痛,这使她无法执行基本任务。一项磁共振研究显示髓外转移袖位于胸椎硬膜内间隙。伴发多发性小结节灶弥漫性粘附于脊髓,与脑脊膜轻脑膜转移性疾病相符。这两种形式的脊柱扩散的发生并不常见,考虑到治疗方法和预后的差异,其影像学上的区别尤为重要。
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引用次数: 2
Case Report of a Rare Cystic Mediastinal Lymphangioma Mimicking Recurrent Pleural Effusion. 罕见的囊性纵隔淋巴管瘤表现为复发性胸腔积液1例报告。
Pub Date : 2019-05-26 eCollection Date: 2019-01-01 DOI: 10.1155/2019/1301845
Fateme Salehi, Mark Landis, Richard Inculet, Daniele Wiseman

Mediastinal lymphangiomas are rare benign congenital malformations, but complications can occur, including infection, cystic hemorrhage, superior vena cava syndrome, airway compromise, and chylothorax. Radiologically, lymphangiomas are well-defined masses, with low attenuation ranging from simple to complex fluid and fat. They often encase adjacent mediastinal structures. We present a case of mediastinal lymphangioma in a young female, who presented with recurrent complex pleural effusions, initially thought to represent an empyema and/or necrotic mass. Despite surgical chest tube and interventional radiology drainage, fluid reaccumulated. Upon further review, the interventional and thoracic radiologist concurred that the complex collection was in fact predominantly extra pleural in location. The patient underwent partial resection after it was discovered intraoperatively that the extra pleural cystic mass was contiguous with and extended deeply into the mediastinum. Histopathology confirmed the diagnosis of lymphangioma.

纵隔淋巴管瘤是罕见的先天性良性畸形,但可发生并发症,包括感染、囊性出血、上腔静脉综合征、气道损害和乳糜胸。放射学上,淋巴管瘤是明确的肿块,低衰减,从简单到复杂的液体和脂肪。它们常包住邻近的纵隔结构。我们报告一个年轻女性纵隔淋巴管瘤的病例,她表现为复发性复杂胸腔积液,最初被认为是脓胸和/或坏死肿块。尽管手术胸管和介入放射学引流,液体再次积聚。经过进一步检查,介入和胸椎放射科医生一致认为,复杂的集合实际上主要位于胸膜外。患者术中发现胸膜外囊性肿块与纵隔相邻并深入纵隔,遂行部分切除。组织病理学证实淋巴管瘤的诊断。
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引用次数: 2
An Unusual Ovarian Mucinous Borderline Tumor with a Large Solid Component. 罕见的卵巢黏液交界性肿瘤伴大实性成分。
Pub Date : 2019-05-22 eCollection Date: 2019-01-01 DOI: 10.1155/2019/1402736
Eito Kozawa, Kaiji Inoue, Mitsutake Yano, Masanori Yasuda, Kosei Hasegawa, Junji Tanaka, Tomoaki Ichikawa, Mamoru Niitsu

Herein, we report magnetic resonance imaging (MRI) findings of a mucinous borderline tumor of the ovary, which we observed as a mainly solid tumor with large solid components in the lower pelvic cavity. The appearance of ovarian epithelial tumors on imaging is often complex. Cystic to solid appearing masses may be observed, and they often resemble epithelial carcinoma. Due to mucinous or hemorrhage components of packed small or microcystic components, MRI depicts slightly high signal intensity on T1-weighted images and low signal intensity on T2-weighted images. Mucinous borderline tumor of the ovary with a large solid component is very rare, but it is clinically important to recognize the possibility of mucinous borderline tumor to avoid unnecessary surgical intervention.

在此,我们报告一个卵巢黏液交界性肿瘤的磁共振成像(MRI)结果,我们观察到这是一个主要的实体瘤,在盆腔下部有很大的实体成分。卵巢上皮性肿瘤的影像学表现通常很复杂。可观察到囊性到实性肿块,通常类似上皮癌。由于填充小或微囊性成分的粘液或出血成分,MRI在t1加权图像上表现为略高信号强度,在t2加权图像上表现为低信号强度。卵巢黏液性交界性肿瘤具有较大的实性成分是非常罕见的,但认识黏液性交界性肿瘤的可能性是临床上重要的,以避免不必要的手术干预。
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引用次数: 3
TB Meningitis and TB Peritonitis: Abdominal Pseudocyst and VP-Shunt Link. 结核性脑膜炎和结核性腹膜炎:腹部假性囊肿和vp -分流链。
Pub Date : 2019-04-28 eCollection Date: 2019-01-01 DOI: 10.1155/2019/4893547
Manzoor Ahmed, Essameldin Ali ElGamal, Anwar Ahmad, Muhammad Badar Zaman

TB meningitis (TBM) carries high morbidity and mortality and is a relatively common extrapulmonary TB in the third world countries. TBM as thick exudative disease manifests on MRI and CT as nodular basal leptomeningitis, hydrocephalus, basal infarcts, and tuberculomas. Hydrocephalus is treated with ventriculoperitoneal shunting (VPS). Shunt malfunction and revision are common. We report a case of multidrug-resistant TBM with spinal involvement and dissemination of the disease via VPS causing TB peritonitis (TBP). TBP presented as a large abdominal pseudocyst around the catheter tip with shunt malfunction. There was no evidence for any other site of extra-CNS disease. TBP per se is relatively less common. This is the first case reporting VPS as a means of TB spread.

结核性脑膜炎(TBM)具有较高的发病率和死亡率,是第三世界国家相对常见的肺外结核。TBM为厚渗出性疾病,在MRI和CT上表现为结节性基底脑膜炎、脑积水、基底梗死和结核瘤。脑积水采用脑室腹腔分流术(VPS)治疗。分流故障和改型是常见的。我们报告一例多药耐药结核性脊髓炎与脊髓受累和疾病传播通过VPS引起结核性腹膜炎(TBP)。TBP表现为导管尖端周围的大腹腔假性囊肿,并伴有分流功能障碍。没有证据表明有任何其他部位的外中枢神经系统疾病。TBP本身相对不太常见。这是第一个报告VPS作为结核病传播手段的病例。
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引用次数: 0
Transcatheter Proximal Coil Blocking with n-Butyl-2-Cyanoacrylate Injection via the Pulmonary Artery Alone for Rasmussen's Aneurysm. 经肺动脉注射正丁基-2-氰基丙烯酸酯近端线圈阻断治疗拉斯穆森动脉瘤。
Pub Date : 2019-04-15 eCollection Date: 2019-01-01 DOI: 10.1155/2019/1725238
Atsushi Ugajin, Hiroyuki Fujii, Hiroyasu Nakamura, Akifumi Fujita, Takahiro Sasaki, Naoko Mato, Hideharu Sugimoto

Rasmussen's aneurysm is a peripheral pulmonary artery pseudoaneurysm (PAP) within a tuberculosis cavity. Because it can be perfused from the bronchial and pulmonary arterial circulations, combined embolization via the bronchial and pulmonary arteries is sometimes required. Herein, we present case of a 51-year-old man with Rasmussen's aneurysm that was successfully treated by proximal coil blocking with n-butyl-2-cyanoacrylate (NBCA) injection via the pulmonary artery alone. With proximal coil blocking, a sufficient amount of NBCA could be injected without unintended reflux of the NBCA cast to the proximal pulmonary artery. To our knowledge, there has been no report that attempted NBCA injection under proximal coil blocking for Rasmussen's aneurysm. Our treatment approach may be safe and effective for infectious lung disease-related PAP, which has to be treated from the pulmonary artery side.

拉斯穆森动脉瘤是结核腔内的外周肺动脉假性动脉瘤。由于它可以从支气管和肺动脉循环灌注,有时需要通过支气管和肺动脉联合栓塞。在此,我们报告一例51岁男性拉斯穆森动脉瘤患者,通过肺动脉注射正丁基-2-氰基丙烯酸酯(NBCA)近端圈阻断成功治疗。在近端线圈阻断的情况下,可以注射足量的NBCA,而不会导致NBCA铸型意外返流至肺动脉近端。据我们所知,目前还没有报道在近端线圈阻断下注射NBCA治疗拉斯穆森动脉瘤。我们的治疗方法对于感染性肺部疾病相关的PAP可能是安全有效的,因为PAP必须从肺动脉侧进行治疗。
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引用次数: 2
Multisystemic Benign Metastasizing Leiomyoma: An Unusual Condition with an Atypical Clinical Presentation. 多系统良性转移性平滑肌瘤:一种不典型临床表现的罕见疾病。
Pub Date : 2019-04-10 eCollection Date: 2019-01-01 DOI: 10.1155/2019/7014248
Fernando Matos, Cristina Santiago, Duarte Silva

Benign metastasizing leiomyoma (BML) is a rarely found entity with few documented cases in the literature, usually occurring in women of reproductive age with a history of myomectomy or hysterectomy. The leiomyomas can metastasize to several organs, the lungs being the most commonly affected. We report a case of a 40-year-old female patient who presented at our institution with low back pain. She underwent a lumbar MR that revealed the presence of an expansive and compressive mass in the body of L4. This mass was biopsied, corresponding to a metastasizing leiomyoma with no malignant characteristics. Subsequently, a CT examination showed several soft tissue density round masses in both lungs, but the most striking feature was a 12 cm mass located in the left iliac crest. There was asymmetrical uterus enlargement, caused by the presence of several leiomyomas. Since the lesions were estrogen and progesterone positive, hormone suppression consisting of oophorectomy followed by anastrozole was the chosen treatment. No signs of progression were observed at the 6-month follow-up. This case is one of the very few that occurred in a woman with no previous uterine intervention, adding further evidence that surgery is not an essential condition for this entity to develop.

良性转移性平滑肌瘤(BML)是一种罕见的实体,文献中很少有病例记录,通常发生在有子宫肌瘤切除术或子宫切除术史的育龄妇女。平滑肌瘤可以转移到几个器官,肺是最常见的影响。我们报告一例40岁的女性患者谁提出在我们的机构腰痛。她接受了腰椎MR检查,发现腰4椎体存在一个膨胀性和压缩性肿块。肿块经活组织检查,为转移性平滑肌瘤,无恶性特征。随后,CT检查显示双肺多个软组织密度圆形肿块,但最显著的特征是位于左髂嵴的12厘米肿块。子宫不对称增大,由几个平滑肌瘤引起。由于病变是雌激素和孕激素阳性,激素抑制包括卵巢切除术后阿那曲唑是选择的治疗。6个月随访未见进展迹象。本病例是极少数发生在没有子宫干预的妇女中的一例,进一步证明手术不是该实体发展的必要条件。
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引用次数: 10
期刊
Case Reports in Radiology
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