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Journal of Radiology Case Reports最新文献

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Nasal obstruction in a 14 year old girl caused by a huge middle turbinate mucocele appearing radiologically as an inverted papilloma. 一名 14 岁女孩因巨大的中鼻甲粘液瘤引起鼻塞,放射学表现为倒置乳头状瘤。
IF 1 Q3 Medicine Pub Date : 2023-08-01 eCollection Date: 2023-09-01 DOI: 10.3941/jrcr.v17i8.4774
William Wakeford, Dimitrios Ioannidis

Introduction: We present a case of a fourteen year old girl who presented with a large intra-nasal mass to the ENT team at a district general hospital in the UK.

Presentation of case: The girl presented predominantly with nasal obstruction and some symptoms of allergic rhinitis. Imaging revealed a large lesion abutting the skull base and causing bony remodelling with marked septal deviation. Based both on CT and MRI imaging, the reporting (non-head and neck) radiologist suggested inverted papilloma as a differential diagnosis. Intra-operative exploration in fact revealed a very large left middle turbinate mucocele extending to the left frontal sinus. The mass was excised endoscopically without complications.

Discussion: Although concha bullosa of the middle turbinate of the nose are common, development of a mucocele within them is far less common and for such a mucocele to develop to this size in a child is extremely rare. The egg shell lining of the lesion can be a tell-tale sign of their aetiology when taken alongside other radiological factors. This case highlights challenges in radiological diagnosis of intra-nasal masses in children, which can lead to delays and increased anxiety.

Conclusion: When assessing nasal masses in children it is important to keep a wide differential due to the challenges of diagnosis. A close conversation should be had with local head and neck radiologists and, of course, where there is a unilateral nasal mass tissue sampling is essential and may be taken as part of a full excision where clinically indicated.

导言:我们介绍了一例 14 岁女孩的病例,她因鼻腔内巨大肿块向英国一家地区综合医院的耳鼻喉科团队求诊:女孩主要表现为鼻塞和一些过敏性鼻炎症状。影像学检查发现,一个巨大的病变与颅底相邻,导致骨质重塑,鼻中隔明显偏曲。根据 CT 和核磁共振成像,报告的放射科医生(非头颈部)建议将倒置乳头状瘤作为鉴别诊断。术中探查实际上发现了一个非常大的左侧中鼻甲粘液瘤,一直延伸到左侧额窦。该肿块经内窥镜切除,无并发症:虽然鼻中鼻甲的圆锥囊肿很常见,但在其中形成粘液瘤的情况却少见得多,而且这种粘液瘤在儿童中发展到如此大的程度也极为罕见。病变的蛋壳状内膜与其他放射学因素结合在一起,可以成为病因的提示性标志。本病例凸显了儿童鼻内肿块放射学诊断的挑战,这可能导致延误和焦虑增加:结论:在评估儿童鼻腔肿块时,由于诊断的挑战性,保持广泛的鉴别是非常重要的。当然,如果是单侧鼻腔肿块,则必须进行组织取样,并在有临床指征的情况下作为全切的一部分。
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引用次数: 0
Pericardial hydatid cyst: The water lily sign as a classical sign in a nonclassical location. 心包水瘤囊肿:睡莲征作为非典型位置的经典征象。
IF 1 Q3 Medicine Pub Date : 2023-08-01 eCollection Date: 2023-09-01 DOI: 10.3941/jrcr.v17i8.5152
Israa Alsulami, Reem Alwasiah, Mohammed Alsalman, Abdulmohsen Alyousef

Hydatid disease is a parasitic infection that usually targets the liver and is rarely seen affecting the heart. Herein, we present an incidentally diagnosed cardiac hydatid cyst with a pathognomonic radiological feature of a water lily sign.

包虫病是一种寄生虫感染,通常针对肝脏,很少影响心脏。在此,我们介绍了一例偶然确诊的心脏包虫囊肿,其放射学特征为睡莲征。
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引用次数: 0
Rosai-Dorfman Disease in a Pediatric Patient: Imaging Findings and Pathology with a brief review of the Literature. 一名儿科患者的罗赛-多夫曼病:影像学检查结果和病理学,以及文献简评。
IF 1 Q3 Medicine Pub Date : 2023-08-01 eCollection Date: 2023-09-01 DOI: 10.3941/jrcr.v17i8.4873
Thomas Hartmann, Nadia Solomon, Gabriel Lerner, Lauren Ehrlich

Rosai-Dorfman Disease, otherwise known as sinus histiocytosis with massive lymphadenopathy, is a rare form of non-Langerhans cell histiocytosis with an estimated incidence of 100 cases per year in the United States. Due to its variable presentation and nonspecific clinical findings, it is particularly difficult to diagnose in pediatric patients. We report a case of an 11-month-old male who presented with a 4-day history of a right groin mass. Ultrasound of the groin and pelvis demonstrated, and MRI of the abdomen and pelvis confirmed an inguinal mass with surrounding lymphadenopathy. Pathology confirmed Rosai-Dorfman Disease and the patient improved after starting oral steroid therapy. To the best of our knowledge, this is the first case of Rosai-Dorfman Disease involving the inguinal region in an infant under 1 year of age reported in the literature. In this case report, we discuss the imaging and histology findings as well as provide a brief literature review for this diagnosis.

罗赛-多夫曼病(Rosai-Dorfman Disease)又称窦性组织细胞增生症伴大量淋巴结病,是一种罕见的非郎格罕氏细胞组织细胞增生症,在美国的发病率估计为每年 100 例。由于其表现多变且临床表现无特异性,因此对儿童患者的诊断尤为困难。我们报告了一例 11 个月大的男性病例,他因右侧腹股沟肿块就诊 4 天。腹股沟和骨盆超声波显示,腹部和骨盆核磁共振成像证实其为腹股沟肿块,周围伴有淋巴结病。病理证实为罗赛-多夫曼病,患者在开始口服类固醇治疗后病情有所好转。据我们所知,这是文献中报道的首例罗赛-多夫曼病累及一岁以下婴儿腹股沟区的病例。在本病例报告中,我们讨论了影像学和组织学检查结果,并对这一诊断进行了简要的文献综述。
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引用次数: 0
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Journal of Radiology Case Reports
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