von Recklinghausen病的罕见泌尿生殖表现:阴囊、阴茎和盆腔内累及膀胱和精索延伸1例报告

Q4 Medicine
Nadia El Mahi, Amal Mojahid, Hajar Siouri, Hamid Ziani, Siham Nasri, Imane Kamaoui, Imane Skiker
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引用次数: 0

摘要

神经纤维瘤病是一组遗传疾病,包括两种主要类型:1型神经纤维瘤病(NF-1)和2型神经纤维瘤病。最常见的形式是NF-1,也被称为冯·雷克林豪森病。这种疾病的临床表现和表现是多变的。在这个报告中,我们提出一个独特的情况下,一个10岁的儿童NF-1谁提出阴囊肿胀与进行性阴茎增大。经过全面的评估,诊断为丛状神经纤维瘤。MRI检查显示肿瘤在盆腔内延伸,影响膀胱和精索。这种罕见的临床表现使本病例特别有趣,并突出了冯·雷克林豪森病的多种表现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rare uro-genital manifestations of von Recklinghausen disease: Scrotal, penile, and intrapelvic involvement with bladder and spermatic cord extension: A case report
Neurofibromatosis is a group of genetic disorders comprising 2 main types: type 1 neurofibromatosis (NF-1) and type 2 neurofibromatosis. The most common form is NF-1, also known as Von Recklinghausen disease. The clinical manifestations and presentation of this condition are variable. In this report, we present a unique case of a 10-year-old child with NF-1 who presented with scrotal swelling associated with progressive penile enlargement. After a thorough evaluation, the diagnosis of a plexiform neurofibroma was made. MRI evaluation revealed an intrapelvic extension of the tumor affecting the bladder and spermatic cords. This rare clinical presentation makes this case particularly interesting and highlights the diverse manifestations of Von Recklinghausen disease.
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来源期刊
Radiology Case Reports
Radiology Case Reports Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
1.10
自引率
0.00%
发文量
1074
审稿时长
30 days
期刊介绍: The content of this journal is exclusively case reports that feature diagnostic imaging. Categories in which case reports can be placed include the musculoskeletal system, spine, central nervous system, head and neck, cardiovascular, chest, gastrointestinal, genitourinary, multisystem, pediatric, emergency, women''s imaging, oncologic, normal variants, medical devices, foreign bodies, interventional radiology, nuclear medicine, molecular imaging, ultrasonography, imaging artifacts, forensic, anthropological, and medical-legal. Articles must be well-documented and include a review of the appropriate literature.
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