伪装成丝虫病的儿童巨大阴囊神经纤维瘤:一种常见疾病的罕见表现。

Q4 Biochemistry, Genetics and Molecular Biology Prague medical report Pub Date : 2024-01-01 DOI:10.14712/23362936.2024.5
Anurag Singh, Gyanendra Singh, Anuragani Verma, Yogendra Narayan Verma
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引用次数: 0

摘要

阴囊神经纤维瘤是一种非常少见的良性肿瘤,尤其是当它影响到青少年且与神经纤维瘤病 I 型无关时。在此,我们报告了一例 17 岁男孩的病例研究,该男孩患有巨大阴囊肿块长达 10 年之久,临床上被伪装成丝虫病。根据细胞学检查结果,初步诊断为良性神经鞘瘤。手术切除了患者的肿块,组织病理学和免疫组化检查确定了神经纤维瘤的诊断。结合临床、术前细胞学、组织学和免疫组化检查结果的阴囊神经纤维瘤病例未见文献报道。本病例扩展了临床医生以前观察到的阴囊肿瘤的鉴别诊断范围。
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A Giant Scrotal Neurofibroma in a Child Masquerading as Filariasis: Uncommon Presentation of a Common Disease.

Neurofibroma of the scrotum is a very uncommon benign neoplasm, specifically when it affects teenagers and is not associated with neurofibromatosis type I. To the best of our knowledge, only a couple of cases of neurofibroma in children have been documented. Here, we report a case study of a 17-year-old boy who had a giant scrotal lump for ten years masquerading clinically as filariasis. A provisional diagnosis of benign nerve sheath neoplasm was made based on cytology findings. The lump was surgically removed from the patient, and a histopathological and immunohistochemistry examination established the diagnosis of neurofibroma. The combined clinical, preoperative cytological, histological, and immunohistochemistry findings were not presented in the literature in any of the formerly documented cases of scrotal neurofibroma. The current case expands the spectrum of differential diagnoses for scrotal tumours that clinicians have previously observed.

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来源期刊
Prague medical report
Prague medical report Medicine-Medicine (all)
CiteScore
1.10
自引率
0.00%
发文量
19
审稿时长
20 weeks
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