Langerhans Cell Histiocytosis in the Nasal Bone: A Rare Case.

Q4 Medicine
Won Ik Ahn, Jong Chang Jang, Dong Jin Yang, Tae Eun Kim, Hyou Chun Park, Dong Kyu Lee, Jae Min Seong
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引用次数: 0

Abstract

Nasal bone involvement of Langerhans cell histiocytosis is rarely reported. Here we present a case of a 13-year-old boy with a palpable nasal mass. Ultrasonography revealed a hypoechoic mass on the left side of the nose. Both CT scanning and MRI showed an osteolytic mass. The lesion seen on MRI was well-defined mass with homogeneous enhancement. Histopathological examination of the resected specimen confirmed the diagnosis of LCH.

Abstract Image

朗格汉斯细胞组织细胞增多症在鼻骨:一个罕见的病例。
朗格汉斯细胞组织细胞增多症累及鼻骨的报道很少。我们在此报告一个13岁男孩的病例,他有可触及的鼻肿块。超声检查显示鼻子左侧有一个低回声肿块。CT及MRI均显示溶骨性肿块。MRI上病灶为清晰的肿块,均质强化。切除标本的组织病理学检查证实了LCH的诊断。
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来源期刊
Journal of the Korean Society of Radiology
Journal of the Korean Society of Radiology Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
0.40
自引率
0.00%
发文量
98
审稿时长
16 weeks
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