Patient with Rosai-Dorfman-Destombes disease: 18F-FDG-PET/CT scan as a diagnostic tool

Luis C. Araujo Cachay
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Abstract

Rosai-Dorfman-Destombes disease (RDD) is a rare non-Langerhans cell histiocytosis, with sinus involvement and massive lymphadenopathy. RDD is usually self-limited; it can appear alone or related to other diseases. We present a 9-year-old male with biopsy of that lesion was taken, giving as result a benign histiocytosis, compatible with RDD. The patient was scanned with full body 18F-FDG PET/CT, the results of the study showed hypermetabolic focal lesions in the sphenoid sinus, ethmoid sinus, and bilateral nasal involvement with hypermetabolic focal injury in the middle third of the left tibia, findings in relation to high-grade expansive injury. The study of 18F-FDG PET/CT demonstrated avid FDG lesions at nodal and extranodal sites, and it also can be used in monitoring and/or evaluating response to treatment.
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rosai - dorfman - desstombes病患者:18F-FDG-PET/CT扫描作为诊断工具
rossai - dorfman - destombes病(RDD)是一种罕见的非朗格汉斯细胞组织细胞病,以窦性病变和大量淋巴结病变为主。RDD通常是自我限制的;它可以单独出现,也可以与其他疾病有关。我们报告一名9岁男性,病变活检结果为良性组织细胞增多症,与RDD相符。对患者进行全身18F-FDG PET/CT扫描,研究结果显示蝶窦、筛窦及双侧鼻部高代谢性局灶性损伤累及左胫骨中三分之一处高代谢性局灶性损伤,与高度扩张性损伤有关。18F-FDG PET/CT的研究显示结节和结外部位有明显的FDG病变,它也可用于监测和/或评估对治疗的反应。
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来源期刊
CiteScore
1.40
自引率
0.00%
发文量
46
审稿时长
12 weeks
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