朗格汉斯细胞组织细胞增多症:成年男性脊柱背侧异常定位。

IF 0.5 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Giovanni Foti, Chiara Longo, Fabio Lombardo, Enrico Piovan, Francesco Colpani, Alberto Beltramello
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引用次数: 0

摘要

本病例报告描述了一例朗格汉斯细胞组织细胞增多症的临床,影像学和病理特征,影响了患有慢性胸椎疼痛的患者。朗格汉斯细胞组织细胞增生症的脊柱定位很少被描述,其特征通常是椎体与溶骨病变的累及。我们的病例表现出几个不寻常的特征,包括患者的年龄和左T10肋椎交界处受累,椎体和肋骨相对保留。钆治疗后脂肪饱和t2w和t1w图像的信号强度增加,为诊断提供了线索。最终通过经皮活检和随后的组织/免疫组织化学研究证实了诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Langerhans cell histiocytosis: unusual dorsal spine localization in an adult male.

Langerhans cell histiocytosis: unusual dorsal spine localization in an adult male.

Langerhans cell histiocytosis: unusual dorsal spine localization in an adult male.

Langerhans cell histiocytosis: unusual dorsal spine localization in an adult male.

This case report describes the clinical, imaging, and pathological features of a case of Langerhans cell histiocytosis affecting a patient suffering from chronic thoracic spine pain. Spinal localizations of Langerhans cell histiocytosis have been rarely described and they are usually characterized by involvement of vertebral bodies with osteolytic lesions. Our case presented with several unusual features that delayed the diagnosis, including the age of patient and the involvement of left T10 costovertebral junction with relative sparing of vertebral body and costal bone. The clues for diagnosis were represented by increased signal intensity both on T 2W fat-saturated and T 1W images after administration of gadolinium. The diagnosis was finally confirmed by means of percutaneous biopsy with subsequent histological/immunohistochemical study.

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来源期刊
BJR Case Reports
BJR Case Reports RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING-
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审稿时长
11 weeks
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