Wang Juan, Zheng Yan, Xiong Ying
Department of Radiology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Department of Pathology, The Fifth Hospital of Xiamen, Xiamen, China.
Front Oncol. 2024 Feb 22;14:1333519. doi: 10.3389/fonc.2024.1333519. eCollection 2024.
ALK-positive histiocytosis is an exceptionally rare neoplasm of histiocytes that predominantly involves the nervous system and can also affect the skin and other parts of the body. Previous relevant literature has provided limited information regarding the imaging manifestations of this disease with neurological involvement.
We reported a case of ALK-positive histiocytosis with multisystem involvement. Together with a comprehensive literature review, the imaging characteristics of this disease in the nervous system were summarized.
A 3-year-old girl with abdominal pain and ambulation difficulty checked in at the Department of Pediatric Neurology. The initial diagnosis was "acute cerebellitis with ataxia" based on the elevated protein level in the cerebrospinal fluid (CSF). However, despite 3 months of treatment, her condition deteriorated. MRI showed an oval-shaped, intradural extramedullary nodule at the T6-T7 level. The patient was ultimately diagnosed as ALK-positive histiocytosis, accompanied by cauda equina and skin involvement. The literature review showed a total of 23 patients who had involvement of the nervous system and provided imaging descriptions. Together with our case, the imaging features were summarized as follows: iso-dense or slightly hyperdense on computed tomography (CT), isointense or iso-hypointense on T2-weighted imaging (T2WI), moderate homogeneous enhancement with mildly/markedly punctate enhancement or/and smooth ring enhancement on contrast-enhanced T1-weighted imaging (T1WI), restricted diffusion on diffuse weighted imaging (DWI), and elevated fluorodeoxyglucose (FDG) uptake on positron-emission tomography/computed tomography (PET/CT).
The multimodal imaging findings of ALK-positive histiocytosis exhibit distinct characteristics, familiarity with which will enhance radiologists' expertise and facilitate accurate diagnosis of this disease.
ALK 阳性组织细胞增多症是一种极其罕见的组织细胞肿瘤,主要累及神经系统,也可影响皮肤和身体其他部位。先前的相关文献关于该疾病累及神经系统的影像学表现提供的信息有限。
我们报告了 1 例多系统受累的 ALK 阳性组织细胞增多症病例。结合全面的文献复习,总结了该疾病在神经系统的影像学特征。
一名 3 岁女童因腹痛和行走困难入住小儿神经科。基于脑脊液(CSF)中蛋白水平升高,初步诊断为“急性小脑炎伴共济失调”。然而,尽管经过 3 个月的治疗,她的病情仍恶化。MRI 显示 T6 - T7 水平有一个椭圆形的硬膜内髓外结节。患者最终被诊断为 ALK 阳性组织细胞增多症,伴有马尾和皮肤受累。文献复习显示共有 23 例累及神经系统并提供了影像学描述的患者。结合我们的病例,影像学特征总结如下:计算机断层扫描(CT)上呈等密度或稍高密度,T2 加权成像(T2WI)上呈等信号或等低信号,对比增强 T1 加权成像(T1WI)上呈中等均匀强化,伴有轻度/明显点状强化或/和平滑环状强化,扩散加权成像(DWI)上有扩散受限,正电子发射断层扫描/计算机断层扫描(PET/CT)上氟脱氧葡萄糖(FDG)摄取增加。
ALK 阳性组织细胞增多症的多模态影像学表现具有独特特征,熟悉这些特征将提高放射科医生的专业水平并有助于准确诊断该疾病。