Curgunlu Asli, Karter Yesari, Oztürk Ayşe
Department of Internal Medicine, Istanbul University Cerrahpaşa Medical Faculty, Istanbul, Turkey
Eur J Intern Med. 2003 Feb;14(1):53-55. doi: 10.1016/s0953-6205(02)00208-x.
Erdheim-Chester disease (ECD) is a rare, non-Langerhans cell histiocytosis. It is characterized by osteosclerosis of the metaphyseal regions of long bones and several extraskeletal manifestations. Clinically, it ranges from an asymptomatic focal process to systemic disease with life-threatening visceral involvement. Until now, only two cases of Erdheim-Chester disease with paraparesis have been reported. Herein we report the first case of Erdheim-Chester disease with the clinical manifestation of paraplegia. Our patient also had diabetes insipidus, pleural and pericardial effusion, retro-orbital and cavernous sinus masses, fibrotic changes in the retroperitoneal, perirenal, and periaortic areas, and epidural space-occupying lesions. We want to emphasize that ECD may be a very rare cause of paraplegia.
厄尔德海姆-切斯特病(ECD)是一种罕见的非朗格汉斯细胞组织细胞增多症。其特征为长骨干骺端区域的骨硬化以及多种骨骼外表现。临床上,它的表现范围从无症状的局灶性病变到伴有危及生命的内脏受累的全身性疾病。到目前为止,仅报道过两例伴有双下肢轻瘫的厄尔德海姆-切斯特病。在此,我们报告首例表现为截瘫的厄尔德海姆-切斯特病病例。我们的患者还患有尿崩症、胸腔和心包积液、眶后及海绵窦肿块、腹膜后、肾周和主动脉周围区域的纤维化改变以及硬膜外占位性病变。我们想强调的是,ECD可能是截瘫的一个非常罕见的病因。