Department of Radiology, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul 137-701, Korea.
Korean J Radiol. 2013 May-Jun;14(3):520-4. doi: 10.3348/kjr.2013.14.3.520. Epub 2013 May 2.
Langerhans cell sarcoma (LCS) is a neoplastic proliferation of Langerhans cells with malignant cytological features and multi-organ involvement that typically has a poor prognosis. We experienced 2 cases of LCS in children less than 2 years of age and report them based primarily on CT and MR findings. Both children had findings of hepatosplenomegaly with low-attenuation nodular lesions, had multiple lymphadenopathy, and had shown recurrent lesions invading the skull during follow-up after chemotherapy.
朗格汉斯细胞肉瘤(LCS)是一种朗格汉斯细胞的肿瘤性增生,具有恶性细胞学特征和多器官受累,通常预后不良。我们在 2 岁以下的儿童中遇到了 2 例 LCS,并主要根据 CT 和 MR 发现报告了这些病例。两个孩子均有肝脾肿大和低衰减结节性病变,有多处淋巴结病,并在化疗后随访期间出现了反复发作的侵犯颅骨的病变。