霍奇金淋巴瘤后发生朗格汉斯细胞组织细胞增多症：来自伊朗的一例报告
Langerhans cell histiocytosis following Hodgkin lymphoma: a case report from Iran.
作者信息
Dehkordi Nahid Reisi, Rajabi Parvin, Naimi Azar, Heidarpour Mitra
机构信息
Assistant Professor of Pediatrics, Department of Pediatrics, Faculty of Medicine, Isfahan University of Medical Science, Isfahan, Iran.
出版信息
J Res Med Sci. 2010 Jan;15(1):58-61.
Abstract
The occurrence of Langerhans Cell Histiocytosis (LCH) in a patient with lymphoma is an indication of a probable relationship between them. The two conditions have similarities both clinically and histopathologically. Occurrence of these two conditions in the same patient, particularly not simultaneously, is rare. According to different management and treatment of these conditions, exact histopathologic evaluation and even using immunohistochemistery (IHC) can prevent misdiagnosis. In this report, a 10 year old boy presented who afflicted with LCH 3 years after diagnosis and treatment of mixed cellularity Hodgkin lymphoma.
摘要
淋巴瘤患者发生朗格汉斯细胞组织细胞增多症（LCH）表明两者之间可能存在关联。这两种病症在临床和组织病理学上都有相似之处。这两种病症出现在同一患者身上，尤其是不同时出现，是很罕见的。根据这些病症的不同管理和治疗方法，进行精确的组织病理学评估甚至使用免疫组织化学（IHC）可以防止误诊。在本报告中，一名10岁男孩在混合细胞型霍奇金淋巴瘤诊断和治疗3年后患上了LCH。
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