Department of Internal Medicine, Carle Foundation Hospital, Urbana, Illinois, USA
Pathology and Lab Sciences, Carle Foundation Hospital, Urbana, Illinois, USA.
BMJ Case Rep. 2021 Apr 16;14(4):e237236. doi: 10.1136/bcr-2020-237236.
Langerhans cell histiocytosis (LCH) is an uncommon group of disorders, which can be either localised or systemic, characterised by abnormal proliferation of monocytes, macrophages and dendritic cells. These disorders represent an aberrant response of myeloid progenitor cells. Bones are the most commonly affected organ but there can be involvement of the skin, lungs, liver and spleen. Renal involvement, however, is rare. LCH is the most commonly seen in children but certain rare forms such as Erdheim-Chester disease can be seen in adults. In this report, we present a case of clear cell renal adenocarcinoma (CCRC) admixed with LCH in a patient with history of smoking and presenting with abdominal pain and heamaturia. Imaging revealed left renal lesion and subsequently left renal nephrectomy was performed with tissue biopsy showing grade 3 clear cell renal cell carcinoma admixed with neoplastic LCH.
朗格汉斯细胞组织细胞增生症(LCH)是一组罕见的疾病,可分为局限性或全身性,其特征是单核细胞、巨噬细胞和树突状细胞的异常增殖。这些疾病代表骨髓祖细胞的异常反应。骨骼是最常受影响的器官,但皮肤、肺部、肝脏和脾脏也可能受累。然而,肾脏受累很少见。LCH 最常见于儿童,但某些罕见形式,如 Erdheim-Chester 病,可发生于成年人。在本报告中,我们介绍了一例吸烟史患者,因腹痛和血尿就诊,其左肾病变,左肾切除术,组织活检显示 3 级透明细胞肾细胞癌伴肿瘤性 LCH。