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中枢性尿崩症:警惕朗格汉斯细胞组织细胞增多症!

Central diabetes insipidus: beware of Langerhans cell histiocytosis!

作者信息

Brys A D H, Vermeersch S, Forsyth R, Velkeniers B, Bravenboer B

机构信息

Department of Internal Medicine, Maastricht University Medical Centre, the Netherlands.

出版信息

Neth J Med. 2018 Dec;76(10):445-449.

Abstract

Langerhans cell histiocytosis (LCH) is a rare disorder, characterised by a monoclonal proliferation of aberrant histiocytes that accumulate in and infiltrate into different organs. When the hypothalamic-pituitary axis is involved, central diabetes insipidus (CDI) can be its first manifestation. Three cases of LCH with central diabetes insipidus were retrospectively analyzed: Case 1 is a 41-year old female presenting with polyuria and polydipsia. Diabetes insipidus was diagnosed and treated with desmopressin. MRI pituitary showed hypophysitis. Subsequently, she developed bone lesions and a biopsy demonstrated LCH. Case 2 is a 51-year old female presenting in 2009 with polyuria and polydipsia. Diabetes insipidus was diagnosed and treated with desmopressin. MRI pituitary revealed hypophysitis. LCH was suspected because of known pulmonary histiocytosis. Coexisting bone lesions were biopsied and confirmed LCH. Case 3 is a 44-year old female presenting with diabetes insipidus. She was treated with desmopressin as well. MRI of the pituitary gland showed impressive thickening of the infundibulum. A few months later, she developed skin lesions and a biopsy revealed LCH. Conclusively, LCH is a rare, elusive and probably underdiagnosed disease with a broad disease spectrum. Due to infiltration of the hypothalamic-pituitary axis, CDI can be the first manifestation, even before LCH is diagnosed. Therefore, LCH should be considered in the diagnostic workup of CDI.

摘要

朗格汉斯细胞组织细胞增多症(LCH)是一种罕见疾病,其特征为异常组织细胞的单克隆增殖,这些组织细胞积聚并浸润到不同器官。当下丘脑 - 垂体轴受累时,中枢性尿崩症(CDI)可能是其首发表现。回顾性分析了3例伴有中枢性尿崩症的LCH病例:病例1为一名41岁女性,表现为多尿和烦渴。诊断为尿崩症并使用去氨加压素治疗。垂体MRI显示垂体炎。随后,她出现骨病变,活检证实为LCH。病例2为一名51岁女性,于2009年出现多尿和烦渴。诊断为尿崩症并使用去氨加压素治疗。垂体MRI显示垂体炎。由于已知有肺部组织细胞增多症,怀疑为LCH。对并存的骨病变进行活检,证实为LCH。病例3为一名44岁女性,表现为尿崩症。也使用去氨加压素治疗。垂体MRI显示漏斗明显增厚。几个月后,她出现皮肤病变,活检显示为LCH。总之,LCH是一种罕见、难以捉摸且可能诊断不足的疾病,疾病谱广泛。由于下丘脑 - 垂体轴的浸润,CDI可能是首发表现,甚至在LCH被诊断之前。因此,在CDI的诊断检查中应考虑LCH。

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