Artigues Barceló A, Guiscafré Fontirroig P, de Miguel Sebastián P, Salgado R M, Albiol Varella M T
Servicio de Medicina Interna, Fundación Hospital de Manacor, Palma de Mallorca.
An Med Interna. 2005 Nov;22(11):535-7. doi: 10.4321/s0212-71992005001100008.
Langerhan's cell histiocytosis (LCH) is a rare disorder in which granulomatous deposits occur at multiple sites within the body. The aetiology is unknown. Is more frequent in children. Presenting symptoms are polyuria and polydipsia, due to diabetes insipidus, other symptoms are skin rash, dyspnea and tachypnea. Diagnosis is reached by biopsy of lesions, in which Langerhan's cell are found. Prognosis is variable, depending the site affected; therefore, treatment must be individually. The hyperprolactinaemia in LCH is very rare and its related with anterior pituitary deficiency. There are not many cases described, all of them during the course of the disease, not as the onset. We describe a 22 year-old woman with Langerhan's cell histiocytosis which initial presentation was fever and hyperprolactinaemia.
朗格汉斯细胞组织细胞增多症(LCH)是一种罕见疾病,其中肉芽肿沉积物出现在身体的多个部位。病因不明。在儿童中更为常见。由于尿崩症,出现的症状为多尿和烦渴,其他症状有皮疹、呼吸困难和呼吸急促。通过对病变进行活检来确诊,活检中可发现朗格汉斯细胞。预后因人而异,取决于受影响的部位;因此,治疗必须个体化。LCH中的高泌乳素血症非常罕见,且与垂体前叶功能减退有关。描述的病例不多,所有病例均在疾病过程中出现,而非在发病时。我们描述了一名22岁患有朗格汉斯细胞组织细胞增多症的女性,其最初表现为发热和高泌乳素血症。