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Laugier–Hunziker syndrome in endocrine clinical practice

机译:Laugier–Hunziker综合征在内分泌临床实践中的应用

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SummaryLaugier–Hunziker syndrome (LHS) is a rare, benign and acquired disorder characterized by hyperpigmentation of the oral cavity and lips along with longitudinal melanonychia. No underlying systemic abnormalities or malignant predisposition is associated with it. In everyday clinical practice, an endocrinologist encounters certain endocrine conditions (e.g. Addison’s disease, McCune–Albright syndrome) that present with, inter alia, mucocutaneous hyperpigmentation. Even though LHS is easily distinguished from endocrine entities mentioned earlier, diagnostic evaluation usually requires skilled and thorough practitioner. Since it is the diagnosis of exclusion, a number of systemic conditions must be ruled out prior to making the final diagnosis. However, its major differential diagnosis is primarily Peutz-Jeghers syndrome, which carries an increased risk of cancer. Here, we report a case of a young woman who was referred to the endocrinologist for diagnostic evaluation of dark-colored lesions of the oral cavity and nails. All performed laboratory tests were within reference range. Endoscopic gastrointestinal evaluation did not reveal neoplastic formations. Owing to an adult-onset, asymptomatic clinical course and negative diagnostic findings, we made a final diagnosis. In this case, target diagnostic evaluation notably reduced the need for additional expensive and invasive procedures and treatments.Learning points:Laugier–Hunziker syndrome is a rare, acquired cause of asymptomatic, benign mucocutaneous hyperpigmentation.Prior to making a final diagnosis, certain medical entities with overlapping clinical features must be excluded.Endocrine conditions that usually present with the hyperpigmentation of the skin and mucous membranes (e.g. Addison’s disease, McCune–Albright syndrome) can be easily ruled out based on clinical and laboratory findings.Its major differential diagnosis, Peutz-Jeghers syndrome is characterized by melanotic macules of the face and mouth, intestinal polyposis and significantly increased risk of different types of cancer, especially gastrointestinal.Anamnesis, physical examination and target diagnostic evaluation reduce the need for additional invasive and expensive procedures and treatment.
机译:小结Laugier–Hunziker综合征(LHS)是一种罕见,良性和获得性疾病,其特征是口腔和嘴唇色素沉着以及纵向黑色素瘤。没有潜在的全身异常或恶性倾向。在日常临床实践中,内分泌科医生会遇到某些内分泌疾病(例如,Addison病,McCune-Albright综合征),其中包括皮肤粘膜色素沉着过多。即使很容易将LHS与前面提到的内分泌实体区分开来,诊断评估通常也需要熟练而透彻的从业人员。由于它是排除疾病的诊断,因此在做出最终诊断之前,必须排除许多系统性疾病。但是,其主要的鉴别诊断主要是Peutz-Jeghers综合征,它增加了患癌症的风险。在这里,我们报告了一名年轻女子的案例,该女子被转诊至内分泌科医生,以对口腔和指甲的深色病变进行诊断评估。所有进行的实验室测试均在参考范围内。内窥镜胃肠道评估未发现肿瘤形成。由于成人发作,无症状临床过程和阴性诊断结果,我们做出了最终诊断。在这种情况下,目标诊断评估显着减少了对其他昂贵和侵入性程序和治疗的需求。学习要点:Laugier-Hunziker综合征是一种罕见的获得性无症状,良性粘膜皮肤色素沉着的原因。在做出最终诊断之前,某些医疗机构根据临床和实验室检查结果,可以很容易地排除通常表现为皮肤和粘膜色素沉着过度的内分泌疾病(例如,艾迪生氏病,麦肯-奥尔布赖特综合症)。 -Jeghers综合征的特征是面部和嘴部黑色素斑,肠息肉病以及显着增加不同类型癌症(尤其是胃肠道癌症)的风险,而病历,体格检查和目标诊断评估减少了对额外侵入性和昂贵程序及治疗的需求。

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