monoclonal gammopathy and skin changes syndrome

  • 文章类型: Case Reports
    苔藓粘液症(LM)是一种特发性皮肤粘液病,和未知意义的单克隆丙种球蛋白病(MGUS)是一种肿瘤前浆细胞疾病,球蛋白单克隆增加。LM合并单克隆丙种球蛋白病的患者通常被诊断为巩膜水肿。然而,我们报告了一例全身性丘疹合并MGUS的78岁男性,最终被诊断为非典型或中间形式的LM,因为它只累及皮肤,病理类型与巩膜水肿不一致。很少有非典型或中间形式的LM报告,因此,LM的非典型或中间形式的过程是不可预测的。我们报告了一例非典型形式的LM的诊断和治疗,以讨论对该疾病的当前认识,以期为本病的临床研究提供参考。
    Lichen myxedematosus (LM) is an idiopathic cutaneous mucinosis disorder, and monoclonal gammopathy of undetermined significance (MGUS) is a preneoplastic plasma cell disease with a monoclonal increase in globulin. Patients with LM combined with monoclonal gammopathy are normally diagnosed with scleromyxedema. However, we report a case of generalized papules combined with MGUS in a 78-year-old man who was eventually diagnosed with atypical or intermediate forms of LM because it only involved the skin, and the pathological type was not consistent with scleromyxedema. Few cases of atypical or intermediate forms of LM have been reported, so the course of atypical or intermediate forms of LM is unpredictable. We report the diagnosis and treatment of a case of atypical forms of LM to discuss the current understanding of the disease, hoping to provide a reference for clinical research on this disease.
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  • 文章类型: Case Reports
    我们报道了一名47岁的男性患者的头部色素沉着,脸和手,最初被诊断为原发性肾上腺功能不全(Addison病)。实验室测试,影像学和体格检查显示亚临床甲状腺功能减退症,高循环催乳素和雌二醇浓度,妇科乳房发育症,淋巴结病,脾肿大和双下肢无力。这些发现使我们考虑该患者是否存在单个或多个疾病。的确,艾迪生的疾病可以代表更广泛的全身性疾病的一个方面。因此,我们做了进一步的检查,并发现高血清M蛋白(5.1%)和血管内皮生长因子[1005.30pg/mL(正常范围0至142pg/mL)]浓度。因此,我们诊断出多发性神经病,器官肿大,内分泌病,单克隆丙种球蛋白病和皮肤变化(POEMS)综合征。因此,当单个疾病不能完全解释一个患者的多种症状和体征时,临床医生应考虑出现更广泛综合征的可能性,并进行更详细的诊断测试.
    We report the case of a 47-year-old male patient with pigmentation of the head, face and hands, who was initially diagnosed as having primary adrenal insufficiency (Addison\'s disease). Laboratory testing, imaging and physical examination revealed subclinical hypothyroidism, high circulating prolactin and oestradiol concentrations, gynaecomastia, lymphadenopathy, splenomegaly and weakness of both lower limbs. These findings led us to consider whether a single or multiple diseases were present in this patient. Indeed, Addison\'s disease can represent one aspect of a wider systemic disease. Therefore, we performed further examinations, and found high serum M protein (5.1%) and vascular endothelial growth factor [1005.30 pg/mL (normal range 0 to 142 pg/mL)] concentrations. As a consequence, we diagnosed polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy and skin changes (POEMS) syndrome. Consequently, when a single disease cannot fully explain the multiple symptoms and signs of one patient, clinicians should consider the possibility of the presence of a wider syndrome and undertake more detailed diagnostic testing.
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