Clinical Appearance of Vitiligo and Piebaldism: A Review Article

Nanda Rachmad Putra Gofur, Aisyah Rachmadani Putri Gofur
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Abstract

Introduction: Vitiligo is idiopathic hypomelanosis characterized by the presence of white macules that can expand. Can affect all parts of the body that contain melanocyte cells, for example, hair and eyes. The cause is unknown, various trigger factors are often reported, for example emotional crisis and physical trauma. Pathogenesis of vitiligo still unclear, there is an association between vitilligo and Hashimoto’s thyroditis, pernicious anemia, and hypoparathyroid melanocytes found in the serum of 80% of vitiligo patients. Moreover, there is disease that similar to vitiligo, called piebaldism. Patches of skin that do not contain pigment that is found at birth and persists for life.The disease is inherited autosomally, due to differentiation and possibly the melanoblast membrane. Discussion: Inheritance of vitiligo can involve genes related to the biosynthesis of melanin, the response to oxidative stress and autoimmune regulation. The macula is white with a diameter of several millimeters to several centimeters, round or oval with defined boundaries, with no other epidermal changes. Hypomelanotic macules are sometimes seen in addition to apigmented macules. In vitiligo macules can be found macules with normal pigmentation or hyperpigmentation called perifollicular repigmentation. Occasionally there is a raised edge of the lesion, erythema and itching, which is called inflammatory. Piebaldism is In the form of skin patches that do not contain pigment on the forehead, median or paramedian, accompanied by white hair. White patches are sometimes also found on the upper chest, abdoment and legs. Normal skin color or hypermelanosis there are areas that are hypomelanosis. Ultrastructural investigation showed no visible melanocytes and melanosomes in hypomelanotic areas. On the other hand, hypemelanotic islets are found with melanocytes that produce melanosomes normally, but if abnormal spheric milanosomes and granules are found, abnormal spherical and ganular melanosomes are also found. Conclusion: It is distinguished from vitiligo which usually does not appear at birth, the shape and distribution are also different. On piebaldism. In piebaldism accompanied by white forlock and the presence of islets with normal pigments in hypomelanotic areas. Differentiated from the nevus with depigmentosus, in the nevus the number of melanocit is normal. If piebaldism is accompanied by abnormalities in the distance of the two pupils or is accompanied by deafness, then the possibility of Waardenburg syndrome should be considered.
白癜风和花斑病的临床表现综述
简介:白癜风是一种特发性低黑素病,其特征是存在可扩大的白色斑点。可以影响身体含有黑素细胞的所有部位,例如头发和眼睛。原因尚不清楚,经常报道各种触发因素,例如情绪危机和身体创伤。白癜风的发病机制尚不清楚,白癜风与桥本甲状腺炎、恶性贫血和80%白癜风患者血清中发现的甲状旁腺功能低下黑色素细胞有关。此外,还有一种与白癜风类似的疾病,叫做花斑病。不含色素的皮肤斑块,在出生时发现并持续一生。由于分化和可能的黑素母细胞膜,本病常染色体遗传。讨论:白癜风的遗传可能涉及与黑色素生物合成、氧化应激反应和自身免疫调节相关的基因。黄斑白色,直径几毫米至几厘米,圆形或椭圆形,边界清晰,无其他表皮变化。除了色素沉着斑外,有时还可见低黑色素斑。在白癜风中,可以发现正常色素沉着或色素沉着的斑点,称为毛囊周围再色素沉着。偶尔病灶边缘隆起,出现红斑和瘙痒,称为炎症。斑疹病是指前额、正中或旁正中出现不含色素的皮肤斑块,并伴有白发。白色斑块有时也出现在上胸部、腹部和腿部。正常肤色或黑色素过多的区域也有浅黑症。超微结构检查未见黑素细胞和黑素体。另一方面,低黑素化胰岛可见正常产生黑素小体的黑素细胞,但如发现异常的球形黑素小体和颗粒,也可发现异常的球形黑素小体和瘤样黑素小体。结论:白癜风不同于一般出生时不出现的白癜风,其形态和分布也有所不同。在斑驳病。在斑疹病中,伴有白色斑纹,在黑色素减退区存在正常色素的胰岛。与有色素沉着的痣不同,痣内黑色素的数量是正常的。如果双瞳距离异常或伴有耳聋,则应考虑Waardenburg综合征的可能性。
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