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唐氏综合征相关粟粒疹样皮肤钙质沉着症:一例新病例并文献复习。

Milia-like calcinosis cutis in Down syndrome: a new case with a review of the literature.

机构信息

Section of Dermatology and Venereology, Department of Medicine, University of Verona, Verona.

出版信息

Dermatol Online J. 2021 Aug 15;27(8). doi: 10.5070/D327854695.

Abstract

We report an 11-year-old girl who presented with white papules on the dorsal and palmar region of the hands bilaterally. The parents reported that the lesions had appeared four months before and some had resolved spontaneously. The girl was suffering from celiac disease, Down syndrome, and alopecia areata treated with topical corticosteroids. At the first visit, the girl presented with alopecia areata, corticosteroid acne, and a dozen white papules located on the hands. On dermoscopy, a whitish structureless area was seen. Histological examination showed the presence of calcium deposits without tissue damage, thus confirming the diagnosis of milia-like idiopathic calcinosis cutis. At 6-month follow up, the lesions had completely disappeared. Milia-like idiopathic calcinosis cutis is a benign cutaneous disorder consisting of calcium deposits in an apparently undamaged dermis and is typically associated with Down syndrome. Up to a quarter of patients have coexisting syringomas. The milia-like papules tend to self-resolve as patients reach adulthood, so a wait-and-see approach is recommended.

摘要

我们报告了一例 11 岁女孩,她双侧手掌背部和掌部出现白色丘疹。父母报告说,这些病变在四个月前出现,有些已经自行消退。该女孩患有乳糜泻、唐氏综合征和斑秃,曾接受过局部皮质类固醇治疗。初次就诊时,该女孩患有斑秃、皮质类固醇性痤疮和十几颗位于手部的白色丘疹。在皮肤镜下,可见白色无结构区域。组织学检查显示存在钙沉积而无组织损伤,从而确诊为粟粒样特发性钙沉着症。6 个月随访时,皮损完全消失。粟粒样特发性钙沉着症是一种良性皮肤疾病,由真皮中明显无损伤的钙沉积引起,通常与唐氏综合征有关。多达四分之一的患者存在共存的汗管瘤。粟粒样丘疹随着患者成年后往往会自行消退,因此建议采取观望态度。

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