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首页> 外文期刊>International journal of dermatology >Lipedematous alopecia: an uncommon clinicopathologic variant of nonscarring but permanent alopecia.
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Lipedematous alopecia: an uncommon clinicopathologic variant of nonscarring but permanent alopecia.

机译:脂溢性脱发:一种非瘢痕性但永久性脱发的罕见临床病理变异。

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摘要

A 52-year-old black woman presented with a 5-year history of gradual swelling and slowed hair growth involving the vertex and both parietal regions of the scalp. Gradually, the swelling progressed to involve the entire scalp, only sparing a peripheral crown. She reported no history of trauma or medications. Slight pruritus of the involved area was the only accompanying symptom. There was no family history of a similar condition. Her past medical history included surgery for ovarian cysts, 10 years previously, and cholelithiasis. Physical examination revealed diffuse hair thinning and alopecia, more prominent along the vertex and parietal regions (Fig. 1a). There was no evidence of scalp inflammation, scaling, or increased hair fragility. The scalp was mildly tender on palpation and had a boggy, spongy consistency. The hairs which still remained in the involved areas were thin, short, and soft (Fig. 1b). The involved area was slightly hypopigmented when compared with adjacent noninvolved scalp. The restof the physical examination was within normal limits. No abnormalities of the hair shaft were observed on microscopic examination of several plucked hairs. Laboratory investigations, including a complete blood cell count, blood chemistry, urinalysis, sedimentation rate, antinuclear antibodies, and serologic tests for syphilis, hepatitis B and C virus, and human immunodeficiency virus, were negative. A computed tomography scan of the skull demonstrated diffuse and regular thickening of subcutaneous fatty tissue of the scalp, disclosing a maximum scalp thickness of 15 mm at the vertex (Fig. 2). The biopsy from the vertex revealed a normal epidermis and dermis, with diffuse loss of hair follicles. The most striking feature consisted of a large increase in thickness of the subcutaneous fatty tissue (Fig. 3a). Pre-existing hair follicles were replaced by vertical fibrous tracts of lamellar fibroplasia with no inflammatory infiltrate (Fig. 3b). Adipocytes showed a normal size and shape, but the connective tissue septa, which are normally present separating the subcutaneous tissue into fat lobules, were lacking, and subcutaneous fatty tissue consisted of a continuous and diffuse sheet of mature adipocytes (Fig. 3c). Orcein stain revealed normal contents of elastic fibers with foci of condensation at the sites of disappeared pre-existing hair follicles (Fig. 3d). Colloidal iron and Alcian blue (pH 2.5) stains revealed no mucin deposits.
机译:一名52岁的黑人妇女有5年的逐渐肿胀和头发生长缓慢的病史,涉及到头皮的顶角和两个顶叶区域。肿胀逐渐蔓延至整个头皮,仅保留了周围的冠部。她没有外伤史或药物治疗史。唯一的症状是受累部位轻微瘙痒。没有类似情况的家族史。她过去的病史包括10年前的卵巢囊肿手术和胆石症。体格检查发现弥漫性的头发稀疏和脱发,在顶和顶区域更为突出(图1a)。没有证据表明头皮发炎,脱屑或头发脆弱。头皮在触诊时有轻微的触痛,并有松软的海绵状稠度。仍留在受累区域的毛发稀薄,短而柔软(图1b)。与邻近的非累及头皮相比,累及区域的色素沉着轻微。其余的体格检查均在正常范围内。通过显微镜检查几根拔出的头发,未观察到发干异常。实验室检查为阴性,包括全血细胞计数,血液化学,尿液分析,沉降率,抗核抗体以及梅毒,乙型和丙型肝炎病毒以及人类免疫缺陷病毒的血清学检查。头颅的计算机断层扫描显示头皮下脂肪组织的扩散和规则增厚,揭示了在顶点的最大头皮厚度为15 mm(图2)。顶点活检显示表皮和真皮正常,毛囊弥漫性丢失。最显着的特征是皮下脂肪组织的厚度大大增加(图3a)。原有的毛囊被片状纤维化的垂直纤维束所取代,没有炎性浸润(图3b)。脂肪细胞显示出正常的大小和形状,但缺乏将皮下组织分隔为小叶的正常存在的结缔组织隔,皮下脂肪组织由成熟的脂肪细胞的连续且分散的片组成(图3c)。 Orcein染色显示弹性纤维含量正常,在已存在的毛囊消失的部位出现凝结点(图3d)。胶态铁和阿尔辛蓝(pH 2.5)染色显示没有粘蛋白沉淀。

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