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   incontinence 在 皮肤病与性病 分类中 的翻译结果: 查询用时:0.708秒
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incontinence    
相关语句
  失禁
    A Case of Incontinence Pigment
    色素失禁症1例
短句来源
    A Case of Incontinence Pigmenti with Pust
    色素失禁症1例
短句来源
    Results : H. E. stain of biopsy specimen revealed that hyperkeratosis and parakeratosis in epidermis, and anomalous thickening in granular layer, and serious liquefaction of basal cell, and incontinence of pigmentation.
    结果:活检组织切片,HE染色示:表皮角化过度伴角化不全,颗粒层不规则增厚,基底细胞液化严重已融合成表皮下大疱,无大疱区域表皮和真皮分界不清。 有较多淋巴细胞在此区域以及血管周浸润,可见“色素失禁”现象。
短句来源
    The skin biopsy revealed that increased pigmentation of the basal layer and increase of melanocytes without incontinence of pigments.
    组织病理学检查示基底层色素增加和黑素细胞增多,无色素失禁
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  incontinence
Reduced contractile activity of the muscles may be one of the reasons for incontinence (enuresis).
      
Other health conditions or life experiences associated with it were hearing, incontinence and lifetime trauma exposure.
      
Risk factors associated with a fall were increasing age, male gender, type of surgery, the use of a rollator and nocturnal urinary incontinence.
      
A woman, aged 49, had a complete sensory and motor deficit of the S2-5 segments with urinary and fecal incontinence due to a neurinoma of the cauda.
      
Weakness in arms, speech difficulties, and urinary incontinence tended to be late symptoms.
      
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Objective:We report a rare case of lichen planus pemphigoides.Methods: Biopsy spci-men from the skin lesion on the back was taken for pathology and immunopathology examination. Results : H. E. stain of biopsy specimen revealed that hyperkeratosis and parakeratosis in epidermis, and anomalous thickening in granular layer, and serious liquefaction of basal cell, and incontinence of pigmentation. Direct immunofluorescence revealed linear C3 and IgG deposition in basement membrane zone(BMZ). The symptom was...

Objective:We report a rare case of lichen planus pemphigoides.Methods: Biopsy spci-men from the skin lesion on the back was taken for pathology and immunopathology examination. Results : H. E. stain of biopsy specimen revealed that hyperkeratosis and parakeratosis in epidermis, and anomalous thickening in granular layer, and serious liquefaction of basal cell, and incontinence of pigmentation. Direct immunofluorescence revealed linear C3 and IgG deposition in basement membrane zone(BMZ). The symptom was disappered and does not relapse in a year. Conclusion: Lichen planus pemphigoides is different from bullous lichen palnus and bullous pemphigoid. Treatment of the patient with fulvicin, tetracycline and niacinamide was good response.

目的:报告和分析一例少见的类天疱疮样扁平苔藓病例。方法:取患者背部皮损活检组织部分行组织病理和免疫病理检查。结果:活检组织切片,HE染色示:表皮角化过度伴角化不全,颗粒层不规则增厚,基底细胞液化严重已融合成表皮下大疱,无大疱区域表皮和真皮分界不清。有较多淋巴细胞在此区域以及血管周浸润,可见“色素失禁”现象。直接免疫荧光显示基底膜有IgG、C3、IgM呈线状沉积。符合类天疱疮样扁平苔藓。经治疗后痊愈,随访一年未见复发。结论:类天疱疮样扁平苔藓临床表现和病理结果不同于大疱性扁平苔藓和大疱性类天疱疮,是一个独立的疾病。可采用灰黄霉素、四环素和烟酰胺治疗。

We reported2cases of middle-aged females,who had first noticed hypo-and hyperpigmented macules on the back8years and16years before respectively.One had shown a nonprogressive lesion since its occurrence,while another gradually developed its extent with the tendency of coalescence of hyperpigmented macules.Both of them showed localized and well de-marcated lesions without squamous,atrophic or telangiectatic conditions.Skin biopsy revealed a slightly focal atrophic epidermis and varying intensity of pigmentation...

We reported2cases of middle-aged females,who had first noticed hypo-and hyperpigmented macules on the back8years and16years before respectively.One had shown a nonprogressive lesion since its occurrence,while another gradually developed its extent with the tendency of coalescence of hyperpigmented macules.Both of them showed localized and well de-marcated lesions without squamous,atrophic or telangiectatic conditions.Skin biopsy revealed a slightly focal atrophic epidermis and varying intensity of pigmentation throughout the basal layer and pigmentary incontinence along with focal liquefaction degen-eration.Crystal violet and Congo red staining were negative.Their clinical and pathologic characteristics coincided with localized dyschromatosis.They were first two cases reported in China.The cause of dyschromatosis is still unknown.It should be distin-guished from dyschromatosis symmetrica hereditaria(DSH)and dyschromatosis universalis hereditaria(DUH).No effective treatment is available.

报告2例中年女性患者,分别于8年或16年前于背部出现色素沉着斑及色素减退斑,其中1例皮损多年未发展;另一例范围逐渐扩大,近年来色素沉着斑有融合倾向。两例患者皮损分布局限,界限清楚,皮损无鳞屑,无萎缩,未见毛细血管扩张。病理示表皮局部轻度萎缩,基底层细胞不同程度色素增加,灶性液化变性伴色素失禁,真皮无特殊改变。结晶紫、刚果红染色均阴性。临床表现及病理特点符合“限局性色素异常症”,本2例患者为国内首报病例,该病病因不清,临床特点不同于遗传性对称性色素异常症和泛发性色素异常症,治疗目前尚无有效办法。

A case of linear and whorled nevoid hypermelanosis is reported. The patient was a 17-year-old female and had pigmentary disorders since she was only two weeks after birth. The lesions were linear and whorled hyperpigmentation following the lines of Blaschko on the whole body except mucous membranes, eyes, palms, and soles. The skin biopsy revealed that increased pigmentation of the basal layer and increase of melanocytes without incontinence of pigments. This patient was diagnosed as linear and whorled...

A case of linear and whorled nevoid hypermelanosis is reported. The patient was a 17-year-old female and had pigmentary disorders since she was only two weeks after birth. The lesions were linear and whorled hyperpigmentation following the lines of Blaschko on the whole body except mucous membranes, eyes, palms, and soles. The skin biopsy revealed that increased pigmentation of the basal layer and increase of melanocytes without incontinence of pigments. This patient was diagnosed as linear and whorled nevoid hypermelanosis. This disease is often confused with other pigmented disorders, such as incontinentia pigmenti, early linear epidermal nevi.

报告1例线状和漩涡状痣样过度黑素沉着病。患者女,17岁。出生2周后周身即出现色素斑,并排列成条纹状或漩涡状,皮损面积广泛,无黏膜、眼睛、掌跖受累,损害至成年仍未消退。组织病理学检查示基底层色素增加和黑素细胞增多,无色素失禁。本病易与色素失禁症和早期线状表皮痣相混淆。

 
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