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鳞状不全角化病中的角质形成细胞。

Corneocytes in scaly parakeratotic diseases.

作者信息

Amer M, Mostafa F F, Tosson Z, Nasr A N

机构信息

Department of Dermatology, University of Zagazig, Faculty of Medicine, Egypt.

出版信息

Int J Dermatol. 1996 Jun;35(6):417-21. doi: 10.1111/j.1365-4362.1996.tb03024.x.

DOI:10.1111/j.1365-4362.1996.tb03024.x
PMID:8737877
Abstract

BACKGROUND AND OBJECTIVES

The stratum corneum of some of the scaly (parakeratotic) diseases was examined with light and scanning electron microscopy (SEM) with the purpose to reveal the importance of this layer in the diagnosis of some of the diseases associated with the formation of scales.

MATERIALS AND METHODS

Two biopsies of the skin surface were taken: one, obtained from 80 patients with various parakeratotic scaly diseases and from 25 control subjects, was processed for light microscopy; the other biopsy for SEM was taken from 10 control subjects and 25 patients. The diagnoses of these patients were: psoriasis (5 patients), erythrodermic psoriasis (2 subjects), parapsoriasis (5 patients), pityriasis rubra pilaris (5 subjects), pityriasis rosea (3 subjects), and seborrheic dermatitis (5 subjects).

RESULTS

The light microscopic studies showed that normal corneocytes are of polygonal shape with their largest diameter measuring 42 microns; these cells lacked nuclei. All parakeratotic cells appeared bizarre in shape, smaller than normal, and the cells contained a nucleus. With SEM, normal cells appeared relatively regular in size and shape, trabeculated, and had a flat surface. Cells examined in all the diseases revealed various sizes, outlines, and trabeculae. Specific surface patterns (print) of diseased cells were: "fish-scale" in psoriasis; "marbled" in parapsoriasis, "rocky stone" in pityriasis rubra pilaris; "heart-shaped" in seborrheic dermatitis, and semicrystalloid in pityriasis rosea.

CONCLUSIONS

Parakeratosis is characterized not only by the retention of the nucleus in keratinocytes, but is also characterized by a cell of smaller size. The specific print of a disease helps in the diagnosis. The print will change with different stages of a disease.

摘要

背景与目的

运用光学显微镜和扫描电子显微镜(SEM)对部分鳞屑性(角化不全)疾病的角质层进行检查,旨在揭示该层在某些与鳞屑形成相关疾病诊断中的重要性。

材料与方法

采集两份皮肤表面活检样本:一份取自80例患有各种角化不全性鳞屑疾病的患者以及25名对照者,用于光学显微镜检查;另一份用于SEM检查的活检样本取自10名对照者和25例患者。这些患者的诊断结果为:银屑病(5例)、红皮病型银屑病(2例)、副银屑病(5例)、毛发红糠疹(5例)、玫瑰糠疹(3例)以及脂溢性皮炎(5例)。

结果

光学显微镜研究显示,正常角质形成细胞呈多边形,最大直径为42微米;这些细胞无细胞核。所有角化不全细胞形状怪异,比正常细胞小,且含有细胞核。通过SEM观察,正常细胞在大小和形状上相对规则,呈小梁状,表面平坦。在所有疾病中检查的细胞呈现出各种大小、轮廓和小梁。患病细胞的特定表面模式(印记)为:银屑病呈“鱼鳞状”;副银屑病呈“大理石状”;毛发红糠疹呈“岩石状”;脂溢性皮炎呈“心形”;玫瑰糠疹呈半晶体状。

结论

角化不全不仅表现为角质形成细胞核的保留,还表现为细胞尺寸较小。疾病的特定印记有助于诊断。印记会随疾病的不同阶段而变化。

相似文献

1
Corneocytes in scaly parakeratotic diseases.鳞状不全角化病中的角质形成细胞。
Int J Dermatol. 1996 Jun;35(6):417-21. doi: 10.1111/j.1365-4362.1996.tb03024.x.
2
Sherlock Holmesian dermatopathology. Parakeratosis as a diagnostic clue.
Am J Surg Pathol. 1978 Mar;2(1):71-80. doi: 10.1097/00000478-197803000-00008.
3
Psoriasiform and related papulosquamous disorders.银屑病样及相关丘疹鳞屑性疾病。
J Cutan Pathol. 1985 Oct;12(5):412-25. doi: 10.1111/j.1600-0560.1985.tb00439.x.
4
Papulosquamous diseases: a review.丘疹鳞屑性疾病:综述
J Am Acad Dermatol. 1985 Apr;12(4):597-624. doi: 10.1016/s0190-9622(85)70084-9.
5
[Ultrastructure of parapsoriasis lesions. Parapsoriasis en plaques and parakeratosis variegata as prelymphoma; differences from pityriasis lichenoides].[副银屑病皮损的超微结构。斑块状副银屑病和斑驳性角化不全作为淋巴瘤前期病变;与点滴状副银屑病的区别]
Z Hautkr. 1982 Aug 15;57(16):1209-24.
6
Exfoliative cytology of psoriasis and other common dermatoses. Quantitative analysis of parakeratotic horny cells in 266 patients.银屑病及其他常见皮肤病的脱落细胞学。266例患者角化不全角质形成细胞的定量分析。
Arch Dermatol. 1972 Oct;106(4):476-83.
7
[Histological differential diagnosis of psoriasis vulgaris and seborrheic eczema of the scalp].[寻常型银屑病与头皮脂溢性湿疹的组织学鉴别诊断]
Hautarzt. 1979 Sep;30(9):478-83.
8
Psoriasis: odd varieties in the adult.银屑病:成人中的罕见类型。
Acta Derm Venereol Suppl (Stockh). 1979;87:90-4.
9
Differential diagnosis of psoriasis.银屑病的鉴别诊断。
Reumatismo. 2007;59 Suppl 1:56-60.
10
Parakeratosis in skin is associated with loss of inhibitor of differentiation 4 via promoter methylation.皮肤的角化不全与分化抑制因子 4 通过启动子甲基化的丢失有关。
Hum Pathol. 2011 Dec;42(12):1878-87. doi: 10.1016/j.humpath.2011.02.005. Epub 2011 Jun 12.

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