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西瓦特皮肤异色病:一项组织病理学与超微结构研究。

Poikiloderma of Civatte: a histopathological and ultrastructural study.

作者信息

Katoulis A C, Stavrianeas N G, Panayiotides J G, Bozi E, Vamvasakis E, Kalogeromitros D, Georgala S

机构信息

2nd Department of Dermatology and Venereology, Attikon University General Hospital, Athens, Greece.

出版信息

Dermatology. 2007;214(2):177-82. doi: 10.1159/000098580.

Abstract

BACKGROUND

Poikiloderma of the face and neck (Civatte) has not been studied in depth for decades, especially as far as the histopathology is concerned.

MATERIAL AND METHODS

We studied 50 consecutive patients with poikiloderma of Civatte (PC). Their evaluation included: history, physical examination, lesional skin biopsy and histological examination of sections stained with hematoxylin-eosin, PAS, Fontana-Masson, acid orcein Giemsa for elastic fibers and toluidine blue for mast cells. In 10 randomly selected subjects, a second skin biopsy was performed and specimens were examined under the electron microscope.

RESULTS

There were 34 females (68%) and 16 males. The mean age at diagnosis was 47.8 years for females and 61.7 years for males. Histological examination revealed an atrophic (62%), flattened (84%) epidermis with hyperkeratosis (92%) and occasional follicular plugging (34%). In some cases, mild hydropic degeneration of the basal cell layer was evident (46%). Melanin was irregularly distributed in the lower epidermis (94%), and melanophages were often present in the dermis (92%). The most prominent and constant feature (100%) was solar elastosis of the papillary dermis. The blood vessels were almost invariably dilated (96%) with a mild perivascular lymphohistiocytic infiltrate (78%), sometimes with plasmacytes (56%). At the ultrastructural level, the epidermis showed only minor changes. The dermoepidermal junction was intact. The most constant findings were swelling and disruption of the collagen fibers as well as focal degeneration of the collagen bundles. Occasionally, several vacuolar spaces were found just under the basal lamina. Melanin-laden macrophages scattered in the dermis were also detected.

CONCLUSIONS

PC shows distinct histological and ultrastructural features, supporting the theory that it represents a separate entity. The histology of PC is characteristic but not pathognomonic. On this basis, the differential diagnosis from Riehl's melanosis, poikiloderma atrophicans et vasculare and other acquired poikilodermas can be made. Ultrastructural findings were consistent with the histological findings. Changes of the dermal connective tissue (solar elastosis) predominated, providing morphological evidence for the role of ultraviolet radiation in the pathogenesis of PC.

摘要

背景

面部和颈部皮肤异色症(西瓦特氏病)几十年来一直未得到深入研究,尤其是在组织病理学方面。

材料与方法

我们对50例连续性面部和颈部皮肤异色症(PC)患者进行了研究。对他们的评估包括:病史、体格检查、皮损皮肤活检以及对苏木精 - 伊红染色、PAS染色、Fontana - Masson染色、酸性orcein Giemsa染色(用于弹性纤维)和甲苯胺蓝染色(用于肥大细胞)的切片进行组织学检查。在10例随机选择的受试者中进行了第二次皮肤活检,并将标本置于电子显微镜下检查。

结果

有34名女性(68%)和16名男性。女性诊断时的平均年龄为47.8岁,男性为61.7岁。组织学检查显示表皮萎缩(占62%)、扁平(占84%),伴有角化过度(占92%),偶尔有毛囊堵塞(占34%)。在某些病例中,基底细胞层有轻度水样变性(占46%)。黑色素在表皮下层分布不规则(占94%),真皮中常可见噬黑素细胞(占92%)。最突出且始终存在的特征(占100%)是乳头层真皮的日光性弹力纤维变性。血管几乎总是扩张的(占96%),伴有轻度血管周围淋巴细胞 - 组织细胞浸润(占78%),有时还有浆细胞(占56%)。在超微结构水平上,表皮仅显示轻微变化。真皮 - 表皮连接完整。最常见的发现是胶原纤维肿胀和断裂以及胶原束的局灶性变性。偶尔,在基膜下方发现几个空泡间隙。在真皮中还检测到散在的含黑色素巨噬细胞。

结论

面部和颈部皮肤异色症显示出独特的组织学和超微结构特征,支持其为一个独立实体的理论。面部和颈部皮肤异色症的组织学具有特征性但并非特异性。在此基础上,可以与里尔氏黑变病、萎缩性血管性皮肤异色症及其他后天性皮肤异色症进行鉴别诊断。超微结构发现与组织学发现一致。真皮结缔组织的变化(日光性弹力纤维变性)占主导,为紫外线辐射在面部和颈部皮肤异色症发病机制中的作用提供了形态学证据。

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