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原发性皮肤淀粉样变:一项临床、组织病理学及免疫荧光研究。

Primary Cutaneous Amyloidosis: A Clinical, Histopathological and Immunofluorescence Study.

作者信息

Mehrotra Krati, Dewan Rupali, Kumar Jagannath V, Dewan Abhinav

机构信息

Senior Resident, Department of Dermatology, Venereology and Leprosy, Dr. Baba Saheb Ambedkar Medical College and Hospital, New Delhi, India.

Professor, Department of Obstetrics and Gynecology, Vardhman Mahavir Medical College and Safdarjang Hospital, New Delhi, India.

出版信息

J Clin Diagn Res. 2017 Aug;11(8):WC01-WC05. doi: 10.7860/JCDR/2017/24273.10334. Epub 2017 Aug 1.

Abstract

INTRODUCTION

Primary Localized Cutaneous Amyloidosis (PLCA) is a relatively rare chronic condition characterized by amyloid deposition in dermis without associated deposits in internal organs. Histopathology of cutaneous amyloidosis using Haematoxylin and Eosin (H&E) stain shows eosinophilic hyaline material in papillary dermis, which can be further confirmed by Congo Red (CR) staining or Direct Immunofluorescence (DIF) Test or immunohistochemistry.

AIM

To assess the concordance between the clinical, histo pathological and DIF findings in various subtypes of (PLCA).

MATERIALS AND METHODS

Data was collected from patients attending the Outpatient Department (OPD) at a tertiary care centre in Karnataka, India, over a period of one and half years. A total of 50 patients with clinical features suggestive of cutaneous amyloidosis were subjected to histopathological examination with H&E, CR stain and immunofluorescence.

RESULTS

Among 50 clinically suspected patients, the most common subtype was macular amyloidosis (70%) and lichen amyloidosis seen only in 16%. A biphasic pattern comprising of both macular and lichen amyloidosis was seen in 14% cases. Extensor aspect of the arm was the most frequently (76%) involved area. All the cases had multiple site involvement. Immunofluorescence positivity was 88% as compared to 86% on histopathology using CR stain. Amyloid deposits were detected in 80% of clinically diagnosed macular amyloidosis cases by histopathology using CR stain and in 85.7% by DIF, whereas in 5.7% cases, it was not detectable by both CR stain and DIF. Both immunofluorescence and CR staining were able to detect amyloid in all the cases of lichen amyloidosis. In biphasic amyloidosis, amyloid was detected in 100% cases on histopathology versus 85.7% cases on immunofluorescence.

CONCLUSION

CR stain and DIF are complimentary to each other for detection of macular amyloidosis. In case of lichen and biphasic amyloidosis, both CR and DIF are comparable modalities.

摘要

引言

原发性局限性皮肤淀粉样变(PLCA)是一种相对罕见的慢性疾病,其特征是淀粉样蛋白沉积于真皮,而内部器官无相关沉积。使用苏木精和伊红(H&E)染色的皮肤淀粉样变组织病理学显示乳头真皮中有嗜酸性透明物质,这可通过刚果红(CR)染色、直接免疫荧光(DIF)试验或免疫组织化学进一步证实。

目的

评估(PLCA)各亚型的临床、组织病理学和DIF结果之间的一致性。

材料与方法

在印度卡纳塔克邦的一家三级医疗中心,收集了门诊(OPD)患者在一年半时间内的数据。共有50例具有皮肤淀粉样变临床特征的患者接受了H&E、CR染色和免疫荧光的组织病理学检查。

结果

在50例临床疑似患者中,最常见的亚型是斑状淀粉样变(70%),苔藓样淀粉样变仅占16%。14%的病例表现为斑状和苔藓样淀粉样变的双相模式。手臂伸侧是最常受累的部位(76%)。所有病例均有多个部位受累。免疫荧光阳性率为88%,而使用CR染色的组织病理学阳性率为86%。在临床诊断为斑状淀粉样变的病例中,80%通过使用CR染色的组织病理学检测到淀粉样蛋白沉积,85.7%通过DIF检测到,而在5.7%的病例中,CR染色和DIF均未检测到。免疫荧光和CR染色在所有苔藓样淀粉样变病例中均能检测到淀粉样蛋白。在双相淀粉样变中,组织病理学检测到淀粉样蛋白的病例为100%,免疫荧光检测到的病例为85.7%。

结论

CR染色和DIF在检测斑状淀粉样变方面相互补充。在苔藓样和双相淀粉样变的情况下,CR和DIF都是可比的方法。

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