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环状肉芽肿不寻常组织学特征的评估:30例病例研究

Evaluating the Unusual Histological Aspects of Granuloma Annulare: A Study of 30 Cases.

作者信息

Chatterjee Debajyoti, Kaur Manveen, Punia R P S, Bhalla Mala, Handa Uma

机构信息

Department of Pathology, Government Medical College and Hospital, Chandigarh, India.

Department of Dermatology, Government Medical College and Hospital, Chandigarh, India.

出版信息

Indian Dermatol Online J. 2018 Nov-Dec;9(6):409-413. doi: 10.4103/idoj.IDOJ_75_18.

Abstract

BACKGROUND

Granuloma annulare (GA) is an uncommon dermatologic disorder that presents as annular, skin-colored to erythematous plaques. Histopathologically, it is characterized by palisaded histiocytic granulomas. A definitive diagnosis of GA is based on clinicopathologic correlation.

OBJECTIVE

The aim of this study was to study the histomorphologic spectrum of GA.

MATERIALS AND METHODS

A total of 30 cases reported as GA over 6 years (2012-2017) were retrieved. The detailed clinical profile and histomorphologic findings on the skin biospies were reviewed.

RESULTS

Majority of the cases (40%) presented in the 6 decade of life with a mean age of 48.3 ± 16.5 years and with a female predominance (77%). The lesions were localized in 22 cases (73%). Asymptomatic to erythematous, annular plaques was the most frequent presentation (60%). GA was not suspected clinically in two cases. Histopathologically, interstitial pattern of infiltrate was most common (44%), whereas granuloma formation and palisaded histiocytes were seen in 4 (13%) and 3 cases (10%), respectively. A mixed pattern was observed in 10 (33%) cases. Collagen degeneration was universal finding (100%) and presence of dermal mucin was noted in 24 cases (80%), both of which were important clues to the diagnosis of GA. Additional features such as presence of plasma cells, eosinophils, and vasculitis were noted in 10 (33%), 6 (20%), and 6 (20%) cases, respectively.

CONCLUSION

The diagnosis of GA may be challenging owing to its diverse morphology. Acquaintance with the varied histomorphology of GA is of utmost importance to render a correct diagnosis and understand the pathogenesis.

摘要

背景

环状肉芽肿(GA)是一种不常见的皮肤病,表现为环状、肤色至红斑性斑块。组织病理学上,其特征为栅栏状组织细胞肉芽肿。GA的确诊基于临床病理相关性。

目的

本研究旨在探讨GA的组织形态学谱。

材料与方法

检索了2012年至2017年6年间报告为GA的30例病例。回顾了皮肤活检的详细临床资料和组织形态学发现。

结果

大多数病例(40%)出现在60岁年龄段,平均年龄为48.3±16.5岁,女性占优势(77%)。22例(73%)病变为局限性。无症状至红斑性环状斑块是最常见的表现(60%)。有2例临床上未怀疑为GA。组织病理学上,浸润的间质模式最常见(44%),而肉芽肿形成和栅栏状组织细胞分别见于4例(13%)和3例(10%)。10例(33%)观察到混合模式。胶原变性是普遍发现(100%),24例(80%)发现真皮粘蛋白,这两者都是GA诊断的重要线索。分别在10例(33%)、6例(20%)和6例(20%)病例中注意到浆细胞、嗜酸性粒细胞和血管炎等其他特征。

结论

由于GA形态多样,其诊断可能具有挑战性。熟悉GA的各种组织形态学对于做出正确诊断和理解发病机制至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fddc/6233004/8833e8bb7eb0/IDOJ-9-409-g001.jpg

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