Chatterjee Debajyoti, Kaur Manveen, Punia R P S, Bhalla Mala, Handa Uma
Department of Pathology, Government Medical College and Hospital, Chandigarh, India.
Department of Dermatology, Government Medical College and Hospital, Chandigarh, India.
Indian Dermatol Online J. 2018 Nov-Dec;9(6):409-413. doi: 10.4103/idoj.IDOJ_75_18.
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.
The aim of this study was to study the histomorphologic spectrum of GA.
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.
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.
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.
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。
本研究旨在探讨GA的组织形态学谱。
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。
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。
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。