Clinico-histopathological Features of Pyoderma Gangrenosum: A Case Series

M. Patel, Digisha Hamirbhai Jotva, N. Dhinoja, R. Patel, Neela M. Patel
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Abstract

Pyoderma Gangrenosum (PG) is a rare, ulcerative, non infectious neutrophilic inflammatory dermatosis and often associated with underlying systemic disorder. The incidence of PG is estimated to be 0.63 per 1,00,000 with the median age at presentation of 59 years. Among its clinical variants, classical PG is the most common. The diagnosis of PG can be difficult. This case series was an attempt to review the new trends for the diagnosis of PG and also to compare them with previous diagnostic criteria. Previously histopathological criteria were included as minor criteria in Su WP et al., classification. More recently proposed diagnostic criteria by Maverkis E et al., include histopathology of skin biopsy from edge of ulcer showing neutrophilic infiltration as a major criteria. Aim of the study is to correlate and stamp the clinically suspected cases of PG with help of histopathology. This retrospective observational case series study was conducted in a tertiary care hospital from May 2018 to April 2020 consisting of 19 cases (15 years to 68 years of age range; 13 males and 6 females). Detailed history, clinical examination and blood investigations were done in all suspected cases of PG followed by histopathological examination of skin biopsy. In 17 cases, lesions were located in lower limb, one case each in buttocks and lower abdomen. The classical, ulcerative form found in 12 cases (63.15%), vegetative form in 3 cases (15.78%), plaque and bullae form were in 2 cases each (10.52%). Pathergy test was positive in 11 cases (57.89%). Histopathological examination showed neutrophilic infiltration in all 19 cases (100%), vasculitis in 11 patients (57.89%), lymphoplasmacytic infiltrate in 6 patients (31.57%), pseudoepitheliomatous hyperplasia in 5 patients (26.31%), mixed inflammatory infiltrate in 4 patients (21%), Epidermal ulceration in 4 patients (21%) and mitosis is seen in 3 patients (15.78%). Histopathology is considered as a main tool which helps clinicians to stamp suspected cases of PG.
坏疽性脓皮病的临床病理特征:一个病例系列
坏疽性脓皮病(PG)是一种罕见的溃疡性、非感染性中性粒细胞性炎症性皮肤病,常伴有潜在的全身性疾病。PG的发病率估计为0.63 / 100,000,发病时的中位年龄为59岁。在其临床变异中,经典PG最为常见。PG的诊断可能很困难。本病例系列旨在回顾PG诊断的新趋势,并将其与以前的诊断标准进行比较。以前的组织病理学标准在Su WP等人的分类中被作为次要标准。Maverkis等人最近提出的诊断标准包括溃疡边缘皮肤活检的组织病理学显示中性粒细胞浸润作为主要标准。本研究的目的是在组织病理学的帮助下对临床疑似PG病例进行关联和标记。本回顾性观察性病例系列研究于2018年5月至2020年4月在一家三级医院进行,包括19例病例(15岁至68岁;13名男性和6名女性)。所有疑似PG病例均行详细病史、临床检查和血液调查,并行皮肤活检组织病理学检查。17例病变位于下肢,臀部和下腹各1例。典型溃疡型12例(63.15%),营养型3例(15.78%),斑块型和大疱型各2例(10.52%)。病理检查阳性11例(57.89%)。19例组织病理检查均见中性粒细胞浸润(100%),血管炎11例(57.89%),淋巴浆细胞浸润6例(31.57%),假上皮瘤性增生5例(26.31%),混合性炎症浸润4例(21%),表皮溃疡4例(21%),有丝分裂3例(15.78%)。组织病理学被认为是帮助临床医生盖章疑似PG病例的主要工具。
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