Dinh Huyenlan, Seyffert Jennifer, Lountzis Nektarios I, Altman Howard B, Oram Christian, Purcell Stephen M
*Department of Dermatology, Lehigh Valley Health Network, Allentown, PA; †School of Osteopathic Medicine, Western University Health Sciences, Pomona, CA; and ‡Advanced Dermatology Associates, LTD, Allentown, PA.
Am J Dermatopathol. 2017 Feb;39(2):140-143. doi: 10.1097/DAD.0000000000000706.
Lichen planus (LP) is a mucocutaneous inflammatory dermatitis of idiopathic origin that can involve the skin, mucous membranes, hair, and nails. LP has an associated set of characteristic histopathologic findings which include hyperkeratosis, vacuolization of the basal layer, Civatte bodies, wedge-shaped hypergranulosis, band-like lymphocytic infiltrate at the dermal epidermal junction, eosinophilic colloid bodies in the papillary dermis, and pigment incontinence. The infiltrate is usually composed of lymphocytes with few histiocytes, mast cells, and macrophages. The presence of plasma cell predominant infiltrate in LP has only been reported in four previous cases and 2 other cases of lichen nitidus. The authors report another 2 cases of LP with predominate plasma cell infiltrate in 2 female patients on the legs. The differential includes a drug-induced lichenoid reaction with predominate plasma cell infiltrate. However, there have been no case reports of that type of reaction. Because plasma cells are seen commonly in certain infectious diseases, malignancy, and macroglobulinemia, it is prudent to rule out those entities. Our patients responded well with a class 1 topical steroid, with improvement of their lower leg lesions within 1 month of treatment.
扁平苔藓(LP)是一种特发性起源的皮肤黏膜炎症性皮炎,可累及皮肤、黏膜、毛发和指甲。LP具有一系列相关的特征性组织病理学表现,包括角化过度、基底层空泡形成、Civatte小体、楔形颗粒层增厚、真皮表皮交界处带状淋巴细胞浸润、乳头真皮内嗜酸性胶体小体以及色素失禁。浸润通常由淋巴细胞组成,伴有少量组织细胞、肥大细胞和巨噬细胞。LP中以浆细胞为主的浸润仅在之前的4例以及另外2例光泽苔藓病例中有报道。作者报告了另外2例腿部女性患者的LP以浆细胞浸润为主。鉴别诊断包括药物性苔藓样反应伴浆细胞浸润为主。然而,尚无该类型反应的病例报告。由于浆细胞常见于某些感染性疾病、恶性肿瘤和巨球蛋白血症,因此谨慎起见应排除这些疾病。我们的患者使用1级外用类固醇治疗反应良好,治疗1个月内小腿病变有所改善。