[Intraepidermal mass of M. leprae in a case of seborrheic keratosis due to Hansen's disease (LLs)].

M Yajima, K Suzuki, M Wen, N Yamada, G Asano
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引用次数: 1

Abstract

A 67-year-old patient has had exanthema in the lower right limb since 51 years ago (16 years old at onset), which underwent repeated remission and recurrence. At present, he has bilateral symmetrical widespread infiltrating exanthema and asymmetrical marked neuralhypertrophy, and has been diagnosed typical LLs (His father had the same disease). The exanthema recurred several years ago, and the patient is being treated for Hansen's disease. He had a dark brown flat elevation with a rough surface and the size of a small finger tip in his right abdominal skin for approximately 20 years. A biopsy was performed, and the specimen was fixed in 10% formalin and paraffin sections were prepared for histopathologic examination. A part of the specimen was processed forscanning electron microscopic examination. Seborrheic keratosis was diagnosed by H & E staining. Acid-fast (FITE) staining, immunohistochemical staining (keratin, S-100 protein, anti-PGL antibody and anti-BCG antibody) and scanning electron microscopy revealed the presence of bacteria (M. leprae) in the dermal foam cells, the matrix with a banded structure and the squamous epithelial cells which normally lack phagocytosis function. Compared to the basal cells of normal epidermis, the basal cells located adjacent to the dermis affected with seborrheic keratosis showed increased proliferation and more marked characteristics of a germinative cell. The degree of differentiation of the basal cells appeared regressed, and they probably possessed augmented phagocytic activity. The phagocytosed bacteria were probably carried by the epidermal cell cycle toward the surface layer. However, bacteria could not be found in the stratum corneum, probably due to an association with the lysosome.

[麻风分枝杆菌表皮内肿物在汉森病(LLs)引起的脂溢性角化病1例]。
患者67岁,51年前(发病时为16岁)出现右下肢体肿大,反复缓解和复发。目前患儿双侧对称性广泛浸润性肿大,神经肥厚不对称,已确诊为典型的LLs(其父同病)。几年前又复发了,病人正在接受汉森氏病治疗。他的右腹部皮肤上有一块深棕色的平坦凸起,表面粗糙,有小指尖那么大,大约有20年了。行活检,10%福尔马林固定标本,制作石蜡切片进行组织病理学检查。对样品的一部分进行扫描电镜检查。h&e染色诊断脂溢性角化病。抗酸(FITE)染色、免疫组化染色(角蛋白、S-100蛋白、抗pgl抗体和抗bcg抗体)和扫描电镜显示,真皮泡沫细胞、带状结构基质和通常缺乏吞噬功能的鳞状上皮细胞中存在细菌(麻风分枝杆菌)。与正常表皮的基底细胞相比,脂溢性角化病患者真皮附近的基底细胞增殖增加,具有更明显的发芽细胞特征。基底细胞分化程度退步,可能具有增强的吞噬活性。被吞噬的细菌可能被表皮细胞周期带到表层。然而,角质层中没有发现细菌,这可能与溶酶体有关。
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