Ohnishi Takamitsu, Watanabe Shinichi
Department of Dermatology, Teikyo University School of Medicine, 11-1, Kaga-2, Itabashi-ku, Tokyo 173-8605, Japan.
J Dermatol Sci. 2003 Oct;33(1):17-21. doi: 10.1016/s0923-1811(03)00131-2.
Nevus sebaceus of Jadassohn (NSJ) is a complex hamartoma in which various kinds of secondary neoplastic or hyperplastic proliferations such as primitive follicular structure (PFS) may arise. Recently, cytokeratin (CK) 20 expressed cells in PFSs and trichoblastomas of NSJs were demonstrated.
To clarify the nature and relationship among these proliferations, those in other secondary neoplasms and precise CK distributions in such lesional epidermis are examined.
49 cases of NSJ were analyzed clinicopathologically and immunohistochemically using ten monoclonal antibodies against involucrin and CKs.
15 of 49 cases possessed PFSs, and six cases, of which five were associated with PFSs, possessed seven lesions of secondary neoplasms: four BCC, two syringocystadenoma papilliferum (SAP) and one trichilemmoma. The age distribution of 15 patients with PFSs was significantly higher than that of the other 34 patients without the PFSs. The six patients with secondary neoplasms were statistically situated in a higher age range than the ten cases with the PFSs alone. Although the CK expression in lesional epidermis of NSJs were similar to that of normal epidermis, CK20 expressed cells were scattered in the PFSs of 11 cases among the 15 NSJs, but not in the other four cases. Three of the four cases were associated with BCC in which CK20 was not expressed.
From the statistical analysis, we presumed that the existence of the PFSs indicates potency to develop secondary neoplasms. Moreover, the absence of CK20 expressed cells (Merkel cells) in the structures was speculated to predict the development of BCC in the future.
Jadassohn皮脂腺痣(NSJ)是一种复杂的错构瘤,其中可能出现各种继发性肿瘤性或增生性增殖,如原始毛囊结构(PFS)。最近,在NSJ的PFS和毛母细胞瘤中发现了细胞角蛋白(CK)20表达细胞。
为阐明这些增殖、其他继发性肿瘤中的增殖以及此类病变表皮中精确的CK分布之间的性质和关系,进行了研究。
对49例NSJ进行临床病理分析,并使用针对内披蛋白和CK的十种单克隆抗体进行免疫组织化学分析。
49例中有15例具有PFS,6例具有继发性肿瘤病变7处,其中5例与PFS相关:4例基底细胞癌(BCC)、2例乳头状汗管囊腺瘤(SAP)和1例毛鞘瘤。15例有PFS患者的年龄分布显著高于其他34例无PFS患者。6例有继发性肿瘤的患者在统计学上年龄范围高于仅10例有PFS的患者。虽然NSJ病变表皮中的CK表达与正常表皮相似,但15例NSJ中有11例的PFS中散在有CK20表达细胞,另外4例则没有。4例中的3例与不表达CK20的BCC相关。
通过统计分析,我们推测PFS的存在表明有发生继发性肿瘤的可能性。此外,推测结构中不存在CK20表达细胞(默克尔细胞)可预测未来BCC的发生。