Secondary Localized Cutaneous Amyloidosis is not Rare in Bowen's Disease and Bowenoid Papulosis.

IF 1.1 Q4 PATHOLOGY
Can Baykal, Ozge Hurdogan, Goncagul Babuna Kobaner, Algun Polat Ekinci, Nesimi Buyukbabani
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引用次数: 3

Abstract

Secondary localized cutaneous amyloidosis is a histopathological finding seen in the dermis, in various benign, premalignant, and malignant skin conditions, without clinical significance. The real incidence is not known. We aimed to investigate the phenomenon of secondary localized cutaneous amyloidosis in Bowen's disease and Bowenoid papulosis. We retrospectively evaluated the data of all cases with histopathological confirmation of Bowen's disease and Bowenoid papulosis between 2006 and 2017 in our Dermatovenereology and/or Pathology departments. Secondary localized cutaneous amyloidosis was observed in three patients with Bowen's disease (3/52; 5.8%) and in three patients with Bowenoid papulosis (3/18; 16.7%). Herein, we present the demographic, clinical and histopathological features of these six cases of secondary localized cutaneous amyloidosis in detail. Although the occurrence of secondary localized cutaneous amyloidosis in epithelial tumors is a well-known phenomenon, its incidence has not been previously reported in Bowen's disease and Bowenoid papulosis. Therefore, our results indicating a high incidence may be particularly important for Bowenoid papulosis, as its association with secondary localized cutaneous amyloidosis has only been shown in one case before. Moreover, in three of six cases, we histologically observed areas of regression with a marked prominence of amyloid deposition. Remarkably, two of these patients had a history of topical application of destructive agents which reveals a possible etiologic relationship between secondary localized cutaneous amyloidosis and cellular apoptosis/necrosis induced by these external agents.

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继发性局部皮肤淀粉样变性在鲍文氏病和鲍文氏样丘疹病中并不罕见。
继发性局限性皮肤淀粉样变是一种组织病理学发现,可见于真皮,在各种良性,癌前和恶性皮肤病,没有临床意义。真正的发病率尚不清楚。我们的目的是探讨继发性局限性皮肤淀粉样变在鲍文氏病和鲍文氏样丘疹病中的现象。我们回顾性评估了2006年至2017年间皮肤性病学和/或病理学部门所有经组织病理学证实的Bowen病和Bowenoid丘疹病病例的数据。3例Bowen病患者继发局限性皮肤淀粉样变(3/52;5.8%)和3例鲍氏样丘疹病(3/18;16.7%)。在此,我们详细介绍了这6例继发性局限性皮肤淀粉样变的人口学、临床和组织病理学特征。虽然上皮性肿瘤继发性局部皮肤淀粉样变的发生是一种众所周知的现象,但其发病率在Bowen病和Bowenoid丘疹病中尚未报道。因此,我们的研究结果表明,鲍氏样丘疹病的高发病率可能特别重要,因为它与继发性局限性皮肤淀粉样变的关联之前只在一个病例中被证实。此外,在6例中的3例中,我们在组织学上观察到淀粉样蛋白沉积明显突出的退化区域。值得注意的是,其中两例患者有局部应用破坏性药物的历史,这表明继发性局部皮肤淀粉样变性与这些外源性药物诱导的细胞凋亡/坏死之间可能存在病因学关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.90
自引率
10.00%
发文量
23
审稿时长
14 weeks
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