首页> 外文期刊>Journal of cutaneous pathology >Primary cutaneous Ewing sarcoma with diffuse S100/SOX10 positivity and pseudoalveolar pattern: An extraordinarily rare case highlighting a potential pitfall with significant repercussions
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Primary cutaneous Ewing sarcoma with diffuse S100/SOX10 positivity and pseudoalveolar pattern: An extraordinarily rare case highlighting a potential pitfall with significant repercussions

机译:具有漫射S100 / SOX10阳性和伪阳光模式的主要皮肤肤色肉瘤:一个非常罕见的案例,突出显示潜在的陷阱

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摘要

Primary cutaneous Ewing sarcoma is a very rare entity with less than 100 cases reported in the literature, sharing the same morphological and immunohistochemical characteristics as their osseous counterparts. Herein, to the best of our knowledge, we report the first case in English literature of a molecularly confirmed Ewing sarcoma with diffuse and strong SOX10 immunoreactivity. This exceedingly rare immunohistochemical finding along with the rarity of this tumor could easily lead to a misdiagnosis with significant repercussions. Our case highlights the difficulty in diagnosing primary cutaneous Ewing sarcoma as well as the pivotal role molecular diagnostics can play in specific scenarios.
机译:原发性皮肤尤因肉瘤是一种非常罕见的实体,文献中报告的病例不到100例,与骨肉瘤具有相同的形态学和免疫组化特征。在此,据我们所知,我们报告了英国文献中第一例经分子证实的尤因肉瘤,具有弥漫性和强SOX10免疫反应性。这种极其罕见的免疫组织化学发现,加上这种肿瘤的罕见性,很容易导致误诊,并产生重大影响。我们的病例强调了诊断原发性皮肤尤因肉瘤的困难,以及分子诊断在特定情况下可以发挥的关键作用。

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