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Primary invasive extramammary Paget disease on penoscrotum: a clinicopathological analysis of 41 cases

机译:阴囊原发性乳腺外Paget病:41例临床病理分析

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To investigate the clinicopathological and immunohistochemical features and prognostic factors for invasive extramammary Paget disease (EMPD) on penoscrotum, we described the clinical presentations, histopathology, and follow-up courses of 41 cases. The age of the patients ranged from 42 to 84 years. All the patients were treated with wide surgical excision, and 14 were confirmed to have lymph node metastasis. During follow-up, 18 patients (43.9%) developed local or distant recurrence, and 13 patients (31.7%) died of the disease. Histologically, glandular formation with true lumina within the epidermis was found in 29 cases, and signet ring cells were seen in 11 cases. In invasive components, nodular/micronodular growth pattern, glandular formation, and strands/solid sheets existed in 95.1% (39/41), 43.9% (18/41), and 24.4% (10/41) of the cases, respectively. More than half of the cases had at least 2 different types of invasive growth pattern. CK7 was diffusely positive in all cases, whereas CK20 was focally positive in 8 cases. GCDFP-15 was expressed to a variable degree in 24 cases. Presence of strands/solid sheets, lymphovascular invasion, and perineural invasion in invasive EMPD were found to be correlated with higher lymph node metastatic rate. Univariate analysis revealed that patients with one of the following prognostic factors: delay in diagnosis more than 7.5 years, depth of invasion more than 1 mm, invasive pattern of strands/solid sheets, marked inflammation, lymphovascular invasion, and lymph node metastasis at diagnosis, had significantly shorter cancer-specific survival. We concluded that invasive EMPD is a rare malignant skin neoplasm with morphological diversity. Invasive pattern of strands/solid sheets is significantly associated with both lymph node metastasis and worse prognosis. Delay in diagnosis, depth of invasion, marked inflammation, lymphovascular invasion, and regional lymph node status are important prognostic factors. (C) 2015 Elsevier Inc. All rights reserved.
机译:为了调查阴囊侵袭性乳房外Paget病(EMPD)的临床病理学和免疫组化特征以及预后因素,我们描述了41例病例的临床表现,组织病理学和随访过程。患者的年龄为42至84岁。所有患者均接受了广泛的手术切除,其中14例被确认具有淋巴结转移。在随访期间,有18例(43.9%)发生局部或远处复发,另有13例(31.7%)因该病死亡。在组织学上,在表皮内发现具有真腔的腺形成29例,并且在11例中发现了印戒细胞。在侵入性组件中,分别有95.1%(39/41),43.9%(18/41)和24.4%(10/41)的病例存在结节/微结节生长模式,腺体形成和股/实心片。超过一半的病例具有至少两种不同类型的侵袭性生长方式。 CK7在所有情况下均为弥漫阳性,而CK20在8例中为局灶性阳性。 GCDFP-15在24例中以不同程度表达。发现在侵入性EMPD中存在股/实心片,淋巴管浸润和神经周浸润与较高的淋巴结转移率相关。单因素分析显示,患者具有以下预后因素之一:诊断延迟超过7.5年,浸润深度超过1毫米,股线/实心片的浸润方式,明显的炎症,淋巴血管浸润以及诊断时的淋巴结转移,癌症特异性生存期明显缩短。我们得出的结论是,侵入性EMPD是一种罕见的恶性皮肤肿瘤,具有形态学多样性。股线/实心床单的浸润模式与淋巴结转移和预后差显着相关。诊断延迟,浸润深度,明显炎症,淋巴血管浸润和区域淋巴结状态是重要的预后因素。 (C)2015 Elsevier Inc.保留所有权利。

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