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Malignant melanoma clinically mimicking pyogenic granuloma: comparison of clinical evaluation and histopathology

机译:恶性黑色素瘤临床模仿化脓性肉芽肿:临床评价和组织病理学的比较

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摘要

Amelanotic melanomas (AMMs) account for a small proportion of all melanomas. They pose a risk of delayed diagnosis and, consequently, poor prognosis. AMMs may atypically present as a pyogenic granuloma-like lesion. This study sought to investigate the prevalence and clinical and histological features of AMM masquerading as pyogenic granuloma. The database of a tertiary medical center was screened for all patients pathologically diagnosed with melanoma in 2005-2016. Those with a suspected primary (i.e. pre-excision) clinical diagnosis of pyogenic granuloma were identified, and their demographic, clinical, histologic, and outcome data were collected from the medical files. Of 2038 patients diagnosed with melanoma, 10 (approximate to 0.5%) had a pyogenic granuloma-like AMM. The mean +/- SD age at lesion presentation was 56 +/- 18.9 years and the mean time from lesion appearance to diagnosis was 91.5 +/- 117.1 months. Nine tumors were located on the skin surface, and one on the oral mucosa. The mean lesion size was 19.6 +/- 14.1mm(2) and the mean Breslow's depth was 6.47 +/- 3.1mm; all tumors presented in the vertical growth phase. Seven (70%) patients had lymph node involvement or metastasis at diagnosis. Two patients died of the disease within 1 year of diagnosis. Given the potential lethality of AMM and the benign nature of pyogenic granuloma, clinician recognition of pyogenic granuloma-like AMMs is crucial. In the presence of a pyogenic granuloma-like lesion, findings of older patient age and large tumor size should raise the index of suspicion and prompt a biopsy study, thereby ensuring early and accurate treatment. Copyright (c) 2018 Wolters Kluwer Health, Inc. All rights reserved.
机译:Amelanotic Melanomas(AMMS)占所有黑色素组的一小部分。它们造成延迟诊断的风险,并因此预后差。 AMMS可以非典型地呈现为一种化脓性肉芽肿样病变。该研究探讨了伪装成神经胶质肉芽肿的患病率和临床和组织学特征。为2005 - 2016年筛查了所有患者的第三级医疗中心的数据库。鉴定了具有疑似初级(即预切除)的临床诊断的那些,并从医疗文件中收集了它们的人口统计学,临床,组织学和结果数据。在2038例患者诊断出黑素瘤,10(近似为0.5%)具有化脓性肉芽肿样的AMM。病变介绍的平均值+/- SD年龄为56 +/- 18.9岁,并且病变外观诊断的平均时间为91.5 +/- 117.1个月。九个肿瘤位于皮肤表面上,一个在口腔粘膜上。平均病变尺寸为19.6 +/- 14.1mm(2),平均Breeslow的深度为6.47 +/- 3.1mm;所有肿瘤均呈现在垂直生长阶段。七(70%)患者患有淋巴结受累或转移诊断。两名患者在诊断后1年内死于该疾病。鉴于AMM的潜在致命性和卵泡肉芽肿的良性性质,临床医生识别脓性肉芽肿样的AMM是至关重要的。在存在的肉芽肿样病变存在下,老年患者年龄和大肿瘤大小的结果应提高怀疑指数并提示活检研究,从而确保早期和准确的治疗。版权所有(c)2018 Wolters Kluwer Health,Inc。保留所有权利。

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