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Pediatric melanoma: Results of a large cohort study and proposal for modified ABCD detection criteria for children

机译:小儿黑色素瘤:一项大型队列研究的结果和修改的儿童ABCD检测标准的建议

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Background: Clinical and histopathologic features of childhood melanoma are poorly characterized. Atypical clinical presentations and ambiguous microscopic findings may contribute to diagnostic delays. Objectives: We sought to determine whether conventional ABCDE melanoma detection criteria (Asymmetry, Border irregularity, Color variegation, Diameter >6 mm, Evolution [any morphologic or symptomatic change in the lesion]) adequately detects pediatric melanoma and to evaluate clinicopathologic and outcome differences between younger and older children. Methods: This was a retrospective study of children given the diagnosis of melanoma (N = 60) or ambiguous melanocytic tumors treated as melanoma (N = 10) before age 20 years from 1984 to 2009 at the University of California, San Francisco. Seventy patients were divided into 2 age groups: 0 to 10 years (N = 19, group A) and 11 to 19 years (N = 51, group B). Clinical, histopathologic, and outcomes data were collected. Main outcome measures were time from diagnosis to death and predictors of metastasis and death. Results: In all, 60% of group A and 40% of group B children did not present with conventional ABCDE criteria. Rather, amelanosis, bleeding, "bumps," uniform color, variable diameter, and de novo development were most common. Histopathological subtypes differed significantly between groups (P = .002). In all, 44% were histopathologically unclassifiable using current melanoma subtypes. Stage IIA disease or higher comprised 92% and 46% of groups A and B, respectively (P = .05). Ten patients died: 1 in group A and 9 in group B. Of these, 70% had amelanotic lesions, and 60% had at least 1 major risk factor. Breslow thickness predicted metastasis (adjusted odds ratio 12.8 [CI 1.4-115]). Limitations: The retrospective design resulted in incomplete data capture. Conclusion: Additional ABCD detection criteria (Amelanotic; Bleeding, Bump; Color uniformity; De novo, any Diameter) used together with conventional ABCDE criteria may facilitate earlier recognition and treatment of melanoma in children.
机译:背景:儿童黑色素瘤的临床和组织病理学特征较差。非典型的临床表现和模糊的显微镜检查结果可能会导致诊断延迟。目的:我们试图确定常规的ABCDE黑色素瘤检测标准(不对称,边界不规则,颜色变化,直径> 6 mm,演变[病变的任何形态学或症状变化])是否能充分检测出小儿黑色素瘤,并评估两者之间的临床病理和结果差异年龄较大的孩子。方法:这是一项回顾性研究,研究对象是1984年至2009年在加利福尼亚大学旧金山分校诊断为黑色素瘤(N = 60)或模棱两可的黑色素细胞瘤(N = 10)的儿童,年龄在20岁至1984年之间。 70名患者分为2个年龄组:0至10岁(N = 19,A组)和11至19岁(N = 51,B组)。收集临床,组织病理学和结果数据。主要结果指标是从诊断到死亡的时间以及转移和死亡的预测因子。结果:总共,A组60%的儿童和B组40%的儿童不符合常规ABCDE标准。相反,最常见的是黑斑病,出血,“肿块”,均匀的颜色,可变的直径和从头发展。各组之间的组织病理学亚型差异显着(P = .002)。使用当前的黑色素瘤亚型,共有44%的患者在组织病理学上无法分类。 IIA或更高阶段的疾病分别占A组和B组的92%和46%(P = 0.05)。 10例患者死亡:A组1例,B组9例。其中70%患有褪黑斑病变,60%至少具有1种主要危险因素。 Breslow厚度可预测转移(校正后的优势比为12.8 [CI 1.4-115])。局限性:追溯设计导致数据捕获不完整。结论:与常规ABCDE标准一起使用的其他ABCD检测标准(Amelanotic,出血,肿块,颜色均匀性,从头开始,任何直径)可有助于早期识别和治疗儿童黑色素瘤。

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