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局限于真皮和/或皮下组织的孤立性黑色素瘤:重新审视分期分类的证据

Solitary melanoma confined to the dermal and/or subcutaneous tissue: evidence for revisiting the staging classification.

作者信息

Bowen G M, Chang A E, Lowe L, Hamilton T, Patel R, Johnson T M

机构信息

Department of Dermatology, University of Michigan, 1910 Taubman Center, Ann Arbor, MI 48109-0314, USA.

出版信息

Arch Dermatol. 2000 Nov;136(11):1397-9. doi: 10.1001/archderm.136.11.1397.

Abstract

BACKGROUND

Several patients presented with a single focus of presumed cutaneous metastatic melanoma with an unknown primary tumor based on clinical and histologic staging criteria of the American Joint Committee on Cancer (AJCC). This population is classified as having stage IV disease by the current AJCC staging system, which carries a dismal prognosis (5%-18% 5-year survival). Our clinical observation was that these patients had a higher survival rate than would be expected for stage IV disease. We believe this population represents a subgroup of primary dermal- and or subcutaneously-derived melanoma that simulates cutaneous metastatic melanoma in histologic and clinical presentation but may differ in behavior.

OBSERVATIONS

The database records of 1800 patients from the University of Michigan Melanoma Clinic, Ann Arbor, were retrospectively reviewed to identify the prevalence and survival for patients diagnosed with a single focus of presumed metastatic melanoma to the skin based on accepted histologic and clinical parameters. The prevalence of this population was 0.61% (11 of 1800 patients). The Kaplan-Meier 8-year survival estimate was 83% (95% confidence interval, 58%-100%).

CONCLUSIONS

By AJCC convention, these cases are classified as stage IV metastatic disease. Our data suggest that these presumed metastatic tumors do not behave like stage IV metastatic disease to the skin via lymphatic or hematogenous spread from an unknown primary site; rather, they are behaving like primary tumors originating in the dermal and/or subcutaneous tissue.

摘要

背景

根据美国癌症联合委员会(AJCC)的临床和组织学分期标准,有几位患者表现为单一病灶的疑似皮肤转移性黑色素瘤,原发肿瘤不明。在当前的AJCC分期系统中,这一群体被归类为IV期疾病,预后很差(5年生存率为5%-18%)。我们的临床观察发现,这些患者的生存率高于IV期疾病的预期生存率。我们认为这一群体代表了原发性真皮和/或皮下来源的黑色素瘤亚组,其在组织学和临床表现上模拟皮肤转移性黑色素瘤,但行为可能不同。

观察结果

对密歇根大学安娜堡分校黑色素瘤诊所1800例患者的数据库记录进行回顾性分析,以确定根据公认的组织学和临床参数诊断为单一病灶疑似皮肤转移性黑色素瘤患者的患病率和生存率。该群体的患病率为0.61%(1800例患者中的11例)。Kaplan-Meier法估计的8年生存率为83%(95%置信区间,58%-100%)。

结论

按照AJCC的惯例,这些病例被归类为IV期转移性疾病。我们的数据表明,这些疑似转移性肿瘤的行为不像通过淋巴管或血行从不明原发部位转移至皮肤的IV期转移性疾病;相反,它们的行为类似于起源于真皮和/或皮下组织的原发性肿瘤。

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