Radović-Kovacević V, Pekmezović T, Adanja B, Jarebinski M, Marinković J, Tomin R
Institute of Dermatovenerology, Clinical Centre of Serbia, Belgrade.
Srp Arh Celok Lek. 1997 May-Jun;125(5-6):132-7.
Cutaneous malignant melanoma (MM) takes only 3% of all malignant tumours of the skin, but for reason of its increased frequency and pronounced tendency to rapid growth and metastases, it causes 60% of total lethal outcomes due to malignant tumours of the skin [1]. Primary MM is a diagnostic problem because of the great variety of its clinical features. Asymmetric configuration, irregular border, speckled color(r)diameter of more than 6 mm, and elevation of the surface, suggest suspicion of malignant alteration, but even then misdiagnosis is possible. For the final diagnosis of MM histopathological confirmation is necessary. The method to use is the extensive excisional biopsy of the lesion and its borders [2]. Histopathological diagnosis is based on microscopic findings which include: histogenetic type of MM, tumour thickness according to Breslow, level of invasion according to Clark, presence of ulceration, grade of lymphocyte infiltration, mitote rate, type of cells, presence of melanin in cells [2, 3].
A five-year survival of patients with cutaneous malignant melanoma (MM) was studied according to sex, age and distinct features of the tumour: site, type of initial therapy, stage of the disease, time from the first signs of the disease to diagnosis of MM, histological findings (histogenetic type, Breslow's tumour thickness, Clark's level of invasion, presence of ulceration, degree of lymphocyte infiltration, number of mitoses, type of cells, intensity of pigmentation) and presence of metastases. The retrospective study included 336 patients with cutaneous MM. There were 185 female (55.1%) and 151 male patients (44.9%), aged 14-83 years, mean age 48.8 years, who were treated at the institute of Oncology and Radiology in Belgrade from 1978 to 1990. The mean follow-up was 60 months (1-144 months). Melanoma in situ had 16 (4.1%) patients. Stage I had 45 patients (14.1%), stage II 163 (48.5%), stage III 83 (24.7%) and stage IV 29 (8.6%) patients. Acral location on hands and feet had 40 (11.9%) patients, on head and neck 36 (10.7%), on the trunk 146 (43.5%) and on the extremities (except hands and feet) 114 (33.9%) patients. Nodular melanoma (NM) was the most frequent histogenetic type revealed in 150 (44.6%) patients, superficial spreading melanoma (SSM) in 105 (31.1%) patients, acral melanoma (AM) in 39 (11.5%) and lentigo malignant melanoma (LMM) in 32 (9.4%) patients (Table 1). Five-year survival rate was calculated according to Kaplan-Meier's method and significance of the difference between some categories was tested by Long-Rank's test; the significance less than 0.05 was accepted.
Statistically highly significant differences in a five-year survival (p < 0.01) were related to sex p = 0.0005, age p = 0.0017, tumour site p = 0.0025, initial therapy p = 0.0036, stage of MM p = 0.0000, histological features of the tumour p = 0.0000 and presence of metastases p = 0.0000. A better five-year survival prognosis was found in female patients (64.5%) compared to male patients 44.5%, aged 27-46 years (87.3%) compared to patients younger than 26 years (43.5%); patients with melanoma on the extremities (except hands and feet) had a better five-year survival (66.7%) compared to patients younger than 26 years (43.5%); patients with melanoma on the extremities (except hands and feet) had a better five-year survival (65.7%) compared to patients with melanoma on the trunk or acral melanoma (47.3%). Higher survival was recorded in the group of patients with the tumour 1.5-3 mm thick, in whom the tumours was excised and regional nodes dissected as the primary therapy (66.9%) compared to those who underwent excision of the tumor only (48.8%). A five-year survival of patients with MM in situ was 100% for those in stage I; 85% in stage II; 42% in stage III, 16% and 0% in stage IV. The patients in whom the diagnosis of MM was established within 10 months after the first signs of the disease had significa
皮肤恶性黑色素瘤(MM)仅占所有皮肤恶性肿瘤的3%,但由于其发病率不断上升,且具有快速生长和转移的明显倾向,它导致了皮肤恶性肿瘤所致总死亡病例的60%[1]。原发性MM是一个诊断难题,因为其临床特征多种多样。不对称形态、边界不规则、颜色斑驳、直径超过6mm以及表面隆起,提示可能存在恶性病变,但即便如此仍有可能误诊。MM的最终诊断需要组织病理学证实。采用的方法是对病变及其边界进行广泛切除活检[2]。组织病理学诊断基于微观检查结果,包括:MM的组织发生类型、根据Breslow法测定的肿瘤厚度、根据Clark法测定的浸润深度、溃疡的存在情况、淋巴细胞浸润程度、有丝分裂率、细胞类型、细胞内黑色素的存在情况[2,3]。
根据性别、年龄以及肿瘤的不同特征:部位、初始治疗类型、疾病分期、从疾病首发症状到MM诊断的时间、组织学检查结果(组织发生类型、Breslow肿瘤厚度、Clark浸润深度、溃疡的存在情况、淋巴细胞浸润程度、有丝分裂数、细胞类型、色素沉着强度)以及转移情况,研究皮肤恶性黑色素瘤(MM)患者的五年生存率。这项回顾性研究纳入了336例皮肤MM患者。其中女性185例(55.1%),男性151例(44.9%),年龄在14 - 83岁之间,平均年龄48.8岁,于1978年至1990年在贝尔格莱德肿瘤与放射研究所接受治疗。平均随访时间为60个月(1 - 144个月)。原位黑色素瘤患者有16例(4.1%)。I期患者45例(14.1%),II期163例(48.5%),III期83例(24.7%)及IV期29例(8.6%)。手部和足部的肢端部位有40例(11.9%)患者,头颈部有36例(10.7%),躯干有146例(43.5%),四肢(除手和脚)有114例(33.9%)患者。结节性黑色素瘤(NM)是最常见的组织发生类型,150例(44.6%)患者为此类型,浅表扩散性黑色素瘤(SSM)105例(31.1%),肢端黑色素瘤(AM)39例(11.5%),雀斑样痣恶性黑色素瘤(LMM)32例(