Laveau F, Picot M C, Dereure O, Guilhou J J, Guillot B
Service de Dermatologie, Hôpital Saint-Eloi, CHU, Montpellier.
Ann Dermatol Venereol. 2001 Sep;128(8-9):893-8.
Melanomas of unknown primary site are rare. To establish their diagnosis the metastatic nature of the lesion must be confirmed clinically and histologically, the melanoid nature by histology and immunohistochemistry. Any primary melanoma must be eliminated by careful examination of the skin and mucosa, and the absence of past surgical excision of skin lesions must be confirmed. We studied the epidemiological, clinic and prognostic characteristics of 19 melanomas of unknown primary site in a series of 646 melanomas.
This retrospective study was conducted on a series of 646 melanomas recruited over a period of 14 years. The epidemiological (age, gender, phototype and family history of melanoma), clinical and prognostic parameters (relapse and global survival rate) were analyzed in 19 patients. Clinical and epidemiological data were compared with the 646 melanomas of the series. The prognostic parameters were compared with the melanomas of the series at the same stage.
The melanomas with unknown primary site represented 2.94 p. 100 of our series and concerned 10 men and 9 women with a median age of 60 years. Eight patients presented stage III melanomas, according to MD Anderson's classification and 11 stage IV. Relapse after surgery was observed in 63 p. 100 of patients and 9 deceased during the observation period. In stage III patients the probability of survival after 2 years was of 51 p. 100 and for stage IV 34 p. 100.
In our series the frequency of melanomas of unknown primary site is comparable to that observed in other studies. Compared to melanomas of known primary site, there was a preponderance in men and in slightly older patients. There was a majority of single glandular localizations and no particular site was preponderant. Survival of Stage III patients was comparable to that of melanomas of know primary site. However, for stage IV patients it appeared better, as has been noted in other series. Treatment of metastatic melanomas of unknown primary site should therefore be the same as that of classical forms. Whenever possible, surgery remains the first indication. Search for the primary site must be orientated by clinical examination including complete examination of the skin and mucosa (ENT, ophthalmologic and genito-urinary), eventually associated with paraclinical investigations, depending on the symptoms.
原发部位不明的黑色素瘤较为罕见。要确诊此类黑色素瘤,必须通过临床和组织学检查证实病变的转移性,通过组织学和免疫组化确定黑色素样特征。必须通过仔细检查皮肤和黏膜排除任何原发性黑色素瘤,并确认既往无皮肤病变手术切除史。我们在646例黑色素瘤系列中研究了19例原发部位不明的黑色素瘤的流行病学、临床和预后特征。
这项回顾性研究针对的是在14年期间招募的646例黑色素瘤患者。分析了19例患者的流行病学(年龄、性别、光型和黑色素瘤家族史)、临床和预后参数(复发和总生存率)。将临床和流行病学数据与该系列中的646例黑色素瘤进行比较。将预后参数与同阶段该系列中的黑色素瘤进行比较。
原发部位不明的黑色素瘤占我们系列的2.94%,涉及10名男性和9名女性,中位年龄为60岁。根据MD安德森分类,8例患者为III期黑色素瘤,11例为IV期。63%的患者术后出现复发,9例在观察期内死亡。III期患者2年后的生存率为51%,IV期为34%。
在我们的系列中,原发部位不明的黑色素瘤的发生率与其他研究中观察到的相当。与已知原发部位的黑色素瘤相比,男性和年龄稍大的患者更为多见。大多数为单腺定位,没有特别突出的部位。III期患者的生存率与已知原发部位的黑色素瘤相当。然而,对于IV期患者,生存率似乎更好,其他系列也有此发现。因此,原发部位不明的转移性黑色素瘤的治疗应与经典类型相同。只要有可能,手术仍然是首选治疗方法。寻找原发部位必须通过临床检查来指导,包括对皮肤和黏膜(耳鼻喉科、眼科和泌尿生殖系统)的全面检查,并根据症状最终结合辅助检查。