Abecassis S, Spatz A, Cazeneuve C, Martin-Villepou A, Clerici T, Lacour J-P, Avril M-F
Service de Dermatologie, Institut Gustave Roussy, Villejuif.
Ann Dermatol Venereol. 2006 Apr;133(4):323-8. doi: 10.1016/s0151-9638(06)70909-7.
Nevus spilus is defined as café-au-lait macules with dark maculopapular speckles. Histologically, it has the aspect of lentigo associated with nevocellular nevus. There are 3 types of nevus spilus: small or medium-sized (<20 cm), giant and zosteriform. Malignant transformation of nevus spilus is rare.
We analyzed the cases of 5 patients presenting melanoma within nevus spilus as well as 20 published cases. The evaluation criteria were: for nevus spilus: size, type, topography, age of onset and presence of dysplastic nevi within the nevus spilus; for melanoma: clinical aspect, histological type, thickness, level and age at diagnosis. The presence of other risk factors for melanoma was noted.
The 14 women and 11 men had a mean age of 49 years at melanoma diagnosis. Type of nevus spilus was: small or medium-sized (15 cases), zosteriform (6 cases) and giant (4 cases). Only 3 nevi spili were<4 cm in diameter. Nevus spilus was present since birth (11 cases), childhood (7 cases), after the age of 20 years (3 cases) and was unspecified in 4 cases. Three of our five patients had other risk factors for melanoma. Two patients were presenting 2 melanomas within nevus spilus. The histological type of melanoma was not specified in 8 cases but SSM was the most common type (13 cases). Median Breslow thickness was 1.25 mm (0.27 to 8 mm) for the 19 cases in which it was specified.
The following criteria appeared to be associated with risk of developing melanoma in nevus spilus patients: nevus spilus present since birth, nevus spilus over 4 cm in diameter, and giant or zosteriform nevus spilus. Development of melanoma within nevus spilus is a rare event. Consequently, guidelines for follow-up of nevus spilus cannot be defined. However, follow-up is recommended, and in particular, self-examination.
斑痣性母斑被定义为带有深色斑丘疹状斑点的咖啡牛奶斑。组织学上,它具有与痣细胞痣相关的雀斑样痣外观。斑痣性母斑有3种类型:小或中型(<20 cm)、巨大型和带状疱疹样型。斑痣性母斑的恶性转化很少见。
我们分析了5例斑痣性母斑内出现黑色素瘤的患者病例以及20例已发表病例。评估标准为:对于斑痣性母斑:大小、类型、部位、发病年龄以及斑痣性母斑内发育异常痣的存在情况;对于黑色素瘤:临床表现、组织学类型、厚度、分期及诊断时的年龄。记录黑色素瘤其他危险因素的存在情况。
14名女性和11名男性在黑色素瘤诊断时的平均年龄为49岁。斑痣性母斑的类型为:小或中型(15例)、带状疱疹样型(6例)和巨大型(4例)。只有3例斑痣性母斑直径<4 cm。斑痣性母斑自出生时就存在(11例)、儿童期(7例)、20岁以后(3例),4例未明确说明。我们的5例患者中有3例有黑色素瘤的其他危险因素。2例患者在斑痣性母斑内出现2处黑色素瘤。8例黑色素瘤的组织学类型未明确,但浅表扩散性黑色素瘤是最常见的类型(13例)。19例明确厚度的病例中Breslow厚度中位数为1.25 mm(0.27至8 mm)。
以下标准似乎与斑痣性母斑患者发生黑色素瘤的风险相关:自出生时就存在的斑痣性母斑、直径超过4 cm的斑痣性母斑以及巨大型或带状疱疹样斑痣性母斑。斑痣性母斑内发生黑色素瘤是罕见事件。因此,无法确定斑痣性母斑的随访指南。然而,建议进行随访,尤其是自我检查。