Mérot Y, Mihm M C
Ann Dermatol Venereol. 1985;112(4):325-36.
Minimal deviation malignant melanoma (MDMM) is a rare melanocytic tumor of the skin that shares both malignant and benign histologic features: 1) a vertical growth phase similar to that of malignant melanomas with expansile nodules invading throughout the reticular dermis (Clark's level IV), and even the subcutaneous fat (Clark's level V); 2) but a monotonous and uniform proliferation of melanocytic cells that are only moderately atypical. A very slight cellular maturation from the top to bottom of the lesions may be observed, but usually there is no maturation at all. By themselves, the cells do not appear as malignant. A borderline variant of MDMM shows identical cytological and growth pattern features, but remains confined to a Clark's level III of invasion. Over the past 14 years, 45 cases (female to male ratio: 1.5:1.0) of MDMM, 8 of which were of the borderline variant, were observed. The lesions appeared as acquired pigmented tumors, 0.5 to 1.0 cm in size which predominated on the trunk. Young adults (mean age: 34 years) were most frequently involved. Based on the cytological characteristics of the cellular proliferation, they could be subdivided in 4 groups: 1) epithelioid and spindle cell type (15 cases); 2) epithelioid type (14 cases); 3) spindle cell type (7 cases); and 4) pigmented spindle cell type (9 cases). The mean thickness of the 45 cases was 3.06 mm (1.24 mm for the borderline lesions; 3.40 mm for the MDMM). Tumors with a spindle cell component appeared thicker than those without. Mitoses were numerous (mean: 3.2/10 high power fields). Each tumor but one showed a junctional component. This appeared as melanocytic hyperplasia or melanocytic nests at the dermoepidermal interface. Moreover, 10 cases (7 MDMM and 3 borderline tumors) disclosed intraepidermal spread of melanocytes. However, as observed with the dermal component of the lesions, these intraepidermal melanocytes never appeared cytologically malignant, although moderate atypism could be observed. At last, an association with a compound or dermal nevus was seen in 8 cases. MDMM appears as a particular subgroup of cutaneous malignant melanomas with distinct and characteristic histologic features. Its differential diagnosis includes blue nevus, especially the cellular variant, combined nevus, spindle and epithelioid cell nevus (Spitz-Allen's nevus) and cutaneous metastasis of malignant melanoma. The most important features for the differential diagnosis are the growth pattern, the absence of cellular maturation, the absence of real malignant cells and moderate cellular atypism.(ABSTRACT TRUNCATED AT 400 WORDS)
微小偏离恶性黑色素瘤(MDMM)是一种罕见的皮肤黑素细胞肿瘤,兼具恶性和良性组织学特征:1)垂直生长期类似于恶性黑色素瘤,有扩张性结节侵入整个网状真皮(克拉克IV级),甚至皮下脂肪(克拉克V级);2)但黑素细胞呈单调且均匀的增殖,仅具有中度异型性。从病变顶部到底部可观察到非常轻微的细胞成熟,但通常根本没有成熟。这些细胞本身并不表现出恶性。MDMM的一种临界变体表现出相同的细胞学和生长模式特征,但仍局限于克拉克III级浸润。在过去14年中,观察到45例MDMM(女性与男性比例为1.5:1.0),其中8例为临界变体。病变表现为后天性色素沉着肿瘤,大小为0.5至1.0厘米,主要位于躯干。最常累及年轻成年人(平均年龄:34岁)。根据细胞增殖的细胞学特征,它们可分为4组:1)上皮样和梭形细胞型(15例);2)上皮样型(14例);3)梭形细胞型(7例);4)色素性梭形细胞型(9例)。45例的平均厚度为3.06毫米(临界病变为1.24毫米;MDMM为3.40毫米)。有梭形细胞成分的肿瘤似乎比没有的更厚。有丝分裂众多(平均:3.2/10个高倍视野)。除1例肿瘤外,每个肿瘤都有交界成分。这表现为真皮表皮交界处的黑素细胞增生或黑素细胞巢。此外,10例(7例MDMM和3例临界肿瘤)出现黑素细胞表皮内播散。然而,正如在病变的真皮成分中观察到的那样,这些表皮内黑素细胞在细胞学上从未表现出恶性,尽管可观察到中度异型性。最后,8例中发现与复合痣或皮内痣有关联。MDMM表现为皮肤恶性黑色素瘤的一个特殊亚组,具有独特且典型的组织学特征。其鉴别诊断包括蓝色痣,尤其是细胞变体、复合痣、梭形和上皮样细胞痣(斯皮茨 - 艾伦痣)以及恶性黑色素瘤的皮肤转移。鉴别诊断的最重要特征是生长模式、细胞成熟的缺乏、真正恶性细胞的缺乏以及中度细胞异型性。(摘要截断于400字)