Longacre T A, Egbert B M, Rouse R V
Division of Surgical Pathology, Stanford University Medical Center, California 94305, USA.
Am J Surg Pathol. 1996 Dec;20(12):1489-500. doi: 10.1097/00000478-199612000-00008.
The clinical, histologic, and immunohistologic features of 22 desmoplastic melanomas (DMM), 10 mixed desmoplastic and spindle-cell melanomas (DMM/SMM), and two cellular spindle-cell melanomas (SMM) were studied. Patients ranged in age from 35 to 91 years (mean, 67) and included 23 men and 11 women. Seventeen cases occurred in sun-damaged skin of the head and neck. 11 were on the extremities, and six on the trunk. Except for two cases, all were Clark's level IV or V. Twenty-two (65%) cases were associated with a recognizable overlying pigmented lesion. Thirty of 32 (94%) DMM and DMM/SMM were clearly positive for S100. S100 staining was limited to < 5% of the spindle cells in two DMM/SMM. All DMM were negative when stained with HMB45. Three DMM/ SMM were immunoreactive with HMB45, as were both SMM. CD68 staining was limited to < 5% of the spindle cells in two of 32 DMM and DMM/SMM and 20% of the cells in one of two SMM. Nine (32%) DMM and DMM/SMM contained significant numbers of spindle cells immunoreactive for SMA but not desmin. In five cases, the number of actin-positive spindle cells. Two color stains for SMA and S100 demonstrated that these smooth-muscle actin positive cells constituted a separate spindle-cell population, consistent with reactive myofibroblasts. This study indicates that the immunohistologic features of desmoplastic melanoma differ from those of conventional melanoma. If a problematic spindle-cell skin lesion is a suspected melanocytic process, HMB45 is unlikely to provide confirmatory (or exclusionary) evidence for the diagnosis of DMM. Similarly, because of the variability in S100 expression in this neoplasm, the absence of S100 staining should not be relied on too heavily to exclude DMM if the clinical and histologic features favor that diagnosis. Caution should be exercised in the interpretation of numerous actin-positive spindle cells in isolation of additional confirmatory or exclusionary data as desmoplastic melanomas may contain significant numbers of these cells.
对22例促纤维增生性黑色素瘤(DMM)、10例促纤维增生性与梭形细胞混合型黑色素瘤(DMM/SMM)以及2例细胞性梭形细胞黑色素瘤(SMM)的临床、组织学和免疫组织学特征进行了研究。患者年龄在35至91岁之间(平均67岁),包括23名男性和11名女性。17例发生于头颈部受阳光损伤的皮肤。11例位于四肢,6例位于躯干。除2例之外,所有病例均为克拉克IV级或V级。22例(65%)与可识别的上方色素沉着病变相关。32例DMM和DMM/SMM中的30例(94%)S100呈明显阳性。在2例DMM/SMM中,S100染色仅限于不到5%的梭形细胞。所有DMM用HMB45染色均为阴性。3例DMM/SMM以及2例SMM与HMB45呈免疫反应阳性。在32例DMM和DMM/SMM中的2例以及2例SMM中的1例中,CD68染色仅限于不到5%的梭形细胞。9例(32%)DMM和DMM/SMM含有大量对平滑肌肌动蛋白(SMA)呈免疫反应阳性但对结蛋白呈阴性的梭形细胞。在5例中,肌动蛋白阳性梭形细胞的数量。SMA和S100的双色染色显示,这些平滑肌肌动蛋白阳性细胞构成一个单独的梭形细胞群体,与反应性肌成纤维细胞一致。本研究表明,促纤维增生性黑色素瘤的免疫组织学特征不同于传统黑色素瘤。如果一个有问题的梭形细胞皮肤病变怀疑是黑素细胞性病变,HMB45不太可能为DMM的诊断提供确诊(或排除)证据。同样,由于该肿瘤中S100表达的变异性,如果临床和组织学特征支持该诊断,不应过于依赖S100染色阴性来排除DMM。在解释大量孤立的肌动蛋白阳性梭形细胞时应谨慎,因为促纤维增生性黑色素瘤可能含有大量此类细胞,还需要额外的确诊或排除数据。