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一项针对具有小细胞形态的成人皮肤恶性黑色素瘤的11例病例研究:着重于诊断难点及不寻常特征。

A study of eleven cutaneous malignant melanomas in adults with small-cell morphology: emphasis on diagnostic difficulties and unusual features.

作者信息

Hanson I M, Banerjee S S, Menasce L P, Prescott R J

机构信息

Department of Histopathology, Royal Bolton Hospital, Bolton, UK.

出版信息

Histopathology. 2002 Feb;40(2):187-95. doi: 10.1046/j.1365-2559.2002.01318.x.

Abstract

AIMS

To describe the clinicopathological and immunohistochemical features of cutaneous malignant melanomas with a pure or mixed small-cell pattern in 11 adult patients, and to discuss the diagnostic difficulties encountered.

METHODS AND RESULTS

Haematoxylin and eosin-stained sections of each case of cutaneous small-cell malignant melanoma, together with locally recurrent skin lesions and, where available, metastatic deposits, were re-examined. Available immunohistochemical sections were evaluated. Clinical follow-up data were obtained in each case. One patient presented with metastatic disease, the others presented with cutaneous lesions. Suggested initial diagnoses included malignant melanoma, non-Hodgkin's lymphoma, Merkel cell carcinoma and sarcoma. All the tumours were in the vertical growth phase. Nine had a junctional component, often inconspicuous. The lesions showed either a pure small-cell pattern or a mixed pattern with more conventional areas. In one case, there was colonization of a basal cell carcinoma by invasive malignant melanoma. Variable retention of small-cell morphology in local recurrences and metastases was observed, although in some cases more typically pleomorphic cells were present. In the cases tested, there was strong immunostaining for S100 protein and NKI-C3, and variable immunostaining for HMB45 and Melan-A. Non-melanocytic markers were negative.

CONCLUSIONS

The possibility of a small-cell malignant melanoma should be considered in the assessment of cutaneous and non-cutaneous small-cell neoplasms. The correct diagnosis requires careful evaluation for junctional activity, melanin production and the use of a panel of melanocytic markers.

摘要

目的

描述11例成年患者中具有单纯或混合小细胞模式的皮肤恶性黑色素瘤的临床病理及免疫组化特征,并讨论所遇到的诊断困难。

方法与结果

重新检查每例皮肤小细胞恶性黑色素瘤、局部复发性皮肤病变以及(如有)转移灶的苏木精-伊红染色切片。评估可用的免疫组化切片。获取每例患者的临床随访数据。1例患者表现为转移性疾病,其他患者表现为皮肤病变。初步诊断建议包括恶性黑色素瘤、非霍奇金淋巴瘤、默克尔细胞癌和肉瘤。所有肿瘤均处于垂直生长期。9例有交界成分,通常不明显。病变表现为单纯小细胞模式或与更典型区域混合的模式。1例病例中,侵袭性恶性黑色素瘤累及基底细胞癌。在局部复发和转移灶中观察到小细胞形态的不同程度保留,尽管在某些病例中存在更具多形性的细胞。在所检测的病例中,S100蛋白和NKI-C3呈强免疫染色,HMB45和Melan-A呈不同程度免疫染色。非黑色素细胞标记物为阴性。

结论

在评估皮肤和非皮肤小细胞肿瘤时应考虑小细胞恶性黑色素瘤的可能性。正确诊断需要仔细评估交界活性、黑色素生成情况并使用一组黑色素细胞标记物。

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