Metcalf J S
Department of Pathology, Medical University of South Carolina, Charleston 29425, USA.
Semin Oncol. 1996 Dec;23(6):688-92.
The diagnosis of malignant melanoma requires clinical recognition of suspect lesions, biopsy, and histologic examination. Histological features which serve to distinguish malignant melanoma from their benign counterparts can be found in both the epidermis and dermis. The intraepidermal component of a common acquired nevus usually consists of more or less uniform theques of melanocytes located at or near the tips of rete ridges. Most melanomas are characterized by less orderly intraepidermal growth with areas in which melanocytes lose their nesting characteristics and are distributed more diffusely, sometimes replacing the basal keratinocytes by confluent growth and sometimes by invading upwards either as single cells or small nests into the upper reaches of the epidermis. Nested melanocytes can be found along the basal layer in malignant melanoma, but these nests are usually quite variable in size and location with respect to the tips of the rete ridges, and they are often irregularly distributed along the breadth of the lesion. The dermal component of malignant melanoma usually shows little tendency towards maturation, unlike that of benign nevi. Mitotic figures are unusual to find in the dermal component of common acquired nevi. When they are present, the possibility of melanoma should be considered. Other cytological features can also be useful in the diagnosis of malignant melanoma, particularly when there is marked cytological atypia; however, in some lesions, the cytological changes are not so pronounced and correct diagnosis depends on evaluation of growth pattern. While distinguishing between melanoma and atypical moles can be difficult, problems also arise in distinguishing melanoma from other neoplastic processes. The most common differential diagnosis includes melanoma, paget's disease, and pagetoid Bowen's disease. Desmoplastic melanoma is frequently difficult to distinguish from spindle cell squamous cell carcinoma and atypical fibroxanthoma. Histochemical and immunocytochemical stains are useful in resolving these problems. The pathology report of a melanoma should include the diagnosis, the maximum thickness of the tumor, the adequacy of the surgical margins (if the lesion has been excised), the presence or absence of ulceration, tumor regression, angiolymphatic invasion, and satellitosis. The inclusion of patients in treatment protocols may require additional information such as the host response of tumor-infiltrating lymphocytes, mitotic index, and Clark's level of invasion.
恶性黑色素瘤的诊断需要对可疑病变进行临床识别、活检及组织学检查。有助于将恶性黑色素瘤与其良性对应物区分开来的组织学特征可见于表皮和真皮。常见后天性痣的表皮内成分通常由位于 rete 嵴尖端或其附近的或多或少均匀的黑素细胞巢组成。大多数黑色素瘤的特征是表皮内生长不太规则,黑素细胞失去巢状特征并更分散地分布,有时通过融合生长取代基底角质形成细胞,有时以单细胞或小巢的形式向上侵入表皮上层。在恶性黑色素瘤中,巢状黑素细胞可沿基底层发现,但这些巢的大小和相对于 rete 嵴尖端的位置通常变化很大,并且它们通常沿病变宽度不规则分布。与良性痣不同,恶性黑色素瘤的真皮成分通常几乎没有成熟的趋势。在常见后天性痣的真皮成分中很少能发现有丝分裂象。当出现有丝分裂象时,应考虑黑色素瘤的可能性。其他细胞学特征在恶性黑色素瘤的诊断中也可能有用,特别是当存在明显的细胞学异型性时;然而,在一些病变中,细胞学变化并不那么明显,正确的诊断取决于对生长模式的评估。虽然区分黑色素瘤和非典型痣可能很困难,但在区分黑色素瘤与其他肿瘤性病变时也会出现问题。最常见的鉴别诊断包括黑色素瘤、佩吉特病和佩吉特样鲍温病。促纤维增生性黑色素瘤常常难以与梭形细胞鳞状细胞癌和非典型纤维黄色瘤区分开来。组织化学和免疫细胞化学染色有助于解决这些问题。黑色素瘤的病理报告应包括诊断、肿瘤的最大厚度、手术切缘的充分性(如果病变已切除)、溃疡的有无、肿瘤消退、血管淋巴管侵犯和卫星灶。将患者纳入治疗方案可能需要额外的信息,如肿瘤浸润淋巴细胞的宿主反应、有丝分裂指数和克拉克侵袭水平。