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Histologically Ambiguous ('Borderline') Primary Cutaneous Melanocytic Tumors: Approaches to Patient Management Including the Roles of Molecular Testing and Sentinel Lymph Node Biopsy

机译:组织学上不明确的(“边界”)原发性皮肤黑素细胞瘤:病人管理的方法,包括分子检测和前哨淋巴结活检的作用。

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Abstract It is well recognized that the pathologic diagnosis of melanocytic tumors can sometimes be difficult. For some atypical melanocytic tumors that do not display clear-cut features of malignancy, it may be difficult or impossible to exclude a diagnosis of melanoma; this includes those showing some resemblance to Spitz nevi, blue nevi, deep penetrating nevi, and possible nevoid melanomas. When there is uncertainty about whether a primary melanocytic tumor is a nevus or a melanoma, we recommend that a second opinion be sought from one or more experienced colleagues. If diagnostic uncertainty persists, the evidence for or against the various differential diagnostic considerations should be presented in the pathology report and a "most likely" or "favored" diagnosis given. Molecular testing of the primary tumor by using techniques such as comparative genomic hybridization or fluorescence in situ hybridization may assist in establishing a diagnosis of melanoma if multiple chromosomal aberrations are identified. However, these tests require further independent validation and are not widely available at present. Complete excision of the lesion is probably mandatory, but plans for further management should be formulated on a case-by-case basis. While the safest course of action will usually be to manage the tumor as if it were a melanoma (taking into account the tumor's thickness and other prognostic variables), this may not always be appropriate, particularly if it is located in a cosmetically sensitive site such as the face. In some cases, it may be appropriate for the surgical oncologist to convey the diagnostic uncertainty to patients and to present them with management choices so that they can decide whether they wish to be managed aggressively (as for a melanoma) or conservatively. While a sentinel lymph node biopsy may be recommended on the basis of the primary tumor characteristics, the clinical significance of lymph node involvement for these tumors is not yet clear, and it may not have the same prognostic implications as nodal involvement from an unequivocal "conventional" melanoma.
机译:摘要众所周知,黑素细胞瘤有时难以进行病理诊断。对于一些没有明显的恶性特征的非典型黑素细胞肿瘤,可能难以或不可能排除黑色素瘤的诊断。这包括那些与斯皮兹痣,蓝色痣,深穿透痣和可能避免的黑色素瘤有些相似之处。如果不确定原发性黑素细胞瘤是痣还是黑色素瘤,我们建议从一个或多个有经验的同事那里寻求第二意见。如果诊断不确定性仍然存在,则应在病理报告中提供支持或反对各种不同诊断考虑因素的证据,并给出“最可能”或“有利”诊断。如果鉴定出多个染色体畸变,则使用比较基因组杂交或荧光原位杂交等技术对原发肿瘤进行分子测试可有助于建立黑色素瘤的诊断。但是,这些测试需要进一步的独立验证,目前尚不能广泛使用。完全切除病灶可能是强制性的,但应根据具体情况制定进一步治疗计划。尽管最安全的方法通常是像对待黑色素瘤一样处理肿瘤(考虑到肿瘤的厚度和其他预后变量),但这可能并不总是合适的,特别是如果它位于美容敏感的部位,例如像脸在某些情况下,外科肿瘤科医生可能会向患者传达诊断的不确定性,并为他们提供管理选择,以便他们可以决定是希望积极治疗(如黑色素瘤)还是保守治疗。虽然可以根据原发性肿瘤的特征推荐前哨淋巴结活检,但对于这些肿瘤,淋巴结受累的临床意义尚不明确,其预后可能与明确的“常规”淋巴结受累没有相同的预后意义。黑色素瘤。

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    《Archives of Pathology & Laboratory Medicine》 |2011年第12期|p.1770-1777|共8页
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    Richard A. Scolyer, MD, FRCPA, FRCPath, Rajmohan Murali, MBBS, FRCPA, Stanley W. McCarthy, MBBS, FRCPA, John F. Thompson, MD, FRACSAccepted for publication October 28, 2009.From the Melanoma Institute Australia, Sydney, NSW, Australia (Drs Scolyer, Murali, McCarthy, and Thompson), Tissue Pathology and Diagnostic Oncology, Royal Prince Alfred Hospital, Camperdown, NSW, Australia (Drs Scolyer, Murali, and McCarthy), the Disciplines of Pathology (Drs Scolyer, Murali, and McCarthy) and Surgery (Dr Thompson), and the Cancer Institute New South Wales Clinical Research Fellows, NSW, Australia (Drs Scolyer and Murali).The authors have no relevant financial interest in the products or companies described in this article.Reprints: Richard A. Scolyer, MD, FRCPA, FRCPath, Tissue Pathology and Diagnostic Oncology, Royal Prince Alfred Hospital, Missenden Road, Camperdown, NSW 2050, Australia (e-mail: richard.scolyer@ sswahs.nsw.gov.au).,;

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