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嗜铬细胞瘤和肾上腺外副神经节瘤的病理学

Pathology of pheochromocytoma and extra-adrenal paraganglioma.

作者信息

Tischler Arthur S, Kimura Noriko, Mcnicol Anne Marie

机构信息

Department of Pathology, Tufts University School of Medicine, Boston, MA 02111, USA, and Department of Pathology, Tohoku Rosai Hospital, Sendai, Japan.

出版信息

Ann N Y Acad Sci. 2006 Aug;1073:557-70. doi: 10.1196/annals.1353.059.

Abstract

The 2004 WHO classification of endocrine tumors defines pheochromocytoma as a tumor arising from chromaffin cells in the adrenal medulla. Closely related tumors in extra-adrenal sympathetic and parasympathetic paraganglia are classified as extra-adrenal paragangliomas. A pheochromocytoma is an intra-adrenal sympathetic paraganglioma. While arbitrary, this nomenclature serves to emphasize important distinctive properties of intra-adrenal tumors that must be taken into account in clinical practice and research. Those include an often adrenergic phenotype, a relatively low rate of malignancy, and a predilection to occur in particular hereditary syndromes. Current roles of pathology are limited to distinguishing primary or metastatic pheochromocytomas/paragangliomas from other endocrine or nonendocrine tumors, and flagging tumors that show features suggestive of malignant potential or syndromic disease. Future roles may involve more definitive assessment of malignancy, genotype-phenotype correlation, and identification of targets for therapy. Pathology practice currently rests mostly on interpretation of conventional histological sections stained with hematoxylin and eosin, with variable ancillary application of immunohistochemical staining. Malignancy is currently defined by the presence of metastases, not local invasion. Local invasion alone is a poor predictor of metastases, and the absence of apparent invasion does not preclude development of metastases. The two types of aggressive behavior might therefore have different biological underpinnings, and those will be resolved most effectively if consistent terminology is employed. In order to be optimally informative, pathology reports must employ consistent nomenclature and incorporate standard elements. Templates or checklists for minimal standard reporting are recommended by several pathology associations, but identification of some recommended and optional elements is currently subjective or inconsistent.

摘要

2004年世界卫生组织(WHO)内分泌肿瘤分类将嗜铬细胞瘤定义为起源于肾上腺髓质嗜铬细胞的肿瘤。肾上腺外交感神经和副交感神经节中的相关肿瘤被归类为肾上腺外副神经节瘤。嗜铬细胞瘤是肾上腺内交感神经副神经节瘤。虽然这种命名有些随意,但它有助于强调肾上腺内肿瘤的重要独特特性,这些特性在临床实践和研究中必须予以考虑。这些特性包括通常的肾上腺素能表型、相对较低的恶性率以及在特定遗传综合征中的易发性。目前病理学的作用仅限于区分原发性或转移性嗜铬细胞瘤/副神经节瘤与其他内分泌或非内分泌肿瘤,并标记出具有恶性潜能或综合征性疾病特征的肿瘤。未来的作用可能涉及对恶性程度进行更明确的评估、基因型-表型相关性研究以及确定治疗靶点。目前病理学实践主要基于对苏木精和伊红染色的传统组织切片的解读,免疫组织化学染色的辅助应用程度不一。目前恶性的定义是存在转移,而非局部侵犯。仅局部侵犯对转移的预测性较差,而且没有明显侵犯并不排除转移的发生。因此,这两种侵袭性行为可能有不同的生物学基础,如果采用一致的术语,将能最有效地解决这些问题。为了提供最有用的信息,病理报告必须采用一致的命名法并纳入标准要素。几个病理学协会推荐了最低标准报告的模板或清单,但目前一些推荐要素和可选要素的确定是主观的或不一致的。

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