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IV型胶原免疫染色可区分2a型多发性内分泌腺瘤中的C细胞增生和微小髓样癌。

Immunostains for collagen type IV discriminate between C-cell hyperplasia and microscopic medullary carcinoma in multiple endocrine neoplasia, type 2a.

作者信息

McDermott M B, Swanson P E, Wick M R

机构信息

Division of Surgical Pathology, Barnes Hospital, Washington University Medical Center, St. Louis, MO 63110, USA.

出版信息

Hum Pathol. 1995 Dec;26(12):1308-12. doi: 10.1016/0046-8177(95)90294-5.

Abstract

At a light microscopic level, the separation of C-cell hyperplasia and microscopic medullary carcinoma of the thyroid (MCT) is difficult, and it ultimately rests on the finding of C cells outside of the thyroid follicular basement membranes (FBMs). To date, this has required ultrastructural examination for proper documentation. The assessment of thyroidectomy specimens from patients with multiple endocrine neoplasia, type 2a (MEN2a), a hereditary condition in which there is widespread C-cell hyperplasia (CCH) and multifocal MCT, presented an opportunity to the authors to assess the entire range of C-cell abnormalities. Total thyroidectomy specimens from 17 patients with MEN2a were examined. In addition to hematoxylineosin (H&E) stains, representative tissue sections were labeled for chromogranin A and collagen type IV (CIV), using the avidin-biotin-peroxidase complex (ABC) method. All patients in the study had multifocal C-cell proliferation that was both diffuse and nodular. Fifteen had microscopic MCTs, which were multifocal in eight instances. Three patterns of C-cell proliferation were recognized in CIV immunostains. The first was characterized by complete investment of C-cells by a continuous rim of CIV, corresponding to FBM and confirming an intrafollicular localization; hence, the diagnosis of CCH was made in such cases. The second pattern was distinctive and was typified by defects in the CIV layer; constituent C-cells assumed an extrafollicular location. These images yielded a diagnosis of micro-MCT. The latter findings were also accompanied by focal reduplication of basement membrane that was apparently tumor derived, producing a micronodular or microlobular configuration. The third pattern represented a combination of the first two, with C-cell nodules that were bounded by CIV and clearly situated in an intrafollicular location; however, focal reduplication of basement membranes was also evident in these cases. The biological significance of the third pattern of CIV staining is uncertain, but it may reflect the presence of a preinvasive proliferation of C-cells that is distinct from "usual" CCH in MEN2a.

摘要

在光学显微镜水平上,甲状腺C细胞增生与微小髓样癌(MCT)的鉴别诊断较为困难,最终要依据甲状腺滤泡基底膜(FBM)外C细胞的发现来判断。迄今为止,这需要进行超微结构检查才能妥善记录。对2a型多发性内分泌腺瘤病(MEN2a)患者的甲状腺切除标本进行评估,MEN2a是一种遗传性疾病,存在广泛的C细胞增生(CCH)和多灶性MCT,这为作者提供了一个评估C细胞异常全貌的机会。对17例MEN2a患者的全甲状腺切除标本进行了检查。除苏木精-伊红(H&E)染色外,采用抗生物素蛋白-生物素-过氧化物酶复合物(ABC)法对代表性组织切片进行嗜铬粒蛋白A和IV型胶原(CIV)标记。研究中的所有患者均有多灶性C细胞增殖,呈弥漫性和结节性。15例有微小MCT,其中8例为多灶性。在CIV免疫染色中识别出三种C细胞增殖模式。第一种模式的特征是CIV连续边缘完全包裹C细胞,对应于FBM,证实为滤泡内定位;因此,此类病例诊断为CCH。第二种模式独特,其特点是CIV层有缺陷;组成C细胞位于滤泡外。这些图像诊断为微小MCT。后者的发现还伴有明显源自肿瘤的基底膜局灶性重复,形成微结节或微叶状结构。第三种模式代表前两种模式的组合,C细胞结节由CIV界定,明显位于滤泡内;然而,这些病例中基底膜的局灶性重复也很明显。CIV染色第三种模式的生物学意义尚不确定,但它可能反映了一种与MEN2a中“常见”CCH不同的C细胞浸润前增殖的存在。

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