Primitive Embryonic-Type Neuroectodermal/Glandular Complexes in Testicular Germ Cell Tumors: A Mimic of Embryonic-Type Neuroectodermal Tumor.

IF 4.5 1区 医学 Q1 PATHOLOGY American Journal of Surgical Pathology Pub Date : 2024-07-01 Epub Date: 2024-05-07 DOI:10.1097/PAS.0000000000002241
Rumeal D Whaley, Thomas M Ulbright
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Abstract

Embryonic-type neuroectodermal elements are often intimately mixed with primitive endodermal-type glands, like those of yolk sac tumors, in germ cell neoplasia in situ (GCNIS)-derived germ cell tumors of the testis. Because the primitive glands mimic tubules or rosettes of embryonic-type neuroectodermal elements, these embryonic-type neuroectodermal/glandular complexes may be misinterpreted as pure lesions of embryonic-type neuroectodermal elements, which, if of sufficient size, may lead to a diagnosis of embryonic-type neuroectodermal tumor, despite that the criteria of the World Health Organization for a "somatic-type malignancy" are not met. A diagnosis of embryonic-type neuroectodermal tumor in the testis may lead to retroperitoneal lymphadenectomy even in clinical stage I patients, and in postchemotherapy resections indicates a poor prognosis. The distinction of the neuroectodermal and glandular elements is not always straightforward based on morphology alone. We, therefore, studied 34 testis-derived germ cell tumors with embryonic-type neuroectodermal/glandular complexes and 2 purely glandular yolk sac tumors to characterize the immunophenotypes and determine an efficient immunohistochemical panel to aid in this differential. We found that GFAP, synaptophysin, and paired-like homeobox 2B (PHOX2B) expression was specific to embryonic-type neuroectodermal elements, although PHOX2B had poor sensitivity. In contrast, positive reactions with antibodies directed against AFP, villin, and CDX2 were specific for the glandular elements, although CDX2 had poor sensitivity. Other markers, including AE1/AE3 cytokeratin, SALL4, glypican 3, SOX2, SOX11, CD56, INSM1, and neurofilament, proved less helpful because of their nonspecificity and/or poor sensitivity. We conclude that the optimal immunohistochemical panel for distinguishing the components of embryonic-type neuroectodermal/glandular complexes includes stains for synaptophysin, GFAP, villin, and AFP.

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睾丸生殖细胞瘤中的原始胚胎型神经外胚层/腺体复合体:胚胎型神经外胚层肿瘤的模拟物
在生殖细胞原位瘤(GCNIS)衍生的睾丸生殖细胞瘤中,胚胎型神经外胚层元件往往与原始内胚层型腺体(如卵黄囊瘤的腺体)密切混合。由于原始腺体模仿胚胎型神经外胚层元件的小管或花冠,这些胚胎型神经外胚层/腺体复合体可能会被误认为是胚胎型神经外胚层元件的纯病变,如果病变足够大,尽管不符合世界卫生组织关于 "体细胞型恶性肿瘤 "的标准,也可能被诊断为胚胎型神经外胚层肿瘤。睾丸胚胎型神经外胚层肿瘤的诊断可能会导致腹膜后淋巴结切除术,即使是临床Ⅰ期患者,化疗后切除也预示着不良预后。仅从形态上区分神经外胚层和腺体并不总是很简单。因此,我们研究了 34 例具有胚胎型神经外胚层/腺体复合体的睾丸源性生殖细胞肿瘤和 2 例纯腺体卵黄囊肿瘤,以确定其免疫表型的特征,并确定一个有效的免疫组化面板来帮助进行鉴别。我们发现,GFAP、突触素和成对类同源染色体 2B(PHOX2B)的表达对胚胎型神经外胚层元素具有特异性,但 PHOX2B 的敏感性较差。相比之下,针对甲胎蛋白、绒毛蛋白和 CDX2 的抗体的阳性反应对腺元具有特异性,但 CDX2 的敏感性较差。其他标记物,包括AE1/AE3细胞角蛋白、SALL4、glypican 3、SOX2、SOX11、CD56、INSM1和神经丝,由于其非特异性和/或敏感性较差,因此作用不大。我们的结论是,区分胚胎型神经外胚层/腺体复合体成分的最佳免疫组化方法包括突触素、GFAP、绒毛蛋白和 AFP 染色。
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来源期刊
CiteScore
10.30
自引率
5.40%
发文量
295
审稿时长
1 months
期刊介绍: The American Journal of Surgical Pathology has achieved worldwide recognition for its outstanding coverage of the state of the art in human surgical pathology. In each monthly issue, experts present original articles, review articles, detailed case reports, and special features, enhanced by superb illustrations. Coverage encompasses technical methods, diagnostic aids, and frozen-section diagnosis, in addition to detailed pathologic studies of a wide range of disease entities. Official Journal of The Arthur Purdy Stout Society of Surgical Pathologists and The Gastrointestinal Pathology Society.
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