Yolk sac tumor of postpubertal-type does not exhibit immunohistochemical loss of SMARCB1/INI1 and SMARCA4/BRG1…but choriocarcinoma?

SMARCA4型 卵黄囊 SMARCB1型 免疫组织化学 病理 绒毛膜癌 发病机制 医学 内淋巴囊 生物 解剖 胚胎 细胞生物学 基因表达 内耳 遗传学 染色质重塑 基因
作者
Costantino Ricci,Francesca Ambrosi,Tania Franceschini,Francesca Giunchi,Eugenia Franchini,Francesco Massari,Veronica Mollica,Federico Bianchi,Maurizio Colecchia,Andres Acosta,Michelangelo Fiorentino
出处
期刊:Pathology Research and Practice [Elsevier BV]
卷期号:241: 154269-154269 被引量:1
标识
DOI:10.1016/j.prp.2022.154269
摘要

The recently described SWI/SNF complex-deficient sinonasal carcinoma (SMARCB1 & SMARCA4) may exhibit a yolk sac-like morphology. Tumors with similar features (yolk sac-like histology combined with the immunohistochemical loss of SMARCB1/INI1 and/or SMARCA4/BRG1) have also been described in other sites, such as the female genital tract. In this study, we immunohistochemically assessed SMARCB1/INI1 and SMARCA4/BRG1 expression to evaluate if these proteins could be involved in the pathogenesis of testicular yolk sac tumors of postpubertal type (YSTpt). Specifically, we analyzed a retrospective case series comprising pure YSTpt and mixed germ cell tumors of the testis (GCTT) with YSTpt components. In the present study, no testicular YSTpt showed loss of SMARCB1/INI1 (0/24, 0%) or SMARCA4/BRG1 (0/24, 0%). However, testicular choriocarcinoma (CHC) and isolated syncytiotrophoblast cells (iSTCs) demonstrated abnormal staining patterns for SMARCA4/BRG1 [CHC: 4/4 (100%); iSTCs: 12/12 (100%), respectively], including focal or diffuse loss of expression in a subset of cases. The results of our study suggest that functional loss of SMARCA4/BRG1 represents a recurrent event that may be relevant for the pathogenesis of a subset of testicular CHC.
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