Department of Respiratory Medicine, Comprehensive Cancer Center, International Medical Center, Saitama Medical University, Saitama, Japan.
Department of Pathology, Comprehensive Cancer Center, International Medical Center, Saitama Medical University, Saitama, Japan.
Thorac Cancer. 2020 Dec;11(12):3609-3613. doi: 10.1111/1759-7714.13700. Epub 2020 Oct 12.
Thymic adenocarcinoma is an extremely rare neoplasm, and little is known about its pathogenesis and clinical characteristics. A 52-year-old man presented to our clinic with severe dyspnea. At initial presentation, massive carcinomatous pleuritis and pericarditis were observed, and a lobulated mass in the anterior mediastinum was found on computed tomography. Cytological examination revealed adenocarcinoma accompanied by signet ring cells; however, his tumor showed aggressive growth without any possibility of treatment, and he died as a result of cancer progression within one month of admission. An autopsy confirmed thymic adenocarcinoma showing various histological features including mucinous, signet ring cell-like, and trabecular features. Immunohistochemically, the tumor cells were positive for cytokeratin (CK) (AE1/AE3) but negative for TTF-1. In addition, some tumor cells were positive for CD5 and KIT. Further examination revealed that tumor cells of the nonmucinous type were positive for CK7, and negative for CK20 and caudal-type homeobox 2 (CDX2). The tumor cells with mucinous and signet ring-like features were positive for CK20 and CDX2 and negative for CK7, indicating enteric differentiation. In particular, tumor cells with signet ring cell-like features indicated widespread lymphangitic carcinomatosis and pulmonary tumor thrombotic microangiopathy (PTTM). The presence of signet ring cell-like features with enteric differentiation is suggestive of a fulminant clinical course due to widespread lymphangiosis carcinomatosa and PTTM in patients with thymic adenocarcinoma. KEY POINTS: Thymic adenocarcinoma is an extremely rare neoplasm. Histological features of thymic adenocarcinoma include mucinous, signet ring cell-like, and trabecular features. Tumor cells with signet ring cell-like features indicate widespread lymphangitic carcinomatosis and pulmonary tumor thrombotic microangiopathy. The presence of signet ring cell-like features with enteric differentiation is associated with a fulminant clinical course.
胸腺腺癌是一种极其罕见的肿瘤,其发病机制和临床特征知之甚少。一名 52 岁男性因严重呼吸困难到我院就诊。初诊时,患者患有大量癌性胸膜炎和心包炎,并在计算机断层扫描中发现前纵隔有分叶状肿块。细胞学检查显示腺癌伴印戒细胞;然而,他的肿瘤呈侵袭性生长,没有任何治疗的可能,在入院后一个月内因癌症进展而死亡。尸检证实为胸腺腺癌,具有多种组织学特征,包括黏液性、印戒细胞样和小梁状特征。免疫组织化学检查显示肿瘤细胞 CK(AE1/AE3)阳性,TTF-1 阴性。此外,一些肿瘤细胞 CD5 和 KIT 阳性。进一步检查显示,非黏液型肿瘤细胞 CK7 阳性,CK20 和尾型同源盒 2(CDX2)阴性。黏液性和印戒细胞样特征的肿瘤细胞 CK20 和 CDX2 阳性,CK7 阴性,提示肠型分化。特别是,具有印戒细胞样特征的肿瘤细胞广泛存在淋巴管癌栓和肺肿瘤血栓性微血管病(PTTM)。具有印戒细胞样特征且伴有肠型分化的肿瘤细胞提示广泛的淋巴管癌栓和 PTTM,使胸腺腺癌患者的临床病程迅速恶化。关键点:胸腺腺癌是一种非常罕见的肿瘤。胸腺腺癌的组织学特征包括黏液性、印戒细胞样和小梁状特征。具有印戒细胞样特征的肿瘤细胞提示广泛的淋巴管癌栓和肺肿瘤血栓性微血管病。具有印戒细胞样特征且伴有肠型分化的肿瘤与暴发性临床病程相关。