假鳞状肺腺癌:10例临床病理学和免疫组织化学研究。

IF 4.5 1区 医学 Q1 PATHOLOGY American Journal of Surgical Pathology Pub Date : 2024-07-01 Epub Date: 2024-05-20 DOI:10.1097/PAS.0000000000002242
David I Suster, Natali Ronen, Saul Suster
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引用次数: 0

摘要

肺假鳞状腺癌是分化不良的非小细胞肺癌的一种不常见的形态变异,表面上与鳞状细胞癌相似。我们对 10 例此类肿瘤进行了研究,其中 4 例为女性,6 例为男性,年龄从 47 岁到 93 岁不等。这些肿瘤均为周围性,大小在 1.5 厘米到 5.5 厘米之间。所有病例的特征都是由大的多角形肿瘤细胞组成的实性巢,这些细胞核不典型,细胞质丰富,细胞边界清晰,采用了模拟鳞状细胞癌的铺路样结构。有些病例的细胞质内有透明包涵体,提示角质化。瘤细胞巢中央常有粉瘤样坏死区。所有病例均未见细胞间桥。肿瘤的细胞质通常会明显变清,从而增强其表皮样外观。在 4 个病例中,可见实性假鳞状区与局灶性鳞状腺癌成分合并,在 1 个病例中,还发现肿瘤内有终止的显微镜下尖头分化灶。一个病例出现了局灶性肉瘤样纺锤细胞区。肿瘤细胞 p40 和 CK5/6 阴性,TTF1 或 Napsin-A 标记阳性,证实为腺癌表型。8名患者获得了临床随访资料,其中6名患者在确诊后6个月至11年间(平均3.1年)死于肿瘤。一名患者死于与手术相关的并发症,一名低分期肿瘤患者在27岁时死于其他原因。实体型腺癌可能会与鳞状细胞癌混淆,可能需要进行免疫组化才能确定其真正的表型。
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Pseudosquamous Adenocarcinoma of the Lung: Clinicopathologic and Immunohistochemical Study of 10 Cases.

Pseudosquamous adenocarcinoma of the lung is an unusual morphologic variant of poorly differentiated non-small cell lung carcinoma that superficially resembles a squamous cell carcinoma. We have examined 10 cases of these tumors in 4 women and 6 men, aged 47 to 93 years. The tumors were all peripheral and measured from 1.5 to 5.5 cm. All cases were characterized by solid nests of large polygonal tumor cells containing atypical nuclei with abundant cytoplasm and sharp cell borders, adopting a pavement-like architecture that simulated squamous cell carcinoma. Some cases demonstrated intracytoplasmic hyaline inclusions suggestive of keratinization. The nests of tumor cells often showed central comedo-like areas of necrosis. Intercellular bridges were not seen in any of the cases. The tumors often displayed marked clearing of the cytoplasm enhancing their epidermoid appearance. In 4 cases, the solid pseudosquamous areas were seen to merge with a focal lepidic adenocarcinoma component, and in 1 case, abortive microscopic foci of acinar differentiation were also noted within the tumor. One case showed focal sarcomatoid spindle cell areas. The tumor cells were negative for p40 and CK5/6 and labeled with TTF1 or Napsin-A, confirming an adenocarcinoma phenotype. Clinical follow-up information was available in 8 patients; 6 patients died of their tumors between 6 months to 11 years after diagnosis (mean: 3.1 y). One patient died of complications related to surgery and one patient with a low-stage tumor died at 27 years from other causes. Solid pattern adenocarcinomas can be confused for squamous cell carcinoma and may require immunohistochemistry to determine their true phenotype.

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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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