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结外肠系膜滤泡树突细胞肉瘤表达角蛋白抗原:哪些陷阱引发诊断线索。

Extranodal Mesenteric Follicular Dendritic Cell Sarcoma Expressing Keratin Antigens: What Pitfalls Initiate Diagnostic Clues.

机构信息

Pathology Section, Dubai Hospital, Dubai, United Arab Emirates.

出版信息

Int J Surg Pathol. 2023 Oct;31(7):1308-1313. doi: 10.1177/10668969221143470. Epub 2022 Dec 26.

Abstract

Extranodal follicular dendritic cell sarcomas are infrequent diagnostically challenging tumors. Because of their rarity, heterogeneous histomorphologic features and variable histologic grades a significant number of extranodal lesions are prone to be misdiagnosed. Even though they have a characteristic immunoprofile, expression of a range of nonspecific markers is well documented. Even though they are typically negative for keratins, few authors have reported lesions expressing keratin. Keratin expressing tumors are more likely to be misinterpreted by pathologists further deterring their inclusion in the differential diagnosis. We report an intraabdominal mesenteric follicular dendritic cell sarcoma in a 44-year-old male that immunophenotypically expressed keratin antigens. The lesion showed a high-grade pleomorphic epithelioid appearance and the initial differential diagnosis included lymphoma, sarcomas, melanoma, and carcinomas. Follicular dendritic cell sarcoma was not considered. Expression of epithelial membrane antigen and keratin further deterred the diagnosis which was reached only after extensive use of immunomarkers. The tumor cells expressed CD21, CD23, and D2-40. Morphologically, the tumor showed some thymoma-like features with occasional TDT-expressing background T-lymphocytes. These features were hints to reconsider our differential diagnosis to include follicular dendritic cell tumors. Awareness of this aberrant staining of epithelial immunomarkers and attention to certain clues should encourage pathologists to consider this entity. Speculative assumptions may explain this unusual keratin expression in some lesions. The histomorphologic and immunohistochemical heterogeneity may suggest different variants and grades of follicular dendritic cell sarcomas. The prevalence, importance, and histogenesis of keratin expression in follicular dendritic cell sarcomas warrant further studies.

摘要

结外滤泡树突状细胞肉瘤是一种罕见的具有挑战性的诊断肿瘤。由于其罕见性、异质性组织形态学特征和不同的组织学分级,相当数量的结外病变容易被误诊。尽管它们具有特征性的免疫表型,但广泛记录了一系列非特异性标志物的表达。尽管它们通常对角蛋白呈阴性,但也有少数作者报道了表达角蛋白的病变。表达角蛋白的肿瘤更有可能被病理学家误诊,这进一步阻碍了它们被纳入鉴别诊断。我们报告了一例 44 岁男性的腹腔肠系膜滤泡树突状细胞肉瘤,其免疫表型表达角蛋白抗原。病变呈高级别多形上皮样外观,最初的鉴别诊断包括淋巴瘤、肉瘤、黑色素瘤和癌。滤泡树突状细胞肉瘤未被考虑。上皮膜抗原和角蛋白的表达进一步阻碍了诊断,只有在广泛使用免疫标志物后才得出诊断。肿瘤细胞表达 CD21、CD23 和 D2-40。形态上,肿瘤具有一些胸腺瘤样特征,偶尔有表达 TDT 的背景 T 淋巴细胞。这些特征提示我们重新考虑我们的鉴别诊断,包括滤泡树突状细胞肿瘤。了解这种上皮免疫标志物的异常染色以及注意某些线索应鼓励病理学家考虑这种实体。推测性假设可以解释一些病变中这种不寻常的角蛋白表达。滤泡树突状细胞肉瘤的组织形态学和免疫组织化学异质性可能提示不同的变体和分级。角蛋白在滤泡树突状细胞肉瘤中的表达的普遍性、重要性和组织发生值得进一步研究。

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