Burke Allen P, Hardy Naomi, Fanaroff Rachel, Legesse Teklu
University of Maryland, Baltimore, MD UNITED STATES.
University of Maryland Medical Center. 22 S. Greene St., Baltimore, MD 21201.
AJSP Rev Rep. 2022 May-Jun;27(3):87-93. doi: 10.1097/PCR.0000000000000506.
Sarcomatoid mesotheliomas can be challenging to diagnose on small biopsy specimens, where limited material may preclude definitive assessment of invasion and lesional cells can have relatively bland cytology with no mesothelial marker expression. We report a case of a patient who presented with a pleural effusion and had subsequent pleural biopsy that showed a bland, uniform spindle cell proliferation in a mildly myxoid background. There was little if any collagen; no chest wall, soft tissue, or fat; and mesothelial markers were negative. The cells were positive for pancytokeratin and GATA3 by immunohistochemistry, and in situ hybridization showed a "negative" result for homozygous loss of CDKN2A; however, there was partial (heterozygous) loss of one allele. A diagnosis of atypical spindle cell proliferation was made based on these findings. Several months later, the patient had a repeat pleural biopsy that showed spindled cells with more pleomorphism, areas of invasion into the chest wall, and the same partial loss of CDKN2A, consistent with a sarcomatoid mesothelioma. This case underscores the challenges present on small biopsy specimens, the fact that sarcomatoid mesotheliomas can be relatively bland appearing with focal pleomorphism, and that heterozygous loss of CDKN2A should be considered a positive result indicative of a neoplastic process.
肉瘤样间皮瘤在小活检标本上的诊断可能具有挑战性,因为有限的取材可能无法对浸润进行明确评估,且病变细胞的细胞学表现可能相对平淡,缺乏间皮标志物表达。我们报告一例患者,该患者出现胸腔积液,随后进行的胸膜活检显示在轻度黏液样背景中有平淡、均匀的梭形细胞增生。几乎没有胶原纤维;未累及胸壁、软组织或脂肪;间皮标志物为阴性。免疫组化显示细胞全细胞角蛋白和GATA3呈阳性,原位杂交显示CDKN2A纯合缺失为“阴性”结果;然而,有一个等位基因部分(杂合)缺失。基于这些发现,诊断为非典型梭形细胞增生。几个月后,患者再次进行胸膜活检,显示梭形细胞具有更多的多形性,有侵犯胸壁的区域,且CDKN2A同样存在部分缺失,符合肉瘤样间皮瘤。该病例强调了小活检标本诊断的挑战,肉瘤样间皮瘤可能表现相对平淡,伴有局灶性多形性,以及CDKN2A杂合缺失应被视为提示肿瘤形成过程的阳性结果这一事实。