Wang Wenle, Tavora Fabio, Sharma Rajni, Eisenberger Mario, Netto George J
Department of Pathology, Johns Hopkins University, Baltimore, MD 21231, USA.
Urol Oncol. 2009 Sep-Oct;27(5):525-8. doi: 10.1016/j.urolonc.2008.04.007. Epub 2008 Jun 4.
Radioimmunoscintigraphy using a radiolabeled antibody against prostate-specific membrane antigen (PSMA) is frequently used to detect prostate carcinoma (PCa) recurrence and metastasis to lymph nodes, soft tissues, and bone. PSMA expression has been shown in occasional nonprostatic neoplasms (e.g., urothelial adenocarcinoma) and in the vasculatures of other malignancies. PSMA expression has not been described in benign neoplasms. Recently, during evaluation of a prostatic carcinoma patient, we encountered a false positive PSMA radioimmunoscintigraphy scan in a pathologically confirmed Schwannoma (SCH) lesion. The current study further evaluates PSMA expression in Schwannomas.
Eleven SCH were retrieved from our surgical pathology archives. Representative sections were immunostained with monoclonal antibody for PSMA. PSMA expression was evaluated in tumor cells and lesional vessels. Extent of staining was calculated as percent of positive cells in highest areas of expression. Positive staining was considered focal, multifocal, or diffuse based on the percent of positive cells: <5%, 5% to 75%, and >75%, respectively.
All 11 SCH showed tumoral and or vascular staining; 7 (7/11) displayed both vascular and tumoral cell staining; the remaining 4 had only vascular staining (2/11) or tumor cell staining (2/11). The extent of tumoral cell and vascular staining varied widely among lesions (tumor cells: focal in 8 and diffuse in 1; vascular: focal in 7, multifocal in 1, and diffuse in 1 lesion).
This is the first report of PSMA expression in a benign neoplasm. Given our finding of frequent expression of PSMA in Schwannomas, they should be clinically considered in the differential diagnosis of a lesion that is positive on PSMA radioimmunoscintigraphy study performed during a metastatic work-up of PCa patient.
使用针对前列腺特异性膜抗原(PSMA)的放射性标记抗体进行放射免疫闪烁显像,常用于检测前列腺癌(PCa)复发以及向淋巴结、软组织和骨骼的转移。PSMA表达已在偶发的非前列腺肿瘤(如尿路上皮腺癌)以及其他恶性肿瘤的脉管系统中被发现。尚未有关于良性肿瘤中PSMA表达的描述。最近,在对一名前列腺癌患者进行评估时,我们在一例病理确诊的神经鞘瘤(SCH)病变中遇到了PSMA放射免疫闪烁显像扫描的假阳性结果。本研究进一步评估了神经鞘瘤中PSMA的表达情况。
从我们的外科病理档案中检索出11例神经鞘瘤。代表性切片用PSMA单克隆抗体进行免疫染色。在肿瘤细胞和病变血管中评估PSMA表达情况。染色范围以最高表达区域中阳性细胞的百分比计算。根据阳性细胞百分比,阳性染色被认为是局灶性、多灶性或弥漫性的:分别为<5%、5%至75%和>75%。
所有11例神经鞘瘤均显示肿瘤和/或血管染色;7例(7/11)同时显示血管和肿瘤细胞染色;其余4例仅有血管染色(2/11)或肿瘤细胞染色(2/11)。肿瘤细胞和血管染色的范围在不同病变中差异很大(肿瘤细胞:8例为局灶性,1例为弥漫性;血管:7例为局灶性,1例为多灶性,1例为弥漫性)。
这是关于PSMA在良性肿瘤中表达的首次报道。鉴于我们发现PSMA在神经鞘瘤中频繁表达,在对PCa患者进行转移灶检查时,若PSMA放射免疫闪烁显像研究显示病变阳性,在鉴别诊断中应临床考虑神经鞘瘤。