Department of Pathology and Laboratory Medicine, Medical College of Wisconsin, Milwaukee, WI 53226, USA.
Ann Diagn Pathol. 2010 Oct;14(5):341-6. doi: 10.1016/j.anndiagpath.2010.04.008.
Paraganglioma of the mediastinum is an extremely uncommon neoplasm, and the concurrent finding of cystic changes has yet to be reported in the literature. We report a case of a 43-year-old man presenting with chest pain and left arm paresthesias. Imaging studies revealed a well-defined cystic lesion located in the anterior mediastinum, with the patient undergoing subsequent surgical resection of the mass. Grossly, the heterogenous mass measured 6.0 × 3.6 × 1.7 cm, with prominent cystic spaces and scattered solid areas. Microscopic examination revealed pseudocystic spaces with proliferation of large epithelioid cells with abundant eosinophilic cytoplasm, moderate pleomorphic nuclei, and prominent nucleoli, in a nested pattern of growth along the cysts walls. Immunohistochemical stains showed strong positivity for chromogranin, synaptophysin, and CD56 in the epithelioid cells, with negative staining for cytokeratin AE1/AE3, confirming the diagnosis of paraganglioma. S-100 was positive in the intervening sustentacular cells throughout the tumor. Cystic paraganglioma of the anterior mediastinum is a rare neoplasm, which , to our knowledge, has not yet been reported in the English literature, and should be added to the differential diagnosis of cystic lesions of the mediastinum.
纵隔副神经节瘤是一种非常罕见的肿瘤,文献中尚未报道同时存在囊性改变。我们报告了一例 43 岁男性,表现为胸痛和左上肢感觉异常。影像学研究显示在前纵隔有一个界限清楚的囊性病变,随后患者接受了肿块的手术切除。大体上,混杂的肿块大小为 6.0×3.6×1.7cm,有明显的囊性空间和散在的实性区域。显微镜下检查显示假囊腔,其中有大量嗜酸性细胞质的大上皮样细胞增生,具有中度多形性核和明显的核仁,呈巢状沿囊壁生长。免疫组织化学染色显示上皮样细胞中嗜铬粒蛋白、突触素和 CD56 强阳性,细胞角蛋白 AE1/AE3 阴性,证实了副神经节瘤的诊断。肿瘤中贯穿的支持细胞中 S-100 阳性。我们认为,前纵隔囊性副神经节瘤是一种罕见的肿瘤,在英文文献中尚未报道,应纳入纵隔囊性病变的鉴别诊断。