Phadke D M, Weisenberg E, Engel G, Rhone D P
Illinois Masonic Medical Center, Metropolitan Group Hospitals, Chicago, IL, USA.
Ann Diagn Pathol. 1999 Aug;3(4):213-9. doi: 10.1016/s1092-9134(99)80053-7.
A Sertoli cell carcinoma of the ovary with lung metastases mimicking neuroendocrine carcinoma is presented. Lung metastases frequently occur. Primary and secondary tumors may exhibit similar growth patterns and differentiating primary from secondary tumors may be troublesome. This process may be more difficult when metastases occur from a tumor in which metastases are uncommon and morphologically resemble only a small portion of the primary tumor. We report the case of a 52-year-old woman who underwent resection of a 4,550-g Sertoli cell tumor of the ovary. Histologically, in addition to the characteristic tubular pattern of growth, 5% of the tumor consisted of poorly differentiated areas with tumor cells in sheets, a high mitotic rate, and areas of necrosis. Eleven months after this surgery she presented at a different institution with multiple pulmonary nodules. Microscopic examination of a subsequently resected lung nodule showed histologic findings similar to those of the poorly differentiated areas of the ovarian tumor and initial immunohistochemical studies showed positive staining for cytokeratin, neuron-specific enolase, and focal positivity for synaptophysin. Without knowledge of the ovarian tumor the lung lesion was interpreted as large-cell neuroendocrine carcinoma. On review of the clinical history and comparison with the previous surgical material, however, both tumors showed similar light microscopy and immunohistochemical reactivity, and a final diagnosis of metastatic Sertoli cell tumor was made. Immunohistochemical staining for inhibin revealed weak positivity in the poorly differentiated areas of the ovarian tumor but not in the lung metastasis. This is one of the rare reports of ovarian Sertoli cell tumor metastasizing to the lungs and it emphasizes the importance of complete clinical histories, ancillary studies, appropriate sampling, and review of archival material in such unusual cases.
本文报道了一例卵巢支持细胞瘤伴肺转移,其形态学表现酷似神经内分泌癌。肺转移较为常见。原发性和继发性肿瘤可能呈现相似的生长模式,鉴别原发性肿瘤与继发性肿瘤可能存在困难。当转移瘤来源于一种转移不常见且形态学仅与原发性肿瘤一小部分相似的肿瘤时,这一过程可能会更加困难。我们报告了一例52岁女性,她接受了卵巢4550g支持细胞瘤切除术。组织学上,除了典型的管状生长模式外,肿瘤的5%由低分化区域组成,这些区域的肿瘤细胞呈片状,有较高的有丝分裂率和坏死区域。该手术后11个月,她因多发肺结节就诊于另一家机构。随后切除的肺结节显微镜检查显示组织学表现与卵巢肿瘤的低分化区域相似,初始免疫组化研究显示细胞角蛋白、神经元特异性烯醇化酶呈阳性染色,突触素呈局灶性阳性。在不了解卵巢肿瘤的情况下,肺部病变被诊断为大细胞神经内分泌癌。然而,回顾临床病史并与之前的手术标本进行比较后,发现两个肿瘤在光镜和免疫组化反应性方面相似,最终诊断为转移性支持细胞瘤。抑制素免疫组化染色显示卵巢肿瘤低分化区域呈弱阳性,但肺转移灶未见阳性。这是卵巢支持细胞瘤转移至肺部的罕见报道之一,强调了在这类不寻常病例中完整临床病史、辅助检查、适当取材及回顾存档材料的重要性。