Suppr超能文献

原发性卵巢黑色素瘤来源于成熟畸胎瘤,原位黑色素瘤存在于伴有同步皮肤基底细胞癌患者的纤毛柱状和鳞状上皮中。

Primary Ovarian Melanoma Arising From a Mature Teratoma With Melanoma In Situ Present in the Ciliated Columnar and Squamous Epithelium in a Patient With Synchronous Skin Basal Cell Carcinoma.

出版信息

Int J Gynecol Pathol. 2021 Jul 1;40(4):383-390. doi: 10.1097/PGP.0000000000000727.

Abstract

Primary ovarian melanoma arising from ovarian teratomas are rarely reported and difficult to accurately diagnose. Cases in the literature rely on a diagnosis of exclusion, and cases of primary ovarian melanoma with pathologic evidence of melanoma in situ are exceedingly rare. We report a case of a 66-yr-old female who presented to emergency department with abdominal pain and bloating. Computed tomography scan showed a 21 cm complex pelvic mass. An urgent laparoscopic bilateral salpingo-oophorectomy was performed. Pathologically the mass was identified as a mature teratoma. Within the cystic teratoma, there was an area showing a sheet arrangement of atypical cells. Those atypical cells were positive for Melan A, Sox10, HMB45, and c-KIT, and negative for PD-L1. Melanoma in situ was present in both the squamous and ciliated columnar epithelium. The melanoma was negative for PD-L1, and no BRAF (codon 600, exons 11, 14, and 15) or c-KIT (exons 2, 9, 10, 11, 13, 14, 15, 17, 18) mutations were identified, thus supporting the so-called triple negative malignant melanoma. A thorough dermatologic exam was conducted and only a 3 mm skin basal cell carcinoma was confirmed on biopsy. At 11 mo of follow-up, the patient is disease free and doing well and no metastatic melanoma has been identified. To the best of our knowledge, this is the first documented case of a primary ovarian melanoma arising in a mature teratoma with evidence of melanoma in situ present in both ciliated columnar and squamous epithelium in a patient with synchronous skin basal cell carcinoma. Our case is positive for c-KIT protein (CD117) by immunohistochemistry, but negative for KIT mutation. More case reports are needed to further characterize the disease.

摘要

原发性卵巢黑色素瘤源于卵巢畸胎瘤的情况极为罕见,且难以准确诊断。文献中的病例依赖于排除性诊断,而具有原位黑色素瘤病理证据的原发性卵巢黑色素瘤则极为罕见。我们报告了一例 66 岁女性因腹痛和腹胀到急诊就诊的病例。计算机断层扫描显示有一个 21cm 的复杂盆腔肿块。紧急行腹腔镜双侧输卵管卵巢切除术。病理上,该肿块被鉴定为成熟的畸胎瘤。在囊性畸胎瘤内,有一个区域显示出典型细胞的片状排列。这些典型细胞对 Melan A、Sox10、HMB45 和 c-KIT 呈阳性,对 PD-L1 呈阴性。原位黑色素瘤存在于鳞状和纤毛柱状上皮中。黑色素瘤对 PD-L1 呈阴性,且无 BRAF(密码子 600,外显子 11、14 和 15)或 c-KIT(外显子 2、9、10、11、13、14、15、17、18)突变,支持所谓的三阴性恶性黑色素瘤。进行了彻底的皮肤科检查,仅在活检中证实有一个 3mm 的皮肤基底细胞癌。随访 11 个月时,患者无疾病且情况良好,未发现转移性黑色素瘤。据我们所知,这是首例在成熟畸胎瘤中发生的原发性卵巢黑色素瘤病例,在鳞状和纤毛柱状上皮中均存在原位黑色素瘤,且患者同时患有皮肤基底细胞癌。我们的病例通过免疫组织化学对 c-KIT 蛋白(CD117)呈阳性,但 KIT 突变呈阴性。需要更多的病例报告来进一步描述该疾病。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验