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Ovarian Sex Cord-Stromal Tumors in Postmenopausal Women and Total Laparoscopical Management
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作者 Andrea Tinelli Marcello Pellegrino +1 位作者 Vincenzo Emanuele Chiuri Antonio Malvasi 《Journal of Cancer Therapy》 2010年第1期31-35,共5页
BACKGROUND: Ovarian sex-cord stromal tumors (SCST) take up 5% of the ovarian neoplasm and may develop in?to?an ovarian mass or a haemoperitoneum. The surgical management of SCST in early-stage adult patients is not we... BACKGROUND: Ovarian sex-cord stromal tumors (SCST) take up 5% of the ovarian neoplasm and may develop in?to?an ovarian mass or a haemoperitoneum. The surgical management of SCST in early-stage adult patients is not well?defined. CASE REPORT: A 69 year-old postmenopausal woman was admitted for metrorrhagia, a right ovary mass and?increasing pelvic pain. Preoperative clinical and instrumental examination suspected an ovarian tumor, and the?laparoscopic right ophorectomy and the frozen section suggested an ovarian SCST. To fast restore and preserve woman?integrity, total laparoscopic hysterectomy (TLH) plus left salpingo-ophorectomy (SO) were performed, without complications?in the short and long term follow-up. CONCLUSION: In the authors’ opinion, the minimally invasive management?of SCST by TLH plus bilateral SO followed by a prolonged surveillance and without intensive surgical staging,?could be an appropriate clinical and surgical choice in elder patient at early stage, since these tumors are slow at?growth, recurring locally and only a long time after initial treatment. We suggest, after a minimally invasive treatment,?a possible “wait and see” option, as in our case report. 展开更多
关键词 MENOPAUSE LAPAROSCOPY OVARIAN Cancer sex cord-stromal OVARIAN tumors GRANULOSA Cell tumors MINIMALLY Invasive Treatment.
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Ovarian endometrioid carcinoma resembling sex cord-stromal tumor:A case report
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作者 Xiao-Xia Wei Yan-Mei He +1 位作者 Wei Jiang Lei Li 《World Journal of Clinical Cases》 SCIE 2020年第12期2623-2628,共6页
BACKGROUND Ovarian endometrioid carcinoma resembling sex cord-stromal tumor(ECSCSs)is rare.CASE SUMMARY We present a rare case of primary ECSCSs in the left ovary.A 39-year-old female patient had persistent dull pain ... BACKGROUND Ovarian endometrioid carcinoma resembling sex cord-stromal tumor(ECSCSs)is rare.CASE SUMMARY We present a rare case of primary ECSCSs in the left ovary.A 39-year-old female patient had persistent dull pain in the lower abdomen for more than 1 mo,and she was initially diagnosed with pelvic inflammatory disease at a hospital.The patient received transabdominal hysterectomy,bilateral salpingo-oophorectomy,and pelvic and para-aortic lymph node dissection at our hospital and finally diagnosed with ECSCSs.After the operation,the patient received eight courses of cisplatinum+etoposide+bleomycin chemotherapy treatment and no evidence of tumor recurrence or metastasis was found in a 2-year follow-up period.CONCLUSION Ovarian endometrioid carcinoma is similar to the ovary sex cord-stromal tumor,especially when the cord-like structure is obvious.The clinical diagnosis for this tumor is difficult before surgery and pathology examination.The necessary immunohistochemical markers are of positive significance for assisting diagnosis and differential diagnosis. 展开更多
关键词 Endometrioid carcinoma sex cord-stromal tumor OVARY Case report
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Sclerosing stromal tumor of the ovary with masculinization,Meig’s syndrome and CA125 elevation in an adolescent girl:A case report 被引量:3
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作者 Qian Chen Yi-Hong Chen +2 位作者 Hui-Yun Tang Yang-Mei Shen Xin Tan 《World Journal of Clinical Cases》 SCIE 2020年第24期6364-6372,共9页
BACKGROUND Sclerosing stromal tumor (SST) is an extremely rare sex cord stromal tumor of theovary. It was first reported and named in 1973. These tumors typically presentwith pelvic/abdominal pain and tenderness, a ma... BACKGROUND Sclerosing stromal tumor (SST) is an extremely rare sex cord stromal tumor of theovary. It was first reported and named in 1973. These tumors typically presentwith pelvic/abdominal pain and tenderness, a mass, and/or abnormal menses,but rarely present with masculinity in children and adolescents. Only 2 cases ofthese tumors have been reported in premenarchal girls, who demonstratedhormonal activity, with a history of the development of a virilizing female due tohyperandrogenism. Here, we report a case of a giant SST with obviousmasculinity combined with Meig’s syndrome and CA125 elevation.CASE SUMMARY A 17-year-old female presented with a 7-year history of the development ofmasculinity and a 2-year history of amenorrhea. She had hirsutism, acne, obviouslaryngeal prominence, and voice deepening. Physical examination showed a malesuprapubic hair pattern and a 4.0 cm × 1.5 cm enlarged clitoris. Laboratory testsshowed that the testosterone level was > 15.00 ng/mL (normal range: 0.14-0.76ng/mL), and androstenedione level was > 10.00 ng/mL (normal range: 0.3-3.3ng/mL). A computed tomography scan of the abdomen and pelvis was carriedout and showed a large, solid and cystic, partly calcified pelvic mass in the rightovary measuring 27.1 cm × 20.0 cm × 11.0 cm, 15 cm above the umbilicus (to thelevel of the upper part of L1). Intraoperative findings at laparotomy revealed alarge tumor arising from the right ovary. Approximately, 500 mL of pale-yellow clear liquid was found in the pelvic cavity. A right salpingo-oophorectomy wasperformed. Microscopic examination and immunohistochemical staining of thesurgical specimen showed an SST of the ovary.CONCLUSION This report is remarkable as our patient was not only diagnosed with an SST ofthe ovary, which is extremely rare in this age group, but was the largest and mostobvious reported patient with this tumor who presented with virilization.Therefore, gynecologists should be aware of this potential complication inadolescent girls with a mass in the ovary. 展开更多
关键词 Ovarian tumor Sclerosing stromal tumor ANDROGENS ADOLESCENT VIRILIZATION Case report sex cord-stromal tumor
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Retiform Sertoli-Leydig Cell Tumor of the Ovary
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作者 Gyu-Bong Yu Seung-Kyu Choi +1 位作者 Yun-Dan Kang Choong-Hak Park 《International Journal of Clinical Medicine》 2016年第9期592-597,共6页
Sertoli-Leydig cell tumor of the ovary is a kind of sex cord-stromal tumor, which occurs between teens and twenties with symptoms including abdominal pain and swelling. The incidence rate is infinitely rare comprising... Sertoli-Leydig cell tumor of the ovary is a kind of sex cord-stromal tumor, which occurs between teens and twenties with symptoms including abdominal pain and swelling. The incidence rate is infinitely rare comprising less than 0.5% of all ovarian tumor. The average age of “retiform Sertoli-Leydig cell tumor” is 17 years as compared to 25 years for Sertoli-Leydig cell tumors as a group. We have experienced this rare case of retiform Sertoli-Leydig cell tumor in a 25-year-old foreign patient with the complaint of palpable mass on the right lower quadrant and an irregular menstrual period. The patient underwent right salpingo-oophorectomy and tumor stage was FIGO stage 1A. We report with a brief review of literature. 展开更多
关键词 Sertoli-Leydig Cell tumor Retiform Pattern sex cord-stromal tumor OVARY
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卵巢性索间质肿瘤的超声表现 被引量:2
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作者 吴春燕 赵新美 +3 位作者 曹迎九 袁岩 吴鹏西 夏钰弘 《中国医学影像技术》 CSCD 北大核心 2014年第6期889-892,共4页
目的探讨卵巢性索间质肿瘤(OSCSTs)的超声表现。方法回顾性分析28例OSCSTs的临床表现、超声资料、手术及病理结果,探讨其声像图特征。结果 28例OSCSTs患者共30个肿瘤,根据超声表现分为3型:①实性型19例,分别为纤维卵泡膜瘤13例、纤维瘤... 目的探讨卵巢性索间质肿瘤(OSCSTs)的超声表现。方法回顾性分析28例OSCSTs的临床表现、超声资料、手术及病理结果,探讨其声像图特征。结果 28例OSCSTs患者共30个肿瘤,根据超声表现分为3型:①实性型19例,分别为纤维卵泡膜瘤13例、纤维瘤4例、卵泡膜瘤2例,表现为低回声肿瘤内见条状阴影,后方回声衰减,瘤体周边可见稀疏血流信号。②规则囊实性型5例,均为纤维卵泡膜瘤囊性变,实性部分回声均匀,囊性部分囊壁光滑。③不规则囊实性型4例,为颗粒细胞瘤及纤维肉瘤各2例,呈单房或多房囊实性肿瘤,囊腔大小不等,囊壁及分隔厚薄不均,可见结节状突起,可探及丰富血流信号。结论部分OSCSTs具有较典型超声表现,结合临床及实验室检查,有助于初步诊断OSCSTs。 展开更多
关键词 卵巢 超声检查 性索间质肿瘤
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