Gastrointestinal Stromal Tumor with Repeated Multiple Cerebral Infarction Mimicking Ovarian Cancer with Trousseau's Syndrome

IF 0.6 Q4 OBSTETRICS & GYNECOLOGY
Misa Kobayashi, Y. Otsuki, Hiroharu Kobayashi, Takashi Suzuki, S. Nakayama, H. Adachi
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引用次数: 1

Abstract

We report a case of gastrointestinal stromal tumor (GIST) with repeated multiple cerebral infarctions mimicking ovarian cancer. A 79-year-old postmenopausal woman had multiple cerebral infarctions with a giant pelvic tumor detected by computed tomography. Ovarian cancer with Trousseau's syndrome was suspected. Through laparoscopic biopsy on the tumor surface, she was diagnosed with left ovarian fibrosarcoma; although, the abdominal cavity could not be observed appropriately. Ovarian fibrosarcoma is an extremely rare tumor and still has no adequate treatment strategy. Complete resection was planned. The tumor was extremely fragile, and gelatinous that it easily bled. Meanwhile, the uterus and bilateral ovaries and fallopian tubes were all normal. The tumor invaded only the peritoneum near the left sacral uterine ligament and sigmoid colon, with no peritoneal dissemination. To completely remove the tumor, we performed total hysterectomy with bilateral salpingo-oophorectomy and omentectomy and sigmoidal and rectal resection with colostomy. Despite resuming her anticoagulant therapy on postoperative day 4, she had recurrent multiple strokes. On histopathological examination, tumor showed spindle cell proliferation with severe atypia, increased mitotic activity, and widespread necrosis. Immunohistochemical studies showed positive staining for c-kit, CD34, and DOG1. Thus, she was diagnosed with GIST. This case was rare and highly malignant, with a high risk of recurrence of GIST because of a giant ruptured tumor that had a mitotic activity of 36/10 high-power fields from the sigmoid colon. Multiple cerebral infarctions mimicking ovarian cancer recurred. Therefore, preoperative diagnosis of an atypical GIST was extremely difficult.
胃肠道间质瘤伴重复多发性脑梗死,模拟卵巢癌伴特鲁索综合征
我们报告一例胃肠道间质瘤(GIST)与重复多发性脑梗死模仿卵巢癌。一位79岁的绝经后妇女,经计算机断层扫描发现多发性脑梗死伴巨大盆腔肿瘤。怀疑卵巢癌合并特鲁索综合征。经腹腔镜肿瘤表面活检,诊断为左卵巢纤维肉瘤;虽然,腹腔不能正常观察。卵巢纤维肉瘤是一种极为罕见的肿瘤,至今仍没有适当的治疗策略。计划完全切除。肿瘤非常脆弱,呈凝胶状,很容易出血。同时,子宫及双侧卵巢、输卵管均正常。肿瘤仅侵袭左侧骶子宫韧带及乙状结肠附近腹膜,无腹膜播散。为了彻底切除肿瘤,我们进行了全子宫切除术并双侧输卵管卵巢切除术和大网膜切除术以及乙状结肠和直肠切除术并结肠造口术。尽管术后第4天恢复了抗凝治疗,但她复发性多发性中风。组织病理学检查显示,肿瘤呈梭形细胞增生伴严重异型性,有丝分裂活性增高,广泛坏死。免疫组化研究显示c-kit、CD34和DOG1染色阳性。因此,她被诊断为GIST。该病例罕见且高度恶性,由于乙状结肠有丝分裂活性为36/10倍视场的巨大破裂肿瘤,GIST复发的风险很高。类似卵巢癌的多发脑梗死复发。因此,术前诊断非典型GIST是非常困难的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Case Reports in Obstetrics and Gynecology
Case Reports in Obstetrics and Gynecology Medicine-Obstetrics and Gynecology
CiteScore
1.30
自引率
0.00%
发文量
64
审稿时长
12 weeks
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