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胃肠道间质瘤伴反复多发性脑梗死,酷似伴有特鲁索综合征的卵巢癌。

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

作者信息

Kobayashi Misa, Otsuki Yoshirou, Kobayashi Hiroharu, Suzuki Takashi, Nakayama Satoru, Adachi Hiroshi

机构信息

Department of Gynecology, Seirei Hamamatsu General Hospital, 2-12-12 Sumiyoshi, Naka-ku, Hamamatsu, Shizuoka 430-8558, Japan.

Department of Pathology, Seirei Hamamatsu General Hospital, 2-12-12 Sumiyoshi, Naka-ku, Hamamatsu, Shizuoka 430-8558, Japan.

出版信息

Case Rep Obstet Gynecol. 2022 Apr 6;2022:5537990. doi: 10.1155/2022/5537990. eCollection 2022.

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.

摘要

我们报告一例胃肠道间质瘤(GIST),其表现为反复多次脑梗死,酷似卵巢癌。一名79岁的绝经后女性出现多次脑梗死,计算机断层扫描发现盆腔有一个巨大肿瘤。怀疑为伴有特鲁索综合征的卵巢癌。通过对肿瘤表面进行腹腔镜活检,诊断为左卵巢纤维肉瘤;不过,腹腔观察并不充分。卵巢纤维肉瘤是一种极其罕见的肿瘤,目前仍没有足够的治疗策略。计划进行完整切除。肿瘤极其脆弱,质地呈胶冻状,极易出血。同时,子宫及双侧卵巢和输卵管均正常。肿瘤仅侵犯左骶子宫韧带和乙状结肠附近的腹膜,无腹膜播散。为完全切除肿瘤,我们进行了全子宫切除术、双侧输卵管卵巢切除术、大网膜切除术以及乙状结肠和直肠切除术并做了结肠造口术。尽管术后第4天恢复了抗凝治疗,但她仍反复出现多次中风。组织病理学检查显示肿瘤呈梭形细胞增殖,具有严重异型性、有丝分裂活性增加及广泛坏死。免疫组化研究显示c-kit、CD34和DOG1呈阳性染色。因此,她被诊断为GIST。该病例罕见且恶性程度高,由于肿瘤巨大且破裂,乙状结肠高倍视野下有丝分裂活性为36/10,GIST复发风险高。酷似卵巢癌的多次脑梗死复发。因此,术前诊断非典型GIST极其困难。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/074a/9007665/352bd00354ca/CRIOG2022-5537990.001.jpg

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