Yahagi Masashi, Ishii Yoshiyuki, Hara Atsuko, Watanabe Masahiko
Department of Surgery, Kitasato University Kitasato Institute Hospital, 5-9-1 Shirokane, Minato-ku, Tokyo, Japan.
Department of Surgery, Kitasato University School of Medicine, 1-15-1 Kitasato, Sagamihara, Kanagawa, Japan.
Surg Case Rep. 2019 Feb 12;5(1):20. doi: 10.1186/s40792-019-0579-8.
Leiomyosarcomas (LMSs) of the colon are extremely rare and highly aggressive. Although treatment of gastrointestinal LMS is not standardized, surgical resection is generally performed. The fact that the tumors are usually large at the time of diagnosis may explain why no report on laparoscopic resection of a colonic LMS has appeared.
A 46-year-old male presented with hematochezia 1 month in duration. Abdominal examination including palpation was normal. The levels of several blood tumor markers were normal. Colonoscopy revealed a polypoid lesion approximately 30 mm in diameter in the sigmoid colon 30 cm from the anal verge. Contrast-enhanced computed tomography revealed that the tumor was 28 mm in diameter, and that no lymph node or distant metastasis was apparent. Histopathological examination of a biopsy specimen revealed spindle-shaped cells exhibiting significant nuclear atypia and a trabecular proliferation pattern upon hematoxylin-eosin staining. Immunohistochemically, the sample was positive for SMA and desmin, and negative for c-kit, DOG-1, CD34, and S-100. Furthermore, the Ki-67 index was > 50%. We thus diagnosed a leiomyosarcoma of the sigmoid colon without any metastasis. We performed laparoscopic sigmoid colectomy and regional lymphadenectomy using five trocars. After complete curative resection, a colorectal end-to-end anastomosis was created employing the double-stapling technique. All surgical margins were negative, and no lymph node metastasis was observed. The postoperative course was uneventful, and the patient was discharged 9 days after operation. No recurrence was noted to 1 year after surgery.
We report the first case of a colonic LMS treated via laparoscopic surgery. Although further work is necessary to assess prognosis and to develop the treatment further, laparoscopic surgery to treat small colonic LMSs may be feasible, being both minimally invasive and curative.
结肠平滑肌肉瘤(LMS)极为罕见且侵袭性强。尽管胃肠道LMS的治疗尚无标准化方案,但通常会进行手术切除。肿瘤在诊断时通常较大,这或许可以解释为何尚无关于腹腔镜切除结肠LMS的报道。
一名46岁男性,便血1个月。包括触诊在内的腹部检查正常。多项血液肿瘤标志物水平正常。结肠镜检查发现距肛缘30 cm的乙状结肠有一个直径约30 mm的息肉样病变。增强计算机断层扫描显示肿瘤直径为28 mm,未见淋巴结及远处转移。活检标本的苏木精-伊红染色显示梭形细胞,核异型性明显,呈小梁状增生模式。免疫组化结果显示,样本平滑肌肌动蛋白(SMA)和结蛋白阳性,c-kit、DOG-1、CD34和S-100阴性。此外,Ki-67指数>50%。因此,我们诊断为乙状结肠平滑肌肉瘤,无转移。我们使用5个套管针进行了腹腔镜乙状结肠切除术和区域淋巴结清扫术。在完整根治性切除后,采用双吻合器技术进行了结直肠端端吻合。所有手术切缘均为阴性,未观察到淋巴结转移。术后过程顺利,患者术后9天出院。术后1年未发现复发。
我们报告了首例通过腹腔镜手术治疗的结肠LMS。尽管需要进一步开展工作来评估预后并进一步完善治疗方案,但腹腔镜手术治疗小型结肠LMS可能是可行的,具有微创性且能达到根治效果。