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经肛门全直肠系膜切除术治疗低位直肠巨大平滑肌肉瘤:1例报告及文献复习

Transanal total mesorectal excision for a large leiomyosarcoma at the lower rectum: a case report and literature review.

作者信息

Hoshino Nobuaki, Hida Koya, Kawada Kenji, Sakurai Takaki, Sakai Yoshiharu

机构信息

Department of Surgery, Kyoto University Graduate School of Medicine, 54 Shogoin-Kawahara-cho, Sakyo-ku, Kyoto, 606-8507, Japan.

Department of Diagnostic Pathology, Kyoto University Graduate School of Medicine, 54 Shogoin-Kawahara-cho, Sakyo-ku, Kyoto, 606-8507, Japan.

出版信息

Surg Case Rep. 2017 Dec;3(1):13. doi: 10.1186/s40792-017-0289-z. Epub 2017 Jan 13.

Abstract

BACKGROUND

Rectal leiomyosarcoma (LMS) is an extremely rare disease. Previously, LMS was not properly distinguishable from gastrointestinal stromal tumor (GIST) until c-kit, a characteristic marker of GIST, was discovered in 1998. No standard therapeutic strategy for gastrointestinal LMS has been established except for surgical resection because of its rarity. Rectal LMS is often accompanied by symptoms, which can enable detection at a small size. However, when a large LMS is detected at the lower rectum, it is difficult to excise due to the narrow pelvic space.

CASE PRESENTATION

We present the case of an 86-year-old man with a large LMS. The LMS was asymptomatic and incidentally found at the lower rectum when he visited another hospital for management of benign prostatic hypertrophy. An abdominoperineal resection of the rectum was performed with combined resection of both seminal vesicles and a part of the prostate because tumor invasion was suspected. We used the hybrid method of laparoscopic and transanal total mesorectal excision (TaTME) approaches to achieve negative surgical margins. Late-onset urethral injury occurred in the postoperative course, which was successfully treated with a urethral catheter. The patient was discharged and received no adjuvant therapy. Local recurrence did not occur, but multiple lung metastases were detected 4 months later and the patient died 12 months after the surgery.

CONCLUSIONS

This is the first report of the hybrid method of laparoscopic and TaTME approaches to remove a large LMS at the lower rectum.

摘要

背景

直肠平滑肌肉瘤(LMS)是一种极其罕见的疾病。此前,在1998年发现胃肠道间质瘤(GIST)的特征性标志物c-kit之前,LMS无法与GIST正确区分。由于其罕见性,除手术切除外,尚未建立胃肠道LMS的标准治疗策略。直肠LMS常伴有症状,这使得其在较小尺寸时就能被检测到。然而,当在直肠下段检测到较大的LMS时,由于盆腔空间狭窄,很难将其切除。

病例介绍

我们报告了一例86岁男性患有巨大LMS的病例。该LMS无症状,在他因良性前列腺增生到另一家医院就诊时偶然在直肠下段被发现。由于怀疑肿瘤侵犯,进行了直肠腹会阴切除术,并联合切除双侧精囊和部分前列腺。我们采用腹腔镜和经肛门全直肠系膜切除术(TaTME)相结合的方法,以实现手术切缘阴性。术后出现迟发性尿道损伤,经尿道导管成功治疗。患者出院,未接受辅助治疗。未发生局部复发,但4个月后检测到多发肺转移,患者术后12个月死亡。

结论

这是首次报道采用腹腔镜和TaTME相结合的方法切除直肠下段巨大LMS的病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d777/5236054/e8233046a7ae/40792_2017_289_Fig1_HTML.jpg

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