Departments of Radiation Medicine, Loma Linda University Medical Center, Loma Linda, California, USA.
Surgical Oncology, Loma Linda University Medical Center, Loma Linda, California, USA.
J Gastrointest Oncol. 2014 Feb;5(1):E7-E12. doi: 10.3978/j.issn.2078-6891.2013.050.
Melanoma of the anorectal mucosa is a rare but highly aggressive tumor. Its presenting symptoms are frequently confused with hemorrhoids, thereby causing a delay in diagnosis. Anorectal melanoma carries with it a very poor prognosis. There is a paucity of data investigating management options for anorectal melanoma, and even fewer data reporting recurrent or refractory cases.
This case documents a 41-year-old female with a long history of hemorrhoids presenting with anorectal discharge. She was incidentally found have anorectal melanoma following surgical resection. Systemic diagnostic work-up demonstrated PET-avid lymphadenopathy in her right groin. She underwent right groin dissection. However, seven months later she recurred in her right groin and a new recurrent mass was found in her pelvis. She underwent a second groin dissection and resection of the pelvic recurrence. This was followed by a course of hypofractionated radiation therapy then systemic immunotherapy.
Surgery has been the mainstay of treatment. However, the extent of surgery has been the topic of investigation. Historically, radical resections have been performed but they result in high rates of post-operative morbidity. Newer studies have compared radical resection with wide local excisions and found comparable outcomes. Anorectal melanoma is frequently a systemic disease. The ideal systemic therapy regimen has not yet been determined but numerous studies show a benefit to multi-agent treatments. Radiation therapy is typically given in the post-operative or palliative setting.
Anorectal mucosal melanoma is a very rare but aggressive disease with a poor prognosis. The overall treatment goal should strive to optimize quality of life and tumor control while minimizing treatment-related morbidities.
肛门直肠黏膜黑色素瘤是一种罕见但高度侵袭性的肿瘤。其表现症状常与痔疮混淆,从而导致诊断延迟。肛门直肠黑色素瘤预后极差。目前针对肛门直肠黑色素瘤的治疗方法的研究数据很少,而报告复发性或难治性病例的数据则更少。
本病例记录了一位 41 岁女性,长期患有痔疮,出现肛门直肠分泌物。在接受痔疮手术后,意外发现患有肛门直肠黑色素瘤。系统诊断检查发现其右侧腹股沟有 PET 阳性淋巴结。她接受了右侧腹股沟淋巴结清扫术。然而,七个月后,她在右侧腹股沟复发,并在骨盆发现新的复发性肿块。她再次接受了右侧腹股沟淋巴结清扫术和骨盆复发病灶切除术。随后进行了分次低分割放疗和全身免疫治疗。
手术一直是主要的治疗方法。然而,手术的范围一直是研究的主题。历史上,曾进行过根治性切除术,但术后并发症发生率高。新的研究比较了根治性切除术与广泛局部切除术,发现两者结果相当。肛门直肠黑色素瘤通常是一种全身性疾病。理想的全身治疗方案尚未确定,但许多研究表明多药物治疗有益。放疗通常在术后或姑息治疗中进行。
肛门直肠黏膜黑色素瘤是一种罕见但侵袭性强、预后差的疾病。总体治疗目标应努力优化生活质量和肿瘤控制,同时将治疗相关的发病率降到最低。