偶然发现肛门黑色素瘤的罕见病例。

IF 0.4 Q4 SURGERY
Journal of Surgical Case Reports Pub Date : 2024-11-25 eCollection Date: 2024-11-01 DOI:10.1093/jscr/rjae728
Nawal Khan, Dondre Irving, Lynn O'Connor
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引用次数: 0

摘要

肛门黑色素瘤是一种罕见的侵袭性极强的恶性肿瘤,预后极差。由于肛门黑色素瘤的表现多变且不明确,常常被误诊为痔疮、息肉或溃疡,并伴有直肠脱垂。由于肛门黑色素瘤很少见,临床医生通常对其怀疑度较低,而且大多数患者在确诊时已出现转移性疾病。我们报告了一例偶然发现患有肛门黑色素瘤的患者。由于辅助化疗或免疫疗法的额外益处一直存在争议,因此及时进行手术切除和局部广泛切除与腹腔镜切除仍是治疗的主流。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A rare account of incidentally discovered anal melanoma.

Anal melanoma is a rare and highly aggressive malignancy that carries a poor prognosis. Due to its variable and ambiguous presentation, it is often misdiagnosed as a hemorrhoid, polyp, or an ulcer with a concomitant rectal prolapse. Clinicians usually have a low suspicion of anal melanoma due to its rarity and most people present with metastatic disease at the time of diagnosis. We report a case of a patient incidentally found to have anal melanoma. Prompt surgical resection with wide local excision versus abdominoperineal resection remains the mainstay of treatment as the added benefit of adjuvant chemoradiation or immunotherapy has been controversial.

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来源期刊
CiteScore
0.70
自引率
0.00%
发文量
559
审稿时长
11 weeks
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