Anorectal balloon cell melanoma: a rare variant.

Q4 Medicine
Autopsy and Case Reports Pub Date : 2023-12-15 eCollection Date: 2023-01-01 DOI:10.4322/acr.2023.459
Priyanka Sameer, Pallavi Srivastava, Saumya Shukla, Nuzhat Husain
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引用次数: 0

Abstract

Balloon cell melanoma is a rare presentation of malignant melanoma, usually on the skin, with less than 100 cases reported. Mucosal BCM is even rarer, with only one case of anorectal BCM reported in English literature. The diagnosis is based on the histopathologic findings of a tumor composed of large, foamy melanocytes, with or without pigmentation, and confirmed by immunohistochemical studies showing expression for melanocytic markers. The foam cell appearance of the tumor cells and the lack of melanin pigment lead to a diagnostic dilemma, mostly when presented at an unusual location. Herein, we report a case of balloon cell melanoma at the anorectal junction in a 73-year-old male patient complaining of constipation and bleeding per rectum. Surgical resection was performed with no evidence of recurrence after three years of close follow-up. We believe this case will raise awareness among the medical community to consider this tumor a differential diagnosis in rectal masses.

肛门直肠气球细胞黑色素瘤:一种罕见的变异。
气球细胞黑色素瘤是一种罕见的恶性黑色素瘤,通常发生在皮肤上,报道的病例不到 100 例。粘膜球形细胞黑色素瘤更为罕见,英文文献中仅有一例肛门直肠球形细胞黑色素瘤的报道。诊断的依据是组织病理学发现的由大的泡沫状黑色素细胞组成的肿瘤,伴有或不伴有色素沉着,并经免疫组化研究证实显示黑色素细胞标记物的表达。肿瘤细胞的泡沫细胞外观和黑色素色素的缺乏导致了诊断上的两难,尤其是在肿瘤位置不寻常的情况下。在此,我们报告了一例肛门直肠交界处的气球细胞黑色素瘤病例,患者 73 岁,男性,主诉便秘和直肠出血。经过三年的密切随访,手术切除后无复发迹象。我们相信这个病例将提高医学界对直肠肿块的鉴别诊断意识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Autopsy and Case Reports
Autopsy and Case Reports Medicine-Internal Medicine
CiteScore
1.20
自引率
0.00%
发文量
60
审稿时长
9 weeks
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