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39岁患者甲下无黑色素性黑色素瘤的罕见部位:一例罕见病例报告

Unusual location of subungual amelanotic melanoma in 39-year-old patient: a rare case report.

作者信息

Karaja Saja Ahmad, Halloum Mai Abdulsalam, Mansour Sanaa Yasser, Almasri Alae Aldin

机构信息

Faculty of Medicine, Hama University.

Ministry of Health, Hama, Syria.

出版信息

Ann Med Surg (Lond). 2024 Feb 28;86(4):2314-2317. doi: 10.1097/MS9.0000000000001860. eCollection 2024 Apr.

Abstract

INTRODUCTION AND IMPORTANCE

Melanoma represents only 1% of all skin cancers. Acral lentigious melanoma (ALM) which usually arises from feet, is the rarest main subtype of melanoma. Subungual melanoma (SUM) is a rare variant of ALM. Amelanotic melanoma (AM) is found only in 4-27.5% of melanomas, and the mean age for patients affected by AM exceeds 50 years. Late diagnosing leads to unfavourable prognosis.

CASE PRESENTATION

The authors present a case of subungual amelanotic melanoma that affected the nail unit of the right thumb which is a rare case, especially when the patient is only 39 years old. The lesion enlarged over a year and was misdiagnosed many times and treated with no response. Sentinel node biopsy was positive and the patient was moved to a specialized hospital for treatment.

CLINICAL DISCUSSION

Diagnosing subungual amelanotic melanoma is challenging, not only because it is the rarest, but also it mimics many benign and malignant neoplasms due to the lack of pigmentation, in addition to the absence of clinical diagnostic features. AM exhibits a high growth rate helping in limiting the window for early detection.

CONCLUSIONS

Lately diagnosed subungual amelanotic melanoma usually associates with an increased risk of metastases, So it should be considered as a cause of any non-healing lesion. Early diagnosing gives patients the best chance for survival.

摘要

引言与重要性

黑色素瘤仅占所有皮肤癌的1%。肢端雀斑样痣黑色素瘤(ALM)通常发生于足部,是黑色素瘤最罕见的主要亚型。甲下黑色素瘤(SUM)是ALM的一种罕见变体。无色素性黑色素瘤(AM)仅在4% - 27.5%的黑色素瘤中出现,且受AM影响的患者平均年龄超过50岁。诊断延迟会导致预后不良。

病例介绍

作者报告了一例影响右手拇指甲单位的甲下无色素性黑色素瘤病例,这是一个罕见病例,尤其是患者年仅39岁。病变在一年多的时间里逐渐增大,多次被误诊且治疗无效。前哨淋巴结活检呈阳性,患者被转至专科医院进行治疗。

临床讨论

诊断甲下无色素性黑色素瘤具有挑战性,不仅因为它最为罕见,还因为缺乏色素沉着以及没有临床诊断特征,它会模仿许多良性和恶性肿瘤。AM生长速度快,这有助于限制早期检测的窗口期。

结论

甲下无色素性黑色素瘤诊断延迟通常与转移风险增加相关,因此应将其视为任何不愈合病变的一个病因。早期诊断为患者提供了最佳的生存机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b76/10990321/7557576bb385/ms9-86-2314-g001.jpg

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