Dunphy Louise, Morhij Rossell, Verma Yash, Pay Andrew
Department of Plastic Surgery, John Radcliffe Hospital, Oxford, UK.
BMJ Case Rep. 2017 Nov 3;2017:bcr-2016-218785. doi: 10.1136/bcr-2016-218785.
Subungual melanoma, an uncommon form of acral melanoma that arises within the nail matrix, accounts for 1%-3% of all cutaneous melanoma in Caucasians. As subungual melanoma presents in a more disguised manner than cutaneous lesions, increased vigilance is required. It most commonly presents as a discolouration of the nail, nail splitting or nail-bed bleeding. Black pigmentation of the adjacent nail fold, termed Hutchinson's sign, may be a diagnostic clue. Treatment of subungual melanoma remains surgical with wide local excision and amputation primary modalities. We present the case of a 61-year-old man with an 18-month history of a left thumb nail-bed abnormality and a 6-week history of left axillary lymphadenopathy. One year earlier, he presented to the emergency department with a purulent discharge from his left thumb but declined nail-bed ablation. He was referred to the 'Hand and Plastic Injuries Clinic' by his general practitioner and diagnosed with a chronic traumatic-induced nail-bed injury. As his symptoms did not improve, he was referred to the 2-week wait Skin Cancer Clinic. The left thumb nail-bed was excised as a nail unit down to bone, and the diagnosis of melanoma was rendered. Left axillary lymphadenopathy was confirmed as metastatic melanoma. He underwent amputation of his left thumb at the interproximal phalangeal joint, and a left axillary node dissection was performed. No residual melanoma was identified in his thumb. Microscopically, his left axillary dissection confirmed 9 out of 36 positive nodes for metastatic melanoma with extracapsular spread. He was staged at IIIC disease. This case report demonstrates missed opportunities to diagnose subungual melanoma and acts as a cautionary tale in considering this pathology in the differential diagnosis of nail-bed lesions with prompt referral for further investigation.
甲下黑色素瘤是肢端黑色素瘤的一种罕见形式,起源于甲母质,在白种人中占所有皮肤黑色素瘤的1%-3%。由于甲下黑色素瘤的表现比皮肤病变更为隐匿,因此需要提高警惕。它最常见的表现是指甲变色、指甲裂开或甲床出血。相邻甲襞的黑色色素沉着,称为哈钦森征,可能是一个诊断线索。甲下黑色素瘤的治疗仍然以手术为主,广泛局部切除和截肢是主要方式。我们报告一例61岁男性,有18个月的左拇指甲床异常病史和6周的左腋窝淋巴结病病史。一年前,他因左拇指脓性分泌物就诊于急诊科,但拒绝甲床切除。他被全科医生转诊至“手部和整形损伤诊所”,诊断为慢性创伤性甲床损伤。由于症状未改善,他被转诊至两周等待期皮肤癌诊所。将左拇指甲床作为一个甲单位切除至骨,诊断为黑色素瘤。左腋窝淋巴结病被确诊为转移性黑色素瘤。他在近节指间关节处接受了左拇指截肢,并进行了左腋窝淋巴结清扫术。在他的拇指中未发现残留的黑色素瘤。显微镜检查显示,他的左腋窝清扫术证实36个阳性淋巴结中有9个为转移性黑色素瘤,伴有包膜外扩散。他被分期为IIIC期疾病。本病例报告展示了诊断甲下黑色素瘤时错过的机会,并作为一个警示故事,提醒在鉴别诊断甲床病变时考虑这种病理情况,并及时转诊进行进一步检查。