Rushing Calvin J, Ivankiv Roman, Bullock Neal M, Rogers Diana E, Spinner Steven M
Resident, Graduate Medical Education, Westside Regional Medical Center, Plantation, FL.
Resident, Graduate Medical Education, Westside Regional Medical Center, Plantation, FL.
J Foot Ankle Surg. 2017 Sep-Oct;56(5):1095-1098. doi: 10.1053/j.jfas.2017.04.008. Epub 2017 May 27.
Onychomatricoma is a rare benign neoplasm of the nail matrix first described by Baran and Kint in 1992. Fewer than 80 cases of onychomatricoma have been described in the literature, 15 of which were initially misdiagnosed and treated as onychomycosis. We present the case of a 66-year-old male with thickening and linear xanthonychia of the hallux nail plate secondary to an onychomatricoma misdiagnosed as onychomycosis. Following biopsy for histopathologic analysis, the lesion and proximal nail matrix were surgically excised. At 12 months post-excision, the patient remains asymptomatic without evidence of recurrence. The purpose of the present case report is to make foot and ankle surgeons more cognizant of the pathology, highlight the nonspecific clinical and radiologic findings, and emphasize the importance of interdisciplinary communication for an accurate clinicopathologic correlation and diagnosis of the lesion. Although rare, onychomatricoma should be considered in the differential diagnosis for patients presenting with onychomycosis failing to respond to antimycologic treatment. The clinical index of suspicion for onychomatricoma should increase when only a singular dystrophic nail is involved. Following diagnostic confirmation by histopathology, complete surgical excision is the treatment of choice.
甲母质瘤是一种罕见的甲母质良性肿瘤,由巴兰和金特于1992年首次描述。文献中报道的甲母质瘤病例不到80例,其中15例最初被误诊为甲癣并按甲癣治疗。我们报告一例66岁男性,其拇趾甲板增厚并呈线状黄甲,继发于被误诊为甲癣的甲母质瘤。在进行活检以进行组织病理学分析后,手术切除了病变组织和近端甲母质。切除术后12个月,患者无症状,无复发迹象。本病例报告的目的是让足踝外科医生更了解这种病理情况,突出其非特异性的临床和影像学表现,并强调多学科沟通对于准确的临床病理关联和病变诊断的重要性。尽管罕见,但对于抗真菌治疗无效的甲癣患者,鉴别诊断时应考虑甲母质瘤。当仅累及单个营养不良甲时,对甲母质瘤的临床怀疑指数应增加。经组织病理学确诊后,完整手术切除是首选治疗方法。