Department of Dermatology, University of Utah Health Sciences Center, Salt Lake City, Utah, USA.
J Am Acad Dermatol. 2010 Apr;62(4):591-6. doi: 10.1016/j.jaad.2009.06.080. Epub 2009 Dec 16.
Little is known about the recurrence/persistence rates of dysplastic nevi (DN) after biopsy, and whether incompletely removed DN should be re-excised to prevent recurrence.
Our purpose was to determine the recurrence rates of previously biopsied DN, and to assess whether biopsy method, margin involvement, congenital features, epidermal location, and degree of dysplasia are associated with recurrence.
Patients having a history of a "nevus biopsy" at least 2 years earlier were assessed for clinical recurrence. Slides of original lesions were re-reviewed by a dermatopathologist.
A total of 271 nevus biopsy sites were assessed in 115 patients. Of 195 DN with greater than 2 years of follow-up, 7 (3.6%) demonstrated recurrence on clinical examination. In all, 98 DN had a follow-up period of at least 4 years with no clinical recurrence. Of 61 benign nevus biopsy sites examined, clinical recurrence was observed in two (3.3%). For all nevi, recurrence was significantly associated with shave biopsy technique but not with nevus dysplasia or subtype, or the presence of positive margin or congenital features.
Most biopsies were performed in a pigmented lesion clinic at a single tertiary referral center. Determinations of nevus recurrence were made on clinical rather than histologic grounds, and follow-up times were limited in some cases.
In this cohort, rates of clinical recurrence after biopsy of DN and benign nevi were extremely low. Re-excision of nevi, including mildly to moderately DN with a positive margin, may not be necessary.
关于活检后发育不良痣(DN)的复发/持续率知之甚少,以及是否应切除未完全切除的 DN 以防止复发。
我们的目的是确定先前活检的 DN 的复发率,并评估活检方法、边缘受累、先天性特征、表皮位置和发育不良程度是否与复发相关。
对至少 2 年前有“痣活检”病史的患者进行临床复发评估。由皮肤科病理学家重新审查原始病变的切片。
在 115 名患者中评估了 271 个痣活检部位。在 195 例随访时间超过 2 年的 DN 中,7 例(3.6%)在临床检查中显示复发。在所有随访时间至少为 4 年且无临床复发的 98 例 DN 中,有 2 例(3.3%)良性痣活检部位出现临床复发。对于所有痣,复发与刮除活检技术显著相关,但与痣发育不良或亚型、阳性边缘或先天性特征无关。
大多数活检是在单一三级转诊中心的色素病变诊所进行的。对痣复发的确定是基于临床而不是组织学依据,并且在某些情况下随访时间有限。
在该队列中,DN 和良性痣活检后的临床复发率极低。对于包括轻度至中度阳性边缘的 DN 在内的痣,再次切除可能没有必要。