Seab J A, Graham J H, Helwig E B
Department of Dermatopathology, Armed Forces Institute of Pathology, Washington, DC 20306-6000.
Am J Surg Pathol. 1989 Jan;13(1):39-44. doi: 10.1097/00000478-198901000-00005.
We report a clinical and histologic study of 70 patients, each with a single melanocytic lesion termed "deep penetrating nevus" (DPN). The lesions are most commonly found on the face, upper trunk, or proximal extremities of patients between the ages of 10 and 30 years. Typically they are darkly pigmented. Histologically they are characterized by loosely organized nests of pleomorphic pigmented cells that penetrate deep into the reticular dermis and often to the subcutaneous fat. Follow-up was obtained from 48 patients. It ranged from 1 to 23 years (mean, 7 years). Despite an initial histologic diagnosis of malignant melanoma in 29% of the cases, there were no local recurrences and no distant metastases. It is important to differentiate DPN from malignant melanoma. The characteristic histologic features of DPN also allow its differentiation from spindle cell and epithelioid cell nevi and blue nevi.
我们报告了一项对70例患者的临床和组织学研究,每位患者均有一个被称为“深部穿透性痣”(DPN)的单一黑素细胞病变。这些病变最常见于10至30岁患者的面部、上躯干或近端肢体。通常它们色素沉着较深。组织学上,其特征是多形性色素细胞巢排列疏松,深入网状真皮,常至皮下脂肪。对48例患者进行了随访。随访时间为1至23年(平均7年)。尽管最初29%的病例组织学诊断为恶性黑色素瘤,但无一例局部复发和远处转移。将DPN与恶性黑色素瘤区分开来很重要。DPN的特征性组织学特征也使其能够与梭形细胞和上皮样细胞痣以及蓝色痣相鉴别。