Dalton Scott R, Fillman Eric P, Altman Coleman E, Gardner Timothy L, Davis Thomas L, Bastian Boris C, Libow Lester F, Elston Dirk M
Department of Pathology, Brooke Army Medical Center, Fort Sam Houston, Texas, USA.
Hum Pathol. 2003 Jul;34(7):706-9. doi: 10.1016/s0046-8177(03)00234-x.
Melanocytic lesions with lichenoid regression may mimic a benign lichenoid keratosis (BLK) histologically. A total of 336 BLKs were reviewed and deeper sections obtained to determine the frequency of this phenomenon. Two cases (0.6%) showed at least 1 melanocytic nest or junctional multinucleated melanocyte (starburst melanocyte) on deeper sections confirmed by MART-1 immunostaining. Both of these cases demonstrated solar elastosis, and 1 case had an effaced rete ridge pattern. Not included in the histological study are 5 additional cases in which the initial slide showed only lichenoid dermatitis, but deeper sections obtained before to the initial sign-out revealed a melanocytic proliferation. These 5 cases would have been signed out as "consistent with BLK" if deeper sections had not been obtained. Fluorescent in situ hybridization (FISH) was performed on 3 cases; in each case, the melanocytes demonstrated a loss of chromosome 9p21 DNA copy number. The finding of nests of genetically altered melanocytes on severely sun-damaged skin strongly suggests that these cases represent lichenoid regression of melanoma in situ. Pathologists should approach a diagnosis of BLK cautiously in the setting of severely sun-damaged skin.
具有苔藓样消退的黑素细胞性病变在组织学上可能类似于良性苔藓样角化病(BLK)。我们回顾了336例BLK,并获取了更深层次的切片以确定这种现象的发生率。有2例(0.6%)在更深层次的切片上显示至少1个黑素细胞巢或交界性多核黑素细胞(星爆样黑素细胞),经MART-1免疫染色证实。这2例均表现为日光性弹力组织变性,其中1例有表皮嵴消失的表现。组织学研究未纳入另外5例,这些病例最初的切片仅显示苔藓样皮炎,但在最初报告之前获取的更深层次切片显示有黑素细胞增殖。如果未获取更深层次的切片,这5例原本会报告为 “符合BLK”。对3例进行了荧光原位杂交(FISH)检测;在每例中,黑素细胞均显示9号染色体p21区域DNA拷贝数缺失。在严重日光损伤的皮肤上发现基因改变的黑素细胞巢强烈提示这些病例代表原位黑素瘤的苔藓样消退。在严重日光损伤的皮肤情况下,病理学家应谨慎做出BLK的诊断。