Kyrpychova Liubov, Vanecek Tomas, Grossmann Petr, Martinek Petr, Steiner Petr, Hadravsky Ladislav, Belousova Irena E, Shelekhova Ksenya V, Svajdler Marian, Dubinsky Pavol, Michal Michal, Kazakov Dmitry V
Sikl's Department of Pathology, Medical Faculty in Pilsen, Charles University in Prague, Pilsen, Czech Republic.
Bioptical Laboratory, Pilsen, Czech Republic.
Am J Dermatopathol. 2018 Oct;40(10):721-726. doi: 10.1097/DAD.0000000000001091.
Adenoid cystic carcinoma (ACC) of the skin is a rare malignant neoplasm histologically identical to homonymous tumors in other organs. Cutaneous ACC has been found to harbor MYB gene activations, either through MYB chromosomal abnormalities or by generation of the MYB-NFIB fusion. In salivary gland ACC, in addition to the MYB gene, alterations in MYBL1, the gene closely related to MYB, have been reported. We studied 10 cases of cutaneous ACC (6 women, 4 men; and age range 51-83 years) for alterations in the MYB, NFIB, and MYBL1 genes, using FISH and PCR. MYB break-apart and NFIB break-apart tests were positive in 4 and 5 cases, respectively. MYB-NFIB fusions were found in 4 cases. The break of MYBL1 was found in 2 cases, and in one of them, the NFIB break-apart probe was positive, strongly indicating a MYBL1-NFIB fusion. In 2 cases, the MYB break-apart test was positive, whereas no MYB-NFIB was detected, strongly suggesting another fusion partner. It is concluded that MYBL1 alterations are detected in primary cutaneous ACC but are apparently less common compared with MYB and NFIB alterations.
皮肤腺样囊性癌(ACC)是一种罕见的恶性肿瘤,在组织学上与其他器官的同名肿瘤相同。已发现皮肤ACC存在MYB基因激活,其方式要么是通过MYB染色体异常,要么是通过产生MYB-NFIB融合。在涎腺ACC中,除MYB基因外,还报道了与MYB密切相关的基因MYBL1的改变。我们使用荧光原位杂交(FISH)和聚合酶链反应(PCR)研究了10例皮肤ACC(6例女性,4例男性;年龄范围51-83岁)的MYB、NFIB和MYBL1基因改变情况。MYB断裂分析和NFIB断裂分析分别在4例和5例中呈阳性。在4例中发现了MYB-NFIB融合。在2例中发现了MYBL1断裂,其中1例中NFIB断裂分析探针呈阳性,强烈提示存在MYBL1-NFIB融合情况。在2例中,MYB断裂分析呈阳性,但未检测到MYB-NFIB,强烈提示存在另一种融合伴侣。得出的结论是,原发性皮肤ACC中可检测到MYBL1改变,但与MYB和NFIB改变相比,其明显较少见。