Kao Andrew S, St Claire Kayla, Bedford Lisa M, Mehregan Darius R, Andea Aleodor A, Kouba David
Wayne State University School of Medicine MI, USA.
Department of Dermatology, Wayne State University MI, USA.
Int J Clin Exp Pathol. 2022 Apr 15;15(4):201-205. eCollection 2022.
Nevoid and myxoid melanoma are rare variants of melanoma; association of the two is a unique finding. Nevoid melanoma is characterized by morphologic resemblance to a nevus, whereas myxoid melanoma demonstrates a basophilic mucinous matrix. We present an atypical case of a melanoma progressing from a nevoid melanocytoma with myxoid changes. A 78-year-old female presented with a pigmented growth on her right thigh. Biopsy demonstrated a biphenotypic melanocytic proliferation composed of a nodule showing epithelioid melanocytes with enlarged nuclei, prominent nucleoli, lack of maturation, and abundant amphophilic cytoplasm with a rare mitotic figure. These findings were suggestive of melanoma along with a nevoid dermal component and myxoid stroma. FISH testing revealed a homozygous loss of 9p21 in the atypical component. SNP-microarray from the nevoid component demonstrated three abnormalities including a gain of whole chromosome 8, as well as loss of a copy of nearly an entire chromosome 9 and 16q most consistent with a melanocytoma.
无色素性和黏液样黑色素瘤是黑色素瘤的罕见变体;两者的关联是一个独特的发现。无色素性黑色素瘤的特征是形态上与痣相似,而黏液样黑色素瘤表现为嗜碱性黏液基质。我们报告了一例非典型病例,黑色素瘤由伴有黏液样改变的无色素性黑素细胞瘤发展而来。一名78岁女性右大腿出现色素沉着性肿物。活检显示为双表型黑素细胞增殖,由一个结节组成,该结节显示上皮样黑素细胞,细胞核增大,核仁突出,缺乏成熟,具有丰富的两性细胞质,有罕见的有丝分裂象。这些发现提示为黑色素瘤,伴有无色素性真皮成分和黏液样基质。荧光原位杂交检测显示非典型成分中9p21纯合缺失。来自无色素性成分的单核苷酸多态性微阵列显示三个异常,包括整条8号染色体的增加,以及几乎整条9号染色体和16q的一个拷贝的缺失,最符合黑素细胞瘤。