Missak Meina, Haig Aaron, Gabril Manal
Pathology and Laboratory Medicine, Schulich School of Medicine and Dentistry, Western University, London, Ontario, Canada.
Case Rep Dermatol. 2021 Feb 4;13(1):98-102. doi: 10.1159/000511696. eCollection 2021 Jan-Apr.
Pilomatrixoma is an uncommon, benign tumor with differentiation towards both the hair matrix and cells arising in the cortex, most frequently appearing in the first or second decade of life. In rare instances, pilomatrixomas can show malignant transformation. Pilomatrix carcinoma is extremely uncommon and has traditionally been considered a tumor of low malignant potential; however, a high local recurrence rate has been reported. There is a paucity of literature on these lesions, with only a few reports describing the spectrum of malignant changes seen in these lesions. In this case report, we present a case of pilomatrixoma in an adult patient showing atypical features. While the tumor is small, there are focal features that suggest progression to malignancy, but do not fulfill the criteria for pilomatrix carcinoma. These focal atypical features include a focal infiltrative pattern at the periphery, with a variable cytological atypia and an increased mitotic rate, up to five mitotic events/high-power field. Irregular foci of central necrosis (comedonecrosis) were present in several lobules. Some of the features identified were similar to a subset of pilomatrixoma, known as "proliferating pilomatrixoma." However, our case did not have the diffuse changes or larger size that has been frequently reported in "proliferating pilomatrixoma." In conclusion, given the lack of focality of the changes, the lesion in our case is best described as a pilomatricoma with atypical features. Furthermore, our case may highlight the need to ensure close clinical follow-up for these lesions with unexpected atypical features that raise concern of recurrence and malignant transformation.
毛母质瘤是一种罕见的良性肿瘤,具有向毛基质和毛囊皮质细胞分化的特性,最常出现在生命的第一个或第二个十年。在罕见情况下,毛母质瘤可发生恶性转化。毛母质癌极为罕见,传统上被认为是一种低恶性潜能的肿瘤;然而,已有报道称其局部复发率较高。关于这些病变的文献较少,仅有少数报告描述了这些病变中所见的恶性变化谱。在本病例报告中,我们展示了一例具有非典型特征的成年患者毛母质瘤。虽然肿瘤较小,但有一些局灶性特征提示有进展为恶性的可能,但不符合毛母质癌的标准。这些局灶性非典型特征包括周边的局灶浸润性模式、不同程度的细胞异型性和有丝分裂率增加,高达每高倍视野5个有丝分裂事件。几个小叶中存在中央坏死(粉刺样坏死)的不规则病灶。所发现的一些特征与毛母质瘤的一个亚型“增殖性毛母质瘤”相似。然而我们的病例没有“增殖性毛母质瘤”中经常报道的弥漫性变化或更大的尺寸。总之,鉴于变化缺乏局灶性,我们病例中的病变最好描述为具有非典型特征的毛母质瘤。此外,我们的病例可能凸显了对于这些具有引发复发和恶性转化担忧的意外非典型特征的病变,需要确保密切临床随访的必要性。