McGregor Stephanie M, Alikhan Mir B, John Rahel A, Kotler Howard, Bridge Julia A, Mujacic Ibro, Kadri Sabah, Segal Jeremy, Krausz Thomas
*Department of Pathology, University of Chicago Medicine §Chicago Otolaryngology Associates, Chicago ‡Dermatopathology, Midwest Diagnostic Pathology, Park Ridge, IL †Department of Pathology and Laboratory Medicine, University of Wisconsin-Madison, Madison, WI ∥Department of Pathology/Microbiology, Pediatrics, and Orthopaedic Surgery, 983135 Nebraska Medical Center, University of Nebraska, Omaha, NE.
Am J Surg Pathol. 2017 May;41(5):717-722. doi: 10.1097/PAS.0000000000000778.
Perivascular epithelioid cell neoplasms (PEComas) are a family of mesenchymal tumors with features of both smooth muscle and melanocytic differentiation, with or without true melanin pigment. The highly variable morphology of PEComas results in a broad differential diagnosis that is also dependent on anatomic site. A subset demonstrates rearrangements involving the TFE3 (Xp11) locus, which can be used in diagnostically difficult cases. Here we describe a case of a melanotic PEComa with NONO-TFE3 fusion occurring in the sinonasal mucosa, as demonstrated by both next-generation sequencing and molecular cytogenetic studies. This case is the first of its kind in the literature and only the second documented PEComa harboring a NONO-TFE3 rearrangement. In light of unequivocal molecular ancillary studies, this case illustrates that PEComa must enter the differential for pigmented lesions of the sinonasal mucosa, where malignant melanoma would be much more likely to occur.
血管周上皮样细胞肿瘤(PEComas)是一类间质性肿瘤,具有平滑肌和黑素细胞分化特征,可有或无真正的黑色素沉着。PEComas高度可变的形态导致广泛的鉴别诊断,这也取决于解剖部位。一部分病例显示涉及TFE3(Xp11)位点的重排,可用于诊断困难的病例。在此,我们描述了一例发生于鼻窦黏膜的伴有NONO-TFE3融合的黑色素性PEComa病例,二代测序和分子细胞遗传学研究均证实了这一点。该病例是文献中首例此类病例,也是第二例记录在案的伴有NONO-TFE3重排的PEComa。鉴于明确的分子辅助研究,该病例表明PEComa必须纳入鼻窦黏膜色素沉着病变的鉴别诊断,而鼻窦黏膜更易发生恶性黑色素瘤。