Modi Shilpi, Goel Deepa, Goyal Pawan, Gupta Aditya
Department of Pathology, Artemis Hospital, Gurgaon, Haryana, India.
Department of Neurosurgery, Artemis Hospital, Gurgaon, Haryana, India.
Asian J Neurosurg. 2020 Oct 19;15(4):1024-1026. doi: 10.4103/ajns.AJNS_144_20. eCollection 2020 Oct-Dec.
Myoepithelial tumor (MET) of bone is an unusual tumor of uncertain differentiation and histogenesis. Although its presence in various bones has been reported sparsely, the presentation in clivus as primary myoepithelial carcinoma (MEC) has never been reported. They resemble their salivary gland counterparts morphologically and immunohistochemically, but harbor distinct molecular phenotype. At present, moderate nuclear atypia is the acceptable criteria to differentiate MEC from myoepithelioma. Because of their rarity, wide histopathological spectrum, and intraosseous location, MET of bone is easily confused with a variety of primary bone and cartilaginous tumors. Application of immunohistochemistry and, if required, molecular testing are required for making a correct diagnosis. In this article, we describe an extremely rare case of a primary MEC arising from the clivus, which owing to unusual location and immunohistochemical profile was diagnostically challenging.
骨肌上皮瘤(MET)是一种分化和组织发生不确定的罕见肿瘤。尽管其在各种骨骼中的存在已有零星报道,但斜坡原发性肌上皮癌(MEC)的病例从未被报道过。它们在形态学和免疫组织化学上与涎腺同类肿瘤相似,但具有独特的分子表型。目前,中度核异型性是区分MEC和肌上皮瘤的可接受标准。由于其罕见性、广泛的组织病理学谱以及骨内位置,骨MET很容易与多种原发性骨和软骨肿瘤混淆。正确诊断需要应用免疫组织化学,必要时还需进行分子检测。在本文中,我们描述了一例极其罕见的起源于斜坡的原发性MEC病例,因其位置特殊和免疫组织化学特征,诊断具有挑战性。