Qari Hiba, Hamao-Sakamoto Aya, Fuselier Clay, Cheng Yi-Shing Lisa, Kessler Harvey, Wright John
Department of Diagnostic Sciences, Texas A&M University Baylor College of Dentistry, 3302 Gaston Avenue Room # 214, Dallas, TX, 75246, USA.
Oral and Maxillofacial Surgery Division, Department of Surgery, UT Southwestern Medical Center, 5323 Harry Hines Blvd, Dallas, TX, 75390-9109, USA.
Head Neck Pathol. 2016 Jun;10(2):192-200. doi: 10.1007/s12105-015-0668-3. Epub 2015 Nov 14.
Phosphaturic mesenchymal tumor (PMT) is a rare neoplasm that secretes fibroblast growth factor-23 (FGF-23) and causes oncogenic osteomalacia. It occurs in adults with equal gender distribution and the most common location is the lower extremities, followed by the head and neck. Besides osteomalacia, the clinical presentation includes bone pain and multiple bone fractures. Microscopic features consist of spindle cells, multinucleated giant cells, and calcifications embedded in a chondromyxoid matrix. Laboratory findings indicate normal calcium and parathyroid levels, hypophosphatemia, and increased levels of FGF-23 that usually revert to normal after surgical removal. Due to its rarity, the purpose of the study was to report 2 new oral cases of PMT and to review the literature in the head and neck. The first case occurred in the gingiva and had been present for 6 years. The second case was a recurrence of a previously diagnosed PMT in the right mandible that metastasized to the lung and soft tissue. The literature review included 53 cases in the head and neck. There was a predilection for extra-oral sites (76%) compared to intra-oral sites (24%) with paranasal sinuses considered the most common location (38%) followed by the mandible (15%). There were 9 recurrences that included 3 malignant cases indicating a potentially aggressive tumor. Due to the indeterminate biological behavior of PMT and its rarity, a comprehensive evaluation of medical, laboratory, radiographic, and histological findings are crucial for a definitive diagnosis and treatment.
磷酸尿性间叶肿瘤(PMT)是一种罕见的肿瘤,可分泌成纤维细胞生长因子23(FGF-23)并导致致癌性骨软化症。它发生于成年人,男女发病率相等,最常见的部位是下肢,其次是头颈部。除骨软化症外,临床表现还包括骨痛和多发性骨折。显微镜下特征包括梭形细胞、多核巨细胞以及嵌入软骨黏液样基质中的钙化。实验室检查结果显示钙和甲状旁腺水平正常,低磷血症,FGF-23水平升高,手术切除后通常恢复正常。由于其罕见性,本研究的目的是报告2例新的口腔PMT病例并回顾头颈部相关文献。第一例发生于牙龈,已存在6年。第二例是先前诊断的右下颌骨PMT复发并转移至肺和软组织。文献回顾包括53例头颈部病例。与口腔内部位(24%)相比,口腔外部位(76%)更易发生,其中鼻窦被认为是最常见的部位(38%),其次是下颌骨(15%)。有9例复发,包括3例恶性病例,表明该肿瘤具有潜在侵袭性。由于PMT生物学行为不确定且罕见,对医学、实验室、影像学和组织学检查结果进行全面评估对于明确诊断和治疗至关重要。