Maher Ossama M, Prieto Victor G, Stewart John, Herzog Cynthia E
Departments of *Pediatrics ‡Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX †Department of Pediatrics, National Cancer Institute, Cairo University, Cairo, Egypt.
J Pediatr Hematol Oncol. 2015 May;37(4):e268-71. doi: 10.1097/MPH.0000000000000313.
Angiomatoid fibrous histiocytoma (AFH) is a soft-tissue tumor of low-grade malignancy and uncommon metastatic behavior. In this study, we describe the clinical findings of a metastatic case of AFH in the pelvis. In addition, we characterize 16 patients in the literature with AFH who metastasized over the last 4 decades. The time of appearance of metastases varied substantially and was reported 5 months to 16 years after primary tumor resection. Nine patients metastasized to lymph nodes. Excision of metastatic lymph nodes was usually curative. Pulmonary metastases were associated with fatal outcome. Long-term monitoring should be considered in patients with AFH.
血管样纤维组织细胞瘤(AFH)是一种低度恶性且具有不常见转移行为的软组织肿瘤。在本研究中,我们描述了1例骨盆部AFH转移病例的临床发现。此外,我们对文献中过去40年里发生转移的16例AFH患者进行了特征分析。转移出现的时间差异很大,报告显示在原发肿瘤切除后5个月至16年出现转移。9例患者发生淋巴结转移。切除转移淋巴结通常可治愈。肺转移与致命结局相关。对于AFH患者应考虑进行长期监测。