Handa Atsuhiko, Fujita Kazutoshi, Kono Tatsuo, Komori Koji, Hirobe Seiichi, Fukuzawa Ryuji
Department of Radiology, Tokyo Metropolitan Children's Medical Center, Tokyo, Japan.
Department of Surgery, Tokyo Metropolitan Children's Medical Center, Tokyo, Japan.
J Med Imaging Radiat Oncol. 2016 Dec;60(6):741-743. doi: 10.1111/1754-9485.12460. Epub 2016 Apr 20.
Perivascular epithelioid cell tumour (PEComa) encompasses a group of mesenchymal tumours composed of histologically and immunohistochemically distinctive perivascular epithelioid cells. A subset of PEComa that typically arises from the falciform ligament and/or ligamentum teres is termed clear cell myomelanocytic tumour of the falciform ligament/ligamentum teres. To date, its imaging findings have not been described. Here, we report the first radiological description of a pathologically confirmed tumour. The patient was a 5-year-old girl with a palpable abdominal mass. US, CT, MR and FDG-PET revealed a midline, well-defined, solid anterior abdominal wall tumour below the rectus abdominis and contiguous with the umbilicus that was hypervascular and FDG avid. Awareness of these imaging findings facilitates the diagnosis of this distinctive tumour.
血管周上皮样细胞瘤(PEComa)是一组由组织学和免疫组织化学上独特的血管周上皮样细胞组成的间叶性肿瘤。PEComa的一个亚组通常起源于镰状韧带和/或圆韧带,被称为镰状韧带/圆韧带透明细胞肌黑色素细胞瘤。迄今为止,其影像学表现尚未见报道。在此,我们报告首例经病理证实肿瘤的影像学描述。患者为一名5岁女童,可触及腹部肿块。超声、CT、磁共振成像(MR)和氟代脱氧葡萄糖正电子发射断层扫描(FDG-PET)显示,在腹直肌下方、与脐相连的中线处有一个边界清晰的实性前腹壁肿瘤,该肿瘤血管丰富且摄取FDG。了解这些影像学表现有助于诊断这种独特的肿瘤。