Pena-Burgos E M, Serra-Del Carpio G, Tapia-Viñe M, Ortiz-Cruz E J, Pozo-Kreilinger J J
Pathology Department, La Paz University Hospital, Madrid, Spain.
Radiology Department, La Paz University Hospital, Madrid, Spain.
J Cutan Pathol. 2023 May;50(5):390-395. doi: 10.1111/cup.14416. Epub 2023 Mar 16.
Glomus tumors (GT) are rare, benign tumors that arise from glomus bodies and usually develop in digital areas. Extradigital GT are exceptional and thigh location is infrequent.
We report a case of a GT of the thigh in a 79-year-old male patient that measured 9.5 cm in maximum size. The GT lay above the muscular fascia without infiltrating it. Internal hypervascularity was seen by spectral Doppler ultrasound. Magnetic resonance image showed a heterogeneous mass with hyperintense and hypointense components and internal lobes with liquid-liquid levels. Histopathology revealed a monotonous round-cell proliferation with central nuclei without atypia or mitotic figures, around small-caliber vessels. These cells expressed smooth muscle actin and pericellular collagen IV. GT of uncertain malignant potential was diagnosed. The mass was completely removed. The patient did not experience local relapse nor distant metastasis.
GT are rare soft tissue tumors whose diagnosis of unusual giant masses in uncommon locations may be delayed and misdiagnosed given the low suspicion.
血管球瘤(GT)是一种罕见的良性肿瘤,起源于血管球,通常发生在手指部位。指外血管球瘤极为罕见,发生于大腿部位的情况更是少见。
我们报告一例79岁男性患者的大腿血管球瘤,最大直径为9.5厘米。该血管球瘤位于肌筋膜上方,未侵犯肌筋膜。频谱多普勒超声显示内部血管丰富。磁共振成像显示为不均匀肿块,有高信号和低信号成分,内部有液-液平面的叶状结构。组织病理学显示围绕小口径血管有单调的圆形细胞增殖,细胞核位于中央,无异型性或有丝分裂象。这些细胞表达平滑肌肌动蛋白和细胞周围IV型胶原。诊断为具有不确定恶性潜能的血管球瘤。肿块被完全切除。患者未出现局部复发或远处转移。
血管球瘤是罕见的软组织肿瘤,鉴于其可疑性低,在不常见部位出现异常巨大肿块时,其诊断可能会延迟并被误诊。