Iezzoni J C, Fechner R E, Wong L S, Rosai J
Department of Pathology, University of Virginia Health Sciences Center, Charlottesville 22908, USA.
Am J Clin Pathol. 1995 Oct;104(4):391-6. doi: 10.1093/ajcp/104.4.391.
Aggressive angiomyxoma (AAM) is a rare, locally infiltrative but nonmetastasizing tumor of the pelvic and perineal soft tissues that occurs almost exclusively in adult females. The authors describe four cases of AAM in adult males that arose in the scrotum. There was some histologic variation among the tumors. One case was focally hypercellular around the blood vessels, two were more densely cellular throughout, and one had cystic degeneration. Three of the tumors were widely infiltrative, and one of the four tumors recurred locally. The clinicopathologic features of these cases are similar to those of AAM occurring in females. In either sex, AAM should be distinguished from benign myxoid tumors with a low risk of local recurrence and fully malignant myxoid tumors with distant metastatic potential.
侵袭性血管黏液瘤(AAM)是一种罕见的、局部浸润但不转移的盆腔和会阴软组织肿瘤,几乎仅发生于成年女性。作者描述了4例发生于成年男性阴囊的AAM病例。这些肿瘤之间存在一些组织学差异。1例在血管周围局灶性细胞增多,2例整体细胞密度更高,1例有囊性变。3例肿瘤呈广泛浸润性生长,4例中的1例发生局部复发。这些病例的临床病理特征与女性发生的AAM相似。无论男女患者,AAM均应与局部复发风险低的良性黏液样肿瘤以及具有远处转移潜能的完全恶性黏液样肿瘤相鉴别。