Department of Pathology, Royal Group of Hospitals Trust, Belfast, Northern Ireland.
Adv Anat Pathol. 2010 Mar;17(2):122-9. doi: 10.1097/PAP.0b013e3181cfe732.
Mullerian adenosarcoma is an uncommon, but not rare, mixed tumor containing a neoplastic but benign or mildly atypical epithelial element and a sarcomatous, usually low-grade, stromal component. The most common site is the uterine corpus but adenosarcoma also occurs in the cervix and ovary and more rarely in the vagina, fallopian tube, arising from peritoneal surfaces, or outside the female genital tract, for example in the intestine. Most uterine cases have a polypoid gross appearance, sometimes resulting in the formation of multiple polyps. Characteristic histologic features include a low power "phyllodes-like" architecture with leaf-like projections lined by a variety of benign Mullerian type epithelia, sometimes with squamous metaplasia. Intraglandular stromal protrusions are a characteristic feature. The stroma may be uniformly cellular but there is typically increased cellularity around the epithelial elements, resulting in the formation of a cambium layer. Using the World Health Organization definition, stromal mitotic activity of 2 or more per 10 high-power fields is required for a diagnosis of adenosarcoma but in practice the diagnosis is made with stromal mitotic activity less than this if the characteristic architecture and cambium layer is present. The stromal component is usually morphologically "low-grade" and of endometrial stromal or fibroblastic type (hormone receptor and CD10 positive). Sometimes it is high grade, resembling undifferentiated sarcoma. Additional features sometimes present include heterologous stromal elements or sex cord-like differentiation. Uterine adenosarcomas are, in general, low-grade neoplasms capable of local recurrence after polypectomy or hysterectomy and much less commonly distant metastasis. The 2 most important adverse prognostic factors, which sometimes coexist, are deep myometrial invasion and sarcomatous overgrowth; the latter is usually associated with morphologically "high-grade" stromal elements with loss of expression of hormone receptors and CD10. Adenosarcoma may be confused with a variety of lesions and one of the main differential diagnoses is adenofibroma in which the stromal component is, by definition, morphologically benign. However, occasional adenofibromas recur or even metastasize. As such, it has been suggested that all adenofibromas should be classified as adenosarcomas, albeit with low-malignant potential. Ovarian adenosarcomas are much more likely to exhibit malignant behavior than their uterine counterparts, probably due to the lack of an anatomic barrier to peritoneal dissemination.
苗勒管腺肉瘤是一种不常见但并非罕见的混合性肿瘤,包含一种肿瘤性但良性或低度非典型上皮成分和一种肉瘤性、通常为低级别、基质成分。最常见的部位是子宫体,但腺肉瘤也发生在宫颈和卵巢,更罕见的发生在阴道、输卵管,源于腹膜表面或女性生殖器官以外的部位,例如在肠。大多数子宫病例具有息肉样大体外观,有时导致多个息肉形成。特征性组织学特征包括低倍镜下“叶状瘤样”结构,由各种良性苗勒型上皮组成叶状突起,有时伴有鳞状化生。腺体内间质突起是一个特征性特征。基质可以是均匀细胞性的,但上皮成分周围通常有更多的细胞,形成形成层。根据世界卫生组织的定义,需要每 10 个高倍视野中有 2 个或更多的基质有丝分裂活动才能诊断为腺肉瘤,但实际上,如果存在特征性结构和形成层,诊断为有丝分裂活动小于这个数目的腺肉瘤。基质成分通常在形态上是“低级别”的,为子宫内膜基质或纤维母细胞类型(激素受体和 CD10 阳性)。有时它是高级别,类似于未分化肉瘤。有时还存在其他特征,包括异源性基质成分或性索样分化。子宫腺肉瘤通常是低级别肿瘤,在息肉切除或子宫切除后可能会局部复发,更罕见远处转移。2 个最重要的不良预后因素,有时共存,是深肌层浸润和肉瘤性过度生长;后者通常与形态上“高级别”的基质成分相关,伴有激素受体和 CD10 的表达丧失。腺肉瘤可能与多种病变混淆,主要的鉴别诊断之一是腺纤维瘤,其中基质成分根据定义在形态上是良性的。然而,偶尔腺纤维瘤会复发甚至转移。因此,有人建议将所有腺纤维瘤都归类为腺肉瘤,尽管其恶性潜能较低。卵巢腺肉瘤比子宫腺肉瘤更有可能表现出恶性行为,可能是因为缺乏腹膜扩散的解剖屏障。