Oliva E, Young R H, Clement P B, Bhan A K, Scully R E
James Homer Wright Pathology Laboratories, Massachusetts General Hospital, Boston 02114, USA.
Am J Surg Pathol. 1995 Jul;19(7):757-68. doi: 10.1097/00000478-199507000-00003.
Thirty-three highly cellular leiomyomas of the uterus from patients 29 to 65 (mean, 46) years of age and six endometrial stromal nodules from patients 41 to 53 (mean, 46) years of age are described. The patients usually presented with irregular uterine bleeding. Twenty-eight of the leiomyomas were intramural and five, submucosal. Eleven of 18 whose consistency is known were soft, fish-flesh, or rubbery, 10 were yellow or yellow-tan; one had a prominent cystic component. The tumors ranged from 0.5 to 15 cm (mean, 4.6 cm) in maximum dimension. On microscopic examination, they were densely cellular and composed of cells that ranged from round to spindle-shaped and had scanty cytoplasm. A focal fascicular pattern was present in all of the cases. Blood vessels were typically large; thick muscular walls and focally dilated lumens were a conspicuous feature of the majority of the neoplasms. Arterioles were evident focally in most of the tumors but were prominent in only one of them. Cleft-like spaces, some representing compressed vessels, others due to internodular edema, were present in 24 of the tumors and were conspicuous in 15 of them. The neoplasms typically exhibited focal irregular extension into the adjacent myometrium, and this feature was conspicuous in 18 of them. They often merged almost imperceptibly with the adjacent myometrium. All tumors were immunoreactive for desmin and 32 of 32 for alpha-smooth muscle actin. Two of the stromal nodules were polypoid intracavitary masses, three were submucosal, and one intramural. Five were completely or predominantly solid with cysts present focally in three of them; one tumor was predominantly cystic. The solid tissue was frequently yellow. Microscopic examination disclosed a diffuse growth of closely packed small cells with scanty cytoplasm and nuclei that lacked atypia. Three neoplasms contained cells with abundant foamy cytoplasm that were immunoreactive for CD68, indicating that they were histiocytes and not neoplastic cells. All the neoplasms had a prominent component of arterioles, which in one tumor had hyalinized walls. Five tumors were entirely well circumscribed and one predominantly well circumscribed with limited extension into the adjacent myometrium. The tumors were immunohistochemically negative for desmin.(ABSTRACT TRUNCATED AT 400 WORDS)
本文描述了33例年龄在29至65岁(平均46岁)患者的子宫高度富细胞平滑肌瘤,以及6例年龄在41至53岁(平均46岁)患者的子宫内膜间质结节。患者通常表现为子宫不规则出血。33例平滑肌瘤中,28例为肌壁间肌瘤,5例为黏膜下肌瘤。已知质地的18例中,11例质地柔软、鱼肉样或橡胶样,10例为黄色或黄棕色,1例有明显的囊性成分。肿瘤最大径0.5至15cm(平均4.6cm)。显微镜下检查,肿瘤细胞密集,由圆形至梭形细胞组成,胞质稀少。所有病例均有局灶性束状结构。血管通常较大;厚的肌壁和局灶性扩张的管腔是大多数肿瘤的显著特征。小动脉在大多数肿瘤中局灶可见,但仅在其中1例中较为突出。24例肿瘤中有裂隙样间隙,部分代表受压血管,部分由于结节间水肿,其中15例较为明显。肿瘤通常表现为局灶性不规则延伸至邻近肌层,18例中此特征明显。它们常与邻近肌层几乎难以察觉地融合。所有肿瘤对结蛋白呈免疫反应,32例对α-平滑肌肌动蛋白均呈免疫反应。6例子宫内膜间质结节中,2例为息肉样腔内肿物,3例为黏膜下肿物,1例为肌壁间肿物。5例完全或主要为实性,其中3例局灶有囊肿;1例肿瘤主要为囊性。实性组织常为黄色。显微镜检查显示,紧密排列的小细胞弥漫性生长伴有稀少胞质,细胞核无异型性。3例肿瘤含有胞质丰富呈泡沫状的细胞,对CD68呈免疫反应,表明它们是组织细胞而非肿瘤细胞。所有肿瘤均有明显的小动脉成分,其中1例肿瘤小动脉壁玻璃样变。5例肿瘤完全边界清楚,1例主要边界清楚,仅有限延伸至邻近肌层。这些肿瘤结蛋白免疫组化阴性。(摘要截断于400字)