Suppr超能文献

共质体血管瘤:两例报告。

Symplastic hemangioma: report of two cases.

作者信息

Goh Seng Geok Nicholas, Dayrit Johannes F, Calonje Eduardo

机构信息

St John's Institute of Dermatology, St Thomas' Hospital, Lambeth Palace Road, London, UK.

出版信息

J Cutan Pathol. 2006 Nov;33(11):735-40. doi: 10.1111/j.1600-0560.2006.00552.x.

Abstract

Symplastic hemangioma is characterized by degenerative atypia of vascular smooth muscle and interstitial cells within a pre-existing vascular lesion with minimal endothelial cell atypia. We describe an additional two cases of this distinctive but poorly recognized entity. On histology, both lesions revealed a cirsoid aneurysm-type appearance with thick-walled and variably dilated blood vessels. The vascular endothelial cells showed mild nuclear hyperchromasia with no multilayering or mitoses. The atypical cells, either located within the vascular smooth muscle wall or within the interstitium, were spindle or epithelioid with varying degrees of hyperchromasia, nuclear enlargement, pleomorphism, and multinucleation. Perivascular hemorrhage, vascular thrombosis, and focal papillary endothelial hyperplasia were uniformly present. The variably fibrous to edematous stroma showed hemosiderin deposits and a mononuclear inflammatory infiltrate. Clusters of adipocytes were present within the superficial dermis. Rare atypical mitoses and occasional bizarre lipoblast-like stromal cells were identified in one tumor. Immunohistochemistry showed focal smooth muscle actin positivity in the pleomorphic cells of the vascular walls. CD68 and CD34 stained occasional stromal cells in the interstitial location. Both the cases showed no recurrence. The bizarre cytologic changes are interpreted as degenerative in nature and probably akin to that observed in ancient schwannoma and uterine symplastic leiomyoma.

摘要

共生型血管瘤的特征是在先前存在的血管病变内血管平滑肌和间质细胞发生退行性异型性,内皮细胞异型性极小。我们描述了另外两例这种独特但认识不足的实体病例。组织学上,两个病变均显示出蔓状动脉瘤样外观,血管壁增厚且不同程度扩张。血管内皮细胞显示轻度核深染,无多层排列或核分裂象。非典型细胞位于血管平滑肌壁内或间质内,呈梭形或上皮样,有不同程度的深染、核增大、多形性和多核现象。血管周围出血、血管血栓形成和局灶性乳头状内皮增生均存在。不同程度的纤维性至水肿性间质可见含铁血黄素沉积和单核炎症浸润。浅真皮内可见脂肪细胞簇。在一个肿瘤中发现了罕见的非典型核分裂象和偶尔的奇异脂肪母细胞样间质细胞。免疫组化显示血管壁多形性细胞中局灶性平滑肌肌动蛋白阳性。CD68和CD34染色显示间质部位偶尔有间质细胞。两例均无复发。奇异的细胞学变化被解释为本质上是退行性的,可能类似于在古老的神经鞘瘤和子宫共生型平滑肌瘤中观察到的情况。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验