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快速生长的先天性血管外皮细胞瘤中的出血并发症。

Hemorrhagic complications in a rapidly growing, congenital hemangiopericytoma.

作者信息

Resnick S D, Lacey S, Jones G

机构信息

School of Medicine, University of North Carolina at Chapel Hill 27514.

出版信息

Pediatr Dermatol. 1993 Sep;10(3):267-70. doi: 10.1111/j.1525-1470.1993.tb00374.x.

Abstract

A 3-week-old infant had a massive hemangioma-like vascular neoplasm that had enlarged rapidly since being noted at birth. Less than a day after this initial evaluation the tumor underwent spontaneous ulceration and the infant had a near-fatal hemorrhage. Histologically, the tumor was a spindle cell neoplasm most consistent with the diagnosis of congenital hemangiopericytoma. Local excision appears to have been curative after almost two years of follow-up. The case is instructive in pointing out the importance of considering nonhemangioma vascular neoplasms in the evaluation of newborns with vascular tumors.

摘要

一名3周大的婴儿患有巨大的血管瘤样血管肿瘤,自出生时被发现以来迅速增大。在初次评估后不到一天,肿瘤发生自发性溃疡,婴儿出现近乎致命的出血。组织学上,该肿瘤是一种梭形细胞瘤,最符合先天性血管外皮细胞瘤的诊断。经过近两年的随访,局部切除似乎已治愈。该病例有助于指出在评估患有血管肿瘤的新生儿时考虑非血管瘤性血管肿瘤的重要性。

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