罕见的Klippel-Trenaunay综合征,表现为慢性髓性白血病。

IF 0.8 4区 医学 Q4 PEDIATRICS
Çağrı Coşkun, Tekin Aksu, Fatma Gümrük, Şule Ünal
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引用次数: 3

摘要

背景:Klippel-Trenaunay综合征(KTS)是一种与毛细血管/静脉/淋巴畸形相关的过度生长综合征,伴有肢体肥大和癌症风险。各种癌症,主要是肾母细胞瘤,在KTS患者中有报道,但没有白血病。慢性髓性白血病(CML)在儿童中也是一种罕见的疾病,没有已知的疾病或综合征易患CML。病例:我们报告一例CML偶然诊断在儿童与KTS时,他是出血的手术左腹股沟血管畸形。结论:本病例反映了可能伴随KTS的多种癌症类型,并为此类患者的CML预后提供了信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A rare case of Klippel-Trenaunay syndrome presenting with chronic myeloid leukemia.

Background: Klippel-Trenaunay syndrome (KTS) is an overgrowth syndrome associated with capillary/venous/ lymphatic malformations with limb hypertrophy and cancer risk. Various cancers, mostly Wilms tumor, have been reported in patients with KTS, but not leukemia. Chronic myeloid leukemia (CML) is also a rare disease in children, where there is no known disease or syndrome to predispose to CML.

Case: We report a case of CML incidentally diagnosed in a child with KTS when he was bleeding from surgery of the left groin for vascular malformation.

Conclusions: This case reflects the variety of cancer types that may accompany KTS and provides information about CML prognosis in such patients.

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来源期刊
CiteScore
1.40
自引率
0.00%
发文量
122
审稿时长
6-12 weeks
期刊介绍: The Turkish Journal of Pediatrics is a multidisciplinary, peer reviewed, open access journal that seeks to publish research to advance the field of Pediatrics. The Journal publishes original articles, case reports, review of the literature, short communications, clinicopathological exercises and letter to the editor in the field of pediatrics. Articles published in this journal are evaluated in an independent and unbiased, double blinded peer-reviewed fashion by an advisory committee.
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