幼儿丛状血管瘤1例
摘要
<正>1病历摘要患儿女,3岁。主因右肩胛部出现片状暗红色斑块半年,于2017年2月就诊于我科门诊。患儿半年前无明显诱因右肩胛部出现片状红斑,轻度隆起,质硬,有轻压痛,无明显瘙痒。曾至当地医院就诊,具体诊断不详,予外用糖皮质激素(种类不详)治疗后无明显好转,后皮损逐渐增大,且原皮损右侧出现新的红色丘疹,为明确诊断遂来我院皮肤科门诊就诊。患儿系第1胎第1产,足月顺产,既往体健,起病以来一般情况良好,否认系统疾病史,家族中无类似疾病患者。
引文
[1]宋志强,郝飞等.丛状血管瘤1例[J].临床皮肤科杂志,2003,32(6):353.
[2]郭金竹,张倩,李邻峰.中心消退的丛状血管瘤1例[J].临床皮肤科杂志,2008,37(10):678-679.
[3]张桂英,田清华,温海泉,等.获得性丛状血管瘤二例[J].国际皮肤性病学杂志,2010,36(4):184-185.
[4]Herron MD,Coffin CM,Vanderhooft SL,et al.Tufted angiomas:variability of the clinical morphology[J].Pediatr Dermatol,2002,19(5):394-401.
[5]Wassef C,Mateus R,Rao BK,et al.In vivo reflectance confocal microscopy features of discoid lupus erythematosus[J].J Drugs Dermatol,2012,11(9):1111-1113.
[6]Xu D,O TM,Shartava A.Isolation,characterization,and in vitro propagation of infantile hemangioma stem cells and an in vivo mouse model[J].J Hematol Oncol,2011,4:54.
[7]Croteau SE,Liang MG,Kozakewich HP,et al.Kaposiform hemangioendothelioma:atypical features and risks of Kasabach-Merritt phenomenon in 107 referrals[J].J Pediatr,2013,162(1):142-147.
[8]Egashira S,Jinnin M,Harada M.Exome sequence analysis of Kaposiform hemangioendothelioma:identification of putative driver mutations[J].An Bras Dermatol,2016,91(6):748-753.
[9]高亚,王怀杰.Kasabach-Merritt现象的过去、现在和未来[J].实用医院临床杂志,2012,9(4):25-27.
[10]Le Huu AR,Jokinen CH,Rubin BP,et al.Expression of prox1,lymphatic endothelial nuclear transcription factor,in Kaposiform he mangioendothelioma and tufted angioma[J].Am J Surg Pathol,2010,34(11):1563-1573.
[11]龚毓宾,孙斌,雷红召,等.Kasabach-Merritt现象的研究进展和治疗[J].中华实用儿科临床杂志,2014,29(10):789-791.
[12]Ishikawa K,Hatano Y,Ichikawa H,et al.The spontaneous regression of tufted angioma.A case of regression after two recurrences and a review of 27 cases reported in the literature[J].Dermatology,2005,210(4):346-348.
[13]Croteau SE,Gupta D.The clinical spectrum of kaposiform hemangioendothelioma and tufted angioma[J].Semin Cutan Med Surg,2016,35(3):147-152.
[14]徐教生,刘笑宇,马琳,等.外用卡替洛尔成功治疗儿童丛状血管瘤和化脓性肉芽肿[J].中华皮肤科杂志,2015,48(12):887-888.
[2]郭金竹,张倩,李邻峰.中心消退的丛状血管瘤1例[J].临床皮肤科杂志,2008,37(10):678-679.
[3]张桂英,田清华,温海泉,等.获得性丛状血管瘤二例[J].国际皮肤性病学杂志,2010,36(4):184-185.
[4]Herron MD,Coffin CM,Vanderhooft SL,et al.Tufted angiomas:variability of the clinical morphology[J].Pediatr Dermatol,2002,19(5):394-401.
[5]Wassef C,Mateus R,Rao BK,et al.In vivo reflectance confocal microscopy features of discoid lupus erythematosus[J].J Drugs Dermatol,2012,11(9):1111-1113.
[6]Xu D,O TM,Shartava A.Isolation,characterization,and in vitro propagation of infantile hemangioma stem cells and an in vivo mouse model[J].J Hematol Oncol,2011,4:54.
[7]Croteau SE,Liang MG,Kozakewich HP,et al.Kaposiform hemangioendothelioma:atypical features and risks of Kasabach-Merritt phenomenon in 107 referrals[J].J Pediatr,2013,162(1):142-147.
[8]Egashira S,Jinnin M,Harada M.Exome sequence analysis of Kaposiform hemangioendothelioma:identification of putative driver mutations[J].An Bras Dermatol,2016,91(6):748-753.
[9]高亚,王怀杰.Kasabach-Merritt现象的过去、现在和未来[J].实用医院临床杂志,2012,9(4):25-27.
[10]Le Huu AR,Jokinen CH,Rubin BP,et al.Expression of prox1,lymphatic endothelial nuclear transcription factor,in Kaposiform he mangioendothelioma and tufted angioma[J].Am J Surg Pathol,2010,34(11):1563-1573.
[11]龚毓宾,孙斌,雷红召,等.Kasabach-Merritt现象的研究进展和治疗[J].中华实用儿科临床杂志,2014,29(10):789-791.
[12]Ishikawa K,Hatano Y,Ichikawa H,et al.The spontaneous regression of tufted angioma.A case of regression after two recurrences and a review of 27 cases reported in the literature[J].Dermatology,2005,210(4):346-348.
[13]Croteau SE,Gupta D.The clinical spectrum of kaposiform hemangioendothelioma and tufted angioma[J].Semin Cutan Med Surg,2016,35(3):147-152.
[14]徐教生,刘笑宇,马琳,等.外用卡替洛尔成功治疗儿童丛状血管瘤和化脓性肉芽肿[J].中华皮肤科杂志,2015,48(12):887-888.