早产儿持续高血压2个月

刘云峰, 韩彤妍, 童笑梅, 王晶, 汤亚南, 崔立刚, 朱小辉, 朴梅花, 王晴晴, 武慧

中国当代儿科杂志 ›› 2018, Vol. 20 ›› Issue (11) : 939-943.

PDF(1712 KB)
HTML
PDF(1712 KB)
HTML
中国当代儿科杂志 ›› 2018, Vol. 20 ›› Issue (11) : 939-943. DOI: 10.7499/j.issn.1008-8830.2018.11.012
论著·病例分析

早产儿持续高血压2个月

  • 刘云峰1, 韩彤妍1, 童笑梅1, 王晶1, 汤亚南1, 崔立刚2, 朱小辉3, 朴梅花1, 王晴晴1, 武慧1
作者信息 +

Persistent hypertension for two months in a preterm infant

  • LIU Yun-Feng1, HAN Tong-Yan1, TONG Xiao-Mei1, WANG Jing1, TANG Ya-Nan1, CUI Li-Gang2, ZHU Xiao-Hui3, PIAO MeiHua1, WANG Qing-Qing1, WU Hui1
Author information +
文章历史 +

摘要

患儿(36周胎龄出生),男,2个月,因咳嗽、呼吸困难入院。入院后发现患儿存在持续性高血压、蛋白尿和惊厥持续状态,影像学提示主动脉及大分支广泛钙化,腹主动脉、右肾动脉局部管腔变窄伴血流速度增快。患儿新生儿期因湿肺、肺动脉高压住院,期间曾发现高血压、蛋白尿。进一步行全外显子组基因高通量测序,发现患儿ENPP1基因存在源自父母的复合杂合突变:c.130C > T(p.Q44X)和.c.1112A > T(p.Y371F)。c.130C > T为无义突变,可造成蛋白质从44个氨基酸之后的部分缺失,为一级致病性突变形式;c.1112A > T为错义突变,为已报道的与特发性婴儿动脉钙化症(ⅡAC)相关的致病性突变。因此确诊为ⅡAC。给予膦酸盐及降压、止惊、呼吸支持等对症治疗,血压维持在正常高限,动脉钙化未恶化。对于持续高血压伴广泛大血管钙化的小婴儿,应注意ⅡAC的可能,尽早行影像学及基因检查确诊。

Abstract

A boy aged 2 months (born at 36 weeks of gestation) was admitted due to cough and dyspnea. After admission, he was found to have persistent hypertension, proteinuria, and persistent convulsion, and imaging examination showed extensive calcification of the aorta and major branches and stenosis of local lumens of the abdominal aorta and the right renal artery with increased blood flow velocity. The boy was admitted during the neonatal period due to wet lung and pulmonary arterial hypertension and was found to have hypertension and proteinuria. Highthroughput whole-exome sequencing was performed and found two compound heterozygous mutations in the ENPP1 gene from his parents, c.130C > T (p.Q44X) and c.1112A > T (p.Y371F). c.130C > T was a nonsense mutation, which could cause partial deletion of protein from 44 amino acids, and was defined as a primary pathogenic mutation. c.1112A > T was a missense mutation which had been reported as a pathogenic mutation associated with idiopathic infantile arterial calcification (ⅡAC). Therefore, he was diagnosed with ⅡAC. He was given phosphonate drugs, antihypertensive drugs, anticonvulsion treatment, and respiratory support. Blood pressure was maintained at the upper limit of normal value. There was no deterioration of arterial calcification. It is concluded that ⅡAC should be considered for infants with persistent hypertension and extensive vascular calcification, and imaging and genetic examinations should be performed as early as possible to make a confirmed diagnosis.

关键词

高血压 / 大动脉 / 钙化 / 婴儿

Key words

Hypertension / Main artery / Calcification / Infant

引用本文

导出引用
刘云峰, 韩彤妍, 童笑梅, 王晶, 汤亚南, 崔立刚, 朱小辉, 朴梅花, 王晴晴, 武慧. 早产儿持续高血压2个月[J]. 中国当代儿科杂志. 2018, 20(11): 939-943 https://doi.org/10.7499/j.issn.1008-8830.2018.11.012
LIU Yun-Feng, HAN Tong-Yan, TONG Xiao-Mei, WANG Jing, TANG Ya-Nan, CUI Li-Gang, ZHU Xiao-Hui, PIAO MeiHua, WANG Qing-Qing, WU Hui. Persistent hypertension for two months in a preterm infant[J]. Chinese Journal of Contemporary Pediatrics. 2018, 20(11): 939-943 https://doi.org/10.7499/j.issn.1008-8830.2018.11.012

参考文献

[1] Rutsch F, Ruf N, Vaingankar S, et al. Mutations in ENPP1 are associated with ‘idiopathic’ infantile arterial calcification[J]. Nat Genet, 2003, 34(4):379-381.
[2] Ruf N, Uhlenberg B, Terkeltaub R, et al. The mutational spectrum of ENPP1 as arising after the analysis of 23 unrelated patients with generalized arterial calcification of infancy (GACI)[J]. Hum Mutat, 2005, 25(1):98.
[3] Bryant JH, Hale-White WA. A case of calcification of the arteries and obliterative endarteritis associated with hydronephrosis in a child aged six months[J]. Guys Hosp Rep, 1901, 55:17-28.
[4] Guimarães S, Lopes JM, Oliveira JB, et al. Idiopathic infantile arterial calcification:a rare cause of sudden unexpected death in childhood[J]. Patholog Res Int, 2010, 2010:185314. doi:10.4061/2010/185314.
[5] 程蓉, 许伟青, 汪洁云. 新生儿特发性动脉钙化症伴腔内血栓形成一例[J]. 中华围产医学杂志, 2007, 10(1):63.
[6] 范松青, 付汐, 李朵. 特发性婴儿动脉钙化症一例[J]. 中华医学杂志, 2008, 88(5):358-359.
[7] 高凤兰, 刘春灵, 张印坡, 等. 婴儿特发性动脉钙化尸检一例[J]. 中华病理学杂志, 2013, 42(11):771-772.
[8] 宋莉莉, 邢轶维, 张芳, 等. 婴儿泛发性动脉钙化一例[J]. 天津医药, 2013, 41(2):175-176.
[9] 李晓卿, 王丽靖, 顾艳敏, 等. 二磷酸盐治疗婴儿特发性动脉钙化症[J]. 中国小儿急救医学, 2014, 21(1):54-55.
[10] 梁小碧, 曾少颖, 李渝芬, 等. 特发性婴儿动脉钙化症二例[J]. 中华儿科杂志, 2014, 52(11):874-876.
[11] Li Q, Brodsky JL, Conlin LK, et al. Mutations in the ABCC6 gene as a cause of generalized arterial calcification of infancy:genotypic overlap with pseudoxanthoma elasticum[J]. J Invest Dermatol, 2014, 134(3):658-665.
[12] Numakura C, Yamada M, Ariyasu D, et al. Genetic and enzymatic analysis for two Japanese patients with idiopathic infantile arterial calcification[J]. J Bone Miner Metab, 2006, 24(1):48-52.
[13] Cheng KS, Chen MR, Ruf N, et al. Generalized arterial calcification of infancy:different clinical courses in two affected siblings[J]. Am J Med Genet A, 2005, 136(2):210-213.
[14] Chong CR, Hutchins GM. Idiopathic infantile arterial calcification:the spectrum of clinical presentations[J]. Pediatr Dev Pathol, 2008, 11(5):405-415.
[15] van der Sluis IM, Boot AM, Vernooij M, et al. Idiopathic infantile arterial calcification:clinical presentation, therapy and long-term follow-up[J]. Eur J Pediatr, 2006, 165(9):590-593.
[16] Shaireen H, Howlett A, Amin H, et al. The mystery of persistent pulmonary hypertension:an idiopathic infantile arterial calcification[J]. BMC Pediatr, 2013, 13:107.
[17] Rani H, Rao R, Rao U, et al. Idiopathic infantile arterial calcification with thrombotic microangiopathy——a unique case[J]. Fetal Pediatr Pathol, 2010, 29(6):413-418.
[18] Zhang E, Owen R, Bruce G, et al. Idiopathic infantile arterial calcification in a 12-year-old girl presenting as chronic mesenteric ischemia:imaging findings and angioplasty results[J]. Pediatr Radiol, 2011, 41(11):1476-1480.
[19] Tran KH, Boechat MI. Idiopathic infantile arterial calcification:imaging evaluation and the usefulness of MR angiography[J]. Pediatr Radiol, 2006, 36(3):247-253.
[20] Whitehall J, Smith M, Altamirano L, et al. Idiopathic infantile arterial calcification:sonographic findings[J]. J Clin Ultrasound, 2003, 31(9):497-501.
[21] Bolster F, Ali Z, Southall P, et al. Generalized arterial calcification of infancy——findings at post-mortem computed tomography and autopsy[J]. Forensic Sci Int, 2015, 254:e7-e12.
[22] Rutsch F, Böyer P, Nitschke Y, et al. Hypophosphatemia, hyperphosphaturia, and bisphosphonate treatment are associated with survival beyond infancy in generalized arterial calcification of infancy[J]. Circ Cardiovasc Genet, 2008, 1:133-140.
[23] Ramjan KA, Roscioli T, Rutsch F, et al. Generalized arterial calcification of infancy:treatment with bisphosphonates[J]. Nat Clin Pract Endocrinol Metab, 2009, 5(3):167-172.
[24] Edouard T, Chabot G, Miro J, et al. Efficacy and safety of 2-year etidronate treatment in a child with generalized arterial calcification of infancy[J]. Eur J Pediatr, 2011, 170(12):1585-1590.
[25] Otero JE, Gottesman GS, McAlister WH, et al. Severe skeletal toxicity from protracted etidronate therapy for generalized arterial calcification of infancy[J]. J Bone Miner Res, 2013, 28(2):419-430.
[26] Ferreira CR, Ziegler SG, Gupta A, et al. Treatment of hypophosphatemic rickets in generalized arterial calcification of infancy (GACI) without worsening of vascular calcification[J]. Am J Med Genet A, 2016, 170A(5):1308-1311.
[27] Nael A, Siaghani PJ, Chen D, et al. Idiopathic infantile arterial calcification:a possible cause of refractory cardiopulmonary failure in infancy[J]. Case Rep Pathol, 2014, 2014:189850. doi:10.1155/2014/189850.
[28] Stojanovic V, Doronjski A, Milak G, et al. Idiopathic arterial calcification of infancy——peritoneal dialysis for treatment of hypertension[J]. Fetal Pediatr Pathol, 2013, 32(6):443-447.
[29] Giovannoni I, Callea F, Travaglini L, et al. Heart transplant and 2-year follow up in a child with generalized arterial calcification of infancy[J]. Eur J Pediatr, 2014, 173(12):1735-1740.
[30] Glatz AC, Pawel BR, Hsu DT, et al. Idiopathic infantile arterial calcification:two case reports, a review of the literature and a role for cardiac transplantation[J]. Pediatr Transplant, 2006, 10(2):225-233.

基金

北京市自然科学基金预探索项目(7173275)资助。

PDF(1712 KB)
HTML

Accesses

Citation

Detail

段落导航
相关文章

/