Primary Intrarenal Neuroblastoma with Hypertension and Disseminated Intravascular Coagulation

被引:5
作者
Shamsian, Bibi Shahin [1 ,2 ]
Kajizadi, Mohammad [1 ]
Rezaei, Nima [3 ,4 ,5 ]
Ghojehvand, Nozar [6 ]
Azma, Roxana [6 ]
Rouzrokh, Mohsen [7 ]
Aghdam, Maryam Kazemi [8 ]
Mesbah, Seyed Malek [6 ]
Ghazizadeh, Farid [1 ]
Arzanian, Mohammad Taghi [1 ]
机构
[1] Shahid Beheshti Univ Med Sci, Pediat Congenital Hematol Disorders Res Ctr, Mofid Childrens Hosp, Tehran 1546815514, Iran
[2] Mofid Children Hosp, Dept Pediat Hematol Oncol, Tehran 1546815514, Iran
[3] Univ Tehran Med Sci, Childrens Med Ctr, Res Ctr Immunodeficiencies, Tehran 14194, Iran
[4] Univ Tehran Med Sci, Mol Immunol Res Ctr, Sch Med, Tehran 14194, Iran
[5] Univ Tehran Med Sci, Sch Med, Dept Immunol, Tehran 14194, Iran
[6] Shahid Beheshti Univ Med Sci, Mofid Childrens Hosp, Dept Pediat Radiol, Tehran 1546815514, Iran
[7] Shahid Beheshti Univ Med Sci, Mofid Childrens Hosp, Dept Pediat Surg, Tehran 1546815514, Iran
[8] Shahid Beheshti Univ Med Sci, Mofid Childrens Hosp, Dept Pediat Pathol, Tehran 1546815514, Iran
关键词
D O I
10.1155/2013/684939
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The primary intrarenal neuroblastoma (IRNB) is a rare condition. Intrarenal neuroblastoma typically results from direct renal invasion from an adrenal neuroblastoma, but true intrarenal neuroblastoma originates either sequestered adrenal rests during the fetal life or intrarenal sympathetic ganglia. Clinical, radiological, and pathological correlation is very essential for diagnosis and appropriate management of this type of unusual cases. The distinction of this rare tumor from Wilms' tumor is an important challenge since both tumors have major differences in prognostic and therapeutic response. We present a 3-year-old boy of primary intrarenal neuroblastoma with extensive abdominal and mediastinal mass, persistent hypertension, and disseminated intravascular coagulation (DIC).
引用
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页数:4
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