Inflammatory Myofibroblastic Tumour

被引：1
|
作者：
Amah, C. C. [1 ]
Obianyo, I. C. [1 ]
Chukwubuike, K. E. [1 ]
Obianyo, N. E. N. [1 ]
Aniume, O., I [2 ]
Okafor, O. C. [2 ]
机构：
[1] UNTH, Dept Paediat Surg, Enugu, Nigeria
[2] UNTH, Dept Pathol, Enugu, Nigeria
来源：
JOURNAL OF PEDIATRIC SURGERY CASE REPORTS | 2019年 / 40卷
关键词：
Tumour in infancy; Inflammatory Myofibroblastic Tumour;
D O I：
10.1016/j.epsc.2018.10.007
中图分类号：
R72 [儿科学];
学科分类号：
100202 ;
摘要：
We report a rare case of Inflammatory Myofibroblastic Tumour (IMT) on the left arm of a 6 month old male infant. The tumour was completely excised and has not recurred in two years. IMT is known to occur in any part of the anatomy of humans, at any age, and in any gender. Reviewing publications of IMT in English literature, this case appears to be one of the few occurring in infancy. IMT, previously classified under inflammatory pseudo-tumour is now known to belong to its own entity. Complete surgical resection is the mainstay of treatment and histology of the tumour gives the ultimate diagnosis.
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收藏
页码：30 / 33
页数：4
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