Low-grade myofibroblastic sarcoma of the sacrum Case report

被引：12

作者：

Humphries, William E., III ^{[1
]}

Satyan, Krishna B. ^{[1
]}

Relyea, Katherine ^{[1
]}

Kim, Eugene S. ^{[2
]}

Adesina, Adekunle M. ^{[3
]}

Chintagumpala, Murali ^{[4
]}

Jea, Andrew ^{[1
]}

机构：

[1] Texas Childrens Hosp, Baylor Coll Med, Dept Neurosurg, Neurospine Program,Div Pediat Neurosurg, Houston, TX 77030 USA

[2] Texas Childrens Hosp, Baylor Coll Med, Dept Surg, Div Pediat Surg, Houston, TX 77030 USA

[3] Texas Childrens Hosp, Baylor Coll Med, Dept Pathol, Div Neuropathol, Houston, TX 77030 USA

[4] Baylor Coll Med, Dept Pediat, Div Pediat Hematol Oncol, Texas Childrens Canc Ctr, Houston, TX 77030 USA

来源：

JOURNAL OF NEUROSURGERY-PEDIATRICS | 2010年 / 6卷 / 03期

关键词：

myofibroblastic sarcoma; sacrectomy; pediatric spine; SACROCOCCYGEAL CHORDOMA; MYOFIBROSARCOMA; EXPERIENCE; MANAGEMENT; DIAGNOSIS; TUMORS; BONE;

D O I：

10.3171/2010.5.PEDS09289

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

Myofibroblastic tumors are soft-tissue neoplasms arising from myofibroblasts, ubiquitous cells sharing ultrastructural features of muscular and fibroblastic cells. Vasudev and Harris described a malignant counterpart of these benign tumors in 1978. Most reported cases of myofibroblastic sarcoma have arisen in the head and neck region and the soft tissues of the extremities. To the best of the authors' knowledge, there have been only 8 previous reports on primary myofibroblastic sarcoma of the bone. The authors report a new case of this rare tumor affecting the sacrum and ilium of a 15-year-old girl and discuss the role of total sacrectomy and lumbopelvic reconstruction for treatment of this disease. (DOI: 10.3171/2010.5.PEDS09289)

引用

页码：286 / 290

页数：5

共 21 条

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