Congenital Ewing's sarcoma of the humerus

H. Y. Hsieh; C. C. Hsiao; W. S. Chen; J. W. Lin; W. J. Chen; Y. L. Wan; S. H. Ng; T. Y. Lee; S. F. Ko

doi:10.1259/bjr.71.852.10319008

Congenital Ewing's sarcoma of the humerus

H. Y. Hsieh, C. C. Hsiao, W. S. Chen, J. W. Lin, W. J. Chen, Y. L. Wan, S. H. Ng, T. Y. Lee, S. F. Ko^*

^*Corresponding author for this work

Department of Medical Imaging and Radiological Sciences

Research output: Contribution to journal › Journal Article › peer-review

21 Scopus citations

Abstract

We report an extremely rare case of Ewing's sarcoma (ES) of the humerus in a Chinese neonate. Plain radiography and magnetic resonance imaging showed extensive neoplastic involvement of the humeral diaphysis and adjacent soft tissues, confirmed on histology and immunohistochemistry as being due to ES. This is the first report of congenital ES in a long bone. Since ultrasound at 20 weeks gestation showed a normal fetal skeleton, the ES may have begun to develop in the late middle or third trimester.

Original language	English
Pages (from-to)	1313-1316
Number of pages	4
Journal	British Journal of Radiology
Volume	71
Issue number	852
DOIs	https://doi.org/10.1259/bjr.71.852.10319008
State	Published - 1998

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@article{043770b7119f4357ae87f5eebe0f97bc,

title = "Congenital Ewing's sarcoma of the humerus",

abstract = "We report an extremely rare case of Ewing's sarcoma (ES) of the humerus in a Chinese neonate. Plain radiography and magnetic resonance imaging showed extensive neoplastic involvement of the humeral diaphysis and adjacent soft tissues, confirmed on histology and immunohistochemistry as being due to ES. This is the first report of congenital ES in a long bone. Since ultrasound at 20 weeks gestation showed a normal fetal skeleton, the ES may have begun to develop in the late middle or third trimester.",

author = "Hsieh, {H. Y.} and Hsiao, {C. C.} and Chen, {W. S.} and Lin, {J. W.} and Chen, {W. J.} and Wan, {Y. L.} and Ng, {S. H.} and Lee, {T. Y.} and Ko, {S. F.}",

year = "1998",

doi = "10.1259/bjr.71.852.10319008",

language = "英语",

volume = "71",

pages = "1313--1316",

journal = "British Journal of Radiology",

issn = "0007-1285",

publisher = "Oxford University Press",

number = "852",

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TY - JOUR

T1 - Congenital Ewing's sarcoma of the humerus

AU - Hsieh, H. Y.

AU - Hsiao, C. C.

AU - Chen, W. S.

AU - Lin, J. W.

AU - Chen, W. J.

AU - Wan, Y. L.

AU - Ng, S. H.

AU - Lee, T. Y.

AU - Ko, S. F.

PY - 1998

Y1 - 1998

N2 - We report an extremely rare case of Ewing's sarcoma (ES) of the humerus in a Chinese neonate. Plain radiography and magnetic resonance imaging showed extensive neoplastic involvement of the humeral diaphysis and adjacent soft tissues, confirmed on histology and immunohistochemistry as being due to ES. This is the first report of congenital ES in a long bone. Since ultrasound at 20 weeks gestation showed a normal fetal skeleton, the ES may have begun to develop in the late middle or third trimester.

AB - We report an extremely rare case of Ewing's sarcoma (ES) of the humerus in a Chinese neonate. Plain radiography and magnetic resonance imaging showed extensive neoplastic involvement of the humeral diaphysis and adjacent soft tissues, confirmed on histology and immunohistochemistry as being due to ES. This is the first report of congenital ES in a long bone. Since ultrasound at 20 weeks gestation showed a normal fetal skeleton, the ES may have begun to develop in the late middle or third trimester.

UR - http://www.scopus.com/inward/record.url?scp=0032426342&partnerID=8YFLogxK

U2 - 10.1259/bjr.71.852.10319008

DO - 10.1259/bjr.71.852.10319008

M3 - 文章

C2 - 10319008

AN - SCOPUS:0032426342

SN - 0007-1285

VL - 71

SP - 1313

EP - 1316

JO - British Journal of Radiology

JF - British Journal of Radiology

IS - 852

ER -

Congenital Ewing's sarcoma of the humerus

Abstract

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