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Research ArticlePediatric Neuroimaging

Differentiating Pediatric Rhabdomyosarcoma and Langerhans Cell Histiocytosis of the Temporal Bone by Imaging Appearance

K.M. Chevallier, R.H. Wiggins, N.A. Quinn and R.K. Gurgel
American Journal of Neuroradiology June 2016, 37 (6) 1185-1189; DOI: https://doi.org/10.3174/ajnr.A4676
K.M. Chevallier
aFrom the Division of Otolaryngology, Head and Neck Surgery (K.M.C. R.H.W., N.Q., R.K.G.), University of Utah, Salt Lake City, Utah
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R.H. Wiggins
aFrom the Division of Otolaryngology, Head and Neck Surgery (K.M.C. R.H.W., N.Q., R.K.G.), University of Utah, Salt Lake City, Utah
bDepartment of Radiology (R.H.W.), University of Utah Hospital, Salt Lake City, Utah.
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N.A. Quinn
aFrom the Division of Otolaryngology, Head and Neck Surgery (K.M.C. R.H.W., N.Q., R.K.G.), University of Utah, Salt Lake City, Utah
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R.K. Gurgel
aFrom the Division of Otolaryngology, Head and Neck Surgery (K.M.C. R.H.W., N.Q., R.K.G.), University of Utah, Salt Lake City, Utah
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Abstract

BACKGROUND AND PURPOSE: Rhabdomyosarcoma and Langerhans cell histiocytosis are malignant lesions that can affect the skull base with similar radiographic characteristics on CT and MR imaging. We hypothesized that location within the temporal bone determined radiographically can provide useful adjunctive information in differentiating these distinct neoplasms.

MATERIALS AND METHODS: We identified patients with Langerhans cell histiocytosis and rhabdomyosarcoma by using an imaging data base and International Classification of Diseases, Ninth Revision codes at a tertiary care academic medical center. Cross-sectional images were reviewed by a neurotologist and neuroradiologist, who evaluated the location of the lesions and scored each subsite—middle ear, mastoid, petrous apex, retrosigmoid/posterior fossa—on a scale of 0 (no involvement), 1 (partial), or 2 (complete involvement).

RESULTS: We identified 12 patients representing 14 cases of Langerhans cell histiocytosis, and 9 patients representing 9 cases of rhabdomyosarcoma. For patients with Langerhans cell histiocytosis, mastoid involvement was rated 23/28 (82%) compared with 6/18 (33%) with rhabdomyosarcoma (P = .001). Langerhans cell histiocytosis was present in only the anterior portion of the temporal bone (petrous apex and middle ear) in 1 case (7.1%) and in the anterior portion of the temporal bone only in 5/9 (55%) cases of rhabdomyosarcoma (P = .018). The cortical bone was more commonly involved in Langerhans cell histiocytosis, 11/28 (39%) of cases compared with 2/18 (11%) cases in rhabdomyosarcoma (P < .05).

CONCLUSIONS: These results indicate that lesions involving only the anterior portion of the temporal bone (petrous apex and middle ear) are more likely to be rhabdomyosarcoma. Lesions involving the mastoid are more likely to be Langerhans cell histiocytosis. This difference in primary location may be helpful in predicting the pathology of these lesions on the basis of imaging.

ABBREVIATIONS:

LCH
Langerhans cell histiocytosis
RMS
rhabdomyosarcoma
  • © 2016 by American Journal of Neuroradiology
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American Journal of Neuroradiology: 37 (6)
American Journal of Neuroradiology
Vol. 37, Issue 6
1 Jun 2016
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Cite this article
K.M. Chevallier, R.H. Wiggins, N.A. Quinn, R.K. Gurgel
Differentiating Pediatric Rhabdomyosarcoma and Langerhans Cell Histiocytosis of the Temporal Bone by Imaging Appearance
American Journal of Neuroradiology Jun 2016, 37 (6) 1185-1189; DOI: 10.3174/ajnr.A4676

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Differentiating Pediatric Rhabdomyosarcoma and Langerhans Cell Histiocytosis of the Temporal Bone by Imaging Appearance
K.M. Chevallier, R.H. Wiggins, N.A. Quinn, R.K. Gurgel
American Journal of Neuroradiology Jun 2016, 37 (6) 1185-1189; DOI: 10.3174/ajnr.A4676
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