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MR and CT findings of cyst degeneration of sphenoid bone in McCune-Albright syndrome: a case report

INTRODUCTION: McCune-Albright syndrome (MAS) is a rare disorder characterized by the classic triad of precocious puberty, polyostotic fibrous dysplasia and café-au-lait pigmented skin lesions. Cystic change is rare in fibrous dysplasia (FD), especially in McCune-Albright syndrome. There were no repo...

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Autores principales: Li, Ping, Zhang, Zai-Ren, Jiang, Ying, Xia, Xu-Dong, Wang, Dan, Li, Xian-Feng
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2804018/
https://www.ncbi.nlm.nih.gov/pubmed/20062549
http://dx.doi.org/10.1186/1757-1626-2-9376
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author Li, Ping
Zhang, Zai-Ren
Jiang, Ying
Xia, Xu-Dong
Wang, Dan
Li, Xian-Feng
author_facet Li, Ping
Zhang, Zai-Ren
Jiang, Ying
Xia, Xu-Dong
Wang, Dan
Li, Xian-Feng
author_sort Li, Ping
collection PubMed
description INTRODUCTION: McCune-Albright syndrome (MAS) is a rare disorder characterized by the classic triad of precocious puberty, polyostotic fibrous dysplasia and café-au-lait pigmented skin lesions. Cystic change is rare in fibrous dysplasia (FD), especially in McCune-Albright syndrome. There were no reports about cyst degeneration in MAS which resulted in abnormal visual acuity and visual fields. Herein, we report a female patient with MAS associated with sphenoid bone cysts which resulted in visual deterioration to describe the computed tomography (CT) and magnetic resonance (MR) imaging findings of cyst degeneration in McCune-Albright syndrome. CASE PRESENTATION: A 20-year-old female presented with right temporal hemianopsia and visual loss in the right eye suddenly. A café-au-lait spot was found on her neck and left shoulder. Endocrinologic examination revealed elevated basal level of serum PRL, FT(3 )and FT(4 )with decreased serum TSH. Fibrous dysplasia (FD) generally manifest as round-glass appearance with well defined borders and cystic areas within involved bone were seen as hypointensity on CT. They were showed as hypointense in T1-weighted sequences and as hyperintense in T2-weighted sequences of MRI. After surgery the right temporal hemianopsia improved. CONCLUSION: CT combined with MRI is the most effective method to evaluate the extent and complications of fibrous dysplasia in patients with MAS. The treatment of surgery can not cure MAS but relieve the symptom.
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spelling pubmed-28040182010-01-10 MR and CT findings of cyst degeneration of sphenoid bone in McCune-Albright syndrome: a case report Li, Ping Zhang, Zai-Ren Jiang, Ying Xia, Xu-Dong Wang, Dan Li, Xian-Feng Cases J Case Report INTRODUCTION: McCune-Albright syndrome (MAS) is a rare disorder characterized by the classic triad of precocious puberty, polyostotic fibrous dysplasia and café-au-lait pigmented skin lesions. Cystic change is rare in fibrous dysplasia (FD), especially in McCune-Albright syndrome. There were no reports about cyst degeneration in MAS which resulted in abnormal visual acuity and visual fields. Herein, we report a female patient with MAS associated with sphenoid bone cysts which resulted in visual deterioration to describe the computed tomography (CT) and magnetic resonance (MR) imaging findings of cyst degeneration in McCune-Albright syndrome. CASE PRESENTATION: A 20-year-old female presented with right temporal hemianopsia and visual loss in the right eye suddenly. A café-au-lait spot was found on her neck and left shoulder. Endocrinologic examination revealed elevated basal level of serum PRL, FT(3 )and FT(4 )with decreased serum TSH. Fibrous dysplasia (FD) generally manifest as round-glass appearance with well defined borders and cystic areas within involved bone were seen as hypointensity on CT. They were showed as hypointense in T1-weighted sequences and as hyperintense in T2-weighted sequences of MRI. After surgery the right temporal hemianopsia improved. CONCLUSION: CT combined with MRI is the most effective method to evaluate the extent and complications of fibrous dysplasia in patients with MAS. The treatment of surgery can not cure MAS but relieve the symptom. BioMed Central 2009-12-22 /pmc/articles/PMC2804018/ /pubmed/20062549 http://dx.doi.org/10.1186/1757-1626-2-9376 Text en Copyright ©2009 Li et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Li, Ping
Zhang, Zai-Ren
Jiang, Ying
Xia, Xu-Dong
Wang, Dan
Li, Xian-Feng
MR and CT findings of cyst degeneration of sphenoid bone in McCune-Albright syndrome: a case report
title MR and CT findings of cyst degeneration of sphenoid bone in McCune-Albright syndrome: a case report
title_full MR and CT findings of cyst degeneration of sphenoid bone in McCune-Albright syndrome: a case report
title_fullStr MR and CT findings of cyst degeneration of sphenoid bone in McCune-Albright syndrome: a case report
title_full_unstemmed MR and CT findings of cyst degeneration of sphenoid bone in McCune-Albright syndrome: a case report
title_short MR and CT findings of cyst degeneration of sphenoid bone in McCune-Albright syndrome: a case report
title_sort mr and ct findings of cyst degeneration of sphenoid bone in mccune-albright syndrome: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2804018/
https://www.ncbi.nlm.nih.gov/pubmed/20062549
http://dx.doi.org/10.1186/1757-1626-2-9376
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