Primary intraosseous glomus tumor: A case report
We reported a rare case of a primary intraosseous glomus tumor in a 53-year-old woman who had a small lytic lesion in the distal phalanx of her left index finger. The radiologic appearance showed a well circumscribed osteolytic lesion without sclerotic rim. Histologic examination revealed solid nest...
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th-cmuir.6653943832-28102014-08-30T02:25:25Z Primary intraosseous glomus tumor: A case report Settakorn J. Chaleoapong P. Rangdaeng S. Arpornchayanon O. Chaiwun B. We reported a rare case of a primary intraosseous glomus tumor in a 53-year-old woman who had a small lytic lesion in the distal phalanx of her left index finger. The radiologic appearance showed a well circumscribed osteolytic lesion without sclerotic rim. Histologic examination revealed solid nests or sheets of polygonal cells surrounding branching vasculatures consistent with a glomus tumor. Curettage resulted in complete removal of the tumor as well as pain alleviation. The patient was well without evidence of recurrent disease following an 18 month follow-up. Despite its rarity, intraosseous glomus tumor should be included in the differential diagnosis of bone lesions in which plain radiography showed a well circumscribed punch-out lesion without sclerotic rim especially those arising in the finger. 2014-08-30T02:25:25Z 2014-08-30T02:25:25Z 2001 Article 01252208 11853310 JMTHB http://www.scopus.com/inward/record.url?eid=2-s2.0-0035523814&partnerID=40&md5=fce8fee27342162c09fee4dfd4f14dbe http://www.ncbi.nlm.nih.gov/pubmed/11853310 http://cmuir.cmu.ac.th/handle/6653943832/2810 English |
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We reported a rare case of a primary intraosseous glomus tumor in a 53-year-old woman who had a small lytic lesion in the distal phalanx of her left index finger. The radiologic appearance showed a well circumscribed osteolytic lesion without sclerotic rim. Histologic examination revealed solid nests or sheets of polygonal cells surrounding branching vasculatures consistent with a glomus tumor. Curettage resulted in complete removal of the tumor as well as pain alleviation. The patient was well without evidence of recurrent disease following an 18 month follow-up. Despite its rarity, intraosseous glomus tumor should be included in the differential diagnosis of bone lesions in which plain radiography showed a well circumscribed punch-out lesion without sclerotic rim especially those arising in the finger. |
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Article |
author |
Settakorn J. Chaleoapong P. Rangdaeng S. Arpornchayanon O. Chaiwun B. |
spellingShingle |
Settakorn J. Chaleoapong P. Rangdaeng S. Arpornchayanon O. Chaiwun B. Primary intraosseous glomus tumor: A case report |
author_facet |
Settakorn J. Chaleoapong P. Rangdaeng S. Arpornchayanon O. Chaiwun B. |
author_sort |
Settakorn J. |
title |
Primary intraosseous glomus tumor: A case report |
title_short |
Primary intraosseous glomus tumor: A case report |
title_full |
Primary intraosseous glomus tumor: A case report |
title_fullStr |
Primary intraosseous glomus tumor: A case report |
title_full_unstemmed |
Primary intraosseous glomus tumor: A case report |
title_sort |
primary intraosseous glomus tumor: a case report |
publishDate |
2014 |
url |
http://www.scopus.com/inward/record.url?eid=2-s2.0-0035523814&partnerID=40&md5=fce8fee27342162c09fee4dfd4f14dbe http://www.ncbi.nlm.nih.gov/pubmed/11853310 http://cmuir.cmu.ac.th/handle/6653943832/2810 |
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1681419929529614336 |