Loss of lingual sensitivity and slightly increased size signaling schwannoma in a patient with mixed conjunctive tissue disease
Identifieur interne : 001201 ( Main/Exploration ); précédent : 001200; suivant : 001202Loss of lingual sensitivity and slightly increased size signaling schwannoma in a patient with mixed conjunctive tissue disease
Auteurs : D. C. Ferreira [Brésil] ; G. Nogueira ; V. A. Cancio ; F. S. Cavalcante ; P. Godefroy ; D. S. C. Sousa ; W. Hespanhol ; K. R. N. Dos Santos ; M. A. B. CavalcanteSource :
- Special Care in Dentistry [ 0275-1879 ] ; 2013-11.
English descriptors
- Teeft :
- Antoni, Benign, Clinical diagnosis, Clinical manifestations, Clinical practice, Conjunctive, Conjunctive tissue disease, Connective tissue disease, Encapsulated, Lesion, Lingual, Lingual schwannoma, Lingual sensitivity, Mctd, Neurofibromatosis type, Oral lesions, Oral manifestations, Oral maxillofac surg, Other pathologies, Schwannoma, Scientific evidence, Scleroderma, Soft palate, Surg, Surgical removal, Unusual case.
Abstract
The purpose of this study was to describe an unusual case of a lingual schwannoma associated with a mixed connective tissue disease (MCTD). A case report. A lingual schwannoma with loss of lingual sensitivity and slightly increased size in an 18‐year‐old patient with MCTD was correctly diagnosed through a biopsy and no reoccurrence was observed one year after the surgical removal of the tumor and sensitivity returned 3 months after surgery. This case was considered uncommon, making the clinical diagnosis challenging in view of the diversity of possibilities for its differential diagnosis, thus showing the importance of a biopsy to confirm the diagnosis and long term follow up in such cases.
Url:
DOI: 10.1111/j.1754-4505.2012.00308.x
Affiliations:
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Le document en format XML
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<front><div type="abstract">The purpose of this study was to describe an unusual case of a lingual schwannoma associated with a mixed connective tissue disease (MCTD). A case report. A lingual schwannoma with loss of lingual sensitivity and slightly increased size in an 18‐year‐old patient with MCTD was correctly diagnosed through a biopsy and no reoccurrence was observed one year after the surgical removal of the tumor and sensitivity returned 3 months after surgery. This case was considered uncommon, making the clinical diagnosis challenging in view of the diversity of possibilities for its differential diagnosis, thus showing the importance of a biopsy to confirm the diagnosis and long term follow up in such cases.</div>
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