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Home > Journals > Minerva Stomatologica > Past Issues > Minerva Stomatologica 2008 January-February;57(1-2) > Minerva Stomatologica 2008 January-February;57(1-2):59-63

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CURRENT ISSUEMINERVA STOMATOLOGICA

A Journal on Dentistry and Maxillofacial Surgery

Official Journal of the Italian Society of Odontostomatology and Maxillofacial Surgery
Indexed/Abstracted in: CAB, EMBASE, Index to Dental Literature, PubMed/MEDLINE, Scopus, Emerging Sources Citation Index

Frequency: Bi-Monthly

ISSN 0926-4970

Online ISSN 1827-174X

 

Minerva Stomatologica 2008 January-February;57(1-2):59-63

    CASE REPORTS

Inflammatory myofibroblastic tumor of the alveolar mucosa of the mandible

A. C. B. R. Johann 1, Caldeira P. C. 1, Abdo E. N. 1, Sousa S. O. M. 2, Aguiar M. C. F. 1, Mesquita R. A. 1

1 Department of Oral Surgery Oral Medicine and Oral Pathology School of Dentistry Universidade Federal de Minas Gerais Belo Horizonte, MG, Brasil
2 Department of Oral Pathology School of Dentistry Universidade de São Paulo, São Paulo, SP, Brasil

Inflammatory myofibroblastic tumor is a rare lesion composed of myofibroblastic spindle cells accompanied by inflammatory infiltrate. The objective of this paper is to report an uncommon case of inflammatory myofibroblastic tumor located in the alveolar mucosa of the mandible. A 33-year-old male presented an asymptomatic tumoral lesion, firm, pedunculated, pink-colored, covered by smooth mucosa, with focal ulceration, measuring 30×20×20 mm, located in the left posterior alveolar mucosa. Clinical diagnosis was soft tissue tumor. An excisional biopsy was made. Microscopic examination showed compact fascicular spindle cells proliferation with a diffuse inflammatory infiltrate of plasma cells, lymphocytes, and eosinophils. Large ganglion-like cells were observed. The lesional cells were immunopos-itive to vimentin, α-smooth muscle actin, muscle specific actin, and CD68. Negative immunostain was observed to S-100, Bcl-2, Ki-67, desmin, CD34, and cytokeratin. A diagnosis of inflammatory myofibroblastic tumor was performed. After 28 months of follow-up there was no recurrence. Although no evidence of oral inflammatory myofibroblastic tumor recurrence or malignant transformation has been reported, it has been observed that in inflammatory myofibroblastic tumor of other regions a prolonged follow-up is necessary after surgical excision.

language: English


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