Literature DB >> 20237988

Collagenous myofibroblastic tumor of the mandible: case report of a unique locally aggressive neoplasm.

Jason W Nash1, Amy C Hessel, Nadarajah Vigneswaran, Adel K El-Naggar.   

Abstract

We report a locally aggressive collagenous myofibroblastic neoplasm of the mandible in an 18-year-old male. Clinically, the lesion presented with rapid growth and irregular mandibular bone destruction. Grossly, the tumor was 10 cm in greatest dimension, light-tan, firm, and involving the posterior one-thirds of the body and inferior half of the left mandibular ramus. Histologically, the lesion was composed of a loose spindle cell proliferation interspersed with periodic dense bands of collagen. The spindle cells reacted positively to smooth muscle actin, calponin, and focally to desmin and were negative for S-100, pan-cytokeratin, CD99, CD34 and caldesmon, supporting myofibroblastic derivation. At our 4 year follow-up, the patient remained free of local recurrence and surgery related complications. The clinicopathologic findings and the differential diagnosis of this lesion is presented and discussed.

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Year:  2009        PMID: 20237988      PMCID: PMC2825531          DOI: 10.1007/s12105-009-0154-x

Source DB:  PubMed          Journal:  Head Neck Pathol        ISSN: 1936-055X


  29 in total

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Review 5.  Primary leiomyosarcoma of bone: a clinicopathologic, immunohistochemical, and ultrastructural study of 33 patients and a literature review.

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6.  Myofibrosarcoma of the head and neck in children.

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Review 7.  Low-grade myofibroblastic sarcoma: analysis of 18 cases in the spectrum of myofibroblastic tumors.

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Review 8.  Clinico-pathologic correlations of myofibroblastic tumors of the oral cavity. II. Myofibroma and myofibromatosis of the oral soft tissues.

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9.  Inflammatory myofibroblastic tumor of the larynx. A clinicopathologic study of eight cases simulating a malignant spindle cell neoplasm.

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Authors:  T Lombardi; C Lock; J Samson; E W Odell
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3.  Myofibroblastoma of the mandible in a 3-year-old child.

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