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1.
Head Neck Pathol ; 9(2): 196-204, 2015 Jun.
Article in English | MEDLINE | ID: mdl-25113037

ABSTRACT

The desmoplastic fibroma (DF) is a rare, fibroblastic lesion of bone that histologically resembles the desmoid tumor of soft tissue. Although classified as benign, it frequently demonstrates aggressive behavior, often causing tooth mobility, extensive bone destruction, and has a moderate to high recurrence rate. We present three cases of DF in the mandible: the first in a 13 year old female involving the mandibular body in the region of teeth #s 27-#28, the second in a 57 year old female with a lesion apical to tooth #30, and the third in a 20-year-old female involving the left posterior mandible. Clinical, histologic, immunohistochemical (IHC) and radiographic features of this rare neoplasm are discussed. The challenges encountered in establishing an accurate diagnosis due to significant microscopic overlap with other spindle cell lesions are also detailed. Additionally, the findings of IHC stains including vimentin, smooth muscle actin, S-100 protein, ß-catenin, HHF-35 and proliferation marker, Ki-67 on 3 cases are reported. The potential for misdiagnosis is high, especially in early lesions, since immunohistochemistry has been reported in literature to be inconsistent when differentiating DFs from other spindle cell lesions. A comparative review of DF and similar entities in the jaws with current considerations in treatment and prognosis is presented.


Subject(s)
Bone Neoplasms/diagnosis , Fibroma, Desmoplastic/diagnosis , Mandibular Neoplasms/diagnosis , Actins/metabolism , Adolescent , Bone Neoplasms/metabolism , Bone Neoplasms/pathology , Female , Fibroma, Desmoplastic/metabolism , Fibroma, Desmoplastic/pathology , Humans , Mandibular Neoplasms/metabolism , Mandibular Neoplasms/pathology , Middle Aged , S100 Proteins/metabolism , Vimentin/metabolism , Young Adult , beta Catenin/metabolism
2.
Head Neck Pathol ; 8(3): 339-48, 2014.
Article in English | MEDLINE | ID: mdl-24202723

ABSTRACT

Intraoral basal cell carcinoma (IOBCC) is an extremely rare entity that bears close microscopic resemblance to and is often confused with the peripheral ameloblastoma (PA). Basal cell carcinomas are thought to arise from pluripotential basal cells present within surface epithelium and adnexal structures, so theoretically they can arise within the oral cavity. Many of the early cases reported as IOBCC actually represent PA. Most of the well documented cases arise from the gingiva. The histologic features of basal cell carcinoma that help separate it from a PA include: tumor arising from surface epithelium, scattered mitotic figures and apoptotic cells, presence of mucoid ground substance and tumor infiltrating widely throughout the connective tissue and often exhibiting a prominent retraction artifact. Clinically IOBCC resemble carcinomas, compared to the benign and innocuous appearance of the PA and typically presents as surface ulcerations varying from rodent ulcer to an ulcerated erythroplakia appearance. This contrasts with the classic "bump on the gum" appearance of PAs with usually intact surface and appearing as small discrete, sessile, exophytic lesions. Importantly, the proliferative basaloid epithelium demonstrates positive immunoreactivity for the anti-epithelial antibody, Ber-EP4, a cell surface glycoprotein. The IOBCC has the potential for local recurrence and aggressive behavior and should be treated with wide surgical excision and close clinical follow up. We present 3 rare cases of IOBCC and discuss the salient histologic, immunohistochemical and clinical features.


Subject(s)
Carcinoma, Basal Cell/pathology , Mouth Neoplasms/pathology , Adult , Aged , Biomarkers, Tumor/analysis , Female , Humans , Immunohistochemistry , Male
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