Page 26 - AAOMP Meeting 2019
P. 26

POSTER ABSTRACTS - TUESDAY, JUNE 11, 2019

               #3 BENIGN FIBROUS HISTIOCYTOMA OF THE JAWBONES. REPORT OF 5 CASES WITH
               REVIEW OF THE LITERATURE
                Dr. Robert Feliciano (New York Presbyterian Queens), Dr. Renee Reich (New York Presbyterian
               Queens), Dr. Chelsea Wilson (New), Dr. Paul Freedman (New York Presbyterian Queens)
               Introduction:  Benign fibrous histiocytomas (BFH) are mesenchymal tumors composed of a mixture of
               fibroblasts and histiocytes arranged in a storiform pattern. This benign neoplasm most often occurs in the
               skin of the lower extremities and rarely affects bone. BFH of bone occur most frequently in the femur,
               pelvis and tibia comprising approximately 1% of all benign bone tumors. Jawbone involvement is
               extremely rare with only 13 cases having been reported in the literature as of 2016. In 2017, we presented
               two new cases at the AAOMP annual meeting. Here we present an additional 3 cases.
               Materials and Methods:  The files of our biopsy service and consultative service were searched from 1984 to
               2019 for cases with the diagnosis of benign fibrous histiocytoma of the jawbone. Three additional cases of
               BFH of the jawbones were identified. These three cases and the two cases presented in 2017 were
               analyzed for their histologic, immunohistochemical and demographic features.
               Results:  Of our five cases of BFH of the jawbone, four involved the mandible and one occurred in the
               maxilla. There was no sex predilection. The age range was 17 to 48 years. The tumors presented as expansile
               painless radiolucent lesions. Histologically, the tumors consisted of spindle shaped cells arranged in a
               storiform pattern. Secondary elements were present consisting of inflammatory cells and foamy histiocytes.
               Immunohistochemical studies revealed CD10, Factor XIIIa and CD68 positivity for three of the five cases.
               Conclusions:  BFH of the jawbones are rare tumors. The addition of our five cases brings the total to 18 cases
               in the literature. The lesions cause painless expansion and appear histologically as spindle cells arranged in a
               storiform patter. Secondary elements may be evident. Staining for CD10, CD 68 and Factor XIIIa may be
               useful is distinguishing these tumors from other spindle cell lesions.


               #4 A CASE REPORT OF LINGUAL BRONCHOGENIC CYST
                Dr. Zahra Aldawood (Department of Oral Medicine, Infection, and Immunity, Harvard School of
               Dental Medicine), Dr. Sook-Bin Woo (Department of Oral Medicine, Infection and Immunity, Harvard
               School of Dental Medicine)
               Bronchogenic cysts are foregut-derived developmental anomalies found along the developmental pathway
               of the foregut. The putative theory of pathogenesis is abnormal budding or branching of epithelial cells
               during the development of tracheobronchial tree. The most common sites are mediastinum and lung (75%
               and 25 % of case respectively) while the head and neck are affected in less than 1% of cases with only rare
               cases reported in the oral cavity. It is usually asymptomatic but if it becomes large, it may cause feeding and
               breathing difficulties. This is a report of a case of a bronchogenic cyst arising in a 6-year-old male. The
               lesion presented as deep mucosal mass in the midline of ventral tongue, measuring 1.1 × 0.7 × 0.7 cm.
               Microscopically, the cyst was lined by pseudostratified columnar epithelium exhibiting many ciliated and
               mucous cells. A focus of cartilage and discontinuous bundles of smooth muscle (smooth muscle actin
               positive) were present adjacent to the lining. Where there was cyst rupture, there was granulation tissue
               associated with many foamy macrophages and acute and chronic inflammation. Three other cases, two in the
               tongue and one in the lower lip vestibule with cutaneous extension, all in the midline, have been reported in
               a 1 day-old, 4 year-old and 3 year-old; all were males. There was no recurrence after excision and this is in
               keeping with the behavior in previous reports. Other developmental cysts including foregut cysts may be
               focally lined with respiratory epithelium but the presence of cartilage is the sine qua non for the diagnosis
               of a bronchogenic cyst.
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