Solitary fibrous tumor of buccal mucosa: A rare entity
Authors
Abstract:
BACKGROUND AND AIM: Solitary fibrous tumor (SFT) is a quite uncommon tumor that commonly occurs in the pleura but occasionally involves an oral cavity. We are reporting this rare case in the oral cavity. The diagnosis depends on microscopic and immunohistochemical features. Patients with these tumors can be carefully treated with local excision, but tumors with positive margins necessitate close follow-up over several years due to the possible late local recurrence. CASE REPORT: A 60-year malepatient came in the maxillofacial department in Abbasi Shaheed Hospital, Karachi, Pakistan with swelling for the past 5 years which slowly increased in size with no history of pain. The excisional biopsy was performed under local anesthesia. Histopathological examination showed a well-circumscribed spindle cell tumor with alternating hypo and hypercellular areas with prominent collagenous stroma. Immunohistochemistry (IHC) investigation led to the positive expression of Cluster of Differentiation 34 (CD34) and Signal Transducer and Activator of Transcription-6 (STAT-6) in the spindle cells, and negative expression of Anti-Smooth Muscle Antibody (ASMA). Recurrent or postoperative complications were not observed over some time. CONCLUSION: SFT in the buccal mucosa of the cheek is a very sporadic condition. It needs to be identified with proper history and clinical examination.
similar resources
Solitary Fibrous Tumor in Buccal Cheek Mucosa
A solitary fibrous tumor is a relatively uncommon neoplasm that usually occurs in the pleura but occurs extremely rarely in the oral cavity. Reported herein is a rare case of a solitary fibrous tumor in the buccal cheek mucosa. A 50-year-old man visited the authors' hospital due to a buccal cheek mass whose size had increased. Excisional biopsy was done under local anesthesia. After the excisio...
full textSolitary fibrous tumor of maxilla: A rare entity
Solitary fibrous tumor (SFT) is a ubiquitous rare mesenchymal neoplasm. Pleura is the favored site of origin and is rare in the oral cavity. SFT occurs across a wide histopathologic spectrum. Fibrous form characterized by hyalinized, thick-walled vessels with opened lumina and strong CD34 reactivity constitute one end and on the other end, a cellular form representing the conventional hemangiop...
full textIntramedullary spinal cord solitary fibrous tumor: A rare clinical entity
Introduction: Solitary Fibrous Tumor (SFT) is a rare tumor that initially was thought to arise from visceral tissue. Later reports documented its occurrence in central nervous system tissue, with most located intracranially. Few reports have mentioned intraspinal SFTs, with the majority being extra-medullary. In this report, we describe a rare presentation of intramedullary SFT. Case descriptio...
full textSolitary fibrous tumor of the buccal space.
Solitary fibrous tumors are submesothelial mesenchymal fibroblastic tumors that typically occur in relation to parietal or visceral pleura. However, the tumor also occurs in extrapleural sites, including the peritoneum, mediastinum, orbit, and oral cavity. With the advent of immunohistochemical testing, certain tumors may be more readily identifiable; however, the diagnosis often must be reache...
full textA Solitary Phlebolith in the Buccal Mucosa: Report of a Rare Entity and Clinicopathologic Correlation.
Pathological conditions can give rise to calcifications within oral mucosa representing either a local or systemic disturbance. Inflammation, trauma, debris acting as nidus and vascular lesions have been attributed as principal causes for occurrence of calcifications within the oral mucosa. Occurrence of multiple calcified thrombi (phleboliths) is considered pathognomonic for hemangiomas and va...
full textKeratocystic Odontogenic Tumor of Buccal Mucosa: A Rare Case Report and Histochemical Comparative Study
Keratocystic odontogenic tumor (KCOT) is a benign intraosseous neoplasm of the jaw occurring most commonly in mandibular ramus molar area with male predilection. Peripheral KCOTs are very uncommon. Here we report a case of keratocyst in buccal mucosa in a 55 years old female patient, the diagnosis of which was based on subjective histological evaluation and further confirmed by immunohistochemi...
full textMy Resources
Journal title
volume 9 issue 2
pages -
publication date 2020-04-01
By following a journal you will be notified via email when a new issue of this journal is published.
Keywords
Hosted on Doprax cloud platform doprax.com
copyright © 2015-2023