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The central giant cell granuloma is an uncommon, benign and proliferative lesion whose etilogy is not well defined. WHO categorize it as a bone-related lesion, not a tumor, although its clinical behavior and radiographic features often are those associated with teeth displacement, root resorption or bone cortical perforation. Here we present a case of cell granuloma in a 23-year-old female patient associated with a painful swelling and facial asymmetry in the left mandibular region. The siginficant increase in size was seen in third trimester of pregnancy. On histopathological analysis, all the classic features were noted and diagnosis of an aggressive central giant cell granuloma was made without any obscruity. Diagnosis of central giant cell granuloma remains a challange for oral pathologists. There are many lesions, e.g. cherubisms, fibrous dysplasia, brown tumor, aneruymal bone cyst, and giant cell tumor which mimic central giant cell granuloma clinically and histologically. These conditions must be ruled out before making a definitive diagnosis central giant cell granuloma. Keywords: Benign tumor, Cherubism, Central giant cell
https://www.ijhsr.org/IJHSR_Vol.13_Issue.2_Feb2023/IJHSR-Abstract14.html, 2023
Central giant cell granuloma (CGCG) is an uncommon, intraosseous, osteolytic, bony lesion of the jaw which is predominantly seen under the age of 30 years with female predominance and is common in the mandibular anterior region. The clinical behavior of the CGCG ranges from slow-growing asymptomatic to large-growing symptomatic osteolytic lesions. The etiology of CGCG is debatable, although, local trauma, inflammation, and hemorrhage have been suggested. Here is a presentation of a case report showing aggressiveness of CGCG with rapid growth involving the anterior region of the mandible associated with paresthesia, pain, mobility, cortical perforation, and showing a completely osteolytic nature. It was diagnosed by histopathological examination and immunohistochemistry. This case was treated surgically with no recurrence seen after a one-year follow-up with a good prognosis. Expansile and osteolytic bony lesions in the jaws or any radiolucency more than 2 cm CGCG should take into consideration as a differential diagnosis.
https://www.ijhsr.org/IJHSR_Vol.11_Issue.4_April2021/IJHSR-Abstract.016.html, 2021
Central giant cell granuloma (CGCG) is an uncommon, benign, intraosseous bony lesion of the mandible and maxilla which is variably aggressive in nature. The incidence of an aggressive and recurrence nature is greatest in a female with a ratio of 2:1. Based on the clinical and radiographic features, Central giant cell granuloma can be classified as aggressive and non-aggressive lesions. Here we report a case of central giant cell granuloma in the posterior mandibular molar region which was aggressive in nature. The clinically and radiographically swelling was evaluated with displaced tooth, pain, cortical expansion, and root resorption. The treatment varies according to the nature of the lesion, this case was treated by conservative excision with continuity of the mandible.
Ibom Medical Journal, 2022
Mandibular aggressive central giant cell granuloma is a rare non-neoplastic giant cell tumour characterised by pain, bone destruction, tooth root resorption, jawbone cortical perforation, and high recurrence rate. This is a case of a 10-year-old boy who presented to the Dental Surgical outpatient clinic of University of Uyo Teaching Hospital with a three-year history of left jaw swelling. The clinical diagnosis was fibrous dysplasia of the left hemi-mandible. Consequently, left hemi-mandibulectomy was performed, and subsequent histopathological diagnosis was aggressive central giant cell granuloma of the mandible. This article presents this rare diagnosis and explores its classification, aetiopathogenesis, clinico-pathological features and management.
Journal of Oral and Maxillofacial Surgery, 2010
Journal of Oral and Maxillofacial Surgery, 1983
2020
Central giant cell granuloma [CGCG] is a relatively uncommon pathological condition accounting for less than 7% of all benign lesions of the jaws. CGCG is a locally aggressive reactive bone lesion with variable clinical behaviour that manifests with pain, cortical perforation, and root resorption. A Case of a 32-year-old male is reported occurring in mandible. The present case is discussed as a diagnostic challenge to distinguish Central giant cell granuloma [CGCG] from Giant cell tumour [GCT], as they show similar biologic behaviour, histopathologic features & prognosis.
2017
Central Giant Cell Granuloma (CGCG) involving either jaw is not a common benign intra-osseous lesion containing giant cells; characterized by osteoclast-like giant cells in a cellular fibrovascular stroma. The true nature of this lesion is controversial and remains unknown: the three competing theories are that it could be reactive lesion, a developmental anomaly or a benign neoplasm. The incidence of CGCG in the general population is estimated to be 0.0001%, with 60% of cases occurring before the age of 30 years. CGCG found more commonly in females and more commonly involve mandible as compared to maxilla, with an epicentre anterior to first molars. This paper presents a rare case of CGCG in a 52 year old female patient involving region posterior to mandibular first molar. As there is paucity in the literature about the CT findings of CGCG, we are presenting a case of CGCG with special emphasis on CT findings, in addition to clinical, histopathological and surgical aspect of the le...
IP International Journal of Maxillofacial Imaging, 2021
Central giant cell granuloma (CGCG) is an uncommon, benign, intraosseous, proliferative lesion of the jaw with an unknown etiology. The incidence in the general population is very low with age predilection generally younger than 30 years with a female predominance. It is usually unifocal and located at the anterior region of the mandible or maxilla, although are more frequently found in the mandible.CGCG is divided into rare aggressive variant and a common non aggressive variant based on clinicoradiographic features. Surgical removal is often the preferred treatment and is characterized by high recurrence rate. The present case is a rare aggressive variant of CGCG seen in posterior mandible in an 8-year-old girl.
JORDI - Journal of Oral Diagnosis
Central giant cell granuloma (CGCG) is a benign intraosseous reactive lesion of jaw with diverse clinical and radiological behaviour pattern. It accounts for 7% of neoplastic bone lesion of jaw with 70% occurring in mandible. CGCG was first considered as giant cell tumor mostly found in epiphyseal region of long bone having both aggressive and non-aggressive pattern. The etiology of the lesion is not defined. Multiple CGCGs of the jaw bones is very rare and, if it occurs, it is usually associated with hyperparathyroidism in majority of the cases. We report an interesting case in which a 33 year old female came with a swelling present on right side of mandible which was asymptomatic. Another swelling was present on left side which was non-evident and asymptomatic. Clinical, radiological and histopathological examination confirmed the lesions as central giant cell granuloma. Biochemical examination showed no signs of hyperparathyroidism. This report represents a very rare entity in which there is idiopathic bilateral CGCG having both aggressive and non-aggressive type of lesion.
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