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Papers by Dipanwita Chakraborty

NL Journal of Dentistry and Oral Sciences, 2024

Juvenile ossifying fibroma is a rare, aggressive, benign fibro-osseous lesion, typically discover... more Juvenile ossifying fibroma is a rare, aggressive, benign fibro-osseous lesion, typically discovered
early as a bony overgrowth, often without symptoms. The recurrence rate for this condition is quite high. This
article presents a case of juvenile ossifying fibroma in a 6-year-old male patient. Upon clinical examination, a
solitary growth on the right side of the patient’s face was observed. A panoramic radiograph, postero-anterior
skull view radiograph, and CT scan were performed. Complete excision with hemi-maxillectomy of the growth
was carried out, followed by surgical reconstruction using an autogenous graft. Biopsy revealed a fibro-osseous
lesion, and the diagnosis given was Juvenile trabecular ossifying fibroma.

Journal of oral medicine, oral surgery, oral pathology and oral radiology, Jun 15, 2024

Journal of Natural Science, Biology and Medicine, 2021

Calcifying epithelial odontogenic tumor (CEOT) is a rare benign odontogenic tumor which can occur... more Calcifying epithelial odontogenic tumor (CEOT) is a rare benign odontogenic tumor which can occur extraosseous or intraosseous. The etiopathogenesis of CEOT is not known. It has a propensity toward mandibular molar ramus region and has no sex predilection. The treatment of choice for CEOT ranges from either enucleation, curettage to enucleation, marginal/segmental resection, and radical and extensive resection (hemimandibulectomy) or hemimaxillectomy. This case report describes an incidence and clinical management of CEOT in a young female patient.

Spindle cell neoplasm is an unusual bimorphic malignant tumor that typically affects the upper ae... more Spindle cell neoplasm is an unusual bimorphic malignant tumor that typically affects the upper aerodigestive tract mucosa but can potentially arise elsewhere in the body. A diverse range of benign and malignant tumors, including those with neural, fibroblastic, vascular, myofibroblastic, myogenic, and epithelial origins, are together referred to as soft tissue spindle cell neoplasms. The average age of occurrence is 51 years for men and 67 years for women, with a predominance of men. There is limited information in the literature about the symptoms of spindle cell neoplasms. These tumors typically have a polypoid form, with a high concentration of dysplastic spindle cell components. They are composed of surface epithelial alterations ranging from mild epithelial dysplasia to invasive carcinoma. The article provides insight into a case of neurofibromatous variant of spindle cell neoplasm. This is an Open Access (OA) journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.

Journal natural science, biology and medicine, 2021

IntroductIon Calcifying epithelial odontogenic tumor (CEOT) or Pindborg tumor is a rare benign od... more IntroductIon Calcifying epithelial odontogenic tumor (CEOT) or Pindborg tumor is a rare benign odontogenic tumor, [1] which constitutes only 0.3%-0.4% of all benign odontogenic tumors. CEOT has two variants: intraosseous and extraosseous, with an incidence rate of 94% and 6%, respectively. [2] Intraosseous type of CEOTs has a propensity to occur in the mandibular molar ramus region, while the extraosseous tumors are frequently discovered in the anterior jaw and involve the gingiva. It is a painless swelling, associated with the crown of an unerupted tooth. The treatment of CEOT ranges from simple excision to extensive resection. The rate of recurrence varies from 10% to 15% and requires periodic follow-up. Here, we present a distinctive case of CEOT of the mandible.

NL Journal of Dentistry and Oral Sciences, 2024

Juvenile ossifying fibroma is a rare, aggressive, benign fibro-osseous lesion, typically discover... more Juvenile ossifying fibroma is a rare, aggressive, benign fibro-osseous lesion, typically discovered
early as a bony overgrowth, often without symptoms. The recurrence rate for this condition is quite high. This
article presents a case of juvenile ossifying fibroma in a 6-year-old male patient. Upon clinical examination, a
solitary growth on the right side of the patient’s face was observed. A panoramic radiograph, postero-anterior
skull view radiograph, and CT scan were performed. Complete excision with hemi-maxillectomy of the growth
was carried out, followed by surgical reconstruction using an autogenous graft. Biopsy revealed a fibro-osseous
lesion, and the diagnosis given was Juvenile trabecular ossifying fibroma.

Journal of oral medicine, oral surgery, oral pathology and oral radiology, Jun 15, 2024

Journal of Natural Science, Biology and Medicine, 2021

Calcifying epithelial odontogenic tumor (CEOT) is a rare benign odontogenic tumor which can occur... more Calcifying epithelial odontogenic tumor (CEOT) is a rare benign odontogenic tumor which can occur extraosseous or intraosseous. The etiopathogenesis of CEOT is not known. It has a propensity toward mandibular molar ramus region and has no sex predilection. The treatment of choice for CEOT ranges from either enucleation, curettage to enucleation, marginal/segmental resection, and radical and extensive resection (hemimandibulectomy) or hemimaxillectomy. This case report describes an incidence and clinical management of CEOT in a young female patient.

Spindle cell neoplasm is an unusual bimorphic malignant tumor that typically affects the upper ae... more Spindle cell neoplasm is an unusual bimorphic malignant tumor that typically affects the upper aerodigestive tract mucosa but can potentially arise elsewhere in the body. A diverse range of benign and malignant tumors, including those with neural, fibroblastic, vascular, myofibroblastic, myogenic, and epithelial origins, are together referred to as soft tissue spindle cell neoplasms. The average age of occurrence is 51 years for men and 67 years for women, with a predominance of men. There is limited information in the literature about the symptoms of spindle cell neoplasms. These tumors typically have a polypoid form, with a high concentration of dysplastic spindle cell components. They are composed of surface epithelial alterations ranging from mild epithelial dysplasia to invasive carcinoma. The article provides insight into a case of neurofibromatous variant of spindle cell neoplasm. This is an Open Access (OA) journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.

Journal natural science, biology and medicine, 2021

IntroductIon Calcifying epithelial odontogenic tumor (CEOT) or Pindborg tumor is a rare benign od... more IntroductIon Calcifying epithelial odontogenic tumor (CEOT) or Pindborg tumor is a rare benign odontogenic tumor, [1] which constitutes only 0.3%-0.4% of all benign odontogenic tumors. CEOT has two variants: intraosseous and extraosseous, with an incidence rate of 94% and 6%, respectively. [2] Intraosseous type of CEOTs has a propensity to occur in the mandibular molar ramus region, while the extraosseous tumors are frequently discovered in the anterior jaw and involve the gingiva. It is a painless swelling, associated with the crown of an unerupted tooth. The treatment of CEOT ranges from simple excision to extensive resection. The rate of recurrence varies from 10% to 15% and requires periodic follow-up. Here, we present a distinctive case of CEOT of the mandible.