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All Journal Indian Journal of Forensic Medicine & Toxicology
Satya Ranjan Misra
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Complex Composite Odontoma: A Cause of Impacted Teeth Satya Ranjan Misra
Indian Journal of Forensic Medicine & Toxicology Vol. 14 No. 4 (2020): Indian Journal of Forensic Medicine & Toxicology
Publisher : Institute of Medico-legal Publications Pvt Ltd

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.37506/ijfmt.v14i4.12982

Abstract

Odontomas are one of the most common odontogenic lesions, earlier considered as mixed odontogenicneoplasms but lately have been accepted as hamartomatous malformations. They are either detectedaccidentally on radiographs or when they are a cause of impeding normal eruption of teeth. Odontomasoriginate from the odontogenic tissue and contain enamel and dentine, hence are referred to as compositelesions. They can be of two types depending on the appearance. If they have masses of calcified structuresresembling multiple miniature teeth then they are called compound odontomas and if they appear as anirregular disorganized radiopaque mass they are referred to as complex odontomas. A case if complexodontoma is reported herewith which led to impacted maxillary molar.
Ameloblastoma: A Common Benign Odontogenic Tumour with Multiple Manifestations Satya Ranjan Misra
Indian Journal of Forensic Medicine & Toxicology Vol. 14 No. 4 (2020): Indian Journal of Forensic Medicine & Toxicology
Publisher : Institute of Medico-legal Publications Pvt Ltd

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.37506/ijfmt.v14i4.12983

Abstract

A myriad of odontogenic cysts and tumours both benign and malignant are seen in the maxilla and themandible. One of the most frequently encountered odontogenic tumour is ameloblastoma and has differentclinical and histologic variants which dictate the treatment plan. It has a properly documented inclinationtowards a local infiltration and tendency of recurrence. Ameloblastoma is a benign intraosseous odontogenicepithelial tumour which is locally invasive and locally destructive, non-functional, intermittent in growth,anatomically benign and clinically persistent. The tumour arises from the epithelial cell rest of malassez,from the walls of odontogenic cyst and from the basal cells.
Acrocephalosyndactyly Syndrome: A Rare Case Report Satya Ranjan Misra
Indian Journal of Forensic Medicine & Toxicology Vol. 15 No. 2 (2021): Indian Journal of Forensic Medicine & Toxicology
Publisher : Institute of Medico-legal Publications Pvt Ltd

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.37506/ijfmt.v15i2.14984

Abstract

Acrocephalosyndactyly or Apert syndrome is a rare disorder in which the fingers and toes are fused,giving the appearance of webbed hand and feet. Also, there is craniosynostosis, leading to severe mid-facehypoplasia and characteristic facial deformities. Here there is a genetic mutation in the fibroblast growthfactor receptor 2 (FGFR2) gene with autosomal dominant inheritance. A case of an 8-year-old male child isreported here with frontal bossing, acrocephaly, prominent ocular hypertelorism with divergent strabismus,saddle-shaped nose, mid-face hypoplasia, crowded anterior teeth, sparse hair and severe bilateral syndactylyof the feet and hands.
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