Maxillary keratocystic odontogenic tumor with calcifications: A review and case report

Naveen, Farzan; Tippu, Shoaib R; Girish, KL; Kalra, Manpreet; Desai, Vela D

doi:10.4103/0973-029x.86692

Cited by 5 publications

(2 citation statements)

References 13 publications

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“…In addition, injured tissue of any kind is predisposed to dystrophic calcification. [ 19 ] In our case, the type of calcification is most likely to be dystrophic as it is the predominant type in syndromic OKCs. Although it was not confirmed, calcification was not evident in our histologic slides.…”

Section: Discussionmentioning

confidence: 74%

An enigma of Gorlin–Goltz syndrome: Two cases reported in mother and daughter

Sahu

Sahoo

Banerjee³

et al. 2019

J Oral Maxillofac Pathol

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Gorlin–Goltz syndrome (GGS) also known as the nevoid basal cell carcinoma syndrome or the nevus–Bifid rib syndrome is an inherited autosomal dominant syndrome. It is caused by genetic alteration produced by a mutation in the “patched” tumor suppressor gene. This rare syndrome is characterized by basal cell carcinoma of skin, multiple odontogenic keratocyst and bifid ribs along with other features such as hypertelorism, sex organ abnormalities, palmar and/or plantar pits and calcification of falx cerebri. Early detection and treatment are essential for patients suffering from this syndrome. Only a few cases of this syndrome with familial background have been reported from India. In this study, we present a rare case of GGS in a mother and her daughter. The purpose of this study is to discuss the role of a dentist in early detection and the need for a multidisciplinary approach for the treatment of this syndrome.

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Section: Discussionmentioning

confidence: 74%

An enigma of Gorlin–Goltz syndrome: Two cases reported in mother and daughter

Sahu

Sahoo

Banerjee³

et al. 2019

J Oral Maxillofac Pathol

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“…Maksilla yerleşimi KCOT'lar daha nadirdir ve yuvarlak, pürüzsüz görünümdedir. Sunulan olguda nadir bir yerleşim olarak maksiller sinus anteriorund agörülmektedir (7,8).…”

Section: Discussionunclassified

Nadir Yerleşimli Geniş Hacimli Keratokistik Odontojenik Tümör

Bilgen¹,

Ural

Bekerecioğlu

2019

Kahramanmaraş Sütçü İmam Üniversitesi Tıp Fakültesi Dergisi

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KCOT (Keratokistik Odontojenik tümör) tüm çene kistlerinin %7,8 ‘ini oluşturmaktadır ve mandibulada daha sık gözlenmektedir. Genellikle bulgu vermeden ilerler. Ancak enfeksiyona sekonder ağrı ve şişlik ortaya çıkabilir. Maksilla yerleşimli KCOT, % 30 oranında oral mukoza ekspansiyonu ile karşımıza çıkar. Çalışmada, nadir bir olgu olarak, sağ yanakta şişlik dışında şikayeti olmayan, tüm maksiller sinüsü kaplamış ve maksillar sinüs anterior duvarının erode etmiş, keratokistik odontojenik tümör ve tedavi yaklaşımımız sunulmaktadır. 37 yaşında erkek hasta yaklaşık 6 aydır sağ malar bölgede 3x3 cm. lik şişlik ve intraoral ekspansiyon nedeniyle opera edildi. Çıkartılan kist duvarı ile histopatolojik imcelemeye gönderildi ve sonuç odontojenik keratokist olarak tespit edildi. Sonuç olarak, Keratokistik odontojenik tümöler, maksiller sinüs içerisinde, bir diş ile birlikte veya diş olmadan ortaya çıkabilir. Hastanın yönetiminde önemli olan, uygun tedavi yönteminin seçimi ve nüks oranı yüksekliği konusunda doğru bilgilendirme ve takiptir.

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Pseudotumeur inflammatoire du sinus maxillaire : un cas

Ayachi

Moatemri

Mziou

et al. 2015

Med Buccale Chir Buccale

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Résumé -Introduction :Les pseudotumeurs inflammatoires sont un groupe rare de tumeurs bénignes d'étiologie inconnue. La localisation cervico-faciale est rare, particulièrement au niveau des sinus para-nasaux. Les auteurs rapportent une nouvelle observation de pseudotumeur inflammatoire au niveau du sinus maxillaire et discutent les caractéristiques cliniques et thérapeutiques de cette entité en se basant sur une revue de la littérature. Observation : Patiente, âgée de 31 ans, ayant consulté pour une tuméfaction jugale droite évoluant depuis trois mois. L'examen clinique a montré un comblement vestibulaire supérieur droit avec une mobilité des dents en regard. La tomodensitométrie a confirmé la présence d'un processus tissulaire dense du sinus maxillaire droit avec érosion des parois osseuses et extension à la fosse nasale homolatérale. Elle a bénéficié d'une exérèse tumorale. L'examen histologique a été en faveur d'une tumeur myofibroblastique inflammatoire du sinus maxillaire. Aucune récidive n'a été notée avec un recul de neuf ans. Discussion : Bien que bénignes, ces pseudotumeurs inflammatoires présentent des caractéristiques cliniques d'agressivité avec un pouvoir lytique mimant une tumeur maligne. Le traitement de ces tumeurs est mal codifié. L'exérèse chirurgicale et les corticostéroïdes représentent les modalités thérapeutiques les plus utilisées.Abstract -Inflammatory pseudotumor of the maxillary sinus : a case report. Introduction: Inflammatory pseudotumors are a rare group of benign neoplasms of unknown etiology. They are uncommon in the head and neck, particularly in the paranasal sinuses. The authors report a new case of an inflammatory pseudotumor of the maxillary sinus, and discuss the clinical and therapeutic characteristics of this entity based on a literature review. Case: The patient, aged 31, consulted for a right cheek swelling lasting for 3 months. Clinical examination showed a right upper vestibular filling with teeth mobility. Computed tomography confirmed the presence of a dense tissue process of the right maxillary sinus with erosion of the bone walls and extension to the ipsilateral nasal cavity. Tumor resection was done, and histological examination showed an inflammatory myofibroblastic tumor of the maxillary sinus. No recurrence was observed with a follow-up of 9 years. Discussion: Although benign, inflammatory pseudotumors often show aggressive clinical behavior, with locally destructive features that mimic a malignant tumor. Their treatment is not well established. Surgical excision and corticosteroids are the most used. Surgeons and pathologists should consider this entity in order to avoid surgery.

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Maxillary keratocystic odontogenic tumor with calcifications: A review and case report

Cited by 5 publications

References 13 publications

An enigma of Gorlin–Goltz syndrome: Two cases reported in mother and daughter

An enigma of Gorlin–Goltz syndrome: Two cases reported in mother and daughter

Nadir Yerleşimli Geniş Hacimli Keratokistik Odontojenik Tümör

Pseudotumeur inflammatoire du sinus maxillaire : un cas

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