scholarly journals A rare case report of simultaneous occurrence of a pediatric pleuropulmonary blastoma and an intralobar pulmonary sequestration

2021 ◽  
Vol 16 (7) ◽  
pp. 1727-1731
Author(s):  
Marjeta Tanka ◽  
Anila Kristo ◽  
Dritan Alushani ◽  
Irena Kasmi ◽  
Nikollaq Leka
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Pulmonary Sequestration ◽  
Pleuropulmonary Blastoma ◽  
Simultaneous Occurrence ◽  
Intralobar Pulmonary Sequestration ◽  
Rare Case Report

Pleuropulmonary blastoma in 3 year old child - A rare case report

2018 ◽  
Vol 7 (1) ◽  
pp. 37-39
Author(s):  
Pramod Shaha ◽  
◽  
Shrishail Adke ◽  
Prakash Patil ◽  
◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Pleuropulmonary Blastoma ◽  
Rare Case Report

scholarly journals Submandibular Abscess due to an Infected Keratocystic Odontogenic Tumor associated with Simultaneous Occurrence of a Traumatic Bone Cyst: A Rare Case Report

2013 ◽  
Vol 14 (1) ◽  
pp. 133-136 ◽  
Author(s):  
Poorandokht Davoodi ◽  
Loghman Rezaei-Soufi ◽  
Mina Jazaeri ◽  
Adineh Javadian Langaroodi ◽  
Seyed Hossein Hoseini Zarch
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Present Report ◽  
Bone Cyst ◽  
Rare Condition ◽  
Odontogenic Tumor ◽  
Simultaneous Occurrence ◽  
Keratocystic Odontogenic Tumor ◽  
Submandibular Region ◽  
Rare Case Report

ABSTRACT Aim The aim of this report is to introduce a rare case in which an infected keratocystic odontogenic tumor (KCOT) was initially diagnosed and treated as a dentoalveolar abscess. Background Keratocystic odontogenic tumor (KCOT) is a benign neoplasm that can be secondarily infected. However, cervical soft tissue abscess formation as a result of an infected odontogenic cyst or tumor is a rare condition few of which have only been described in the existing literature. Also, there has been a single report regarding the coincidence of a traumatic bone cyst and a keratocytic odontogenic tumor to date. Case report The patient was a 29-year-old male, complaining of fever, pain and swelling in the left submandibular region. The panoramic radiography showed a well-defined and partially corticated radiolucency between the roots of the second and third left mandibular molars. In addition, a well-corticated radiolucent lesion was incidentally found on the right side of the mandible, which, following surgical exploration, was diagnosed as a traumatic bone cyst. Conclusion In the present report, an infected KCOT manifested as a cervical abscess, coincided with a traumatic bone cyst. Clinical significance From the clinical point of view, it is of paramount significance to prevent misdiagnosis of similar presentations as pulp and periapical lesions, which may lead to mistreatment and thus complications. How to cite this article Davoodi P, Rezaei-Soufi L, Jazaeri M, Javadian Langaroodi A, Hoseini Zarch SH. Submandibular Abscess due to an Infected Keratocystic Odontogenic Tumor associated with Simultaneous Occurrence of a Traumatic Bone Cyst: A Rare Case Report. J Contemp Dent Pract 2013;14(1): 133-136.

scholarly journals Simultaneous occurrence of triple teeth and double teeth in primary dentition: A rare case report and review of the literature

2020 ◽  
Vol 8 (7) ◽  
pp. 1277-1286
Author(s):  
Marianne Lagarde ◽  
Anne‐Laure Bonnet ◽  
Nina Douangmala ◽  
Marina Traing ◽  
Elisabeth Dursun
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Primary Dentition ◽  
Simultaneous Occurrence ◽  
Review Of The Literature ◽  
Rare Case Report ◽  
Double Teeth

Primary neuroendocrine carcinoma of renal: a rare case report

2014 ◽  
Author(s):  
Tadeusz Budlewski ◽  
Dorota Szydlarska ◽  
Norbert Szalus ◽  
Jolanta Kijek ◽  
Beata Ewa Chrapko
Keyword(s):  
Case Report ◽  
Neuroendocrine Carcinoma ◽  
Rare Case ◽  
Rare Case Report

Combination of turner syndrome and congenital adrenal hyperplasia: a rare case report

2017 ◽  
Author(s):  
Ivana Sagova ◽  
Dušan Pavai ◽  
Matej Stančik ◽  
Helena Urbankova ◽  
Juliana Gregova ◽  
...  
Keyword(s):  
Case Report ◽  
Congenital Adrenal Hyperplasia ◽  
Turner Syndrome ◽  
Rare Case ◽  
Adrenal Hyperplasia ◽  
Rare Case Report
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