scholarly journals Pre-eruptive Intra-Coronal Resorption: A report of two cases and review of the literature

2021 ◽  
Author(s):  
Michelle Briner Garrido ◽  
Joanne Briner Prenafeta ◽  
Rohan Jagtap ◽  
Christopher D. Matesi ◽  
Andres Briner
Keyword(s):  
Pediatric Patients ◽  
Radiographic Finding ◽  
Rare Condition ◽  
Review Of The Literature ◽  
Variable Depth ◽  
Radiographic Findings ◽  
Second Molar ◽  
Unerupted Tooth ◽  
Mandibular Second Molar

Pre-eruptive intracoronary resorption is a rare condition mainly affecting pediatric patients. It is a radiographic finding in the dentin of the crown of an unerupted tooth just below the enamel-dentin junction. It is visualized in radiographs as a radiolucent coronal lesion of variable depth; it is well-defined and located in the dentin adjacent to the amelodentinal limit of an unerupted tooth. Historically, this lesion was misdiagnosed as caries and was misnamed pre-eruptive caries, when in reality they were pre-eruptive intracoronal resorptions. We present two rare cases of pre-eruptive intracoronary resorption in patients that needed radiographs for orthodontic purposes. The Oral & Maxillofacial Radiologist detected the existence of pre-eruptive intracoronary resorption in mandibular second premolars and mandibular second molar. These radiographic findings provided the clinician with the advantage of knowing this condition before teeth eruption, allowing for conservative treatment and periodic radiographic follow-up.

A Rare Case of Congenital Missing Mandibular Second Molar: Report and Review of Literature

2020 ◽  
Author(s):  
Deepashri H Kambalimath
Keyword(s):  
Tooth Development ◽  
Rare Condition ◽  
Review Of Literature ◽  
Indian Literature ◽  
Missing Teeth ◽  
Second Molar ◽  
The World ◽  
Mandibular Second Molar ◽  
Sporadic Cases ◽  
Genetic And Environmental Factors

Congenital missing permanent second molar is an extremely rare condition. Non syndromic mandibular second molar agenesis associated with other anomalies has occasionally been reported in literature, but isolated sporadic cases are rarely observed. Number of interactions between genetic and environmental factors during the process of tooth development might be the causative etiology for agenesis. This report presents an isolated case of hypodontia with absence of bilateral mandibular second molar agenesis in a healthy 18 year old female patient is presented and literature review on prevalence of most missing teeth with incidence of missing second molar in various regions of the world and in various regions of Indian continent is presented. No such case has been reported in Indian literature so far.

Extensive Extraneural Metastases of Cerebral Glioblastoma in a Pediatric Patient: An Extreme Case Report and Comprehensive Review of the Literature

2021 ◽  
pp. 1-6
Author(s):  
Kadir Oktay ◽  
Dogu Cihan Yildirim ◽  
Arbil Acikalin ◽  
Kerem Mazhar Ozsoy ◽  
Nuri Eralp Cetinalp ◽  
...  
Keyword(s):  
Case Report ◽  
Pediatric Patients ◽  
Extreme Case ◽  
Rare Condition ◽  
Review Of The Literature ◽  
Pertinent Literature ◽  
Cervical Lymph Nodes ◽  
Case Presentation ◽  
Comprehensive Review ◽  
Extraneural Metastases

<b><i>Introduction:</i></b> Extraneural metastases of glioblastoma are very rare clinical entities, especially in pediatric patients. Because of their rarity, they can be confused with other pathological processes. <b><i>Case Presentation:</i></b> We report a case of 16-year-old boy with extensive extraneural metastases of glioblastoma. Lung, liver, cervical lymph nodes, skin, and bone metastases were detected in the patient. <b><i>Conclusion:</i></b> We describe the presentation, evaluation, and diagnosis of this rare condition with regard to pertinent literature.

scholarly journals Subgaleal hematoma evacuation in a pediatric patient: A case report and review of the literature

2020 ◽  
Vol 11 ◽  
pp. 243
Author(s):  
Tye Patchana ◽  
Hammad Ghanchi ◽  
Taha Taka ◽  
Mark Calayag
Keyword(s):  
Pediatric Patients ◽  
Neonatal Period ◽  
Clinical Course ◽  
African American Female ◽  
Review Of The Literature ◽  
Hair Pulling ◽  
Imaging Characteristics ◽  
Subgaleal Hematoma ◽  
History Of

Background: Subgaleal hematoma (SGH) is generally documented within the neonatal period and is rarely reported as a result of trauma or hair braiding in children. While rare, complications of SGH can result in ophthalmoplegia, proptosis, visual deficit, and corneal ulceration secondary to hematoma extension into the orbit. Although conservative treatment is preferential, expanding SGH should be aspirated to reduce complications associated with further expansion. Case Description: A 12-year-old African-American female with no recent history of trauma presented with a chief complaint of headache along with a 2-day history of enlarging 2–3 cm ballotable bilateral frontal mass. Hematological workup was negative. The patient’s family confirmed a long history of hair braiding. The patient was initially prescribed a period of observation but returned 1-week later with enlarging SGH, necessitating surgical aspiration. Conclusion: SGH is rare past the neonatal period, but can be found in pediatric and adolescent patients secondary to trauma or hair pulling. Standard workup includes evaluation of the patient’s hematological profile for bleeding or coagulation deficits, as well as evaluation for child abuse. Although most cases of SGH resolve spontaneously over the course of several weeks, close follow-up is recommended. The authors present a case of a 12-year-old female presenting with enlarging subgaleal hemorrhages who underwent surgical aspiration and drainage without recurrence. A literature review was also conducted with 32 pediatric cases identified, 20 of which were related to hair pulling, combing, or braiding. We review the clinical course, imaging characteristics, surgical management, as well as a review of the literature involving subgaleal hemorrhage in pediatric patients and hair pulling.

Virilizing Adrenocortical Tumors in Childhood: Eight Cases and a Review of the Literature

PEDIATRICS ◽  
1985 ◽  
Vol 76 (3) ◽  
pp. 437-444
Author(s):  
Phillip D. K. Lee ◽  
Robert J. Winter ◽  
Orville C. Green
Keyword(s):  
Linear Growth ◽  
Pediatric Patients ◽  
Serum Levels ◽  
Dehydroepiandrosterone Sulfate ◽  
Benign Disease ◽  
Review Of The Literature ◽  
Histologic Diagnosis ◽  
Abdominal Sonography ◽  
Definitive Therapy

Eight cases of adrenocortical tumor are presented with a review of the literature. Although such tumors are rare, they are important causes of inappropriate virilization and Cushing's syndrome in childhood. Clinical virilization with or without hypercortisolism was found in all eight children, who were 5 years old or younger. Excessive linear growth was noted, despite evidence of hypercortisolism. Serum levels of dehydroepian-drosterone, dehydroepiandrosterone sulfate, testosterone, and cortisol were elevated in all cases tested and appear to be useful diagnostic alternatives to the more traditional determinations of urine 17-ketosteroids and 17-hydroxycorticosteroida. Abdominal sonography and computed tomography have proven to be reliable tools for tumor localization. Surgical resection was the definitive therapy in all patients, and perioperative steroid replacement was essential. Histologic diagnosis appeared to have little bearing on prognosis, and the majority of pediatric patients have had clinically benign disease. At a mean follow-up of 3 years, seven of the eight children were alive and had no evidence of tumor recurrence.

scholarly journals Ameloblastic Carcinoma in a 2-Year-Old Child: A Case Report and Review of the Literature

2020 ◽  
Vol 2020 ◽  
pp. 1-7
Author(s):  
Ngoc Bao Vu ◽  
Ngoc Tuyen Le ◽  
Risa Chaisuparat ◽  
Pasutha Thunyakitpisal ◽  
Ngoc Minh Tran
Keyword(s):  
Rare Case ◽  
Pediatric Patients ◽  
Root Resorption ◽  
Immunohistochemical Analysis ◽  
Incisional Biopsy ◽  
Review Of The Literature ◽  
Ameloblastic Carcinoma ◽  
Valuable Contribution ◽  
Radiographic Findings ◽  
The Right

Ameloblastic carcinoma (AC) is a rare malignant odontogenic tumor in pediatric patients, only 22 cases have been reported in literature since 1932. We present an extremely rare case in which AC occurred in a 2-year-old girl, who had a tumor in the right mandible. Radiographic findings showed a multilocular, poorly defined, and mixed radiolucent-radiopaque lesion in the region of teeth #84 to #85, with bone and tooth root resorption. Computed tomography revealed buccal cortex destruction, tumor infiltration of soft tissue, and enlarged nodes. Incisional biopsy showed histomorphological features of AC. Immunohistochemical analysis exhibited a positive result for Cytokeratin (CK) 19 and overexpression of p53 and Ki67. The patient underwent right hemimandibulectomy and neck dissection. The final pathology was consistent with the initial diagnosis of AC. The patient did not exhibit signs of recurrence or metastasis within 2 years postoperatively. Given the rarity of this disease and the age of the patient, this report constitutes a valuable contribution to the current literature.

scholarly journals Management guidelines for amelogenesis imperfecta: a case report and review of the literature

2021 ◽  
Vol 15 (1) ◽  
Author(s):  
M. Roma ◽  
Puneet Hegde ◽  
M. Durga Nandhini ◽  
Shreya Hegde
Keyword(s):  
Case Report ◽  
Treatment Plan ◽  
Rare Condition ◽  
Amelogenesis Imperfecta ◽  
Radiographic Findings ◽  
Case Presentation ◽  
Management Guidelines ◽  
Dental Tissues ◽  
Entire Treatment

Abstract Background Rehabilitation of the entire dentition with amelogenesis imperfecta (AI) tends to pose a great challenge to the clinician. Most of the cases of amelogenesis imperfecta are reported to be associated with skeletal and dental deformities which results in severe sensitivity of the dental tissues. Case presentation This clinical case report marks out the total restoration of the oral condition of a young Indian patient diagnosed with the hypoplastic type of amelogenesis imperfecta. Fixed metal ceramic prosthesis were planned to strengthen the masticatory activity, aesthetics, to banish the dental sensitivity and to build up the general persona of the patient. The patient was followed-up at 6 months, 1 year and 2 years intervals. Functional and esthetic impairment was not visible after the follow up period and the treatment outcome was successful. The entire treatment plan was intended to enhance the functional, esthetic and the masticatory component of the occlusal architecture. Conclusion This case report details the presentation, characteristic radiographic findings, and management of a patient with an extremely rare condition of amelogenesis imperfecta.

scholarly journals Tropheryma whipplei Endocarditis: Case Presentation and Review of the Literature

2018 ◽  
Vol 6 (1) ◽  
Author(s):  
Michael McGee ◽  
Stephen Brienesse ◽  
Brian Chong ◽  
Alexander Levendel ◽  
Katy Lai
Keyword(s):  
Heart Failure ◽  
Rare Condition ◽  
Tropheryma Whipplei ◽  
Review Of The Literature ◽  
Case Presentation ◽  
Gastrointestinal Manifestations ◽  
Presenting Symptoms ◽  
Physician Awareness ◽  
Culture Negative

Abstract Whipple’s disease is a rare infective condition, classically presenting with gastrointestinal manifestations. It is increasingly recognized as an important cause of culture-negative endocarditis. We present a case of Whipple’s endocarditis presenting with heart failure. A literature review identified 44 publications documenting 169 patients with Whipple’s endocarditis. The average age was 57.1 years. There is a clear sex predominance, with 85% of cases being male. Presenting symptoms were primarily articular involvement (52%) and heart failure (41%). In the majority of cases, the diagnosis was made on examination of valvular tissue. Preexisting valvular abnormalities were reported in 21%. The aortic valve was most commonly involved, and multiple valves were involved in 64% and 23% of cases, respectively. Antibiotic therapy was widely varied and included a ceftriaxone, trimethoprim, and sulfamethoxazole combination. The average follow-up was 20 months, and mortality was approximately 24%. Physician awareness is paramount in the diagnosis and management of this rare condition.

scholarly journals Desmoplastic Ameloblastoma of the Mandible

2013 ◽  
Vol 52 (191) ◽  
Author(s):  
Soniya Adyanthaya ◽  
Pushparaja Shetty
Keyword(s):  
Cortical Bone ◽  
Radiographic Finding ◽  
Odontogenic Tumor ◽  
Anterior Portion ◽  
Radiographic Findings ◽  
Anatomical Distribution ◽  
Bone Expansion ◽  
Radiolucent Lesion

The Desmoplastic Ameloblastoma exhibits important differences in anatomical distribution, histologicappearance and radiographic findings compared with the classic type of ameloblastoma. We describea case of desmoplastic variant of ameloblastoma localized in the mandibular anterior portion of thejaw, extending posteriorly in the left side. The tumor was expansile, slowly growing and painless.The radiographic finding showed diffuse, radiolucent lesion with cortical bone expansion. Surgicalexcision was performed and follow-up examination done after two years disclosed no recurrence.The purpose of this article is to assist in better understanding of this variant of odontogenic tumor._______________________________________________________________________________________Keywords: Ameloblastoma; desmoplasia; mandible; odontogenic tumor.

scholarly journals Role of follow-up imaging after resection of brain arteriovenous malformations in pediatric patients: a systematic review of the literature

2017 ◽  
Vol 19 (2) ◽  
pp. 149-156 ◽  
Author(s):  
Joaquin E. Jimenez ◽  
Zachary C. Gersey ◽  
Jason Wagner ◽  
Brian Snelling ◽  
Sudheer Ambekar ◽  
...  
Keyword(s):  
Systematic Review ◽  
Pediatric Patients ◽  
Surgical Removal ◽  
Review Of The Literature ◽  
Brain Arteriovenous Malformation ◽  
Integral Role ◽  
Meta Analyses ◽  
Mesh Database

OBJECTIVE Pediatric patients are at risk for the recurrence of brain arteriovenous malformation (AVM) after resection. While there is general consensus on the importance of follow-up after surgical removal of an AVM, there is a lack of consistency in the duration of that follow-up. The object of this systematic review was to examine the role of follow-up imaging in detecting AVM recurrence early and preventing AVM rupture. METHODS This systematic review was performed using articles obtained through a search of the literature contained in the MeSH database, according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. RESULTS Search results revealed 1052 articles, 13 of which described 31 cases of AVM recurrence meeting the criteria for inclusion in this study. Detection of AVM occurred significantly earlier (mean ± SD, 3.56 ± 3.67 years) in patients with follow-up imaging than in those without (mean 8.86 ± 5.61 years; p = 0.0169). While 13.34% of patients who underwent follow-up imaging presented with rupture of a recurrent AVM, 57.14% of those without follow-up imaging presented with a ruptured recurrence (p = 0.0377). CONCLUSIONS Follow-up imaging has an integral role after AVM resection and is sometimes not performed for a sufficient period, leading to delayed detection of recurrence and an increased likelihood of a ruptured recurrent AVM.

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