scholarly journals Orthodontic Extrusion of an Impacted Maxillary Incisor due to Compound Odontome in an 11-year-old Male Child: A Case Report

2021 ◽  
Vol 4 (3) ◽  
pp. 193-196
Author(s):  
Ashima Goyal ◽  
Gauba Krishan ◽  
Sanjeev K Singh ◽  
Mrinalini Rathore
Keyword(s):  
Case Report ◽  
Male Child ◽  
Maxillary Incisor ◽  
Orthodontic Extrusion

scholarly journals Blake's Pouch Cyst: A Case Report

2017 ◽  
Vol 06 (02) ◽  
pp. 122-125
Author(s):  
Saurabh Verma ◽  
M. Sridhar ◽  
S. Shashivadhanan ◽  
Manish Garg
Keyword(s):  
Genetic Counseling ◽  
Case Report ◽  
Literature Review ◽  
Posterior Fossa ◽  
Clinical Management ◽  
In Utero ◽  
Prenatal Ultrasound ◽  
Male Child ◽  
Imaging Studies ◽  
Initial Imaging

AbstractIt is a rare and underdiagnosed entity. The adagium “one only sees what one knows” is certainly true in cases of Blake's pouch cyst, as all types of posterior fossa cysts and cyst-like malformations may present nearly identical on initial imaging studies. Only one case of Blake's pouch cyst has been reported from this country, except for a case in utero, in which a diagnosis of Blake's pouch cyst was made on prenatal ultrasound and later confirmed by MRI. In this report we describe a case of Blake's pouch cyst in a 9-month-old male child along with the principles of diagnosis of Blake's pouch cyst, in combination with literature review. Differentiating Blake's pouch cyst from other posterior fossa cysts and cyst-like malformations and recognizing the accompanying hydrocephalus that are essentially noncommunicating have important implications not only on clinical management but also on genetic counseling, which is unnecessary in case of Blake's pouch cyst.

scholarly journals AVID triad: a case report

2020 ◽  
Vol 8 (5) ◽  
pp. 1918
Author(s):  
Manoj M. C. ◽  
Lokesh Kumar T.
Keyword(s):  
Case Report ◽  
Corpus Callosum ◽  
Fetal Mri ◽  
Male Child ◽  
Imaging Findings ◽  
Mri Imaging ◽  
History Of ◽  
Interhemispheric Cyst

Asymmetric ventriculomegaly, interhemispheric cyst and dysgenesis of the corpus callosum (AVID) constitutes a rare imaging triad. Additional findings include subcortical and subependymal heterotopia, polymicrogyria, fused thalami, deficient falx, and hydrocephalus. The knowledge of this triad helps us to diagnose prenatally by sonography and fetal MRI. In this case report authors present MRI Imaging findings in a case of AVID syndrome in a 6year old male child presenting with history of seizures and delayed milestones.

scholarly journals Bannayan-Riley-Ruvalcaba Syndrome, Rare Etiology of Intestinal Hamartomatouspolyposis: A case report

2019 ◽  
Vol 43 (1) ◽  
pp. 62-65
Author(s):  
Zannatul Ferdous Sonia ◽  
Md Rukunuzzaman ◽  
ASM Bazlul Karim ◽  
Afsana Yasmin ◽  
Shashi Bhushan Thakur
Keyword(s):  
Case Report ◽  
Child Health ◽  
Rectal Bleeding ◽  
Autosomal Dominant ◽  
Medical Literature ◽  
Congenital Disorder ◽  
Male Child ◽  
Colonoscopic Polypectomy

Bannayan-Riley-Ruvalcaba syndrome (BRRS) is a rare autosomal dominant congenital disorder, characterized bymacrocephaly, lipomas, hamartomas, and pigmented macule in genitalia.Several dozen cases have been reported in the medical literature, but no case has been reported in Bangladesh. We report a case of BRRS in a 11-year-old male child with recurrent per rectal bleeding with hamartomatouscolonic polyposis & multiple subcutaneous lipomas on the anterior abdominal wall.In addition, patient had macrocephaly, intellectual impairment.Bleeding polyps were removed by colonoscopic polypectomy. Bangladesh J Child Health 2019; VOL 43 (1) :62-65

scholarly journals TADs assisted Camouflage Orthodontic Treatment of Class II Division 1 Malocclusion in a Non Growing Patient: A case report

2018 ◽  
Vol 8 (2) ◽  
pp. 55-59
Author(s):  
Ankita Gupta ◽  
Trilok Shrivastava
Keyword(s):  
Case Report ◽  
Class Ii ◽  
Maxillary Incisor ◽  
Mandibular Incisor ◽  
Anterior Crowding ◽  
Skeletal Class ◽  
Curve Of Spee ◽  
Skeletal Class Ii ◽  
Division 1 ◽  
Class Ii Division 1

Class II, Division I malocclusion has been described as the most frequent treatment problem in orthodontic practice. Aim & objectives of the present case report was to evaluate the management of skeletal Class II division 1 malocclusion in non growing patient with extraction of upper first premolars. Clinical and cephalometric evaluation revealed skeletal Class II with Angles Class II division 1 malocclusion with mild mandibular anterior crowding and increased overjet, severe maxillary incisor proclination, mild mandibular crowding, exaggerated curve of spee, convex profile, incompetent lips, increased overjet and overbite. Maxillary first premolars were extracted followed by en-masse retraction of anteriors with the help of temporary anchorage devices (TADs) to avoid anchorage loss. Mandibular incisor was extracted to correct curve of spee. Following treatment marked improvement in patient’s smile, facial profile and lip competence were achieved and there was a remarkable increase in the patient’s confidence and quality of life.

scholarly journals Cytodiagnosis of Rosai–Dorfman disease masquerading as lymphoma: A case report with brief review of literature

2018 ◽  
Vol 10 (04) ◽  
pp. 460-463
Author(s):  
Manjari Kishore ◽  
Prajwala Gupta ◽  
Arvind Ahuja ◽  
Minakshi Bhardwaj
Keyword(s):  
Case Report ◽  
Sinus Histiocytosis ◽  
Male Child ◽  
Differential Diagnoses ◽  
Review Of Literature ◽  
Massive Lymphadenopathy ◽  
Rosai Dorfman Disease ◽  
Cytological Features

ABSTRACTRosai–Dorfman disease (RDD) or sinus histiocytosis with massive lymphadenopathy (SHML) is a self-limiting, benign histiocytic disorder. We report a case of RDD mimicking lymphoma clinically and cytologically in a 3-year-old male child. The present case highlights the importance of cytology in the diagnosis of RDD along with cytological features of other differential diagnoses.

scholarly journals Living foreign body: Leech inside the nasal cavity causing epistaxis

2017 ◽  
Vol 13 (2) ◽  
pp. 178-179
Author(s):  
Sriti Manandhar ◽  
S Chettri ◽  
S Shah ◽  
BP Sah ◽  
S Shilpakar ◽  
...  
Keyword(s):  
Case Report ◽  
Foreign Body ◽  
Nasal Cavity ◽  
Neck Surgery ◽  
Male Child ◽  
Left Nostril

This is a case report of a three years old male child presented in the Otolaryngology and Head & Neck Surgery with chief complain of bleeding from the left nostril since seven days with nasal itching which was later diagnosed to be living foreign body leech causing epistaxis.Health Renaissance 2015;13(2): 178-179

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