Esthesioneuroblastoma in a young child. Case report

1997 ◽  
Vol 20 (1) ◽  
pp. 59-61 ◽  
Author(s):  
B�lent G�l ◽  
Sezer Kula�oglnu ◽  
Muammer Y�kse ◽  
Handan Dogan ◽  
Ali Ihsan �kten
Keyword(s):  
Case Report ◽  
Young Child

Efficacy of immediate physiotherapy after surgical release of zygomatico-coronoid ankylosis in a young child: A case report

2021 ◽  
pp. 1-7
Author(s):  
Krzysztof Dowgierd ◽  
Anna Lipowicz ◽  
Małgorzata Kulesa-Mrowiecka ◽  
Wojciech Wolański ◽  
Paweł Linek ◽  
...  
Keyword(s):  
Case Report ◽  
Young Child ◽  
Surgical Release

Bullous pemphigoid associated with ulcerative colitis in a young child: A case report

2020 ◽  
Vol 33 (6) ◽  
Author(s):  
Yang Wang ◽  
Yuanyuan Xiao ◽  
Yunzhu Li ◽  
Libing Fu ◽  
Feihong Yu ◽  
...  
Keyword(s):  
Ulcerative Colitis ◽  
Case Report ◽  
Young Child ◽  
Bullous Pemphigoid

Bullosis Diabeticorum in a Young Child: Case Report of a Very Rare Entity and a Literature Review

2017 ◽  
Vol 41 (2) ◽  
pp. 129-131 ◽  
Author(s):  
Anca Chiriac ◽  
Irina Costache ◽  
Cristian Podoleanu ◽  
Adrian Naznean ◽  
Simona Stolnicu
Keyword(s):  
Case Report ◽  
Young Child ◽  
Literature Review ◽  
Rare Entity ◽  
Bullosis Diabeticorum

scholarly journals Young child with painful edema and purpura: a case report

2021 ◽  
Vol 47 (1) ◽  
Author(s):  
Sarah Contorno ◽  
Giorgio Cozzi ◽  
Irene Berti ◽  
Egidio Barbi ◽  
Andrea Taddio
Keyword(s):  
Differential Diagnosis ◽  
Child Abuse ◽  
Case Report ◽  
Young Child ◽  
Sickle Cell ◽  
Benign Condition ◽  
Sickle Cell Crisis

Abstract Background We reported the case of a two-old-year boy with a painful acute hemorrhagic edema. This is a self-limited benign condition: usually, affected children are well appearing and this strongly support the diagnosis. In the opposite, in our case, we observed a painful presentation of the edema. Therefore, we demonstrated that rarely, this condition could have also a painful presentation. Conclusions This case report helps clinician to know that also acute hemorrhagic edema could have a painful presentation, so we must considered it in the differential diagnosis with sepsis, sickle cell crisis and child abuse. We believe that these findings will be of interest to pediatricians.

scholarly journals A Giant Cell Fibroma and Focal Fibrous Hyperplasia in a Young Child: A Case Report

2012 ◽  
Vol 2012 ◽  
pp. 1-5 ◽  
Author(s):  
Rodney J. Vergotine
Keyword(s):  
African American ◽  
Case Report ◽  
Young Child ◽  
Giant Cell ◽  
Clinical Impact ◽  
The Other ◽  
African American Female ◽  
Distinct Entity ◽  
Anterior Maxilla ◽  
Attached Gingiva

A case of two fibrotic lesions of the oral mucosa in a 17-month-old African-American female is reported. Both lesions occurred on the anterior maxilla, one lesion pedunculated on the buccal attached gingiva and the other lesion sessile on the palate. Histological examination characterized the buccal lesion as focal fibrous hyperplasia (FFH) and the palatal lesion as a giant cell fibroma (GCF). A case is made for continuing the consideration of GCF as a histologically distinct entity from FFH but that no difference in clinical impact between the two lesions exists.

scholarly journals A Young Child with Sickle Cell Beta Thalassemia: A Case Report and Review of Literatures

2013 ◽  
Vol 21 (2) ◽  
pp. 245-249
Author(s):  
Md. Abid Hossain Mollah ◽  
Ekhlasur Rahman ◽  
Saiful Islam ◽  
AKM Amirul Morshed ◽  
Farzana Rahman Munmun ◽  
...  
Keyword(s):  
Case Report ◽  
Young Child ◽  
Sickle Cell ◽  
Beta Thalassemia ◽  
Medical College

J Dhaka Medical College, Vol. 21, No. 2, October, 2012, Page 245-249 DOI: http://dx.doi.org/10.3329/jdmc.v21i2.15368

scholarly journals A Solitary Ventral Scapular Osteochondroma causing Pseudo-winging of Scapula: A Case Report

2021 ◽  
Vol 11 (7) ◽  
Author(s):  
Eknath Pawar ◽  
Nihar Modi ◽  
Amit Kumar Yadav ◽  
Jayesh Mhatre ◽  
Sachin Khemkar ◽  
...  
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Soft Tissue ◽  
Young Child ◽  
Chest Wall ◽  
Rare Case ◽  
Rare Presentation ◽  
Medial Border ◽  
Soft Tissue Masses ◽  
Scapular Region

Introduction: Winging of scapula is defined as a failure of dynamic stabilizing structures that anchor the scapula to the chest wall, leading to prominence of the medial border of scapula. It could be primary, secondary, or voluntary. Primary winging could be true winging due to neuromuscular causes or pseudo-winging due to osseous or soft-tissue masses. A scapular osteochondroma is a very rare presentation site and causes pseudo-winging leading to pushing away of the scapula away from the chest wall presenting as medial border prominence. Here, we are reporting a rare case of a scapular osteochondroma causing a pseudo-winging of the scapula. Case Report: A 2-year-old male child presented with painless, immobile, and non-fluctuant swelling over the left scapular region, insidious in onset and progressive in nature. On examination, a non-tender, immobile swelling was palpable with a painless and unrestricted range of motion at the shoulder joint. After evaluating radiographs and CT scan, the patient was diagnosed to have a ventral scapular osteochondroma leading to pseudo-winging of the scapula. Conclusion: Despite the rarity, a differential diagnosis of a scapular osteochondroma should be kept in mind while examining a young child presenting with a winged scapula. Keywords: Scapula, osteochondroma, pseudo-winging.

scholarly journals A CASE REPORT ON MULTISYSTEMIC INFLAMMATORY SYNDROME- CHILDREN HOW THE DIAGNOSIS AND TREATMENT COULD BE CHALLENGING

2021 ◽  
Vol 9 (11) ◽  
pp. 183-187
Author(s):  
S.U. Basnayake ◽  
◽  
T.G Dissanayakege ◽  
Keyword(s):  
Immune Response ◽  
Case Report ◽  
Young Child ◽  
Treatment Options ◽  
Severe Illness ◽  
Immunological Reaction ◽  
Case Definitions ◽  
Diagnosis And Management ◽  
Inflammatory Syndrome

Although COVID 19 infections in children are generally mild and non-fatal, there is increasing recognition of a multisystem inflammatory syndrome in children (MIS-C) associated with COVID-19, leading to severe illness and long-term sequelae. Even though there is some evidence that the MIS-C is a post-viral immunological reaction to COVID-19, understanding of the immune response induced by SARS-CoV-2 remains unclear.Various local and international guidelines are being widely practiced in the diagnosis and management of patients with MIS-C. A case report of a young child who was diagnosed and managed as MIS-C is discussed here. The diagnostic challenges with the available case definitions and currently accepted treatment options are elaborated herein.

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