scholarly journals Pediatric Isolated Sinonasal Schwannoma: A New Case Report and Literature Review

2016 ◽  
Vol 2016 ◽  
pp. 1-3 ◽  
Author(s):  
Xiao-Hui Ma ◽  
Hai-Chun Zhou ◽  
Can Lai ◽  
Kun Zhu ◽  
Xuan Jia
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Nasal Cavity ◽  
Maxillary Sinus ◽  
Paranasal Sinuses ◽  
Pediatric Patients ◽  
Age Group ◽  
Pediatric Age ◽  
Pediatric Age Group ◽  
Group A

Schwannomas of the paranasal sinus are uncommon. Less than 4% of schwannomas involve the nasal cavity and paranasal sinuses, even less in the pediatric age group. A case of schwannoma arising in maxillary sinus in a 2.5-year-old Chinese boy is reported. The basis for discussion of this case is the exceptional rarity of sinonasal schwannoma in pediatric patients.

Atypical Osteoid Osteoma of sacral region in pediatric age group: a case report

2017 ◽  
pp. 28-31
Author(s):  
Shashi Sharma ◽  
Sakshi Dewan ◽  
Naveen Bhardwaj ◽  
Mir Aziz ◽  
Shilpa Singh ◽  
...  
Keyword(s):  
Case Report ◽  
Osteoid Osteoma ◽  
Age Group ◽  
Pediatric Age ◽  
Sacral Region ◽  
Pediatric Age Group ◽  
Group A

scholarly journals Methotrexate Treatment in Children with Febrile Ulceronecrotic Mucha-Habermann Disease: Case Report and Literature Review

2015 ◽  
Vol 2015 ◽  
pp. 1-4
Author(s):  
Isil Bulur ◽  
Hilal Kaya Erdoğan ◽  
Zeynep Nurhan Saracoglu ◽  
Deniz Arık
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Relevant Literature ◽  
High Fever ◽  
Age Group ◽  
Pediatric Age ◽  
Pityriasis Lichenoides ◽  
Pediatric Age Group ◽  
Disease Case ◽  
Methotrexate Treatment

Febrile Ulceronecrotic Mucha-Habermann disease is a rare and potentially fatal variant of pityriasis lichenoides et varioliformis acuta and is characterized by high fever, constitutional symptoms, and acute oncet of ulceronecrotic lesions. We present an 11-year-old male with Febrile Ulceronecrotic Mucha-Habermann disease who was cured with methotrexate and review the use of methotrexate for this disorder in the pediatric age group with the relevant literature.

scholarly journals Urinary lithiasis in the pediatric age group: Case report and literature review

2017 ◽  
Vol 3 (1) ◽  
pp. 11-13
Author(s):  
Carrel Mavuta Zalula ◽  
◽  
Guylain Bilali ◽  
Alexis Mupepe Kumba ◽  
Olivier Mukuku ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Age Group ◽  
Pediatric Age ◽  
Group Case ◽  
Pediatric Age Group ◽  
Urinary Lithiasis

Dual Chronic Ossified Epidural Hematomas Presented with Seizures 23 Years after Head Injury in an Adult Male: Case Report and Literature Review

2018 ◽  
Vol 15 (01) ◽  
pp. 041-042
Author(s):  
Vivek Agrawal ◽  
Pramod Giri
Keyword(s):  
Case Report ◽  
Head Injury ◽  
Literature Review ◽  
Rare Case ◽  
Age Group ◽  
Pediatric Age ◽  
Rare Entity ◽  
Presenting Symptoms ◽  
Pediatric Age Group

AbstractThe authors report a rare case of dual chronic ossified epidural hematomas (EDHs) in a 35-year-old man with complaint of seizures after 23 years of head injury. Ossified EDH is a rare entity, and it commonly presents in pediatric age group. Presenting symptoms include headache and very rarely seizures. Asymptomatic cases may produce symptoms after decades; hence, regular follow-up is required. Treatment includes craniotomy or conservative management.

scholarly journals Malignant Rhabdoid Tumor of the Mediastinum: A Case Report and Literature Review

2019 ◽  
Vol 9 ◽  
pp. 7
Author(s):  
Wing Ki Ng ◽  
Boon Ping Toe ◽  
Hin Yue Lau
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Rare Case ◽  
Rhabdoid Tumor ◽  
Malignant Rhabdoid Tumor ◽  
Imaging Features ◽  
Age Group ◽  
Pediatric Age ◽  
Pediatric Age Group ◽  
Aggressive Tumor

Malignant rhabdoid tumor (MRT) of the mediastinum is an aggressive tumor that is extremely rare. To date, only 24 cases of the mediastinal MRT have been reported in adults and 9 cases in the pediatric age group under the age of 18 years. We report a rare case of such tumor and review the literature on its clinical and imaging features as well as its treatment and prognostic outcomes.

Sign in / Sign up

Export Citation Format

Share Document