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.

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 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.

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.

Isolated Tuberculosis of Patella in a Child: A Case Report and Literature Review

2017 ◽  
Vol 2 (2) ◽  
pp. 101-103
Author(s):  
Ganesh S Dharmshaktu ◽  
Pankaj Singh
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Rare Case ◽  
Case Reports ◽  
Age Group ◽  
Effective Management ◽  
Skeletal Tuberculosis ◽  
Pediatric Age Group ◽  
Antitubercular Treatment ◽  
High Index Of Suspicion

ABSTRACT The patella is an uncommon site for skeletal tuberculosis. Its incidence is limited to a few anecdotal case reports or series in the literature. The presence of this clinical entity in the pediatric age group is even rarer. A high index of suspicion and early clinicoradiological diagnosis are the mainstay of treatment coupled with compliant antitubercular treatment. The effective management also mitigates its spread to whole of the knee joint and subsequent arthrosis. A rare case of patella tuberculosis with effective management and good functional outcome in a 9-year-old male child is presented here with relevant details. How to cite this article Dharmshaktu GS, Singh P. Isolated Tuberculosis of Patella in a Child: A Case Report and Literature Review. Int J Adv Integ Med Sci 2017;2(2):101-103.

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

scholarly journals Inguinal Hernia with Incarcerated Loop of Sigmoid Colon and Impacted Hard Fecolith in an Infant: Rare Presentation

2021 ◽  
Vol 8 (4) ◽  
pp. 01-03
Author(s):  
Parveen Kumar ◽  
Nitin jain
Keyword(s):  
Case Report ◽  
Inguinal Hernia ◽  
Sigmoid Colon ◽  
Rare Case ◽  
Age Group ◽  
Pediatric Age ◽  
Rare Presentation ◽  
Incarcerated Inguinal Hernia ◽  
Pediatric Age Group ◽  
History Of

Incarcerated inguinal hernia is not an uncommon occurrence and the rate of incarceration in inguinal hernias has been variably reported between 3 and 16% with higher incidence among infants. Sigmoid colon as a content of hernia is itself an uncommon occurrence and associated impacted large and hard fecolith makes it a rare case in pediatric age group. Only single published case report could be found depicting these findings in young age group. Here we report 1-year-old child presented with 24 hours history of obstructed left-sided inguinal hernia. On exploration loop of sigmoid colon was identified with impacted fecolith.

Primary meningeal sarcoma (fibrosarcoma) of cervical spine in an 11 yr old boy: An extremely rare case report

2017 ◽  
Vol 31 (2) ◽  
pp. 203-206
Author(s):  
Kumar Pradeep ◽  
Verma Pawan Kumar ◽  
Das Srikant ◽  
Gupta Ashok
Keyword(s):  
Case Report ◽  
Cervical Spine ◽  
Rare Case ◽  
Malignant Potential ◽  
Age Group ◽  
Pediatric Age ◽  
Rare Tumor ◽  
Pediatric Age Group ◽  
Rare Case Report ◽  
Meningeal Sarcoma

Abstract Primary meningeal sarcoma is a rare tumor in pediatric age group. Here we were reporting an extremly rare case report of an 11 year old boy presented with quadriparesis and bladder involvement. MRI revealed a cervical dural based tumor with extension to cord parenchyma and neural foramina involving paravertebral tissue. The histopathology revealed mesenchymal tumor with malignant potential which on immunohistochemical (IHC) study found to be vimentin positive fibrosarcoma.

MALIGNANT RHABDOID TUMOR MIMICKING HEPATOBLASTOMA: A CASE REPORT AND LITERATURE REVIEW

2006 ◽  
Vol preprint (2007) ◽  
pp. 1
Author(s):  
Lars Wagner ◽  
Jennifer Garrett ◽  
Edgard Ballard ◽  
D. Hill ◽  
Arie Perry ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Rhabdoid Tumor ◽  
Malignant Rhabdoid Tumor
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