scholarly journals Spontaneous Rupture of Hydatid Cyst of the Liver in Pediatric Age Group Four Rare Cases with Literature Review

2021 ◽  
Vol 43 (1) ◽  
pp. 35-41
Author(s):  
Professor Abdulrahman sulaiman
2006 ◽  
Vol 13 (4) ◽  
pp. 219-221 ◽  
Author(s):  
Jeff SW Wong ◽  
Calvin SH Ng ◽  
Tak Wai Lee ◽  
Anthony PC Yim

The present report describes a case of severe airway obstruction caused by endobronchial tuberculosis in an 11-year-old girl who was successfully treated by bronchoscopic balloon dilation. This case illustrates the insidious presentation and the increasingly important role of bronchoscopic intervention in the management of endobronchial tuberculosis. In addition, a brief literature review of the condition in the pediatric age group is included.


2016 ◽  
Vol 2016 ◽  
pp. 1-3 ◽  
Author(s):  
Xiao-Hui Ma ◽  
Hai-Chun Zhou ◽  
Can Lai ◽  
Kun Zhu ◽  
Xuan Jia

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.


2015 ◽  
Vol 2015 ◽  
pp. 1-4
Author(s):  
Isil Bulur ◽  
Hilal Kaya Erdoğan ◽  
Zeynep Nurhan Saracoglu ◽  
Deniz Arık

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.


Author(s):  
Amisha . ◽  
Paras Malik ◽  
Monika Pathania ◽  
Vyas Kumar Rathaur

Disorders of color variation can be localized or generalized, congenital or acquired, acute or chronic. Among the various causes of generalized skin darkening encountered in the pediatric age group, acquired universal melanosis aka Carbon Baby Syndrome is an uncommon hypermelanotic condition, with a histologic appearance of extensive epidermal melanization. The authors report one such case of a 4-year old boy with progressive darkening of skin starting at the age of 1 year and involving the entire body surface in the absence of any other systemic alterations. The disease prevalence, etiology, mechanism and prognosis are still unknown.


2017 ◽  
Vol 3 (1) ◽  
pp. 11-13
Author(s):  
Carrel Mavuta Zalula ◽  
◽  
Guylain Bilali ◽  
Alexis Mupepe Kumba ◽  
Olivier Mukuku ◽  
...  

2018 ◽  
Vol 15 (01) ◽  
pp. 041-042
Author(s):  
Vivek Agrawal ◽  
Pramod Giri

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.


2019 ◽  
Vol 9 ◽  
pp. 7
Author(s):  
Wing Ki Ng ◽  
Boon Ping Toe ◽  
Hin Yue Lau

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.


1997 ◽  
Vol 26 (4) ◽  
pp. 208-213 ◽  
Author(s):  
Çağatay Önal ◽  
Orhan Barlas ◽  
Metin Orakdöğen ◽  
Kemal Hepgül ◽  
Nail İzgi ◽  
...  

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