MEDIASTINAL MALIGNANT TRITON TUMOR: RARE CASE SERIES

CHEST Journal ◽  
2019 ◽  
Vol 155 (6) ◽  
pp. A334
Author(s):  
I. Chaudhry ◽  
N. Alayyaf
Keyword(s):  
Rare Case ◽  
Case Series ◽  
Malignant Triton Tumor

scholarly journals Mediastinal malignant triton tumor: A rare case series and review of literature

2019 ◽  
Vol 62 ◽  
pp. 115-119
Author(s):  
Ikram Chaudhry ◽  
Thabet Algazal ◽  
Ahsan Cheema ◽  
Aman Al Faraj ◽  
Noor Al Malki ◽  
...  
Keyword(s):  
Rare Case ◽  
Case Series ◽  
Review Of Literature ◽  
Malignant Triton Tumor

scholarly journals Overgrowth syndrome in neonates: a rare case series with a review of the literature

2019 ◽  
Vol 12 (1) ◽  
pp. e225640
Author(s):  
Aakash Pandita ◽  
Astha Panghal ◽  
Girish Gupta ◽  
Kirti M Naranje
Keyword(s):  
Lower Limb ◽  
Rare Case ◽  
Case Series ◽  
Port Wine Stain ◽  
Port Wine ◽  
Review Of The Literature ◽  
Term Neonates ◽  
Overgrowth Syndrome ◽  
Klippel Trenaunay Syndrome

We present here two-term neonates presenting with right lower limb hypertrophy, a port-wine stain, acral abnormalities and clubfeet. These neonates had overlapping features of Klippel Trenaunay syndrome and congenital lipomatous overgrowth, vascular malformation, epidermal nevi and scoliosis/skeletal abnormalities. Such overgrowth syndrome has not been previously described in the literature. Both the neonates are doing well and are under regular follow-up.

scholarly journals A rare case of recurrent malignant triton tumor in a male with NF1: Case report and mini-review

2016 ◽  
Vol 21 ◽  
pp. 121-124 ◽  
Author(s):  
B. Aykut ◽  
K. Wieczorek ◽  
P. Schirmacher ◽  
M.W. Büchler ◽  
K. Hoffmann
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Malignant Triton Tumor

scholarly journals Distraction Osteogenesis for Micrognathia in Cipto Mangunkusumo Hospital : A Case Series

1970 ◽  
Vol 2 (1) ◽  
Author(s):  
Grace Boaz ◽  
Prasetyanugraheni Kreshanti ◽  
Siti Handayani ◽  
Kristaninta Bangun
Keyword(s):  
Distraction Osteogenesis ◽  
Rare Case ◽  
Young Patients ◽  
Case Series ◽  
Genetic Syndromes ◽  
Mandibular Hypoplasia ◽  
Distraction Device ◽  
Mandibular Body ◽  
Inferior Border ◽  
Gradual Distraction

Background: Micrognathia is usually associated with genetic syndromes, characterized by mandibular hypoplasia causing a receding chin. The overall incidence of micrognathia was 1 per 1600 births, makes it a rare case. Severe micrognathia can be a neonatal emergency due to airway obstruction by the tongue in the small oral cavity. One method for correcting micrognathia is distraction osteogenesis. Lack of experience due to rare incidence of case, expensive cost of distraction device and technical complexity of the operation can be obstacles to this management. Patient and Method: We report two cases of micrognathia corrected with distraction osteogenesis conducted in Cipto Mangunkusumo Hospital from 2011-2012. The method consists of implantation of bilateral distraction device to the inferior border of the mandibular body. The patients then followed postoperatively. Result: Mandibular lengthening by gradual distraction is a proper method for young patients with micrognathia. Despite our minimal experience and intricate kind of method, we are trying to improve our skill in the future. Summary: Distraction osteogenesis is one method for correcting congenital mandibular hypoplasia. 

scholarly journals A Rare Case Series: Impacted Distomolars

2019 ◽  
Vol 7 (23) ◽  
pp. 4078-4081
Author(s):  
Fareedi Mukram Ali ◽  
Waseem Hassan Aridhi ◽  
Abdulmohsen Moussa Hommadi ◽  
Rawan Ali Altharawi ◽  
Muzaffer Ali Khan
Keyword(s):  
Rare Case ◽  
Case Reports ◽  
Case Series ◽  
Dental Arch ◽  
Supernumerary Teeth ◽  
Maxillary Region

BACKGROUND: The occurrence of multiple supernumerary teeth in individuals without any associated syndrome is rare. Supernumerary teeth may occur in any region of the dental arch and are frequently observed in the maxillary region. But the occurrence of distomolars is rare, particularly mandibular distomolars are extremely rare. CASES PRESENTATION: In this paper, we present a series of case reports of maxillary and mandibular distomolars. CONCLUSION: The occurrence of distomolars is rare, but when detected patients should be kept under observation.

scholarly journals Imatinib mesylate induced erythroderma: A rare case series

2015 ◽  
Vol 11 (4) ◽  
pp. 993 ◽  
Author(s):  
Sandeep Kaur ◽  
Sumir Kumar ◽  
BharatBhushan Mahajan ◽  
RajaParamjeet Singh Banipal ◽  
Amarbir Singh
Keyword(s):  
Imatinib Mesylate ◽  
Rare Case ◽  
Case Series
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