Syringosubarachnoid shunting in treatment of syringomyelia: a literature review and a clinical case report

2017 ◽  
Vol 81 (3) ◽  
pp. 58 ◽  
Author(s):  
V. S. Klimov ◽  
Yu. S. Gulay ◽  
A. V. Evsyukov ◽  
G. I. Moysak
2021 ◽  
Vol 1 (1) ◽  
pp. 15-21
Author(s):  
Rodrigo Cristhian Avelino Bezerra ◽  
Jonas Nogueira Ferreira Maciel Gusmão ◽  
Bruno Frota Amora Silva ◽  
Rodrigo Lemos Alves ◽  
Eliardo Silveira Santos ◽  
...  

The styloid process is a bone projection that originates in the tympanic portion of the temporal bone. The enlongation of the styloid process, or the ossification of the styloid process, can originate a series of symptoms such as dysphagia, odynophagia, facial pain, otalgia, headache, tinnitus and trismus, establishing the clinical picture of Eagle Syndrome. In this report, we present an important clinical case of adult patient diagnosed with Eagle’s Syndrome who underwent surgery for reduction of the enlongated styloid process, by intraoral approach, added to a literature review study.


2011 ◽  
Vol 126 (1) ◽  
pp. 76-78 ◽  
Author(s):  
G P Davies ◽  
I J M Johnson

AbstractObjective:To report the first case of treatment of Nager syndrome associated conductive hearing loss with bone-anchored hearing aids, in a three-year-old boy.Method:Clinical case report and current literature review regarding the use of bone-anchored hearing aids in the treatment of conductive hearing loss in children.Results:A three year eight month old boy with Nager syndrome was successfully treated for conductive hearing loss using bilateral bone-anchored hearing aids.Conclusion:This is the first case report of the use of bone-anchored hearing aids to treat Nager syndrome associated conductive hearing loss. Treatment was safe and successful in this case.


Author(s):  
S. V. Ivanova ◽  
S. A. Kuleva ◽  
E. A. Mikhailova ◽  
E. M. Senchurov ◽  
R. I. Khabarova ◽  
...  

The article presents a clinical case of simultaneous multiple primary tumors (the left adrenal neuroblastoma and the right lower parathyroid adenoma) in the child 11 years old.The literature describes several cases of primarily multiple tumors, one of which was neurogenic, requiring an individual approach to treatment. The relationship between the occurrence of polyneoplasia and genetic mutations is discussed. 


2014 ◽  
Author(s):  
S.C. TEIXEIRA ◽  
C.C. ARY ◽  
R.R. SILVA ◽  
G.C. FILHO ◽  
E.M.L. RIBEIRO

2014 ◽  
Author(s):  
S.C. TEIXEIRA ◽  
L.R. SOUZA ◽  
F.L.F. MOREIRA ◽  
G.C. FILHO ◽  
E.M.L. RIBEIRO

2021 ◽  
Vol 100 (3) ◽  
pp. 258-266
Author(s):  
D.T. Utalieva ◽  
◽  
S.B. Babakhanova ◽  
E.Yu. Ilyina ◽  
N.A. Andreeva ◽  
...  

In recent decades, there has been marked progress in understanding the biology of the most common extracranial solid tumor of childhood – neuroblastoma (NB), which led to a significant improvement in treatment outcomes due to stratification of patients into risk groups, intensification of treatment of patients with metastatic disease and the presence of unfavorable molecular genetic markers. Survivors who have received multimodal therapies, including chemotherapy, high-dose therapy and autologous peripheral stem-cell transplantation, 131I-metaiodobenzylguanidine (131I-MIBG) therapy, radiation therapy, and immunotherapy have a high risk of developing long-term side effects of treatment (LT SE). The study of the nature and frequency of LT SE after completion of therapy in patients with NB is important to ensure the quality of life and minimize severe health disorders. This article presents a literature review and description of a clinical case report of primary hypothyroidism in a high-risk patient with NB who received multicomponent treatment, including 131I-metaiodobenzylguanidine therapy due to the persistence of MIBG-positive foci after the induction chemotherapy.


2012 ◽  
Vol 6 (3) ◽  
pp. 296-301 ◽  
Author(s):  
Ilson Sepúlveda ◽  
Carolina Delgado ◽  
Paulo Flores ◽  
Ornella Salvatori

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