This interesting paper from Germany & Hungary (Attila Torkos et al, Hearing Research Volume 235, Issues 1-2, January 2008, Pages 8-14) reported that inner ear spiral gangion cells (for molecular biology studies) obtained from manual dissection are less pure compared to specimen obtained via laser micro-dissection

Editor’s choice :  Need Inner ear cells..? Get Laser!

...?

Tumour stage, tumour volume & npc...?

This recent study from China (Ching-Chi Lee et al, Acta Oto-Laryngologica, Volume 128, Issue 1 2008 , pages 93 - 97) observed that primary tumor volume is a better prognostic indicator than tumor stage in individuals with nasopharyngeal carcinoma.

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 Box: otolaryngologyinafrica.net

January 18 2008

Vol 7, No 7

Otorhinolaryngology news

In this issue

· Inner ear cells & Laser…?

· Gene mutations for hearing conservation…?

· Tumour stage, volume, & NPC

· Cases of The Year

Text Box: Biodun Olusesi
 Newsletter Editor
View Page in French

Journal Watch: Purinergic signaling in the inner ear. J.H.Lee & D.C. Marcus, 2008

 

 1. Home page of otolaryngologyinafrica.net re-designed for accessibility

2.    A new forum for ENT patients and clinicians launched, For Details, click HERE

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4. Papers delivered at the 16th ORLSON Scientific Meeting held November 21—24, 2007 can be viewed  HERE

5. Forum topic : Chloramphenicol Ototoxicity. Read the preview HERE

6. Blog Topic: Gas Flaring and Otorhinolaryngology

 

 Till Next Week,

 Biodun

This study from USA (Rodney Z Dial et al. JARO - Journal of the Association for Research in Otolaryngology, Volume 8, Number 4 / December, 2007,422-434) reported that mutations involving na-K ATPase and NKCC1 results in hearing conservation with implications in future prevention of Presbycusis and NIHL

Genetic mutation for hearing conservation...?

ABSTRACT: The cochlear implant can restore speech perception in patients with sensorineural hearing loss. However, it is ineffective for those without an implantable cochlea or a functional auditory nerve. These patients can be implanted with the auditory brainstem implant (ABI), which stimulates the surface of the cochlear nucleus. Unfortunately, the ABI has achieved limited success in its main patient group [i.e., those with neurofibromatosis type 2 (NF2)] and requires a difficult surgical procedure. These limitations have motivated us to develop a new hearing prosthesis that stimulates the midbrain with a penetrating electrode array. We recently implanted three patients with the auditory midbrain implant (AMI), and it has proven to be safe with minimal movement over time. The AMI provides loudness, pitch, temporal, and directional cues, features that have shown to be important for speech perception and more complex sound processing. Thus far, all three patients obtain enhancements in lip reading capabilities and environmental awareness and some improvements in speech perception comparable with that of NF2 ABI patients. Considering that our midbrain target is more surgically exposable than the cochlear nucleus, this argues for the use of the AMI as an alternative to the ABI. Fortunately, we were able to stimulate different midbrain regions in our patients and investigate the functional organization of the human central auditory system. These findings provide some insight into how we may need to stimulate the midbrain to improve hearing performance with the AMI.

 

 

Abstract: 

Isolating cells from the cochlea to perform molecular biology assessment presents a challenge, because it is not possible to dissect pure cell pools by conventional methods. Thus, we set out to demonstrate that laser microdissection and pressure catapulting (LMPC) is superior to conventional manual cochlea dissection for this purpose. Spiral ganglions (SG) were isolated from neonatal rat cochleae by manual dissection and LMPC. Also, modioli were manually dissected. Total RNA was isolated from all three cell pools. In order to demonstrate contamination of the dissected cell pool, we determined the expression of type II iodothyronine deiodinase (D2), claudin 11 (Cld-11), neurofilament light chain (NF-L) and glyceraldehyde-3-phosphate dehydrogenase (GAPDH) transcripts by RT-PCR. The results showed that LMPC is not only a suitable method for selectively dissecting cochlear tissues, but in addition the molecular markers confirmed pure spiral ganglion cell pools without indication for any contamination by other cells. This indicates that LMPC is capable of providing a pure SG cell pool in contrast to conventional manual dissection. Therefore, LMPC presents a new technique for cochlear tissue separation improving the validity of molecular biological studies of the inner ear

 

© Copyright Dr 'Biodun Olusesi,  2005 - 2008

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Abstract:

Conclusions. Primary tumor volume (PTV) has a close relationship with survival rates of patients with nasopharyngeal carcinoma (NPC) who were treated with concurrent chemoradiotherapy (CCRT) or radiotherapy. Besides the current AJCC staging system, measurement of PTV may be needed to predict prognosis of NPC and adjust treatment strategy. Objectives. We conducted a retrospective study to elucidate the effect of PTV on treatment outcomes in patients with NPC who were treated with CCRT or radiotherapy. Patients and methods. A total of 66 patients with newly diagnosed NPC were enrolled in this study. Computed tomography (CT)-derived or magnetic resonance imaging (MRI)-derived PTV was calculated. The correlation between AJCC disease stage, PTV, and disease-specific survival was analyzed. Correlations between different prognostic factors were assessed using a Cox regression model. Results. The median PTV for the whole series was 12.01 ml (range 1.25-166.58 ml). The median PTV was 3.45 ml in T1 disease, 7.96 ml in T2 disease, 17.95 ml in T3 disease, and 64.73 ml in T4 disease. Disease stage and T stage carried no prognostic significance (p=0.25 and p=0.30, respectively). Four categories of PTV (<12.5 ml, 12.5-25 ml, 25-50 ml and >50 ml) had prognostic significance (p=0.02). Survival analysis demonstrated a significant difference in overall survival with larger tumor volume (risk ratio 5.447; p=0.044)

Text Box: Cases of The Year—Guess & Win

 

Go to Outstanding Cases of the year—Guess & Win

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