TY - JOUR
T1 - Rate of spiral ganglion cell loss in idiopathic sudden sensorineural hearing loss
AU - Ungar, Omer J.
AU - Handzel, Ophir
AU - Santos, Felipe
N1 - Publisher Copyright:
© 2018, Otology & Neurotology, Inc.
PY - 2018
Y1 - 2018
N2 - Objective: To calculate the spiral ganglion neural decay rate among patients diagnosed with idiopathic sudden sensorineural hearing loss (ISSNHL). Study Design: Retrospective. Setting: Temporal bone histopathology bank. Patients: Subjects diagnosed during life with unrecovered unilateral ISSNHL. Intervention(s): Spiral ganglion cell count in the bilateral reconstructed Rosenthal canal. Main Outcome Measure(s): Decay rate of spiral ganglion cells. Results: Nine patients were enrolled. The average age of ISSNHL diagnosis and death was 52 and 63 years, respectively. The total and segmental SGCC decay shows a temporal dependency. The time lag between the ISSNHL event and death was linearly proportional to the SGCC decay. Subjects who died less than 5 years from diagnosis of ISSNHL had no more than 13% loss of their total SGCC, and no more than 14% of SGCC per Rosenthal canal segment. When a longer period passed from ISSNHL diagnosis to death (19–20 yr), a loss of 16% and 13 to 18% of total and segmental SGCC occurred, respectively. Conclusions: SGCC decline from ISSNHL diagnosis through life.
AB - Objective: To calculate the spiral ganglion neural decay rate among patients diagnosed with idiopathic sudden sensorineural hearing loss (ISSNHL). Study Design: Retrospective. Setting: Temporal bone histopathology bank. Patients: Subjects diagnosed during life with unrecovered unilateral ISSNHL. Intervention(s): Spiral ganglion cell count in the bilateral reconstructed Rosenthal canal. Main Outcome Measure(s): Decay rate of spiral ganglion cells. Results: Nine patients were enrolled. The average age of ISSNHL diagnosis and death was 52 and 63 years, respectively. The total and segmental SGCC decay shows a temporal dependency. The time lag between the ISSNHL event and death was linearly proportional to the SGCC decay. Subjects who died less than 5 years from diagnosis of ISSNHL had no more than 13% loss of their total SGCC, and no more than 14% of SGCC per Rosenthal canal segment. When a longer period passed from ISSNHL diagnosis to death (19–20 yr), a loss of 16% and 13 to 18% of total and segmental SGCC occurred, respectively. Conclusions: SGCC decline from ISSNHL diagnosis through life.
KW - Cochlear histopathology
KW - Cochlear nerve cell count
KW - Spiral ganglion cells count
KW - Sudden hearing loss
UR - http://www.scopus.com/inward/record.url?scp=85056590000&partnerID=8YFLogxK
U2 - 10.1097/MAO.0000000000001992
DO - 10.1097/MAO.0000000000001992
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C2 - 30303937
AN - SCOPUS:85056590000
SN - 1531-7129
VL - 39
SP - e944-e949
JO - Otology and Neurotology
JF - Otology and Neurotology
IS - 10
ER -