Sudden deafness in a patient with secondary syphilis

2009 ◽  
Vol 123 (11) ◽  
pp. 1262-1265 ◽  
Author(s):  
F W Ibrahim ◽  
M K Malu

AbstractObjectives:To emphasise the importance of considering a diagnosis of early acquired syphilis in all sexually active adults, and to review the ENT manifestations and treatment of acquired syphilis.Case report:A 24-year-old woman presented with sudden hearing loss, and subsequently developed clinical features suggestive of secondary syphilis. She was seen in the departments of ENT, dermatology, rheumatology and infectious diseases before a correct diagnosis was made. Treatment resulted in only partial recovery of hearing.Conclusions:With the exponential rise in syphilis cases in the UK, there has been a re-emergence of presenting manifestations that had previously become rare. Early syphilis should be considered in all sexually active adults who present with deafness, as prompt diagnosis and treatment are crucial for maximum recovery.

2012 ◽  
Vol 19 (4) ◽  
pp. 268-271
Author(s):  
Tuba Bayindir ◽  
Erkan Karatas ◽  
Zekeriya Cetinkaya

1997 ◽  
Vol 116 (4) ◽  
pp. 541-544 ◽  
Author(s):  
J SCHREIBSTEIN ◽  
C MACDONALD ◽  
L COX ◽  
L MCMAHON ◽  
D BLOOM

2014 ◽  
Vol 128 (11) ◽  
pp. 1015-1017 ◽  
Author(s):  
M Diao ◽  
F Tian ◽  
J Sun

AbstractBackground:Sudden sensorineural hearing loss rarely occurs in patients with chronic myeloid leukaemia.Case report:We present a case report of a patient who presented with sudden sensorineural hearing loss as the first manifestation of chronic myeloid leukaemia, and review the mechanisms responsible for sudden sensorineural hearing loss in leukaemic patients.Results:A 31-year-old female presented to our clinic with unilateral sudden sensorineural hearing loss and tinnitus. Pure tone audiometry revealed profound sensorineural hearing loss in the left ear at all frequencies. During an investigation into her hearing loss, the patient was found to have chronic myeloid leukaemia.Conclusion:Every case of sudden sensorineural hearing loss must be carefully evaluated, and haematological disorders must be considered in the differential diagnosis of sudden hearing loss.


2020 ◽  
Vol 10 (8) ◽  
pp. 561
Author(s):  
Jan Sroubek ◽  
Ladislava Janouskova ◽  
Jan Klener

Intradural spinal arteriovenous fistulas (sAVF) are spinal vascular lesions that usually manifest due to myelopathy or local symptoms caused by venous congestion and ischemia. In addition, perimedullary arteriovenous fistulas (PMAVF) in particular may rupture and cause subarachnoid or intramedullary hemorrhage along with relevant symptoms. Subarachnoid hemorrhage (SAH) can propagate into cranial space with clinically dominant symptoms and signs of typical aneurysmal intracranial SAH. The standard workup for cerebral SAH, after excluding an intracranial source of hemorrhage, is usually limited to a cervical spine MRI; therefore, thoracolumbar sources of hemorrhage can be missed, or their diagnosis may be delayed. Here we present a case of a pregnant patient who presented with cerebral SAH. The source of hemorrhage was not initially identified, leading to a presumptive diagnosis of benign pretruncal non-aneurysmal SAH. The correct diagnosis of spinal thoracolumbar PMAVF was revealed 2.5 months later due to the progression of local symptoms. While the diagnosis was being refined and endovascular treatment was being planned (but delayed due to pregnancy), there was a recurrence of intraconal hemorrhage followed by brainstem hemorrhage. This led to significant clinical deterioration. The PMAVF was then treated microsurgically and the patient experienced partial recovery.


1997 ◽  
Vol 830 (1 Immunologic D) ◽  
pp. 319-321 ◽  
Author(s):  
M. P. ORLANDO ◽  
S. MASIERI ◽  
M. A. PASCARELLA ◽  
A. CIOFALO ◽  
F. FILIACI

2013 ◽  
Vol 8 (2) ◽  
pp. 114-116
Author(s):  
Shuai Zhang ◽  
Zhang Guanping ◽  
Wei Fanqing ◽  
Liu Tianrun ◽  
Long Zhen ◽  
...  

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