Delayed diagnosis of multiple sclerosis in a patient with schizoaffective disorder: a case of ‘diagnostic overshadowing’

2014 ◽  
Vol 49 (2) ◽  
pp. 186-187 ◽  
Author(s):  
Brad Hayhow ◽  
Frank Gaillard ◽  
Dennis Velakoulis ◽  
Mark Walterfang
CNS Spectrums ◽  
2011 ◽  
Vol 16 (4) ◽  
pp. 95-98
Author(s):  
Afroz Shamim ◽  
Cathy L. Budman

AbstractMultiple sclerosis (MS) and Neuro-Behçet's disease (NBD) have been associated with a range of neuropsychiatric symptoms, including fatigue, cognitive impairment, depression, bipolar disorder, anxiety, sexual dysfunction, and other behavioral disturbances that are characterized by remissions and exacerbations at different points during the course of the disease. We present an interesting case of NBD in a 48-year-old female who had previously been diagnosed with MS. Exploration of this patient's various neuropsychiatric symptoms, their misattribution first to psychopathology and then subsequently to a variety of neurological problems exemplifies the potential pitfalls in diagnosis of a seemingly rare disorder. The role of psychosocial stress-related inflammatory changes in the patient's behavioral and neurological symptoms is explored as well as the potential psychological and medical effects of delayed diagnosis and treatment.


QJM ◽  
2020 ◽  
Vol 113 (Supplement_1) ◽  
Author(s):  
A A Tohamy ◽  
M S Swelam ◽  
D M Abdelgawad ◽  
H A Aref

Abstract © 2018 Institute of Psychiatry, Ain Shams University Copyright r 2018 Institute of Psychiatry, Ain Shams University. Unauthorized reproduction of this article is prohibited. Background MS is an inflammatory and neurodegenerative disease. Early inflammatory activity might have a profound impact on the risk of developing early disability, and might be a risk factor for early transition into the progressive phase of the illness. However, there are a number of barriers implementing early MS diagnosis and treatment as the patients may delay consulting a physician about their neurological symptoms or may be reluctant to start DMT. Objective The aim of this study is to highlight the causes of delayed diagnosis of multiple sclerosis in Egypt to shorten the time of diagnosis and improve the prognosis for patients with MS. Patients and Methods Retrospective descriptive study .500 Patients coming to multiple sclerosis unit at Ain Shams University hospitals with delayed diagnosis of MS for more than 2 years had been screened. A questionnaire could be applied on 320 patients out of 500. Contacting (direct and via phone calls) the patients for evaluating the causes of delayed diagnosis of MS was done. Results In this study we found number of significant factors adversely affected a timely diagnosis including the age at onset finding that those younger at onset of MS (vs. older) experienced diagnostic delays (P-value = 0.005) and denial of symptoms which was a leading cause for delayed time to first doctor consultation and delayed diagnosis of MS (P-value =0.009). Also there was a correlation between types of MS and delayed diagnosis as we found that PPMS versus RRMS had delayed diagnosis for more than 2 years. Meanwhile, sensory symptoms at onset of the disease were associated with longer diagnostic delay. Although the first specialties the patients visit were ophthalmology and orthopedic services, that the most common Source of referral to a neurologist was suggestion by family and media. Conclusion multiple causes significantly affect time to diagnosis of MS including age at onset of the disease, denial of symptoms sensorial symptoms at the disease onset and referral delay from other specialties.


2020 ◽  
pp. 1-7
Author(s):  
Simón Cárdenas-Robledo ◽  
Lorena Lopez-Reyes ◽  
Laura Estefanía Arenas-Vargas ◽  
Michael Steven Carvajal-Parra ◽  
Claudia Guío-Sánchez

Neurology ◽  
2018 ◽  
Vol 90 (16) ◽  
pp. e1435-e1441 ◽  
Author(s):  
Dalia L. Rotstein ◽  
Hong Chen ◽  
Andrew S. Wilton ◽  
Jeffrey C. Kwong ◽  
Ruth Ann Marrie ◽  
...  

ObjectiveWe sought to better understand the reasons for increasing prevalence of multiple sclerosis (MS) by studying prevalence in relation to incidence, mortality rates, sex ratio, and geographic distribution of cases.MethodsWe identified MS cases from 1996 to 2013 in Ontario, Canada, by applying a validated algorithm to health administrative data. We calculated age- and sex-standardized prevalence and incidence rates for the province and by census division. Incidence and prevalence sex ratios for women to men were computed.ResultsThe prevalence of MS increased by 69% from 1.57 (95% confidence interval [CI]: 1.54–1.59) per 1,000 in 1996 (n = 12,155) to 2.65 (95% CI: 2.62–2.68) in 2013 (n = 28,192). Incidence remained relatively stable except for a spike in 2010, followed by a subsequent decline in 2011–2013, particularly among young people and men. Mortality decreased by 33% from 26.7 (95% CI: 23.5–30.3) per 1,000 to 18.0 (95% CI: 16.4–19.8) per 1,000. The incidence sex ratio was stable from 1996 to 2009, then declined in 2010, with partial rebound by 2013. MS prevalence and incidence showed no consistent association with latitude.ConclusionIn this large, population-based MS cohort, we found stable incidence and increasing prevalence of MS; the latter largely reflected declining mortality. A spike in incidence in 2010 among younger patients and men at a time of widespread media coverage of MS suggests that these groups may be vulnerable to delayed diagnosis. We did not find a latitudinal gradient; however, most Ontarians live between the 42nd and 46th parallels, reducing our ability to detect an effect of latitude.


2021 ◽  
pp. 1-2
Author(s):  
Torri Clerici Valentina ◽  
◽  
Bianchi-Marzoli Stefania ◽  

Susac Syndrome (SuS) is a rare disease, characterized by an autoimmune endothelopathy, that involves brain, retina and inner ear. We describe a case of a young woman affected by inner ear-predominant SuS, initially suspected for demyelinating disease, with delayed diagnosis and irreversible hearing ischemic damage, but good prognosis, treated according to current recommendations


2016 ◽  
Vol 24 (4) ◽  
pp. 480-494 ◽  
Author(s):  
Luke A Squires ◽  
Nefyn Williams ◽  
Val L Morrison

To explore experiences and perceptions of assistive technology, 14 people with multiple sclerosis, 5 carers and 4 occupational therapists participated in focus groups. Transcripts were analysed thematically drawing from illness self-regulation theory. Identified themes are as follows: critical multiple sclerosis events (developing symptoms/disability, delayed diagnosis and coping, public reaction and multiple sclerosis progression to assistive technology), matching assistive technology for continued use (acceptance of multiple sclerosis and assistive technology, realistic expectations, occupational therapist responsiveness, timing is crucial and carers and others) and impact of assistive technology (promoting or losing independence, stigma and embarrassment and redefining the carer). Acceptance and communication among those involved ensures assistive technology matches needs and maximises health and psychosocial outcomes.


2013 ◽  
Vol 8 (3) ◽  
pp. 199-200 ◽  
Author(s):  
Unax Lertxundi ◽  
Rafael Palacios ◽  
Fernando Gutierrez ◽  
Saioa Domingo-Echaburu ◽  
Monserrat Garcia ◽  
...  

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