A case report of delayed diagnosis and treatment of paediatric multiple sclerosis: A lesson from paediatric neurology

2019 ◽  
Vol 405 ◽  
pp. 334
Author(s):  
N. Waill Saadi ◽  
Q. Abed Fahad
2021 ◽  
Vol 8 (2) ◽  
Author(s):  
Fuentes S ◽  

Multiple sclerosis can often present with nonspecific symptoms leading to difficulty in establishing a diagnosis early in the disease process. Early diagnosis and treatment is of importance due to the associated decrease in disability for those that get treatment sooner. Here we present a case with a patient the presented with changes in vision and paresthesias. Her initial workup from the neurologist was negative and further workup was delayed until her symptoms worsened. After worsening symptoms, MRI revealed that multiple sclerosis was the cause of her symptoms.


2019 ◽  
Vol 27 ◽  
pp. 49-54
Author(s):  
Piotr Bogucki ◽  
Ewa Nagańska ◽  
Marta Jurek ◽  
Dorota Hoffman-Zacharska ◽  
Anna Kutkowska-Kaźmierczak ◽  
...  

2000 ◽  
Vol 71 (3) ◽  
pp. 327-329 ◽  
Author(s):  
Giovanni Zatti ◽  
Fabio D'Angelo ◽  
Alberto Giughello

2019 ◽  
Vol 61 (9) ◽  
pp. 1039-1049 ◽  
Author(s):  
Sophie Duignan ◽  
Wallace Brownlee ◽  
Evangeline Wassmer ◽  
Cheryl Hemingway ◽  
Ming Lim ◽  
...  

Author(s):  
William Mundo ◽  
Amber Berning ◽  
Yiannis Koullias ◽  
Daniel B Chastain ◽  
Neil Stone ◽  
...  

Abstract Cryptococcus species are ubiquitous in the environment with a global distribution. Whilst causing disease predominantly in immunocompromised hosts such as those with advanced HIV, HIV-uninfected patients are increasingly recognized to be affected. The most common forms of infection are cryptococcal pneumonia and meningitis. HIV-uninfected patients and extrapulmonary infections have worse outcomes, likely due to delayed diagnosis and treatment. Cryptococcus infections involving chylothorax or chyloabdomen have rarely been reported in humans. We describe a case of fulminant disseminated cryptococcosis with fungemia, peritonitis, and empyema in a patient with chronic chylothorax treated with an indwelling pleurovenous shunt. Key autopsy findings included cryptococcal organisms identified on calcified lymphadenopathy, pleural adhesions, and pericardium. We discuss the importance of identifying patients with non-traditional risks factors for cryptococcal disease, such as lymphopenia and hypogammaglobulinemia, and the potential implications of pleurovenous catheters in Cryptococcus dissemination.


Author(s):  
Masoud Ghiasian ◽  
Mohammad Faryadras ◽  
Maryam Mansour ◽  
Elham Khanlarzadeh ◽  
Shahir Mazaheri

2021 ◽  
Vol 14 ◽  
pp. 117954762110498
Author(s):  
Haya Mohammed Kheir ◽  
Mouhannad Dayoub ◽  
Nour Haidar ◽  
Hanin Mansour ◽  
Ammar Omran ◽  
...  

Intestinal diffuse ganglioneuromatosis is a rare, benign, neoplastic condition characterized by disseminated proliferation of neural elements. It has an established association with several systemic disorders including: multiple endocrine neoplasia IIB (MEN IIB) and von Recklinghausen’s disease. However, isolated GNs are very rare and sporadic. We report a case of a 6-year-old patient was referred to the emergency department due to a colon perforation during endoscopy. He then underwent sigmoidectomy and the pathologic studies revealed prominent signs of diffuse ganglioneuromatosis. Unfortunately, the patient died the day after because of the late diagnosis and treatment. Such presentation emphasizes the importance of considering diffuse ganglioneuromatosis, among other causes, in patients with intractable GI symptoms despite medical treatment.


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