scholarly journals Myointimal Hyperplasia in a Patient with Neuromyelitis Optica (Devic’s Disease) after the Creation of an Arteriovenous Graft

2017 ◽  
Vol 9 (3) ◽  
pp. 252-255 ◽  
Author(s):  
Christina Rao ◽  
Stephanie Fox ◽  
Sapan S. Desai

Neuromyelitis optica, also known as Devic’s disease, is an autoimmune disorder that leads to the inflammation and demyelination of nerves. Devic’s disease primarily affects the optic nerve and spinal cord, but can lead to a significant loss of function throughout the body if not treated with steroid therapy or plasmapheresis. We recently saw a 62-year-old patient who received plasmapheresis for Devic’s disease through a PTFE arteriovenous graft in her left arm. Her graft clotted without warning, and percutaneous thrombolysis was not successful. A new vascular access was achieved with the use of an immediate-cannulation PTFE graft, and the patient received plasmapheresis immediately after her operation. However, the patient returned within 2 weeks with a thrombosed graft. Extensive myointimal fibrosis was noted within the brachial artery and axillary vein during a graft thrombectomy. Subsequent placement of a new arteriovenous fistula in her contralateral arm was eventually successful. Myointimal fibrosis may be a sequela of symptomatic antibody-positive Devic’s disease, and avoidance of synthetic materials may be indicated in this patient population to avoid exacerbation of an autoimmune response.

2009 ◽  
Vol 13 (1) ◽  
pp. 58
Author(s):  
SGP Kumuduni ◽  
Athula Dissanayaka

2008 ◽  
Vol 255 (5) ◽  
pp. 710-715 ◽  
Author(s):  
J. F. Rivera ◽  
J. F. Kurtzke ◽  
V. J. A. Booth ◽  
T. Corona

2007 ◽  
Vol 28 (4) ◽  
pp. 209-211 ◽  
Author(s):  
M. Capobianco ◽  
S. Malucchi ◽  
A. di Sapio ◽  
F. Gilli ◽  
A. Sala ◽  
...  

1994 ◽  
Vol 24 (2) ◽  
pp. 75-76 ◽  
Author(s):  
H A M Nazmul Ahasan ◽  
A K M Rafiqueuddin ◽  
M A Jalil Chowdhury ◽  
M A Azhar ◽  
Faisal Kabir

2021 ◽  
Vol 22 (16) ◽  
pp. 8946
Author(s):  
Karina Maciak ◽  
Sylwia Pietrasik ◽  
Angela Dziedzic ◽  
Justyna Redlicka ◽  
Joanna Saluk-Bijak ◽  
...  

Multiple sclerosis (MS) and Devic’s disease (NMO; neuromyelitis optica) are autoimmune, inflammatory diseases of the central nervous system (CNS), the etiology of which remains unclear. It is a serious limitation in the treatment of these diseases. The resemblance of the clinical pictures of these two conditions generates a partial possibility of introducing similar treatment, but on the other hand, a high risk of misdiagnosis. Therefore, a better understanding and comparative characterization of the immunopathogenic mechanisms of each of these diseases are essential to improve their discriminatory diagnosis and more effective treatment. In this review, special attention is given to Th17 cells and Th17-related cytokines in the context of their potential usefulness as discriminatory markers for MS and NMO. The discussed results emphasize the role of Th17 immune response in both MS and NMO pathogenesis, which, however, cannot be considered without taking into account the broader perspective of immune response mechanisms.


2007 ◽  
Vol 13 (3) ◽  
pp. 433-436 ◽  
Author(s):  
J.A. Cabrera-Gómez ◽  
J. Galarraga-Inza ◽  
R.M. Coro-Antich ◽  
Y. Real-González ◽  
M. Cristofol-Corominas ◽  
...  

Neuromyelitis optica (NMO) has been attributed to different underlying pathological events. The aim of this paper is to present the first case report of a patient with Down's syndrome (DS) who died of a fulminant NMO. A 29-year-old woman with DS developed acute transverse myelitis, with complete visual loss and swollen optic discs. Two days later, she developed quadriplegia, respiratory arrest and died. The anatomical study demonstrated typical findings of DS in the brain without demyelinating lesions. A severe destruction of medulla and cervical cord with a very high degree of demyelination of the optic nerves was typical of monophasic NMO (Devic's disease). Most of the cases of NMO in Cuba are of the relapsing form, but this case report is the first one with monophasic NMO and DS with a very aggressive course. The link of the pathogenetic relationship between DS and NMO remains unclear; it may well be coincidence but the fact that the patient died very shortly after the onset suggests, at least on clinical grounds, that the presence of DS could have accelerated the fatal evolution of NMO. Multiple Sclerosis 2007; 13: 433-436. http://msj.sagepub.com


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