Common Presentation in an Uncommon Disease: Case Report of a Patient With Primary Diffuse Leptomeningeal Melanocytosis

2011 ◽  
Vol 29 (33) ◽  
pp. e816-e818 ◽  
Author(s):  
Arunee Dechaphunkul ◽  
Kanita Kayasut ◽  
Thakul Oearsakul ◽  
Kittidet Koonlaboon ◽  
Patrapim Sunpaweravong
1970 ◽  
Vol 3 (2) ◽  
pp. 188-190
Author(s):  
Charu Jain ◽  
VK Malik ◽  
Reny Kamboj ◽  
Sanjeev Kumar ◽  
Sandeep Kumar ◽  
...  

Background: Alport Syndrome is an uncommon disease. Case: We report a case of a young Indian male who presented with the characteristic ocular findings and systemic features of Alport Syndrome. Conclusion: Any young patient with a chronic renal disease should have a careful ophthalmologic examination for Alport Syndrome. Key words: Alport Syndrome, hereditary nephritis, lenticonus, deafness, retinopathy DOI: http://dx.doi.org/10.3126/nepjoph.v3i2.5275 Nepal J Ophthalmol 2011; 3(2): 188-190


2019 ◽  
Vol 84 (3) ◽  
pp. 97-100
Author(s):  
Barbara Igielska-Bela ◽  
◽  
Marek Krzemiński

2021 ◽  
Vol 2021 ◽  
pp. 1-4
Author(s):  
K. Shah ◽  
A. Ahmed ◽  
K. Kaveh ◽  
A. Frugoli ◽  
M. Hammoudi

In this case report, we describe an unusual pathogen F. nucleatum-induced empyema, followed by the development of Guillain–Barré syndrome (GBS). Although many pathogens have been associated with GBS, this may be one of the few in the literature to describe an association with F. nucleatum infection.


Author(s):  
Mitchell W. Couldwell ◽  
Samuel Cheshier ◽  
Philipp Taussky ◽  
Vance Mortimer ◽  
William T. Couldwell

Moyamoya is an uncommon disease that presents with stenoocclusion of the major vasculature at the base of the brain and associated collateral vessel formation. Many pediatric patients with moyamoya present with transient ischemic attacks or complete occlusions. The authors report the case of a 9-year-old girl who presented with posterior fossa hemorrhage and was treated with an emergency suboccipital craniotomy for evacuation. After emergency surgery, an angiogram was performed, and the patient was diagnosed with moyamoya disease. Six months later, the patient was treated for moyamoya using direct and indirect revascularization; after surgery there was excellent vascularization in both regions of the bypass and no further progression of moyamoya changes. This case illustrates a rare example of intracerebral hemorrhage associated with moyamoya changes in the posterior vascularization in a pediatric patient and subsequent use of direct and indirect revascularization to reduce the risk of future hemorrhage and moyamoya progression.


2004 ◽  
Vol 80 (5) ◽  
pp. 425-8 ◽  
Author(s):  
Carolina Prando-Andrade ◽  
Piedad Agudelo-Florez ◽  
Juan A. Lopez ◽  
Maria Aparecida de Souza Paiva ◽  
Beatriz T. Costa-Carvalho ◽  
...  

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