Hypersomnia in Whipple disease: case report
نویسندگان
چکیده
منابع مشابه
Renal amyloidosis in Whipple disease: a case report
INTRODUCTION Whipple disease is a rare systemic infection caused by Tropheryma whippelii that usually manifests with joint pain, weight loss, diarrhoea and abdominal pain. However, in some cases the infection may involve other organs and tissues. CASE PRESENTATION We report on a 44-year-old man with Whipple disease which led to renal amyloidosis and end-stage renal failure. In this case, the ...
متن کاملBilateral panuveitis associated with Whipple disease – case report
PURPOSE To describe a clinical case and literature review of Whipple disease. METHODS A 65-year-old male with bilateral decreased visual acuity for 3 weeks as well as bilateral hypoacusia, vertigo, disequilibrium, headache and decreased strength in the right upper limb for 4 months. The clinical work-up revealed a bilateral panuveitis and an ischemic cerebellar stroke. RESULT The diagnosis ...
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SUMMARY: Kawasaki is an acute multisystemic disease affecting Predominantly. Children below 4 years of age. Having a Self- limited Course, it often Presents as Vasculitis. The Principal Complications are Stomatitis, conjunctivitis. Lymphadenopathy, Skin rashes as well as involvment of cardiovascular, alimentary and nervous system. In this article we report the First case of Kawasaki Disease ...
متن کاملPrimary Whipple disease of the brain: case report with long-term clinical and MRI follow-up
Whipple disease (WD) is a rare systemic disorder caused by the bacteria Tropheryma whipplei. In its classic form, it manifests with gastrointestinal problems including diarrhea, abdominal pain, and weight loss. However, various other systems can be affected, including the central nervous system (CNS). Even more rarely, the CNS is primarily affected without gastrointestinal symptoms and with a n...
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Introduction: Castleman's disease is a rare lymphoproliferative disorder which may be confused with other causes of lymphadenopathy. Case Report: Here we report a case of unicentric Castleman's disease presenting with cervical lymphadenopathy. The patient was treated with complete surgical excision of lesion and was disease free at the time of reporting this article. This case has been reported...
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ژورنال
عنوان ژورنال: Arquivos de Neuro-Psiquiatria
سال: 2006
ISSN: 0004-282X
DOI: 10.1590/s0004-282x2006000500030