polyneuropathies/треска

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Dengue hemorrhagic fever complicated with acute idiopathic scrotal edema and polyneuropathy.

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We report a case of an adult with dengue hemorrhagic fever who developed acute idiopathic scrotal edema and glove-and-stocking polyneuropathy. A 54-year-old man who had fever, chills, bone pain, and skin rash for 4 days was admitted. We diagnosed dengue hemorrhagic fever because of fever, gum

Subdural haematoma and axonal polyneuropathy complicating dengue fever.

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The authors report a case of dengue fever presenting with aseptic meningoencephalitis and developing subdural haematoma and pure motor quadriparesis due to axonal polyneuropathy. This 27-year-old female patient presented to us during the latter part of the dengue epidemic in India in 2010. She had

Ankylosing spondylitis. An unusual manifestation of familial Mediterranean fever. Report of a case complicated by amyloidosis and polyneuropathy.

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We report a case of familial Mediterranean fever (FMF) with typical clinical and roentgenological findings of ankylosing spondylitis. The spinal involvement in FMF is discussed. A second unusual feature of this case is the occurrence of polyneuropathy which could possibly be ascribed to the slowly

Q fever as a cause of pure sensory polyneuropathy -- the six-year itch: a follow-up of an indigenous Swedish case.

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Q fever is common worldwide but extremely rare as a cause of clinical disease in Sweden. Complications such as meningitis and Guillain-Barré syndrome are not uncommon. Chronic polyneuropathy caused by Q fever has until now never been reported in the English-speaking medical community. The first

[Polyneuropathy and Q fever].

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[Anatomo-clinical conference. Pitié-Salpêtrière Hospital. Case No. 3-1991. Prolonged fever, polyneuropathy and diabetes in a 50-year-old man].

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Guillain-Barré polyneuropathy associated with mediterranean spotted fever: case report.

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[Chest pain, fever, persistent pulmonary nodules and polyneuropathy in a 55-year-old man (clinico-pathologic conference)].

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[Clinicopathological conference. XVI. Polyneuropathy, elevated ESR and fever].

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[Familial Mediterranean fever and familial amyloidotic polyneuropathy].

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[Hereditary diseases accompanied with aberrant catecholamine metabolism, in special reference to catecholamine sensitive periodic fever and familial amyloid polyneuropathy (author's transl)].

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Eosinophilic Granulomatosis with Polyangiitis Presented as Acute Polyneuropathy and Cerebral Vasculitis.

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Eosinophilic granulomatosis with polyangiitis (EGPA) is an immune related systemic disease that is caused by vasculitis affecting multiple organ systems. It is characterized by asthma, fever, eosinophilia, cardiac problems, renal injury, and peripheral neuropathy. In this report, we describe a

Antineutrophil cytoplasmic autoantibody-negative antiproteinase 3 syndrome presenting as vasculitis, endocarditis, polyneuropathy and Dupuytren's contracture.

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Antiproteinase 3 antibodies (antiPR3) are assumed to be subtypes of antineutrophil cytoplasmic autoantibodies (ANCA), with a high specificity for active Wegener's granulomatosis and microscopic polyangiitis. Thus, antiPR3 positivity in ELISA, together with negativity in indirect immunofluorescence

A rare case of critical illness polyneuropathy and literature review.

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A 40- year-old Male was admitted to the first hospital of Jilin University with the complaint of 4 days of fever and headache and aggravation of weakness in his lower extremities accompanied with dysuria and disturbance of consciousness for one day. He had tachycardia, tachypnea and elevated white

POEMS (polyneuropathy, organomegaly, endocrinopathy, M protein, skin lesions) syndrome: a South America's report.

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The POEMS syndrome, also known as Crow-Fukase syndrome, is an unusual systemic disorder described mainly in Asian individuals. It is characterized by the presence of (P)polyneuropathy, (O)organomegaly, (E)endocrinopathy, (M) M-protein, and (S) skin changes. Several other associated conditions such

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