Systemic vasculitis in a child mimicking mercury poisoning

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Systemic vasculitis in a child mimicking mercury poisoning

Results A 12 year-old girl was admitted to our hospital with complaints of weakness, weight loss (10 kg in the last month), excessive sweating, and abdominal and joint pains. Her complaints started 6 weeks prior to admittance when she began to suffer from intermittent fever, acrodynia and back and abdominal pain. Also she was found to have red painful hands, a blood pressure 170/120 mm Hg, and ...

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Postoperative spinal infection mimicking systemic vasculitis with titanium-spinal implants

BACKGROUND Secondary systemic vasculitis after posterior spinal fusion surgery is rare. It is usually related to over-reaction of immune-system, to genetic factors, toxicity, infection or metal allergies. CASE DESCRIPTION A 14 year-old girl with a history of extended posterior spinal fusion due to idiopathic scoliosis presented to our department with diffuse erythema and nephritis (macroscopi...

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Angiotropic large cell lymphoma with mononeuritis multiplex mimicking systemic vasculitis.

Angiotropic large cell lymphoma (ALCL), the so-called malignant angioendotheliomatosis, is characterised by proliferation of tumorous cells within small vessels. Manifestations in the CNS and cutaneous lesions prevail in the clinical presentation, although any organ can be involved. The recent classification of this lymphoma as part of the large cell lymphomas has modified the therapeutic appro...

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[Mercury poisoning].

Certain heavy metals such as mercury, lead, arsenic and cadmium are toxic even in reduced concentrations in blood. Their accumulation in the body causes serious illnesses. The most important heavy metals in human pathology are: mercury (Hg), cadmium (Cd), arsenic (As) and lead (Pb). The author mentions the heavy metal sources of poisoning, their toxicokinetics and toxicodynamics, clinical featu...

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Degos' disease mimicking vasculitis.

Introduction Degos’ disease is a rare disorder with multisystem involvement and unknown etiology. This entity was first described by Degos in 1942 (1,2). Other synonyms for this disease are malignant atrophic papulosis, atrophic papulosquamous dermatitis, fatal cutaneous-intestinal syndrome, and thromboangiitis cutaneointestinalis disseminata (3). It has been more commonly reported in whites, m...

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ژورنال

عنوان ژورنال: Pediatric Rheumatology

سال: 2014

ISSN: 1546-0096

DOI: 10.1186/1546-0096-12-s1-p364