DC Field | Value | Language |
dc.contributor.author | Sadovici, Victoria | - |
dc.contributor.author | Cebanu, Mariana | - |
dc.contributor.author | Salaru, Virginia | - |
dc.date.accessioned | 2021-12-21T15:00:40Z | - |
dc.date.available | 2021-12-21T15:00:40Z | - |
dc.date.issued | 2014 | - |
dc.identifier.citation | SADOVICI, Victoria, CEBANU, Mariana, SALARU, Virginia. Case report: a 55 old woman with preudotumor cerebri, urticarial vasculuitis and suspected Sjogren syndrome. In: MedEspera: the 5th Internat. Medical Congress for Students and Young Doctors: abstract book. Chișinău: S. n., 2014, p. 76. | en_US |
dc.identifier.uri | http://repository.usmf.md/handle/20.500.12710/19502 | - |
dc.description | Internal Medicine Department, State Medical
and Pharmaceutical University "Nicolae Testemitanu”, Chisinau, Republic of Moldova | en_US |
dc.description.abstract | Case report: We report a case of a 55 old woman presenting complaints of severe and permanent
headache with progressive decrease of visual acuity (VA) for 6 months, xerophtalmia, xerostomia and
urticarial eruption. The medical history of the patient is marked by autoimmune thyroiditis and active
tobacco smoking (10 cigarettes / day during 20 years). The physical examination was remarkable by a
normal body mass index and skin lesions specific for urticarial vasculitis. The remainder of examination
was normal. The CBC, biochemical, auto-antibodies and radiological examinations were normal too.
The evaluations included the assessment of the cephalalgia: complete neurologic examination, fundus
examination, MR1 of the brain and a lumbar puncture. The results have revealed a papilledema, a
decrease of VA and an elevation of the opening pressure at the lumbar puncture. The diagnosis
conclusion was the presence of pseudotumor cerebri, which is a disorder clinically manifested by
chronically elevated intracranial pressure of unknown etiology associated with visual abnormalities. The
skin biopsy revealed small vessels wall deposits of IgG and C3, and a polynuclear perivascular infiltrate.
The last question was the etiology of the Sicca syndrome, who is supposed to be a Sjogren syndrome.
The Shirmer test and the salivary gland scintigraphy confirmed our suspicion. We proceeded to salivary
gland biopsy, whose result is on pending.
Conclusion: We report a case of a smoking woman who presents a pseudotumor cerebri, urticarial
vasculutis where was suspected Sjogren syndrome, defined as a systemic chronic inflammatory disorder
characterized by lymphocytic infiltrates in exocrine glands. If the principle of parsimony is used, the three
entities can be linked: to our known, in the medical literature where are few case reports concerning the
association of Sjogren syndrome and pseudotumor cerebri as a very rare neurological complication. In its
turn, the urticarial vasculitis is a known manifestation of Sjogren syndrome. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Ministry of Health of the Republic of Moldova, State Medical and Pharmaceutical University Nicolae Testemitanu, Medical Students and Residents Association | en_US |
dc.relation.ispartof | MedEspera: The 5th International Medical Congress for Students and Young Doctors, May 14-17, 2014, Chisinau, Republic of Moldova | en_US |
dc.subject | Sjogren Syndrome | en_US |
dc.subject | Urticarial Vasculuitis | en_US |
dc.title | Case report: a 55 old woman with preudotumor cerebri, urticarial vasculuitis and suspected Sjogren syndrome | en_US |
dc.type | Other | en_US |
Appears in Collections: | MedEspera 2014
|