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- IRMS - Nicolae Testemitanu SUMPh
- 1. COLECȚIA INSTITUȚIONALĂ
- MedEspera: International Medical Congress for Students and Young Doctors
- MedEspera 2014
Please use this identifier to cite or link to this item:
http://hdl.handle.net/20.500.12710/19502
Title: | Case report: a 55 old woman with preudotumor cerebri, urticarial vasculuitis and suspected Sjogren syndrome |
Authors: | Sadovici, Victoria Cebanu, Mariana Salaru, Virginia |
Keywords: | Sjogren Syndrome;Urticarial Vasculuitis |
Issue Date: | 2014 |
Publisher: | Ministry of Health of the Republic of Moldova, State Medical and Pharmaceutical University Nicolae Testemitanu, Medical Students and Residents Association |
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. |
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. |
metadata.dc.relation.ispartof: | MedEspera: The 5th International Medical Congress for Students and Young Doctors, May 14-17, 2014, Chisinau, Republic of Moldova |
URI: | http://repository.usmf.md/handle/20.500.12710/19502 |
Appears in Collections: | MedEspera 2014
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