Case Report of International Journal of Case Reports
Mononeuropathy Multiplex – Case Report of An Unusual Manifestation of Primary Sjögren’s Syndrome
Andreia Freitas1, Filipa Santos Borges1, Sara Beça2, Carina Silva1
1Serviço de Medicina Interna, Centro Hospitalar Vila Nova de Gaia/Espinho, Vila Nova de Gaia; 2Servicio de Medicina Interna, Hospital Clínic Barcelona, Barcelona, Spain
Sjögren’s Syndrome (SS) is a chronic autoimmune disease characterized by exocrinopathy, with xerophthalmia and xerostomia. Patients with SS may exhibit extra-glandular features such as neurologic symptoms. Peripheral neuropathy is the most common neurological complication of primary SS (pSS). We report a case of a 71-year-old female with pSS admitted to the Internal Medicine ward due to sensorimotor symptoms and petechiae. From the extensive study carried out, emphasis is given to elevation of inflammatory markers and to nerve conduction study compatible with mononeuritis of multiple nerves. The diagnosis of mononeuropathy multiplex (MM) secondary to pSS was made. She was started on corticosteroid therapy, which allowed complete regression of the petechiae as well as symptomatic and functional improvement. However, new sensorimotor deficits were noted a few days later. The decision was made to start cycles of cyclophosphamide in association with corticosteroid and physical therapies, leading to deficit improvement. Currently, the patient is in remission with low-dose corticosteroid therapy.
Keywords: Sjögren’s Syndrome; Mononeuropathy Multiplex; Peripheral Nervous System; Autoimmune Diseases; Vasculitides
How to cite this article:
Andreia Freitas, Filipa Santos Borges, Sara Beça, Carina Silva.Mononeuropathy Multiplex – Case Report of An Unusual Manifestation of Primary Sjögren’s Syndrome. International Journal of Case Reports, 2022, 6:281. DOI: 10.28933/ijcr-2022-10-2305af
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