Mixed connective tissue disease presenting as quadriparesis in a female
Journal Title: Indian Journal of Case Reports - Year 2018, Vol 4, Issue 5
Abstract
Mixed connective tissue disease (MCTD), or overlap syndrome, is a multisystem autoimmune disease characterized by a combination of clinical features similar to those of polymyositis, systemic sclerosis, and rheumatoid arthritis. MCTD patients present with a distinct rise (high titers) of anti-U1 ribonucleoprotein antibody in serum. Here, we present the case of a 45-year-old female who presented with subacute onset weakness on all four limbs and later on diagnosed as overlap syndrome with severe myositis.
Authors and Affiliations
Madiha Ali, Yuvraj Sharma, Akshay Kumar Sharma, Amol G Andhale, Sourya Acharya
Gastric schwannoma: An important differential for gastric submucosal tumors - A rare case report
Schwannomas are slow-growing asymptomatic neoplasms that rarely occur in the gastrointestinal (GI) tract. It is a submucosal tumor arising in the neural plexus of the stomach. We herein describe the case of a 60-year-old...
A case of maxillary sinus carcinoma: An occult aggressive entity
Carcinoma of the maxillary sinus is a rare aggressive entity. Squamous cell carcinoma of maxillary sinus has the highest incidence among the tumors developing within the sinonasal compartment and has one of the worst out...
Multidetector computed tomography findings in a case of top of basilar syndrome
Stroke is a condition in which poor blood flow to the brain results in cell death. In India, almost 2,00,000 strokes are reported a year. Basilar artery occlusion syndrome accounts for 1–4% of all strokes. Top of the bas...
Lingual mandibular bone defect: A case report and review
Lingual mandibular bone defect is an asymptomatic radiolucent lesion of the mandible and usually encountered during routine radiographic examinations. It is essential to diagnose this lesion because of its resemblance wi...
Gastric duplication cyst: A rare congenital anomaly
Gastrointestinal (GI) duplication is defined as a spherical structure, with a muscular coat lined by a mucous membrane in the alimentary tract is a rare congenital anomaly. In this report, we present a case of a 14-year-...