Systemic Lupus Erythematosus Patient with Bicytopenia and Motor Aphasia

نویسندگان

چکیده

Background: Systemic lupus erythematosus (SLE) is a chronic inflammatory autoimmune condition with unclear cause that shows broad ranging clinical symptoms, course and prognosis. Cerebrovascular illness, severe symptom SLE in the central nervous system by neuropsychiatric (NPSLE). Aphasia considered to be one of rarer signs, produced secondary antiphospolipid syndrome (APS), cerebrovascular NPSLE. Case: A 37 years-old married woman has background miscarriage speech blocking, motor aphasia, had nasal voice was diagnosed NPSLE APS. After initiating therapy cyclophospamide aspilet patient’s improved significantly. Conclusion: APS needs bear mind patients or thrombosis. The diagnosis based on history, clinical, laboratory examinations which include phospholipid antibodies, There dramatic improvement after 12 days 500 mg oral 100 daily therapy.

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Refractory Angioedema in a Patient with Systemic Lupus Erythematosus

Angioedema secondary to C1 inhibitor deficiency has been rarely reported to be associated with systemic lupus erythematosus. A genetic defect of C1 inhibitor produces hereditary angioedema, which is usually presented with cutaneous painless edema, but edema of the genital area, gastrointestinal and laryngeal tracts have also been reported.In lupus patients, angioedema may be the result of an ac...

متن کامل

Neurobrucellosis in systemic lupus erythematosus

Background: Brucellosis is a zoonotic infection which is endemic in many countries. It is a multisystem disease which may present with a broad spectrum of clinical manifestations and complications. Neurobrucellosis is an uncommon complication of brucellosis. Case presentation: A 25-year-old woman with a history of lupus for 5 months referred to the emergency ward of Shahid Beheshti Hosp...

متن کامل

Fever of unknown origin in a male patient with systemic lupus erythematosus

Background: Systemic lupus erythematosus (SLE) is an inflammatory autoimmune disorder which is uncommon in men. It has a wide variety of clinical presentations. Case Report: We report a 21-year-old male presented with one month history of fever, loss of appetite, weight loss and reduced hair growth with an examination revealing an oral ulcer, cervical and axillary lymphadenopathy simulating ...

متن کامل

Pyoderma gangrenosum in a patient with antiphospholipid antibody negative systemic lupus erythematosus: A case report

In any description of leg ulcers in systemic lupus erythematosus (SLE), pyoderma gangrenosum (PG) earns a mention at least for its being quite rare in such patients. The causative role of aPL (antiphospholipid antibody) in dermatological manifestations of SLE is undermined by the occurrence of PG in aPL negative SLE patients. To the best of our knowledge, there are only two reports of PG in aPL...

متن کامل

refractory angioedema in a patient with systemic lupus erythematosus

angioedema secondary to c1 inhibitor deficiency has been rarely reported to be associated with systemic lupus erythematosus. a genetic defect of c1 inhibitor produces hereditary angioedema, which is usually presented with cutaneous painless edema, but edema of the genital area, gastrointestinal and laryngeal tracts have also been reported. in lupus patients, angioedema may be the result of an a...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: International journal of research publications

سال: 2021

ISSN: ['2708-3578']

DOI: https://doi.org/10.47119/ijrp100771520211953