[The 490th case: arthralgia, amenorrhea, aphasia].

Zhonghua Nei Ke Za Zhi

Department of Rheumatology and Clinical Immunology, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, National Clinical Research Center for Dermatologic and Immunologic Diseases, Key Laboratory of Rheumatology and Clinical Immunology, Ministry of Education, Beijing 100730, China.

Published: December 2021

AI Article Synopsis

  • A 25-year-old woman presented with joint pain, irregular menstruation, and a recent speech disorder, leading to a diagnosis of premature ovarian failure and subsequent hormone replacement therapy.
  • After experiencing a stroke and additional symptoms, she was diagnosed with systemic lupus erythematosus and antiphospholipid syndrome based on positive antibody tests.
  • Treatment with high-dose glucocorticoids and other medications led to the return of her menstrual cycle, indicating her amenorrhea was likely related to autoimmune oophoritis from her lupus rather than any medication side effects.

Article Abstract

A 25-year-old woman was admitted to Peking Union Medical Hospital presented with arthralgia for 5 years, amenorrhea for 16 months, and speech disorder for 3 months. This patient has been afflicted by intermittent pain in metacarpophalangeal and proximal interphalangeal joints of both hands for 5 years. Her menstruation has been irregular 1 year ago and rapidly progressed to amenorrhea. Laboratory tests revealed postmenopausal sex hormones levels (estradiol<5 ng/L, follicle-stimulating hormone 62.5 IU/L, luteinizing hormone 58.71 IU/L) and no antral follicles were seen in gynecologic ultrasound. She was diagnosed with premature ovarian failure and treated with hormone replacement therapy, still with no ovulation. Numbness and weakness of right arm has recurrently occurred to her 4 months ago, and persistent weakness of right limbs combined with motor speech disorder occurred 1 month later. Magnetic resonance angiography was suggestive of ischemic stroke. Hormone replacement therapy was discontinued. Comprehensive laboratory tests revealed positive anti-dsDNA, anti-SSA/SSB, anticardiolipin and anti-βGPⅠ antibodies. Systemic lupus erythematosus (SLE), antiphospholipid syndrome (APS) was diagnosed. Since no drug with gonadal toxicity had been applied to the patient before, her amenorrhea was considered to be due to autoimmune oophoritis secondary to SLE. After treated with high-dose glucocorticoid, mycophenolate mofetil and hydroxychloroquine for 4 months, her menstruation recurred and regularly occurred till now. In some cases, amenorrhea in SLE patient might be resulted from autoimmune oophoritis associated with lupus flare, instead of use of drug with gonadal toxicity.

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http://dx.doi.org/10.3760/cma.j.cn112138-20210425-00308DOI Listing

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[The 490th case: arthralgia, amenorrhea, aphasia].

Zhonghua Nei Ke Za Zhi

December 2021

Department of Rheumatology and Clinical Immunology, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, National Clinical Research Center for Dermatologic and Immunologic Diseases, Key Laboratory of Rheumatology and Clinical Immunology, Ministry of Education, Beijing 100730, China.

Article Synopsis
  • A 25-year-old woman presented with joint pain, irregular menstruation, and a recent speech disorder, leading to a diagnosis of premature ovarian failure and subsequent hormone replacement therapy.
  • After experiencing a stroke and additional symptoms, she was diagnosed with systemic lupus erythematosus and antiphospholipid syndrome based on positive antibody tests.
  • Treatment with high-dose glucocorticoids and other medications led to the return of her menstrual cycle, indicating her amenorrhea was likely related to autoimmune oophoritis from her lupus rather than any medication side effects.
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