Premature ovarian failure in juvenile systemic lupus erythematosus patient: A rare presentation

Author:

Tekgöz Nilüfer1ORCID,Taş Demet2,Çelikel Elif1,Özlü Sare Gülfem3,Acar Banu1

Affiliation:

1. Department of Pediatric Rheumatology, Ankara City Hospital, Turkey

2. Department of Adolescent Medicine, Ankara City Hospital, Turkey

3. Department of Pediatric Nephrology, Ankara City Hospital, Turkey

Abstract

A 16-year-old girl was admitted to the hospital for the absence of a menstrual bleeding over 10 mounts. She has had regular menstrual periods since she was 13 years old and no history of systemic disease. Laboratory tests showed low estrogen (<11.8 ng/L, range 16–238 ng/L), elevated FSH (follicle stimulating hormone) (138.3 U/L), low AMH (anti-Mullerian hormone) (<0.01 µg/L), normal prolactin (7 μg/L), and thyroid hormone levels (TSH: 1.5 mU/L). The ovaries were prepubertal in size and diagnosed with primer ovarian failure. ANA titers, antiphospholipid antibody, and direct coombs were positive. Microscopic hematuria and nephritic proteinuria (34 mg/m2/hour) were also detected and renal biopsy was revealed stage 3–5 lupus nephritis. Premature ovarian failure is an extremely rare disease in childhood. When POF is detected in the adolescent, it is important to investigate the etiology. In this way, it may be possible to diagnose diseases with high morbidity and mortality that may cause POF.

Publisher

SAGE Publications

Subject

Rheumatology

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