2021, Number 12
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Ginecol Obstet Mex 2021; 89 (12)
Adult granulosa cell tumor
López-González E, Sillero-Castillo A, Escribano-Cobalea M
Language: Spanish
References: 15
Page: 1002-1008
PDF size: 199.95 Kb.
ABSTRACT
Background: Systemic lupus erythematosus (SLE) is a chronic, multisystemic disease
of unknown etiology, whose clinical manifestations are heterogeneous. Pericardial
involvement is the most common cardiac complication; however, the development of
cardiac tamponade is rare, and even more so in pregnant patients presenting with SLE.
Objective: To present the clinical characteristics, diagnosis, treatment, and evolu-
tion of cardiac tamponade in a pregnant patient that presents with systemic lupus
erythematosus.
Clinical case: A 24-year-old patient, who is 27.5 weeks pregnant, presenting with
anasarca, dyspnea that evolved to orthopnea and stabbing chest pain for three weeks.
Her chest X-ray showed cardiomegaly grade II, congestive lung fields and pleural
effusion at the level of cardiophrenic sinuses. The echocardiogram found a 500 mL
pericardial effusion with evidence of cardiac tamponade. Progressive deterioration with
compromised lung capacity, and the appearance of acute renal failure with progressive
increases in creatinine; showing hemodynamic instability characterized by paradoxical
pulse and hypotension. With positive Antinuclear Antibodies (ANA) and proteinuria,
renal biopsy reports histopathological patterns corresponding to lupus nephritis, treated
with steroid pulses and intravenous cyclophosphamide in a risk-benefit assessment,
with subsequent satisfactory maternal-fetal evolution.
Conclusion: Cardiac tamponade is not common in patients with SLE, and it is
even rarer as the initial manifestation, even more so during pregnancy. It is a clinical
emergency and requires multidisciplinary management since pregnancy in a patient
with SLE implies an increased risk of systemic complications.
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