Splenic infarction in a 12-year-old female
leading to the diagnosis of systemic lupus
erythematosus
Dublin Core
Title
Splenic infarction in a 12-year-old female
leading to the diagnosis of systemic lupus
erythematosus
leading to the diagnosis of systemic lupus
erythematosus
Subject
Systemic lupus erythematosus, Lupus, Splenic infarct, Pediatric, Rheumatologic
Description
Abstract
Background Systemic lupus erythematosus is an autoimmune inflammatory disease with extremely variable
presentations. While a facial rash is the most common finding, other symptoms can include arthralgias, fatigue, and
cytopenias. Abdominal symptoms are much less common presentations of lupus. Antiphospholipid syndrome is a
related autoimmune disorder causing vascular thrombosis. Children with lupus frequently have antiphospholipid
antibodies. We present a rare case of a 12-year-old female with a splenic infarction leading to a new diagnosis of lupus
with associated antiphospholipid syndrome.
Case presentation A previously healthy 12-year-old female presented with prolonged and recurrent fever, nausea,
body aches and left sided abdominal pain. Her evaluation revealed anemia, thrombocytopenia, and proteinuria.
A computed tomography of the abdomen showed a splenic infarction. While admitted to the hospital, she
underwent extensive oncologic and rheumatologic testing. This evaluation resulted in a diagnosis of systemic
lupus erythematosus. The patient’s hospital course was complicated by acute respiratory failure and myocarditis
requiring intensive care unit transfer and care. Her symptoms and cytopenias gradually improved on oral steroids,
hydroxychloroquine, and cyclophosphamide infusions.
Conclusions Splenic infarction is less a distinct entity, but rather a symptom of an underlying disorder. Common
etiologies include hypercoagulable states, infection, and oncologic and rheumatologic diseases. Patients with splenic
infarctions are more likely to have longer hospital stays and higher mortality. This case is a reminder that a practitioner
should consider hospitalization and further evaluation when splenic infarction is diagnosed, as this can be a signal of
serious systemic disease.
Keywords Systemic lupus erythematosus, Lupus, Splenic infarct, Pediatric, Rheumatologic
Background Systemic lupus erythematosus is an autoimmune inflammatory disease with extremely variable
presentations. While a facial rash is the most common finding, other symptoms can include arthralgias, fatigue, and
cytopenias. Abdominal symptoms are much less common presentations of lupus. Antiphospholipid syndrome is a
related autoimmune disorder causing vascular thrombosis. Children with lupus frequently have antiphospholipid
antibodies. We present a rare case of a 12-year-old female with a splenic infarction leading to a new diagnosis of lupus
with associated antiphospholipid syndrome.
Case presentation A previously healthy 12-year-old female presented with prolonged and recurrent fever, nausea,
body aches and left sided abdominal pain. Her evaluation revealed anemia, thrombocytopenia, and proteinuria.
A computed tomography of the abdomen showed a splenic infarction. While admitted to the hospital, she
underwent extensive oncologic and rheumatologic testing. This evaluation resulted in a diagnosis of systemic
lupus erythematosus. The patient’s hospital course was complicated by acute respiratory failure and myocarditis
requiring intensive care unit transfer and care. Her symptoms and cytopenias gradually improved on oral steroids,
hydroxychloroquine, and cyclophosphamide infusions.
Conclusions Splenic infarction is less a distinct entity, but rather a symptom of an underlying disorder. Common
etiologies include hypercoagulable states, infection, and oncologic and rheumatologic diseases. Patients with splenic
infarctions are more likely to have longer hospital stays and higher mortality. This case is a reminder that a practitioner
should consider hospitalization and further evaluation when splenic infarction is diagnosed, as this can be a signal of
serious systemic disease.
Keywords Systemic lupus erythematosus, Lupus, Splenic infarct, Pediatric, Rheumatologic
Creator
Melanie M. Randall1*, Salomon H. Alvarado1
, Andrew Gurewitz2
, Brian G. Chen3
, Joel A. Labha1
and
Fairuz Despujos Harfouche1
, Andrew Gurewitz2
, Brian G. Chen3
, Joel A. Labha1
and
Fairuz Despujos Harfouche1
Date
2025
Contributor
Peri Irawan
Format
pdf
Language
english
Type
text
Files
Collection
Citation
Melanie M. Randall1*, Salomon H. Alvarado1
, Andrew Gurewitz2
, Brian G. Chen3
, Joel A. Labha1
and
Fairuz Despujos Harfouche1, “Splenic infarction in a 12-year-old female
leading to the diagnosis of systemic lupus
erythematosus,” Repository Horizon University Indonesia, accessed April 22, 2026, https://repository.horizon.ac.id/items/show/13260.
leading to the diagnosis of systemic lupus
erythematosus,” Repository Horizon University Indonesia, accessed April 22, 2026, https://repository.horizon.ac.id/items/show/13260.