Abstract
A 30-year-old #Ethiopian female presented to the emergency department
with intermittent worsening left lower quadrant pain and bilateral upper
extremity pain. Past medical history is significant for sickle cell
#anemia. Physical exam including vital signs were unremarkable except for
tenderness to palpation in bilateral upper extremity and left lower
quadrant (posterior greater than anterior). Complete blood count
revealed only mild anemia (Hemoglobin 10.1 mg/dL), but was otherwise
unremarkable, as was the comprehensive metabolic panel. #Erythrocyte
sedimentation rate (ESR) and C-reactive protein (CRP) were elevated at
71 mm/hr and 12.3mg/L.A 30-year-old Ethiopian female presented to the emergency department
with intermittent worsening left lower quadrant pain and bilateral upper
#extremity pain. Physical exam including vital signs were unremarkable
except for tenderness to palpation in bilateral upper extremity and left
lower quadrant (posterior greater than anterior). Complete blood count
revealed only mild anemia (Hemoglobin 10.1 mg/dL), but was otherwise
unremarkable, as was the comprehensive metabolic panel. Erythrocyte
sedimentation rate (ESR) and C-reactive protein (CRP) were elevated at
71 mm/hr and 12.3mg/L. The patient did not have #hemoglobinuria,
avascular #necrosis, #splenic infarcts, and significant drop in her
hemoglobin/ hematocrit, or other non-osseous stigmata to suggest this
process could be from acute on chronic bone infarct in this patient with
history of sickle cell anemia. Past medical history is significant for
sickle cell anemia. Patient had normal LDH, no leukopenia/lymphopenia
and no clinical signs.
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