Aim: To describe our experience with alveolar hemorrhage (AH) in systemic l
upus erythematosus (SLE),
Methods: Review of medical records and pertinent medical literature using M
EDLINE and reference lists from retrieved publications.
Patients: Seven patients with SLE admitted with episodes of AH (n = 11),
Results: Six patients were female, and one was male. Mean age at the time o
f AH was 31.1 years. Mean duration of SLE was 4.5 years. AH occurred within
3 weeks of SLE onset in two patients. Recurrent AH was observed in four pa
tients. Six patients were already receiving treatment for SLE at the time o
f AH. AH patients presented with dyspnea and new pulmonary infiltrates. Hem
optysis occurred in only 54%, All patients had BAL within 48 h of presentat
ion, Temperature greater than or equal to 39 degreesC (102.2 degreesF) acco
mpanied 82% of episodes. Glomerulonephritis was the most common nonpulmonar
y SLE manifestation (74%), Treatment with empiric IV antibiotics was initia
ted in 10 episodes. Initial treatment included high-dose corticosteroids (p
rednisone, 1 to 3 mg/kg/d [n = 2]; or IV methylprednisolone, 1 g/d [n = 9],
with or without oral cyclophosphamide, 2 to 3 mg/kg/d [n = 7]). Plasmapher
esis (three to four sessions) was added in five episodes for persistent AH.
All patients survived,
Conclusions: AH may mimic pneumonia, Hemoptysis may not be evident. Infecti
on must be aggressively excluded, especially since many patients with AH ar
e already receiving immunosuppressive therapy. AH frequently recurs despite
ongoing immunosuppression, Although high mortality rates have been reporte
d with AH in SLE, we observed 100% survival.