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ORIGINAL ARTICLES |
Spontaneous perinephric hematoma in the absence of anticoagulation, arteritis, or trauma is uncommon. We report the case of a postpartum patient with nephrolithiasis who initially presented to the obstetric service with a spontaneous perinephric hemorrhage.
A 26-year-old G4P3 Asian female presented to the obstetric service at 38 weeks with severe unremitting low back pain and a known history of nephrolithiasis. A limited intravenous pyelogram (IVP) was performed, which showed a filling defect consistent with a nonobstructing right distal ureteric stone (Figure 1). She was made pain-free and labor was augmented the following day, complicated by a drop in her hematocrit from 33.1 % prior to delivery to 27.6 % on postpartum day 1. She was discharged from the hospital and presented five days later with headache, nausea, and vomiting. On physical exam, she was afebrile with a blood pressure of 164/92 and pulse of 61. She had right upper quadrant (RUQ) abdominal tenderness with no palpable masses. Liver transaminases were elevated. Bilirubin, platelet count, coagulation studies, and urinalysis were normal. A RUQ abdominal ultrasound showed a right perinephric fluid collection and computerized tomography (CT) scan of the abdomen showed a 9 cm dense lateral fluid collection contained within Gerotaís fascia and without extravasation of contrast (Figures 2a and b). A right ureteral stent was placed with subsequent spontaneous passage of the stone. Renal magnetic resonance imaging (MRI) and renal angiography revealed no evidence of neoplastic or vascular abnormalities.
Spontaneous perinephric hematomas are uncommon. Renal tumors, vasculopathies,
infectious disease, nephritis, and blood dyscrasias are the most commonly reported
etiologies.1-4 Ten cases of renal hemorrhage associated
with parturition have been reported.5-10 In these
cases, the etiology of the bleeding was obscure, with no detectable pathology to
account for the sudden onset of hemorrhage.9 We
report the first case of a spontaneous perinephric hematoma associated with urolithiasis
in pregnancy. As shown by her negative MRI and angiography, the patient had none
of the previously reported risk factors for spontaneous hemorrhage, to include tumors,
vasculopathies, infections, and blood dyscrasias. Nephrolithiasis in pregnancy should
be considered a risk factor for spontaneous perinephric hematoma, along with the
aforementioned disorders.


Contrast enhanced computerized tomography scan showing a right perinephric hematoma within Gerota's fascia and without contrast extravasation.
