November 2005
Fig.1
Fig2.
Fig3.
Fig4.
History: A 25-year old African-American female, with
a past medical history significant for systemic lupus erythematosus
(SLE) complicated by class IV membranoproliferative glomerular
nephritis, on chronic prednisone therapy, presented to the hospital
September
24, 2005 with the chief complaint of bilateral "burning feet,"
along with an exquisitely painful, retiform, purpurpic eruption
on bilateral feet, calves, knees, thighs, and the left elbow.
She stated she had been taking a shower the morning prior to admission,
looked down and saw what appeared to be a bruise on the left knee
and "purple toes." Over the next 24 hours, the eruption
spread to involve the aforementioned locations. She stated the
pain was so severe that she was unable to rest her legs on the
bed. Furthermore, any subtle palpation of the lesions caused her
to scream out in pain. She denied a history of any similar rash.
In fact, the only history of a rash she had in the past was a
malar rash. She did complain of significant arthralgias present
in her fingers and ankles. She denied fevers, chills, headaches,
mental status changes, shortness of breath, diarrhea, or other
constitutional symptoms.
One month prior to presentation, she was hospitalized with a left lateral calf cellulitis and abscess, which was incised, drained, and debrided on August 9, 2005. MRI was negative at that time for osteomyelitis. The final cultures grew oxacillin-sensitive Staphylococcus Aureus, Escherichia coli, Stentotrophomonas, and Bacteroides fragilis. At the time of admission, she was taking Bactrim-DS along with Flagyl.
Past Medical History: 1) SLE: diagnosed at during
childhood. Anti-ds-DNA positive (9/11/05) in a high titer at 1:3083.
ANA, Anti-Sm, anti-ribonuclear protein, and SS-A were positive.
The lupus was complicated by pleural effusions, anemia, and renal
disease.
2) Membranoproliferative glomerular nephritis (Class IV):
Secondary to the lupus. Confirmed by renal biopsy March 2005.
Baseline creatinine was 1.1 mg/dl on 9/16/05.
Physical Exam:Vital signs in the ER demonstrated a temperature of 39.9 C, a heart rate ranging from 130-150, and a blood pressure of 155/95. She was a thin woman, in significant pain, crying and moaning. Skin examination demonstrated a non-blanchable, non-palpable, well-demarcated, retiform purpura without overlying ulceration present on bilateral feet (Figs 1-2), lateral thighs, shins, the left knee (Fig3), the left elbow (Fig4), and faintly on bilateral dorsal hands. This rash was extremely painful to any touch. There was also a 5 x 10 cm ulceration, without erythema, foul smell, or drainage, located on the left lateral calf, at the previous surgical debridement site. There was no ocular or oral involvement.
Admission Laboratory
Creatinine: 3.6 (0.6-1.4); BUN: 63 (8-25); Plasma protein:
5.2 (6.5-8.5); Albumin: 2.3 (3.6-5.0); Bili: 0.3 (0.3-1.1); Alk
Phos: 90 (38-126); AST: 66 (11-47); ALT: 60 (7-53)
Urinalysis:
Protein: +3; Glucose: negative; Ketones: trace; Bili: +1; Blood:
+3; Nitrites: negative; Leukocyte esterase: +2 RBC: 50 (0-3 HPF);
WBC: 30 (0-5HPF); Bacteria: trace; Coarse granular casts: 2 or
more (none)
CBC: WBC: 10.7 (3.8-9.8); Hgb: 8.6 (12.1-15.1); Hct: 24.9 (36.1-44.3);
Plt: 93K (140-440K);
Haptoglobin: 282 (27-220)
PT: 17.1 (11-15.5): INR: 1.33 (0.8-1.2): PTT: 47.6 (23-35):
D-dimer: >20 (0.22-0.5)
Fibrinogen: 407 (150-400)
ESR: 61 (0-20): CRP: 306 (<10): Anti-ds-DNA: 1:4052: Lupus
anticoagulant: 1.3 (0-1)
Anticardiolipin antibodies: 18.2 (0-9)Blood cultures: negative:
Urine cultures: negative
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