Pyomyositis in the setting of complicated diverticulitis: case report
International Journal of General Medicine
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Pyomyositis in the setting of complicated
diverticulitis: case report
This article was published in the following Dove Press journal:
International Journal of General Medicine
James Sun 1
David Leor Kashan 1
Jolita Marie Auguste 1
Akella Chendrasekhar 2
1
Department of Surgery, State
University of New York, Downstate
Medical Center, Brooklyn, NY, USA;
2
Department of Surgery, Richmond
University Medical Center, Staten
Island, NY, USA
Abstract: Pyomyositis is typically thought of as a disease of the tropics. However, it is
becoming more prevalent in temperate regions, and may be underdiagnosed. Here, pyomyositis
is encountered as a complication of perforated diverticulitis, which has not been previously
reported. A 61-year-old Caucasian man initially presented in respiratory distress and was
diagnosed with respiratory failure due to COPD exacerbation. The patient was taking highdose prednisone, 60 mg daily for the past 2 years. Initially, he was afebrile, normotensive,
tachycardic to 178 beats/minute and tachypneic to 28 breaths/minute, requiring noninvasive
ventilation to maintain oxygenation. Blood tests revealed leukocytosis of 16.7×103/μL, and
blood cultures grew Escherichia coli. Broad-spectrum antibiotics were started but leukocytosis and bacteremia persisted on repeated tests. On the seventh hospital day, a CT scan of the
abdomen was performed for complaints of abdominal pain, and the patient was diagnosed
with Hinchey stage 3 diverticulitis. A Hartmann’s procedure was performed with intraoperative findings of purulent peritonitis. Intraoperative cultures grew E. coli and vancomycinresistant Enterococcus faecium. The patient continued to have leukocytosis of 15.1×103/μL
despite surgical therapy. He began to complain of left lower extremity pain, and a CT scan
on hospital day 24 revealed gluteal intramuscular abscesses, which were percutaneously
drained. Persistent symptoms prompted another CT scan on hospital day 28, which revealed
additional intramuscular abscesses in the vastus lateralis muscle, which was also drained, with
subsequent resolution of pain and normalization of inflammatory markers. This is the first
case demonstrating pyomyositis as a complication of diverticulitis. While the mechanism of
pyomyositis may not be unique, it is important to recognize the potential complications of
frequently encountered diseases. In this critically ill and immunosuppressed patient, there
was delayed diagnosis of both diverticulitis and pyomyositis, but the patient quickly improved
once the diseases were recognized and treated.
Keywords: abscess, immunosuppression, steroid use, COPD, intramuscular infection
Introduction
Correspondence: James Sun
SUNY Downstate Department of
Surgery, 450 Clarkson Ave, Box 40,
Brooklyn, NY 11203, USA
Tel +1 718 270 5800
Fax +1 718 270 2826
Email
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http://dx.doi.org/10.2147/IJGM.S141581
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Pyomyositis is defined as an acute, primary, intramusuclar infection that is hematogenously disseminated from transient bacteremia.1,2 This condition was first described
by Scriba as a disease of the tropics.1–4 It was nearly 100 years before the first reported
case in North America by Levin et al and its prevalence has been increasing.5 To the
author’s knowledge, it has only been associated with a surgical disease of the abdomen
in a report described by Ea et al as a complication of laparoscopy.6 We submit a case
of pyomyositis as an adverse outcome of complicated diverticulitis to underscore the
importance of this disease as a consideration in a surgical patient.
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Sun et al
International Journal of General Medicine downloaded from https://www.dovepress.com/ by 213.32.59.119 on 13-Jul-2018
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Case report
A 61-year-old Caucasian male initially presented with
COPD exacerbation with delirium, visual hallucinations and
altered mental status. The patient had been taking high-dose
prednisone 60 mg daily for 2 years for COPD. On presentation, the patient was afebrile with a temperature of 98.3°F,
normotensive with a blood pressure of 140/85, tachycardic to
178 beats/minute and tachypneic to 28 breaths/minute, with
oxygen saturation of 98% on bilevel positive airway pressure
ventilation. Blood tests were significant for leukocytosis of
16.7×103/μL, with a left shift of 89.1% and a lactic acid of 5.8
mmol/L. He was admitted to the medical service for respiratory failure secondary to COPD exacerbation. The patient
was treated with piperacillin/tazobactam and vancomycin
empirically. Leukocytosis improved and blood cultures from
admission grew Escherichia coli resistant to ampicillin and
levofloxacin, confirmed on repeated blood culture.
On the fifth hospital day, the source of bacteremia was
not identified and routine evaluations of the urinary tract
and lungs failed to show evidence of infection. The patient
had complaints of left flank pain; however, with improved
leukocytosis and no other sources of infection, work-up was
deferred. On the seventh hospital day, persistent abdominal
pain prompted CT imaging of the abdomen, which revealed
a 14×3.7×7.2 cm abscess along the medial wall of the left
psoas muscle (Figure 1) and 2 additional abscesses at the
L5–S1 level; 5.4×3.6 cm in the midline and 3.4×2.3 cm left
of midline, and intramuscular air in the left gluteal muscles.
The patient was diagnosed with Hinchey stage 3 complicated diverticulitis and the surgery service was consulted.
A Hartmann’s procedure and abdominal washout was performed, with intraoperative findings of purulent peritonitis.
Figure 1 Initial CT-scan showing abscess with air–fluid level abutting left psoas
muscle, indicated by red arrow.
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The patient was taken back to the operating room for two
additional abdominal washouts during the following week.
Cultures of the peritoneal fluid from the init (...truncated)