Abstract
Introduction: Mucormycosis is an opportunistic life-threatening infection
whose incidence has significantly risen during the last two decades.
Gastrointestinal form is very rare, with the stomach as the most common site
of infection, followed by the colon and ileum. Risk factors include
uncontrolled diabetes mellitus, corticosteroid use, organ transplantation.
We report a patient with a history of rheumatoid arthritis who has developed
gastrointestinal mucormycosis. To the best of our knowledge, this is the
first such case reported in the literature. Case report: A 53-year-old
female patient with a prior medical history of rheumatoid arthritis was
admitted to the hospital due to persisting diarrhea. Physical examination
revealed diffuse abdominal tenderness to palpation, without meteorism and
peritoneal signs. Laboratory results demonstrated systemic inflammation, so
antibiotic therapy was administered. An abdominal computed tomography
findings revealed inflammation of the rectum and the left colon. Colonoscopy
findings were indicative of Crohn?s disease. Additionally, the patient had
developed profuse rectal bleeding and consequently underwent emergency
surgery. Subtotal colectomy with ileostomy and partial gastrectomy was
performed. Patient?s condition rapidly worsened after operation and she died
due to multi-organ failure. Histologic findings of resection specimens
discovered chronic active colitis and extensive gastric necrosis associated
with dense mixed inflammatory infiltration and numerous nonseptate and
90-degree branching hyphae. Diagnosis of invasive gastric mucormycosis was
obtained, but unfortunately, several days after the patient?s death.
Conclusion: It is very important to obtain high awareness among clinicians
of this deadly infection to achieve a prompt diagnosis and effective
therapy.
Publisher
National Library of Serbia
Subject
Pharmacology (medical),General Medicine