A fatal pseudo-tumour: disseminated basidiobolomycosis.

BMC Infect Dis

Department of Internal Medicine, Division of Infectious Diseases, Tropical Medicine and AIDS, Academic Medical Center, Amsterdam, The Netherlands.

Published: September 2006

Background: Basidiobolomycosis is a rare disease caused by the fungus Basidiobolus ranarum, member of the class Zygomycetes, order Entomophthorales, found worldwide. Usually basidiobolomycosis is a subcutaneous infection but rarely gastrointestinal manifestations have been described; 13 adults and 10 children and a few retroperitoneal or pulmonary cases. In gastrointestinal basidiobolomycosis the colon is most frequently involved, usually presenting with subacute mild abdominal pain. In contrast to children only very few described adult patients had hepatic masses. Definitive diagnosis requires culture, serological testing can be helpful. The fungal morphology and the Splendore-Hoeppli phenomenon are characteristic histological features. There are no prominent risk factors. Usually surgery and prolonged antifungal therapy are required.

Case Presentation: A 61 year old man presented with progressive left abdominal pain and constipation since a few months. Colonoscopy showed an obstructing tumour in the descending colon, and a hemicolectomy was performed. Histology showed inflammation, possibly caused by a fungal or parasitic infection, without definite identification of an organism. A few weeks postoperatively a CT scan made because of abdominal discomfort, revealed a livermass (6 cm). Treatment with metronidazole, directed against an amoebic liver abscess, was unsuccessful. He developed a marked eosinophilia (27.7%). A liver biopsy was performed and the patient was referred to a university hospital.A repeated CT scan showed a livermass of 9 cm diameter. Review of colon and liver biopsy samples showed extensive necrosis and histiocytes, multinucleated giant cells and numerous eosinophils. Grocott stained sections contained unusually large hyphae surrounded by strongly eosinophilic material in haematoxylin and eosin stained sections (Splendore-Hoeppli phenomenon). A presumptive diagnosis of Basidiobolus spp. infection was made and treated with amphotericin B (Itraconazol contra-indicated because of renal insufficiency). A few days later the patient died of a septic shock. After autopsy Basidiobolus ranarum was cultured from liver, gallbladder and colon.

Conclusion: Our patient died of gastrointestinal basidiobolomycosis with an obstructing colon tumour and a large hepatic mass. This was a rare presentation of basidiobolomycosis and the second fatal case described worldwide.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1574330PMC
http://dx.doi.org/10.1186/1471-2334-6-140DOI Listing

Publication Analysis

Top Keywords

basidiobolus ranarum
8
gastrointestinal basidiobolomycosis
8
abdominal pain
8
splendore-hoeppli phenomenon
8
liver biopsy
8
stained sections
8
patient died
8
basidiobolomycosis
6
fatal pseudo-tumour
4
pseudo-tumour disseminated
4

Similar Publications

Article Synopsis
  • Basidiobolomycosis is a rare fungal infection typically presenting as a chronic skin infection, but gastrointestinal cases, like the one reported in a 31-year-old woman, can occur and are harder to diagnose.
  • The patient's symptoms developed after bariatric surgery, leading to a misdiagnosis of ulcerative colitis; extensive surgical intervention revealed granulomatous inflammation indicative of basidiobolomycosis.
  • The case emphasizes the need for healthcare providers to be vigilant for basidiobolomycosis in patients with ulcerative lesions, especially if accompanied by eosinophilia and abdominal masses.
View Article and Find Full Text PDF
Article Synopsis
  • Basidiobolomycosis is a rare fungal infection triggered by the Basidiobolus ranarum fungus, often misdiagnosed as other conditions.
  • A 53-year-old Saudi man with abdominal pain and diarrhea was diagnosed with complicated diverticulitis, and upon surgical examination, significant fungal infection was discovered alongside inflammation characterized by eosinophils and granulomas.
  • Timely identification through special histological stains is crucial for accurate diagnosis and requires prompt antifungal treatment for better patient recovery.
View Article and Find Full Text PDF

Gastrointestinal basidiobolomycosis (GIB) is a rare fungal infection caused by the , and it possesses a significant challenge to diagnose it as it presents with non-specific symptoms that often mimic cancer. Herein, we report a case of GIB in a 51-year-old male from the central region of Saudi Arabia, a non-endemic region of GIB, which was initially misdiagnosed as colon cancer. A 51-year-old man presented with abdominal pain for two-months, non-bloody diarrhea, loss of appetite, and weight loss.

View Article and Find Full Text PDF

Gastrointestinal basidiobolomycosis (GIB) is a rare fungal infection caused by Basidiobolus ranarum, a saprophytic fungus that belongs to the class of Basidiobolomycetes. It mainly infects immunocompetent individuals and is mainly found in arid tropical and subtropical regions, including Southwestern America, Saudi Arabia, Africa, and Asia. Not surprisingly, a great number of human infections have been reported from these warm, humid climate regions that are felicitous for the growth of this fungus, especially from the southern region of Saudi Arabia and Arizona in the United States of America.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!