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A fatal pseudo-tumour: disseminated basidiobolomycosis

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 1...

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Autores principales: van den Berk, Guido EL, Noorduyn, L Arnold, van Ketel, Ruud J, van Leeuwen, Jeannouel, Bemelman, Willem A, Prins, Jan M
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1574330/
https://www.ncbi.nlm.nih.gov/pubmed/16978407
http://dx.doi.org/10.1186/1471-2334-6-140
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author van den Berk, Guido EL
Noorduyn, L Arnold
van Ketel, Ruud J
van Leeuwen, Jeannouel
Bemelman, Willem A
Prins, Jan M
author_facet van den Berk, Guido EL
Noorduyn, L Arnold
van Ketel, Ruud J
van Leeuwen, Jeannouel
Bemelman, Willem A
Prins, Jan M
author_sort van den Berk, Guido EL
collection PubMed
description 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.
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spelling pubmed-15743302006-09-23 A fatal pseudo-tumour: disseminated basidiobolomycosis van den Berk, Guido EL Noorduyn, L Arnold van Ketel, Ruud J van Leeuwen, Jeannouel Bemelman, Willem A Prins, Jan M BMC Infect Dis Case Report 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. BioMed Central 2006-09-15 /pmc/articles/PMC1574330/ /pubmed/16978407 http://dx.doi.org/10.1186/1471-2334-6-140 Text en Copyright © 2006 van den Berk et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
van den Berk, Guido EL
Noorduyn, L Arnold
van Ketel, Ruud J
van Leeuwen, Jeannouel
Bemelman, Willem A
Prins, Jan M
A fatal pseudo-tumour: disseminated basidiobolomycosis
title A fatal pseudo-tumour: disseminated basidiobolomycosis
title_full A fatal pseudo-tumour: disseminated basidiobolomycosis
title_fullStr A fatal pseudo-tumour: disseminated basidiobolomycosis
title_full_unstemmed A fatal pseudo-tumour: disseminated basidiobolomycosis
title_short A fatal pseudo-tumour: disseminated basidiobolomycosis
title_sort fatal pseudo-tumour: disseminated basidiobolomycosis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1574330/
https://www.ncbi.nlm.nih.gov/pubmed/16978407
http://dx.doi.org/10.1186/1471-2334-6-140
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