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1731. Disseminated Metacestode Infection Due to an Unknown Versteria Species

BACKGROUND: A 68-year-old woman with hypogammaglobulinemia and prior treated lymphoma presented with fever and abdominal pain. Evaluation revealed numerous nodules in the lung, eye, brain, and liver (Figure 1). Initial lung and liver biopsies showed necrotizing granulomas with no organisms and negat...

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Autores principales: Lehman, Bethany, Leal, Sixto, Procop, Gary W, O’Connell, Elise M, Nash, Theodore, Jones, Stephen, Braunthal, Stephanie, Cruise, Michael, Mukhopadhyay, Sanjay, Banzon, Jona
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6252536/
http://dx.doi.org/10.1093/ofid/ofy209.137
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author Lehman, Bethany
Leal, Sixto
Procop, Gary W
O’Connell, Elise M
Nash, Theodore
Jones, Stephen
Braunthal, Stephanie
Cruise, Michael
Mukhopadhyay, Sanjay
Banzon, Jona
author_facet Lehman, Bethany
Leal, Sixto
Procop, Gary W
O’Connell, Elise M
Nash, Theodore
Jones, Stephen
Braunthal, Stephanie
Cruise, Michael
Mukhopadhyay, Sanjay
Banzon, Jona
author_sort Lehman, Bethany
collection PubMed
description BACKGROUND: A 68-year-old woman with hypogammaglobulinemia and prior treated lymphoma presented with fever and abdominal pain. Evaluation revealed numerous nodules in the lung, eye, brain, and liver (Figure 1). Initial lung and liver biopsies showed necrotizing granulomas with no organisms and negative serology and cultures. After progression while on broad-spectrum antibiotics for 4 months, an open liver biopsy revealed numerous nodular lesions and a mass made up of multifocal coalescing cystic lesions. The mass consisted of a degenerating 3-layered membrane without scoleces characterized by a wavy protuberant ciliated eosinophilic outer layer, subjacent degenerating cells with pyknotic nuclei, and loose connective tissue suggestive of a bladder wall and calcareous corpuscles in a matrix of granulomatous inflammation with areas of necrosis (Figure 2). This was diagnostic of disseminated metacestodes (larval stage) of a cestode (tapeworm). Treatment with praziquantel and albendazole led to improvement of symptoms and lesions. Disseminated cestode infections other than due to Echinococcus species are rare in humans. Sequencing was pursued due to the unusual findings. METHODS: DNA was extracted from liver tissue followed by targeted amplification of the cestode COX1 gene. PCR products confirmed to be 134 bp, as expected for a cestode COX1 gene, then inserted into a 2.1 Topo vector and cloned. Five separate isolates were sequenced, and 4 were interpretable. The 129-bp consensus sequence is shown in Figure 3. Basic Local Alignment Search Tool (NCBI BLAST) was used to find highly similar sequences. RESULTS: The sequence matched to Versteria sp. (T. mustelae) COX1 gene from a mink in Oregon (accession KT223034) with 98% identity. CONCLUSION: Metacestodes have the propensity to proliferate and rarely disseminate. There is one reported case of Versteria sp. causing a lethal disseminated infection of an orangutan. This is the first report of a Versteria sp. disseminated infection in a human and is singular because the patient survived. The patient likely accidentally ingested ova shed from a tapeworm in a mink or similar mammalian host. Histopathologic assessment is crucial in diagnosing cestode infection. COX1 gene sequencing is useful for cestode identification. [Image: see text] [Image: see text] [Image: see text] DISCLOSURES: All authors: No reported disclosures.
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spelling pubmed-62525362018-11-28 1731. Disseminated Metacestode Infection Due to an Unknown Versteria Species Lehman, Bethany Leal, Sixto Procop, Gary W O’Connell, Elise M Nash, Theodore Jones, Stephen Braunthal, Stephanie Cruise, Michael Mukhopadhyay, Sanjay Banzon, Jona Open Forum Infect Dis Abstracts BACKGROUND: A 68-year-old woman with hypogammaglobulinemia and prior treated lymphoma presented with fever and abdominal pain. Evaluation revealed numerous nodules in the lung, eye, brain, and liver (Figure 1). Initial lung and liver biopsies showed necrotizing granulomas with no organisms and negative serology and cultures. After progression while on broad-spectrum antibiotics for 4 months, an open liver biopsy revealed numerous nodular lesions and a mass made up of multifocal coalescing cystic lesions. The mass consisted of a degenerating 3-layered membrane without scoleces characterized by a wavy protuberant ciliated eosinophilic outer layer, subjacent degenerating cells with pyknotic nuclei, and loose connective tissue suggestive of a bladder wall and calcareous corpuscles in a matrix of granulomatous inflammation with areas of necrosis (Figure 2). This was diagnostic of disseminated metacestodes (larval stage) of a cestode (tapeworm). Treatment with praziquantel and albendazole led to improvement of symptoms and lesions. Disseminated cestode infections other than due to Echinococcus species are rare in humans. Sequencing was pursued due to the unusual findings. METHODS: DNA was extracted from liver tissue followed by targeted amplification of the cestode COX1 gene. PCR products confirmed to be 134 bp, as expected for a cestode COX1 gene, then inserted into a 2.1 Topo vector and cloned. Five separate isolates were sequenced, and 4 were interpretable. The 129-bp consensus sequence is shown in Figure 3. Basic Local Alignment Search Tool (NCBI BLAST) was used to find highly similar sequences. RESULTS: The sequence matched to Versteria sp. (T. mustelae) COX1 gene from a mink in Oregon (accession KT223034) with 98% identity. CONCLUSION: Metacestodes have the propensity to proliferate and rarely disseminate. There is one reported case of Versteria sp. causing a lethal disseminated infection of an orangutan. This is the first report of a Versteria sp. disseminated infection in a human and is singular because the patient survived. The patient likely accidentally ingested ova shed from a tapeworm in a mink or similar mammalian host. Histopathologic assessment is crucial in diagnosing cestode infection. COX1 gene sequencing is useful for cestode identification. [Image: see text] [Image: see text] [Image: see text] DISCLOSURES: All authors: No reported disclosures. Oxford University Press 2018-11-26 /pmc/articles/PMC6252536/ http://dx.doi.org/10.1093/ofid/ofy209.137 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Abstracts
Lehman, Bethany
Leal, Sixto
Procop, Gary W
O’Connell, Elise M
Nash, Theodore
Jones, Stephen
Braunthal, Stephanie
Cruise, Michael
Mukhopadhyay, Sanjay
Banzon, Jona
1731. Disseminated Metacestode Infection Due to an Unknown Versteria Species
title 1731. Disseminated Metacestode Infection Due to an Unknown Versteria Species
title_full 1731. Disseminated Metacestode Infection Due to an Unknown Versteria Species
title_fullStr 1731. Disseminated Metacestode Infection Due to an Unknown Versteria Species
title_full_unstemmed 1731. Disseminated Metacestode Infection Due to an Unknown Versteria Species
title_short 1731. Disseminated Metacestode Infection Due to an Unknown Versteria Species
title_sort 1731. disseminated metacestode infection due to an unknown versteria species
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6252536/
http://dx.doi.org/10.1093/ofid/ofy209.137
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