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Diagnostic Approach for Classic Compared With Localized Whipple Disease

BACKGROUND: Whipple disease (WD), a rare systemic infection caused by Tropheryma whipplei, can be a diagnostic challenge due to its variable presentation. The role of T. whipplei polymerase chain reaction (PCR) is unclear as small bowel biopsy with Periodic acid-Schiff (PAS) staining remains the dia...

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Autores principales: Crews, Nicholas R, Cawcutt, Kelly A, Pritt, Bobbi S, Patel, Robin, Virk, Abinash
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6030902/
https://www.ncbi.nlm.nih.gov/pubmed/29992176
http://dx.doi.org/10.1093/ofid/ofy136
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author Crews, Nicholas R
Cawcutt, Kelly A
Pritt, Bobbi S
Patel, Robin
Virk, Abinash
author_facet Crews, Nicholas R
Cawcutt, Kelly A
Pritt, Bobbi S
Patel, Robin
Virk, Abinash
author_sort Crews, Nicholas R
collection PubMed
description BACKGROUND: Whipple disease (WD), a rare systemic infection caused by Tropheryma whipplei, can be a diagnostic challenge due to its variable presentation. The role of T. whipplei polymerase chain reaction (PCR) is unclear as small bowel biopsy with Periodic acid-Schiff (PAS) staining remains the diagnostic gold standard. Individualized diagnostic approaches based on variable clinical manifestations are underutilized. We investigated the methodologies employed at our institution to diagnose WD. METHODS: We retrospectively collected all cases of WD diagnosed from 1994 to 2016. Microbiology laboratory and anatomic pathology databases were queried. Case characteristics and disease clinical phenotypes (classical, localized WD arthritis, and localized central nervous system [CNS] disease) were described. The diagnostic approach and testing yield were analyzed and reported. RESULTS: Thirty-three cases of WD were diagnosed (18 classic WD [CWD], 9 localized WD arthritis [LWD], 6 CNS WD). Misdiagnosis and delay in diagnosis were frequent. Diagnostic approach and test yield differed by classical vs localized WD involvement. Small bowel tissue biopsy PAS stain/PCR was overwhelmingly positive (86%/92%) in CWD, yet seldom positive (12%/42%) in LWD (P < .001). Affected joint synovial fluid PCR was frequently positive in both CWD (100%, 3/3) and LWD (85%, 6/7). CONCLUSIONS: These results support the role of small bowel biopsy PAS stain/PCR in the diagnosis of CW, though this approach may be of limited utility in LWD or CNS WD without gastrointestinal symptoms. Affected joint synovial fluid or cerebrospinal fluid PCR was frequently positive in both CWD and LWD, supporting its diagnostic usefulness.
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spelling pubmed-60309022018-07-10 Diagnostic Approach for Classic Compared With Localized Whipple Disease Crews, Nicholas R Cawcutt, Kelly A Pritt, Bobbi S Patel, Robin Virk, Abinash Open Forum Infect Dis Major Article BACKGROUND: Whipple disease (WD), a rare systemic infection caused by Tropheryma whipplei, can be a diagnostic challenge due to its variable presentation. The role of T. whipplei polymerase chain reaction (PCR) is unclear as small bowel biopsy with Periodic acid-Schiff (PAS) staining remains the diagnostic gold standard. Individualized diagnostic approaches based on variable clinical manifestations are underutilized. We investigated the methodologies employed at our institution to diagnose WD. METHODS: We retrospectively collected all cases of WD diagnosed from 1994 to 2016. Microbiology laboratory and anatomic pathology databases were queried. Case characteristics and disease clinical phenotypes (classical, localized WD arthritis, and localized central nervous system [CNS] disease) were described. The diagnostic approach and testing yield were analyzed and reported. RESULTS: Thirty-three cases of WD were diagnosed (18 classic WD [CWD], 9 localized WD arthritis [LWD], 6 CNS WD). Misdiagnosis and delay in diagnosis were frequent. Diagnostic approach and test yield differed by classical vs localized WD involvement. Small bowel tissue biopsy PAS stain/PCR was overwhelmingly positive (86%/92%) in CWD, yet seldom positive (12%/42%) in LWD (P < .001). Affected joint synovial fluid PCR was frequently positive in both CWD (100%, 3/3) and LWD (85%, 6/7). CONCLUSIONS: These results support the role of small bowel biopsy PAS stain/PCR in the diagnosis of CW, though this approach may be of limited utility in LWD or CNS WD without gastrointestinal symptoms. Affected joint synovial fluid or cerebrospinal fluid PCR was frequently positive in both CWD and LWD, supporting its diagnostic usefulness. Oxford University Press 2018-06-13 /pmc/articles/PMC6030902/ /pubmed/29992176 http://dx.doi.org/10.1093/ofid/ofy136 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 Major Article
Crews, Nicholas R
Cawcutt, Kelly A
Pritt, Bobbi S
Patel, Robin
Virk, Abinash
Diagnostic Approach for Classic Compared With Localized Whipple Disease
title Diagnostic Approach for Classic Compared With Localized Whipple Disease
title_full Diagnostic Approach for Classic Compared With Localized Whipple Disease
title_fullStr Diagnostic Approach for Classic Compared With Localized Whipple Disease
title_full_unstemmed Diagnostic Approach for Classic Compared With Localized Whipple Disease
title_short Diagnostic Approach for Classic Compared With Localized Whipple Disease
title_sort diagnostic approach for classic compared with localized whipple disease
topic Major Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6030902/
https://www.ncbi.nlm.nih.gov/pubmed/29992176
http://dx.doi.org/10.1093/ofid/ofy136
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