Tropheryma whipplei infection mimicking sarcoidosis with an atypical course: a molecularly confirmed diagnosis without PAS-positive intestinal disease
4 affiliations
- 1Department of Internal Medicine, Kantonsspital Graubünden, Chur, Switzerland
- 2Department of Infectious Diseases, Kantonsspital Graubünden, Chur, Switzerland
- 3Department of Nuclear Medicine, Kantonsspital Graubünden, Chur, Switzerland
- 4Department of Pneumology, Kantonsspital Graubünden, Chur, Switzerland
Abstract
Introduction: The bacterium Tropheryma whipplei causes Whipple’s disease, a rare chronic infection that can involve virtually any organ, especially in the late phase, and mimic inflammatory or neoplastic conditions. The interval from first symptoms to diagnosis is typically several years. Case description: A 68-year-old man was referred for pulmonary re-evaluation 2 years after a non-caseating hilar lymph-node granuloma had led to a diagnosis of stage I (nodal) sarcoidosis. His records revealed a 3-year history of lymphadenopathy with persistently elevated C-reactive protein and a two-year history of recurrent fever and fatigue. Corticosteroid therapy for ankle synovitis caused symptomatic worsening, prompting further investigation. Extensive infectious, oncological, rheumatological and tropical-medicine workup was unrevealing. Detailed history-taking revealed a 6 kg weight loss and epigastric discomfort, and a prior short antibiotic course for incipient pneumonia had produced transient improvement, making an atypical infectious aetiology, specifically Whipple’s disease, plausible. An endobronchial ultrasound–guided lymph-node aspirate and subsequently a stool sample were both positive for T. whipplei by quantitative polymerase chain reaction (qPCR), whereas cerebrospinal fluid PCR was negative, establishing systemic disease without central nervous system involvement. Oral doxycycline plus hydroxychloroquine produced fast and sustained clinical and biochemical remission at 1 year. Surveillance duodenal histology was periodic acid–Schiff -negative and structured clinical follow-up was arranged. Conclusion: Whipple’s disease is a great mimicker, but a treatable one, and should be considered in cases of chronic inflammation without evidence of a pathogen in primary microbiological analysis and in cases of sarcoidosis with an atypical course, particularly if symptoms do not improve or worsen while on corticosteroids.
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BibTeX
@article{bohinikova2026tropheryma,
title = {{Tropheryma whipplei infection mimicking sarcoidosis with an atypical course: a molecularly confirmed diagnosis without PAS-positive intestinal disease}},
author = {Lucia Bohinikova and Marco Seneghini and Michael Benjamin Fischer and Marc Daniel Wermke and Andrea Quadri},
journal = {European Journal of Case Reports in Internal Medicine},
year = {2026},
month = oct,
doi = {10.12890/2026_007539},
url = {https://doi.org/10.12890/2026_007539},
note = {CC BY-NC-ND},
}
RIS
TY - JOUR
TI - Tropheryma whipplei infection mimicking sarcoidosis with an atypical course: a molecularly confirmed diagnosis without PAS-positive intestinal disease
AU - Lucia Bohinikova
AU - Marco Seneghini
AU - Michael Benjamin Fischer
AU - Marc Daniel Wermke
AU - Andrea Quadri
PY - 2026
DA - 2026/10/01
JO - European Journal of Case Reports in Internal Medicine
DO - 10.12890/2026_007539
UR - https://doi.org/10.12890/2026_007539
AB - Introduction: The bacterium Tropheryma whipplei causes Whipple’s disease, a rare chronic infection that can involve virtually any organ, especially in the late phase, and mimic inflammatory or neoplastic conditions. The interval from first symptoms to diagnosis is typically several years. Case description: A 68-year-old man was referred for pulmonary re-evaluation 2 years after a non-caseating hilar lymph-node granuloma had led to a diagnosis of stage I (nodal) sarcoidosis. His records revealed a 3-year history of lymphadenopathy with persistently elevated C-reactive protein and a two-year history of recurrent fever and fatigue. Corticosteroid therapy for ankle synovitis caused symptomatic worsening, prompting further investigation. Extensive infectious, oncological, rheumatological and tropical-medicine workup was unrevealing. Detailed history-taking revealed a 6 kg weight loss and epigastric discomfort, and a prior short antibiotic course for incipient pneumonia had produced transient improvement, making an atypical infectious aetiology, specifically Whipple’s disease, plausible. An endobronchial ultrasound–guided lymph-node aspirate and subsequently a stool sample were both positive for T. whipplei by quantitative polymerase chain reaction (qPCR), whereas cerebrospinal fluid PCR was negative, establishing systemic disease without central nervous system involvement. Oral doxycycline plus hydroxychloroquine produced fast and sustained clinical and biochemical remission at 1 year. Surveillance duodenal histology was periodic acid–Schiff -negative and structured clinical follow-up was arranged. Conclusion: Whipple’s disease is a great mimicker, but a treatable one, and should be considered in cases of chronic inflammation without evidence of a pathogen in primary microbiological analysis and in cases of sarcoidosis with an atypical course, particularly if symptoms do not improve or worsen while on corticosteroids.
SN - 2284-2594
ER -