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Why Is Whipple's Disease Still a Challenging Diagnosis? A Case Report and Brief Review of Literature
Ana Filipa Viegas1, Andreia M Lopes1, Gabriela Venade1
1Department of Internal Medicine, Centro Hospitalar Tondela-Viseu, Viseu, PRT.
Abstract:
Whipple's disease (WD) is a rare multisystemic infectious disease caused by Tropheryma whipplei. The pathogenesis of Whipple's disease remains unknown and clinical experience relies solely on various case reports published in the literature. The disease may occur at any age, with most studies describing patients in their fifth decade. Classic WD mainly affects the gastrointestinal tract, but extraintestinal commitment can occur, with the most common manifestations being arthralgias, lymphadenopathy, fever, and neurological symptoms. We present a case of a 69-year-old woman who presented with fever, macular rash, abdominal pain, lymphadenopathy, pleural and pericardial effusion, weight loss, and severely altered mental status over seven days. Initial workup tests only revealed leucopenia, thrombocytopenia, and hyperferritinemia. Since the fever persisted despite antibiotic treatment, an extensive workup was required until the final diagnosis of classic WD through histological examination of duodenal biopsies. Treatment with ceftriaxone was implemented for two weeks, followed by trimethoprim-sulfamethoxazole 160/800mg bid for 12 months. The patient presented full recovery and no recurrence after three years of follow-up. Even though WD was first described more than a century ago, WD is an elusive disease with a wide variety of clinical findings, leading to a still significant delay in diagnosis. WD should be considered in the differential diagnosis of rheumatologic disorders, chronic abdominal pain or diarrhea, neurological manifestations not suggestive of any other specific disease, non-caseating granulomatous diseases, and cases of lymphadenopathies. The authors aim to add additional clinical data and raise awareness for a rare condition that can be lethal if not timely treated. More studies and recommendations are needed concerning screening patients and treatment, with an urgent need to improve the delay in diagnosis.
Insights
Whipple's disease (WD) is a rare bacterial infection. This case highlights a delayed diagnosis in a 69-year-old woman, emphasizing the need for increased awareness and improved diagnostic strategies for this elusive condition.
Area of Science:
- Infectious Diseases
- Gastroenterology
- Rheumatology
Background:
- Whipple's disease (WD) is a rare multisystemic infectious disease caused by *Tropheryma whipplei*, with unknown pathogenesis.
- WD commonly affects the gastrointestinal tract but can present with diverse extraintestinal manifestations, including arthralgias, lymphadenopathy, fever, and neurological symptoms.
Observation:
- A 69-year-old woman presented with acute onset of fever, rash, abdominal pain, lymphadenopathy, effusions, weight loss, and altered mental status.
- Initial laboratory findings included leukopenia, thrombocytopenia, and hyperferritinemia; fever persisted despite empirical antibiotic treatment.
Findings:
- Diagnosis of classic WD was confirmed via histological examination of duodenal biopsies after extensive workup.
- Treatment with ceftriaxone followed by trimethoprim-sulfamethoxazole resulted in full recovery and no recurrence at three-year follow-up.
Implications:
- WD is an elusive disease with varied presentations, often leading to diagnostic delays; it should be considered in the differential diagnosis of various conditions.
- Increased clinical awareness, improved screening, and further research are crucial to expedite diagnosis and management of potentially lethal Whipple's disease.
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