Whipple's disease

Whipple's disease

Whipple's disease
Low magnification micrograph of Whipple's disease showing the characteristic foamy appearing infiltrate of the lamina propria. Duodenal biopsy. H&E stain.
Classification and external resources
ICD-10 K90.8
ICD-9-CM 040.2
DiseasesDB 14124
MedlinePlus 000209
eMedicine article/183350 article/1166639
MeSH D008061

Whipple's disease is a malabsorption but may affect any part of the body including the heart, brain, joints, skin, lungs and the eyes.[1] Weight loss, diarrhea, joint pain, and arthritis are common presenting symptoms, but the presentation can be highly variable and approximately 15% of patients do not have these classic signs and symptoms.[2] Whipple's disease is significantly more common in men, with 87% of the patients being male.[3] When recognized and treated, Whipple's disease can usually be cured with long-term antibiotic therapy; untreated, the disease is ultimately fatal.


  • Signs and symptoms 1
  • Mechanism 2
  • Diagnosis 3
  • Treatment 4
  • Epidemiology 5
  • History 6
  • See also 7
  • References 8
  • External links 9

Signs and symptoms

The most common symptoms are diarrhea, abdominal pain, weight loss, and joint pains. The joint pains may be due to migratory non-deforming arthritis, which may occur many years before any digestive tract symptoms develop; they tend to involve the large joints but can occur in any pattern and tend not to damage the joint surface to the point that the joint becomes deformed. Fever and chills occur in a small proportion of people.[4]

In its more advanced form, malabsorption (insufficient absorption of nutrients from the diet) leads to wasting and the enlargement of lymph nodes in the abdomen. Neurological symptoms (discussed below) are more common in those with severe abdominal disease. Chronic malabsorptive diarrhea leads to the poor absorption of fat, causing steatorrhea (fatty, offensive stool), flatulence, and abdominal distension. Protein-losing enteropathy may also occur, causing depletion of albumin, a blood protein, which may lead to peripheral edema caused by the lowered oncotic pressures.[4]

Darkening of the skin occurs in almost half; some also have skin nodules. Various eye problems, such as uveitis, may occur; this is typically associated with deteriorating vision and pain in the affected eye. Endocarditis (infection of the heart valve) has been reported in a small number of cases, sometimes in people with no other symptoms of Whipple's disease; this is typically noticed as breathlessness and leg swelling due to fluid accumulation as the heart is unable to pump fluid through the body.[4]

10–40% of people with Whipple's disease have problems related to involvement of the brain; the symptoms relate to the part of the brain that is affected. The most common problems are dementia, memory loss, confusion, and decreased level of consciousness. Eye movement disturbances and myorhythmia (rapidly repetitive movements of the muscles) of the face, together referred to as oculomasticatory myorhythmia, are highly characteristic for Whipple's disease. Weakness and poor coordination of part of the body, headaches, seizures, as well as a number of more uncommon neurological features, are present in some cases.[4]


T. whipplei is one of the actinomycetes, and is a distant relative of Mycobacterium avium-intracellulare, and Mycobacterium paratuberculosis explaining in part why Whipple's disease is similar to the diseases caused by these bacteria.[5] The disease is common in farmers and those exposed to soil and animals, suggesting that the infection is acquired from these sources.[4]

Individuals who are most susceptible to the disease are those with decreased ability to perform intracellular degradation of ingested pathogens or particles, particularly in the macrophages. Several studies indicate that defective T-lymphocyte (particularly TH1 population) function may be an important predisposing factor for the disease.[6] In particular circulating cells that are CD11b (also known as integrin alpha) expressive, are reduced in susceptible individuals. CD11b has a vital role in activation of macrophages to destroy intracellularly ingested T. whipplei bacteria.[5]


High magnification micrograph showing the characteristic foamy macrophages in the lamina propria. H&E stain.

Common clinical signs and symptoms of Whipple's disease include diarrhea, steatorrhea, abdominal pain, weight loss, migratory arthropathy, fever, and neurological symptoms.[7] Weight loss and diarrhea are the most common symptoms that lead to identification of the process, but may be preceded by chronic, unexplained, relapsing episodes of non-destructive seronegative arthritis, often of large joints.[8]

Diagnosis is made by PCR-based assay is also available.[4] PCR can be confirmatory if performed on blood, vitreous fluid, synovial fluid, heart valves, or cerebrospinal fluid.[9] PCR of saliva, gastric or intestinal fluid, and stool specimens is highly sensitive, but not specific enough, indicating that healthy individuals can also harbor the causative bacterium without the manifestation of Whipple's disease, but that a negative PCR is most likely indicative of a healthy individual.[4]

Endoscopy of the duodenum and jejunum can reveal pale yellow shaggy mucosa with erythematous eroded patches in patients with classic intestinal Whipple's disease, and small bowel X-rays may show some thickened folds. Other pathological findings may include enlarged mesenteric lymph nodes, hypercellularity of lamina propria with "foamy macrophages", and a concurrent decreased number of lymphocytes and plasma cells, per high power field view of the biopsy.


Treatment is with penicillin, ampicillin, tetracycline, or co-trimoxazole for one to two years.[2] Any treatment lasting less than a year has an approximate relapse rate of 40%. Recent expert opinion is that Whipple's disease should be treated with doxycycline with hydroxychloroquine for 12 to 18 months.[3] Sulfonamides (sulfadiazine or sulfamethoxazole) may be added for treatment of neurological symptoms.[3]


The disease is regarded as extremely rare, with an incidence (new number of cases per year) of one case per million people. The patients are predominantly male (86% in a survey of American patients), although in some countries the rate of women receiving a diagnosis of Whipple's disease has increased in recent years. It occurs predominantly in those of Caucasian ethnicity, suggesting a genetic predisposition in that population.[4]

T. whipplei appears to be an environmental organism that is commonly present in the gasterointestinal tract but remains asymptomatic.[4] Several lines of evidence suggest that some defect—inherited or acquired—in immunity is required for it to become pathogenic.[10] The possible immunological defect may be specific for T. whipplei, since the disease is not associated with a substantially increased risk of other infections.[11]

The disease is usually diagnosed in middle age (median 49 years). Studies from Germany have shown that age at diagnosis has been rising since the 1960s.[4]


Whipple described the disease in 1907 in a paper in the now-defunct Bulletin of Johns Hopkins Hospital. The patient was a 35-year-old medical missionary. Whipple referred to the disease as "intestinal lipodystrophy".[1] It was long presumed to be an infectious disease, but the causative organism was only fully identified in 1992.[12] In 2003, doctors from Johns Hopkins Hospital, together with a French expert in the disease, applied novel diagnostic methods to stored tissue samples from Whipple's original patient, and demonstrated T. whipplei in these tissues.[3][13]

See also


  1. ^ a b Whipple, G. H. (1907). "A hitherto undescribed disease characterized anatomically by deposits of fat and fatty acids in the intestinal and mesenteric lymphatic tissues". Bulletin of the Johns Hopkins Hospital 18: 382–93. 
  2. ^ a b Bai, J. C., Mazure, R. M., Vazquez, H.; et al. (October 2004). "Whipple's disease". Clin. Gastroenterol. Hepatol. 2 (10): 849–60.  
  3. ^ a b c d Fenollar, F., Puéchal, X., Raoult, D. (January 2007). "Whipple's disease". New England Journal of Medicine 356 (1): 55–66.  
  4. ^ a b c d e f g h i j k Schneider, T., Moos, V., Loddenkemper, C., Marth, T., Fenollar, F., Raoult, D. (March 2008). "Whipple's disease: new aspects of pathogenesis and treatment". Lancet Infect Dis 8 (3): 179–90.  
  5. ^ a b Strayer DL, Rubin R, Rubin E (2008). Rubin's pathology: clinicopathologic foundations of medicine. Philadelphia: Wolters Kluwer/Lippincott Williams & Wilkins. p. 583.  
  6. ^ Marth T (November 2001). "The diagnosis and treatment of Whipple's disease". Curr Allergy Asthma Rep 1 (6): 566–71.  
  7. ^ Longo, D; Faucy, A; Kasper, D; Hauser, S; Jameson, J; Loscalzo, Joseph (2012). Harrison's Principles of Internal Medicine (18th ed.). McGraw Hill Professional. 
  8. ^ Puéchal, X. (2009). "Maladie de Whipple". La Revue de Médecine Interne 30 (3): 233–241.  
  9. ^ SJ McPhee, MA Papadakis. Current Medical Diagnosis and Treatment 2012 McGraw-Hill ISBN 978-0-07-176372-1
  10. ^ Marth, T. (2009). "New Insights into Whipple's Disease – A Rare Intestinal Inflammatory Disorder". Digestive Diseases 27 (4): 494–501.  
  11. ^ Deriban, G.; Marth, T. (2006). "Current concepts of immunopathogenesis, diagnosis and therapy in Whipple's disease". Current medicinal chemistry 13 (24): 2921–2926.  
  12. ^ Relman, D. A., Schmidt, T. M., MacDermott, R. P., Falkow, S. (July 1992). "Identification of the uncultured bacillus of Whipple's disease". N. Engl. J. Med. 327 (5): 293–301.  
  13. ^ Dumler JS, Baisden BL, Yardley JH, Raoult D (April 2003). "Immunodetection of Tropheryma whipplei in intestinal tissues from Dr. Whipple's 1907 patient". N. Engl. J. Med. 348 (14): 1411–2.  

External links

  • "Whipple's Disease". National Digestive Disease Information Clearinghouse NDDIC. 
  • "European Network on Tropheryma whipplei infection". Retrieved 2010-11-15. 
  • Whipple's disease at Merck Manual of Diagnosis and Therapy Home Edition