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Whipple's disease classification

Introduction

Overview

Overview

Whipple’s disease may be classified into two groups of acute and chronic infection. It might be classified as systemic or localized based on the organ involvement. It has four different clinical manifestations: Acute infection, asymptomatic carrier state, the classic Whipple’s disease, and localized chronic infection.

Classification

Classification

  • Whipple’s disease may be classified to two groups of acute and chronic based on the duration.[1][2]


Whipple’s disease classification based on the duration:

 
 
 
 
 
 
 
 
 
 
 
 
 
Whipple’s disease classification
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Acute
 
 
 
 
 
 
 
Chronic
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Gastroenteritis
 
Pneumonia
 
Bacteremia
 
Asymptomatic carrier state
 
 
Classic Whipple’s disease
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Chronic localized infection
 
 
 
 
 
 


Whipple’s disease classification based on organ involvement:

 
 
 
 
 
 
 
 
Whipple’s disease classification
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Systemic involvement
 
 
 
 
 
 
 
 
 
 
 
 
 
Localized involvement
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Heart
 
CNS
 
Eye
 
Lung
 
Bone
 
Serosa
 
Skin
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
• Blood culture negative endocarditis
• Adhesive pericarditis
• Myocardial fibrosis
 
• Encephalitis
• Progressive dementia
• Cerebellar ataxia
• Personality changes
• Hemiparesis
• Seizure
• Wernicke’s encephalopathy
• Hypothalamic involvement
• Supranuclear ophthalmoplegia
 
• Uveitis
• Vitritis
• Retinitis
• Retrobulbar neuritis
• Papilledema
 
• Chronic cough
• Dyspnea
 
• Arthritis
• Spondylodiscitis
 
• Pleuritic chest pain
 
• Hyperpigmentation
 
 
References

References

  1. ↑ 1.0 1.1 Marth, Thomas (2009). “New Insights into Whipple’s Disease – A Rare Intestinal Inflammatory Disorder”. Digestive Diseases. 27 (4): 494–501. doi:10.1159/000233288. ISSN 1421-9875.
  2. ↑ Schneider, Thomas; Moos, Verena; Loddenkemper, Christoph; Marth, Thomas; Fenollar, Florence; Raoult, Didier (2008). “Whipple’s disease: new aspects of pathogenesis and treatment”. The Lancet Infectious Diseases. 8 (3): 179–190. doi:10.1016/S1473-3099(08)70042-2. ISSN 1473-3099.
  3. ↑ Relman, David A.; Schmidt, Thomas M.; MacDermott, Richard P.; Falkow, Stanley (1992). “Identification of the Uncultured Bacillus of Whipple’s Disease”. New England Journal of Medicine. 327 (5): 293–301. doi:10.1056/NEJM199207303270501. ISSN 0028-4793.
  4. ↑ Street, Sara; Donoghue, Helen D; Neild, GH (1999). “Tropheryma whippelii DNA in saliva of healthy people”. The Lancet. 354 (9185): 1178–1179. doi:10.1016/S0140-6736(99)03065-2. ISSN 0140-6736.
  5. ↑ Ectors N, Geboes K, De Vos R, Heidbuchel H, Rutgeerts P, Desmet V, Vantrappen G (1992). “Whipple’s disease: a histological, immunocytochemical and electronmicroscopic study of the immune response in the small intestinal mucosa”. Histopathology. 21 (1): 1–12. PMID 1378814.
  6. ↑ Marth T, Strober W (1996). “Whipple’s disease”. Semin. Gastrointest. Dis. 7 (1): 41–8. PMID 8903578.

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Sadaf Sharfaei M.D.[2]