|Year : 2007 | Volume
| Issue : 4 | Page : 215-217
Etiopathogenesis of pruritus due to systemic causes: Implications for treatment
Uday Khopkar, Sushil Pande
Department of Dermatology, Seth GS Medical College and KEM Hospital, Mumbai - 400012, India
Department of Dermatology, Seth GS Medical College and KEM Hospital, Parel, Mumbai - 400 012
Source of Support: None, Conflict of Interest: None
|How to cite this article:|
Khopkar U, Pande S. Etiopathogenesis of pruritus due to systemic causes: Implications for treatment. Indian J Dermatol Venereol Leprol 2007;73:215-7
|How to cite this URL:|
Khopkar U, Pande S. Etiopathogenesis of pruritus due to systemic causes: Implications for treatment. Indian J Dermatol Venereol Leprol [serial online] 2007 [cited 2020 Jun 6];73:215-7. Available from: http://www.ijdvl.com/text.asp?2007/73/4/215/33632
Pruritus is one of the most troublesome symptoms seen in dermatologic practice. Severe pruritus can undoubtedly affect quality of life and can have serious psychological implications. Satisfactory management of pruritus unassociated with any skin lesions still remains a distant goal though breakthroughs in our understanding of pruritus are on the horizon.
Cutaneous inflammatory disorders are associated with release of chemical mediators like histamine. That skin inflammation leads to pruritus is clear from the fact that anti-inflammatory agents including steroids relieve pruritus in such patients. Antihistamines provide relief from pruritus in allergic disorders by competitively or non-competitively blocking histamine and by producing sedation.
However, when pruritus is not due to any primary skin disease, dermatologists find themselves on less familiar ground. Proven causes of pruritus due to systemic diseases are: uremic pruritus, hepatobiliary pruritus, pruritus due to hematological causes like polycythemia vera, leukemia, lymphomas (especially Hodgkin's disease), multiple myeloma, pruritus due to endocrine disorders and multiple sclerosis. The less proven causes are carcinoid syndrome, iron deficiency anemia, diabetes and intestinal parasites. Our understanding of the pathomechanism of pruritus of systemic origin has considerably improved in the last few years. Drugs based on these mechanisms are likely to produce better results than the use of antihistamines alone.
| Uremic Pruritus|| |
The link between uremia due to chronic renal failure and pruritus is an established one. However, in uremia associated with acute renal failure, pruritus is classically absent. Uremic pruritus is of multifactorial origin and common causes suggested are uremic xerosis, secondary hyperparathyroidism, hypervitaminosis-A, uremic neuropathy, elevated serum histamine levels and iron deficiency anemia. Of these, uremic xerosis is perhaps the most important cause of uremic pruritus. 
The level of uremic pruritus is directly proportional to the severity of uremic xerosis; the more intense the xerosis, the greater the amount of pruritus. ,,, Uremic xerosis is secondary to full-thickness skin dehydration resulting from diminished sweating and low levels of skin surface lipids due to atrophy of the eccrine and sebaceous glands respectively. However, Yosipovitch et al.  and Stεhle-Bδckdahl et al.  did not find a correlation between the severity of pruritus and objective parameters of skin dryness. Nevertheless, it illustrates that even if uremic xerosis is not ' the' cause of uremic pruritus, it can adversely affect pruritus by reducing the threshold for itch. Impaired perfusion of the skin demonstrated in patients of medical renal disease may also contribute to the skin dehydration process.  Liberal application of emollients improves cutaneous hydration and relieves pruritus in a significant proportion of patients with uremia.
Pruritus appears at advanced stages of renal failure. Uremia causes severe paroxysms of pruritus (especially during the summer) in 25% of patients with chronic renal failure.  Generally, dialysis, both hemodialysis and peritoneal dialysis, helps in treatment of pruritus. Occasional concern is about complement activation by dialyzer membrane and aggravation of pruritus. Now, with the use of increasingly more biocompatible membranes the problem is more theoretical than practical.
Nordal et al. reviewed the relationship between secondary hyperparathyroidism and uremic pruritus and suggested the treatment of secondary hyperparathyroidism for the amelioration of uremic pruritus. Secondary hyperparathyroidism leads to calcium phosphate deposition in the skin that causes degranulation of mast cells and release of serotonin and histamine. Uremic patients with pruritus were found to have numerous mast cells in the skin, elevated serum histamine, parathyroid hormone and serum ferritin levels as compared to uremic patients without pruritus.  Despite the evidence for release of histamine, there was no correlation found between plasma histamine levels and severity of itching in uremic patients suggesting that plasma histamine does not play a significant role in uremic pruritus.  Probably for the same reason, the role of antihistamines is best described as marginal in the treatment of uremic pruritus. However, serotonin antagonists like ondansetron and granisetron were found to be effective, safe and well tolerated for the treatment of uremic pruritus in Hemodialysis patients in some recent trials.  Similarly, mast cell stabilizer and anti-serotonin drug, ketotifen also gives encouraging results in the treatment of uremic pruritus. ,
The hypothesis that release of cytokines initiates uremic pruritus is supported by the successful use of narrow band UVB therapy (NB-UVB) in the treatment of uremic pruritus. The NB-UVB therapy supposedly depletes the mast cell in the uremic skin to reduce the itching.  Renal transplantation is curative in uremic pruritus and uremic changes of the skin and generalized pruritus disappear upon restoration of kidney function after renal transplantation. 
| Hepatobiliary Pruritus|| |
Pruritus is one of the common disabling symptoms of hepatobiliary diseases. Although, in the majority of cases, it is associated with jaundice, it may occur in the absence of it. Pruritus in cholestatic hepatobiliary diseases is due to bile acid, bile acid derivatives or endogenous opiates that undergo enterohepatic circulation. , Opiates are thought to be involved in the development of hepatobiliary pruritus because opiate agonists induce opioid receptor-mediated scratching activity of central origin. Further, the increase in central opioidergic tone in cholestasis and reduction of scratching activity by opiate antagonists (naltrexone) in cholestatic patients support their role. , Naltrexone (50 mg/day), an opiate antagonist, is found to be beneficial but only in small controlled trials.  Bile acid binding resin like cholestyramine (4-6 g taken 30 min before meal) still remains the drug of choice for the pruritus associated with primary biliary cirrhosis and primary sclerosing cholangitis.  Malabsorption, constipation and decreased absorption of other medications are some unwanted effects of cholestyramine. In cases of 'surgical' jaundice, surgical intervention will relieve obstruction in the extrahepatic biliary tree to improve pruritus. The common causes include gall stones, calculus cholecystitis, carcinoma of head of pancreas and obstruction of biliary tree by metastases. Biliary stenting by endoscopic retrograde cholangiopancreatography (ERCP) provides another therapeutic option in inoperable malignancies affecting the extra-hepatic biliary tract.
Ursodeoxycholic acid (USDA), 13-15 mg/kg/day is a choleretic bile acid that replaces naturally occurring taurate- and glycate-rich bile acids and improves pruritus in intrahepatic cholestasis of pregnancy but is not useful for other forms of cholestatic jaundice.
Pruritus of primary biliary cirrhosis and pediatric cholestatic disorders has shown improvement with rifampicin, but the underlying mechanism and magnitude of benefits are not clear.  Limited data on the efficacy and potential for hepatotoxicity precludes its routine use in these conditions.
| Pruritus of Endocrine Causes|| |
Common endocrine disorders associated with pruritus are hypothyroidism and hyperthyroidism. Skin in hypothyroidism is dry, coarse and myxedematous. It is postulated that decrease in sebaceous gland activity, decreased sweat secretion and low epidermal sterol synthesis contribute to xerosis.  Supplementation of thyroid hormone and use of emollients is helpful. In hyperthyroidism, skin becomes warm and moist. Vasodilatation leads to increased blood flow of the skin and increase in skin temperature that decreases the threshold for itching. 
Contrary to popular belief, diabetes mellitus is not a cause of generalized pruritus. However, localized pruritus due to anogenital candidiasis is certainly common in diabetics.
| Pruritus and Hematological Disorders|| |
A large number of hematological disorders are associated with pruritus in the absence of 'itchy skin lesions'. Causes include polycythemia vera, Hodgkin's disease, myeloma and leukemia. 'Bath itch' of polycythemia occurs after contact with water and lasts for about 30-60 min, the exact mechanism of which is unknown. While normal serum tryptase levels is a good evidence against mast cell degranulation in these cases, elevated histamine levels are consistently observed.  Despite this, the role of antihistamines in the relief of pruritus is limited. Venesection and aspirin have been used with variable results.
Pruritus is a well-recognized symptom of Hodgkin's lymphoma (HD) that is present in approximately 30% of cases of HD.  Paroxysms of generalized itching and hyperhidrosis have been observed. Pruritus in HD was earlier considered as a sign of active disease warranting aggressive chemotherapy, but this is no longer accepted today. Pruritus in HD is reported to resolve after the initiation of chemotherapy indicating strong etiologic association. 
Causes of central neurogenic pruritus are multiple sclerosis, stroke and spinal tumors. The mechanism of central pruritus and central pain appears the same in such cases. 
| Conclusion|| |
Better understanding of the pathophysiology of pruritus invariably has implications for specific treatment. With increasing understanding of the role of chemical mediators, central neural mechanisms, immune cells and cytokines, newer drugs are being explored for the alleviation of pruritus. Thus, in future, we may use specific drugs to treat each of the systemic causes of pruritus providing succor to our distressed patients.
| References|| |
|1.||Szepietowski JC, Reich A, Schwartz RA. Uraemic xerosis. Nephrol Dial Transplant 2004;19:2709-12. |
|2.||Szepietowski JC, Sikora M, Kunsztal M, Salomon J, Magott M, Szepietowski T. Uremic pruritus: A clinical study of maintenance haemodialysis patients. J Dermatol 2002;29:621-7. |
|3.||Balaskas EV, Chu M, Uldall RP, Gupta A, Oreopoulos DG. Pruritus in continuous ambulatory peritoneal dialysis and hemodialysis patients. Perit Dial Int 1992;13:527S-32. |
|4.||Morton CA, Lafferty M, Hau C, Henderson I, Jones M, Lowe JG. Pruritus and skin hydration during dialysis. Nephrol Dial Transplant 1996;11:2031-6. |
|5.||Young AW, Sweeney EW, David DS, Cheigh J, Hochgelerenl EL, Sakai S, et al . Dermatologic evaluation of pruritus in patients on hemodialysis. NY State J Med 1973;73:2670-4. |
|6.||Stεhle-Bδckdahl M. Uremic pruritus. Clinical and experimental studies. Acta Derm Venereol Suppl (Stockh) 1989;145:1-38. |
|7.||Yosipovitch G, Reis J, Tur E, Sprecher E, Yarnitsky D, Boner G. Sweat secretion, stratum corneum hydration, small nerve function and pruritus in patients with advanced chronic renal failure. Br J Dermatol 1995;133:561-4. |
|8.||Weiss T, Windthorst C, Weiss C, Kreuzer J, Bommer J, Kübler W. Acute effects of haemodialysis on cutaneous microcirculation in patients with peripheral arterial occlusive disease. Nephrol Dial Transplant 1998;13:2317-21. |
|9.||Robinson-Bostom L, DiGiovanna JJ. Cutaneous manifestations of end-stage renal disease. J Am Acad Dermatol 2000;43:975-86. |
|10.||Dimkoviζ N, Djukanoviζ L, Radmiloviζ A, Bojiζ P, Juloski T. Uremic pruritus and skin mast cells. Nephron 1992;61:5-9. |
|11.||De Filippi C, Regazzini R, Piazza V, Galli F, Pisati P, Sacchi S, et al . Uraemic pruritus is not related to plasma histamine concentrations. Clin Exp Dermatol 1995;20:294-6. |
|12.||Layegh P, Mojahedi MJ, Malekshah PT, Pezeshkpour F, Vahedian M, Nazemian F, et al . Effect of oral granisetron in uremic pruritus. Indian J Dermatol Venereol Leprol 2007;73:231-4. [PUBMED] |
|13.||Francos GC, Kauh YC, Gitllen SD, Schulman ES, Besarab A, Goyal S, et al . Elevated plasma histamine in chronic uremia: Effects of Ketotifen of prutitus. Int J Dermatol 1991;30:884-9. |
|14.||Szepietowski JC, Morita A, Tsuji T. Ultraviolet B induces mast cell apoptosis: A hypothetical mechanism of ultraviolet B treatment for uraemic pruritus. Med Hypotheses 2002;58:167-70. |
|15.||Altmeyer P, Kachel HG, Schδfer G, Fassbinder W. Normalization of uremic skin changes following kidney transplantation. Hautarzt 1986;37:217-21. |
|16.||Jones EA, Bergasa NV. Pruritus of cholestasis. Hepatology 1999;29:1003-6. |
|17.||Jones EA, Bergasa NV. Evolving concepts of the pathogenesis and treatment of the pruritus of cholestasis. Can J Gastroenterol 2000;14:33-40. |
|18.||Lidofsky SD. Jaundice. In: Feldman M, Friedman LS, Brandt LJ, Editors. Sleisenger Fordtran's Gastrointestinal and Liver Disease, 8 th Edn. philadelphia: W. B. Saunders; 2006 p. 314. |
|19.||Levy C, Lindor KD. Treatment options for primary biliary cirrhosis and primary sclerosing cholangitis. Curr Treat Options Gastroenterol 2003;6:93-103. |
|20.||Greaves MW. Pathophysiology and clinical aspects of pruritus. In: Freedberg IM, Eisen AZ, Wolff K, Austen KF, Goldsmith LA, Katz SI, editors. Fitzpatrick's dermatology in general medicine. 6 th ed. McGraw-Hill: New York; 2003. p. 398-403. |
|21.||Buchanan JG, Ameratunga RV, Hawkins RC. Polycythemia vera and water-induced pruritus: Evidence against mast cell involvement. Pathology 1994;26:43-5. |
|22.||Krajnik M, Zylicz Z. Pruritus in advanced internal diseases. Pathogenesis and treatment. Neth J Med 2001;58:27-40. |
|23.||Omidvari SH, Khojasteh HN, Mohammadianpanah M, Monabati A, Mosalaei A, Ahmadloo N. Long-term pruritus as the initial and sole clinical manifestation of occult Hodgkin's disease. Indian J Med Sci 2004;58:250-2. [PUBMED] |
|24.||Canavero S, Bonicalzi V, Massa-Micon B. Central neurogenic pruritus: A literature review. Acta Neurol Belg 1997;97:244-7. |
|This article has been cited by|
||Cutaneous manifestations of systemic non-Hodgkin lymphomas (NHL): study and review of literature
| ||M. Carlesimo,A. Narcisi,A. Rossi,I. Saredi,D. Orsini,S. Pelliccia,M.A. Aloe Spiriti,E. Mari,M.C. Cox |
| ||Journal of the European Academy of Dermatology and Venereology. 2013; : n/a |
|[Pubmed] | [DOI]|
||Innovative Management of Pruritus
| ||Jamison D. Feramisco, Timothy G. Berger, Martin Steinhoff |
| ||Dermatologic Clinics. 2010; 28(3): 467 |
|[VIEW] | [DOI]|
||Etiopathogenesis of pruritus due to systemic causes: Implications for treatment
| ||Khopkar U, Pande S |
| ||Indian J Dermatol Venereol Leprol. 2007; 73(4): 215-217 |
|[VIEW] | [PDF]|