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Colchicine in dermatology
2 Department of Dermatology, Gandhi Medical College and Hospital, Musheerabad, Hyderabad - 500048, India
Angoori Gnaneshwar Rao
Department of Dermatology, Gandhi Medical College and Hospital, Musheerabad, Hyderabad - 500048
|How to cite this article:
Konda C, Rao AG. Colchicine in dermatology. Indian J Dermatol Venereol Leprol 2010;76:201-205
Colchicine, a toxic natural product, which is the active principle of the plant, Colchicum autumnale (autumn crocus or meadow saffron), and other plants of Colchiaceae family. It is a nitrogen-containing substance often described erroneously as an alkaloid, although its biosynthetic precursor, demecolcine, is an alkaloid.  It has been known since antiquity for its medicinal uses. It is still in use today for the treatment of gout and familial Mediterranean fever.  Under suitable qualified medical supervision, isolates from the seeds and tubers of these plants have been used in the treatment of certain skin disorders. Colchicine, was first isolated in 1820 by the two French chemists P.S. Pelletier and J. Caventon.  We briefly review here the pharmacological and the therapeutic profiles of colchicine in dermatology.
Mechanism of Action
Anti-mitoticIts capacity to interrupt mitosis is due to its linkage to dimers of tubulin, a dimeric protein in microtubules.  The microtubular toxicity will cause cessation of mitosis in metaphase and interference in cellular mobility.
Anti-inflammatoryColchicine reduces mobility, adhesiveness, and chemotaxis of polymorphonuclear cells. It interferes with intercellular adhesion molecules, selectins, thus inhibiting T-lymphocyte activation and its adhesion to endothelial cells. ,
It impairs cellular secretion of procollagen and increases collagenase production that promotes a larger collagenolytic action. 
Immunosuppressive actionIt inhibits cell-mediated immune responses,  by inhibiting immunoglobulin secretion, IL-1 production, histamine release and HLA-DR expression.
Other pharmacological effects Decrease of the corporal temperature, depression of the respiratory center, increased response to sympathomimetic agents, contraction of blood vessels, hypertension by central vasomotor stimulation, and alteration of the neuromuscular function. [Figure - 1]
Pharmacology and Pharmacokinetics
It occurs as pale to greenish yellow crystals or powder. When exposed to ultra-violet radiation, it oxidizes into a dark color  and is transformed into different photoisomers.  Hence, it must be shielded from exposure to sunlight. It is rapidly absorbed when taken orally; peak plasma levels are reached between 30 and 120 min after ingestion. Fifty percent of the drug circulates and links to plasma proteins. The drug is metabolized in the liver, and the majority is eliminated through bile in the feces. It is also distributed in spleen and kidney. Overall, 10-20% of the dose is eliminated unchanged in the urine.
Dosages and Administration
Acute goutInitial dose is 1 mg, reduced to 0.5 mg every 2-3 h, until pain relief is achieved or gastrointestinal toxicity occurs. Course may be repeated after at least 3 drug-free days. Maximum dose: 6 mg/course. Should be stored in an airtight container and protected from light. Initiation of allopurinol treatment must be preceded by daily oral colchicine for at least 2 weeks. This is done as sudden discontinuation of allopurinol results in rapid re-elevation of serum uric acid to pre-treatment levels. Continuation of colchicine for several weeks or months after initiation of allopurinol is recommended by most experts. In patients with tophi, it is advised to continue colchicine prophylaxis until all tophi have dissolved, which often takes years.
Prophylaxis of recurrent gouty arthritisAdult: 0.5-0.6 mg once daily. Dosage range: 0.6 mg every other day to 0.6 mg tid.
Intravenous preparation (iv)It is given in 0.9% saline (but not in 5% dextrose as it may precipitate) in a dose of 0.5 mg/mL (2 mL). Single intravenous dosages should not exceed 2-3 mg, and cumulative total dosages for an attack should not be more than 4-5 mg. The administration of iv colchicine is contraindicated in patients with renal failure, extrahepatic biliary obstruction, or patients with combined renal and hepatic insufficiency. Although not approved by the Food and Drug Administration (FDA), intravenous (iv) colchicine has been an accepted treatment for acute gout symptoms. Several additional iv uses include treatment of familial Mediterranean fever, pericarditis, primary biliary cirrhosis, amyloidosis, and Behçet′s syndrome. ,,
It should not be given intramuscularly or subcutaneously, as it causes severe local irritation.
Uses in Dermatology
Until now, there was no formal indication approved by the FDA for colchicine use in dermatology; however, several uncontrolled studies have showed exciting results [Table - 1], mainly in neutrophilic dermatoses.
GoutColchicine controls acute attacks by suppressing monosodium urate crystal-induced NACHT-LRR-PYD-containing protein-3 (NALP3) inflammasome-driven caspase-1 activation, IL-1b processing and release, and L-selectin expression on neutrophils.  It will not prevent the formation of cutaneous tophi and may, actually increase the development of tophi, by preventing the inflammatory response. Hence, hyperuricemia must be controlled at the same time.
Papulosquamous DermatosesPsoriasis was one of the first cutaneous diseases to be treated with colchicine. Wahba and Cohen used oral colchicine in 22 psoriasis patients and found greater than 50% improvement in 11 patients. The results were better in those whose lesions were small papules and plaques.  Kaidbey et al. observed usefulness of topical colchicine in patients with recalcitrant plaque psoriasis.  This drug is effectively used in psoriatic arthritis.  However, it was not found beneficial in a larger study. Colchicine was found to be effective in generalized pustular psoriasis and palmoplantar pustulosis. ,, It is likely that colchicine has a limited therapeutic value in psoriasis.
Recurrent aphthous stomatitisColchicine in the dose of 0.6 mg twice or thrice daily was found to decrease morbidity. 
Behcet′s syndromeColchicine was found to be effective in Behcet′s syndrome in the treatment of ocular, articular, oral, and genital lesions. ,, It was postulated that by blocking phagocytosis, colchicine may increase superoxide scavenging activity of neutrophils which is impaired in this syndrome.
Sweet′s syndromeImprovement with a daily dose of 1.5 mg colchicine was found in Sweet′s syndrome. 
Bullous diseasesSeveral bullous diseases can be treated with colchicine.
Dermatitis herpetiformisSilvers et al. used colchicine at the dose of 1.2-1.8 mg/day to treat patients with dermatitis herpetiformis.  They found it useful as alternate therapy in those who could not take sulfonamides.
Linear IgA diseaseAram found colchicine to be very useful in patients who failed to respond to dapsone.  The good response to colchicine in this disease may be based on the fact that there are many neutrophils.
Epidermolysis bullosa acquisita (EBA)Megahed and Scharrffetter-Kochanek described successful treatment of EBA with colchicine. 
Chronic bullous dermatosis of childhoodColchicine was found to be very useful in chronic bullous dermatosis of childhood (CBDC) with G6PD deficiency. 
In all the immunobullous dermatoses listed where colchicine is used, dapsone is the better choice and colchicine is an alternative where the patient cannot take dapsone due to G6PD deficiency or some other reason or dapsone is not effective in a particular patient.
Leucocytoclastic vasculitis (LCV) and Urticarial vasculitis Several case reports have described the beneficial effects of colchicine in this condition with involvement of the skin, with or without joint manifestations, and also in urticarial vasculitis.  Colchicine was effective in urticarial vasculitis associated with hypocomplementemia. It reduces neutrophilic chemotaxis and motility in both these conditions.
SclerodermaSome authors have described beneficial effects in localized and systemic scleroderma,  whereas others have not. Colchicine′s action on production, regulation of collagen, adhesion molecules, and matrix digester enzymes justifies its use in this disease.
AmyloidosisCutaneous lesions develop in upto 40% of patients with systemic amyloidosis, both primary and secondary. This drug prevents amyloid deposition and slows disease progression in amyloidosis associated with familial Mediterranean fever.  Amyloid originates from degenerated epidermal cells in susceptible subjects. Colchicine probably blocks the release of lysosomal enzymes within these cells thereby preventing conversion of the cells tonofilaments into amyloid.  Oral colchicine is useful in the management of primary cutaneous amyloidosis. 
Miscellaneous Colchicine was found to be effective in erythema nodosum leprosum, , pyoderma gangrenosum,  severe cystic acne,  calcinosis cutis,  keloids, sarcoid, condyloma acuminata,  fibromatosis,  relapsing polychondritis,  primary anetoderma,  subcorneal pustular dermatosis,  erythema nodosum,  scleredema,  and actinic keratosis. 
Colchicine is usually well tolerated. Gastrointestinal (GI) adverse effects are the most frequent and include diarrhea, nausea, vomiting, and abdominal pain. The GI side effects are due to increase in gut motility by neural mechanisms as well as by inhibition of mitosis in its rapid turnover mucosa. Symptoms decrease on reducing the dose. The iv administration of the drug avoids the occurrence of these gastrointestinal side effects. Long-term therapy may induce steatorrhea, malabsorption with reduced absorption of vitamin B 12 , fat, sodium, potassium, nitrogen, xylose, and other actively transported sugars. It can cause decreased serum cholesterol and carotene concentrations.
Bone marrow suppression -agranulocytosis, thrombocytopenia, and aplastic anemia occurs after prolonged treatment. Colchicine-induced leukopenia occurs with accidental or intentional overdose and prompt administration of G-CSF must be considered in such cases.
Myopathy and neuropathy occur particularly in patients with renal impairment. Colchicine induces autophagic vacuolar changes in muscle. Myopathy presents as proximal muscle weakness, with rise in creatinine phosphokinase, abnormal proximal muscle fibrillations, and axonal neuropathy. Myopathy recovers on withdrawal of colchicine. Neuropathy resolution is more prolonged. Azoospermia is a reported side effect. 
Dermatological adverse effects include urticaria,  toxic epidermal necrolysis,  and precipitation of porphyria cutanea tarda. Alopecia occurs 2-3 weeks after the onset of therapy and involves face, axilla, and pubic area. 
Colchicine has been known for centuries as a poison. Advice on the dangers of colchicine varies from one source to the next. Until recently, there was no maximum dose of colchicine stated in the approved dosage guidelines. There have been published cases of death occurring after colchicine doses as little as 6 or 7 mg.  Overdosage can lead to cholera-like syndrome with dehydration, hypokalemia, hyponatremia, metabolic acidosis, renal failure, and ultimately shock. Respiratory distress syndrome, disseminated intravascular coagulation, and bone marrow suppression occur. Patients may develop convulsions, delirium, muscle weakness, neuropathy, and muscle paralysis. After prolonged therapy, leukopenia, aplastic anemia, myopathy and alopecia can occur. Colchicine intoxication is characterized by multi-organ involvement and by the poor prognosis associated with administration of large amounts of the drug. Therapy is basically supportive and symptomatic because of the rapid distribution and binding of colchicine to the affected tissues. Use of anticolchicine antibodies is a novel approach still in an experimental stage. 
The coadministration of colchicine with known inhibitors or substrates of CYP3A4 may inhibit its metabolism resulting in toxicity such as by macrolide antibiotics. It may increase the serum concentration of cyclosporine, and verapamil, and vice versa. It may cause malabsorption of vitamin B 12 leading to megaloblastic anemia. Coadministration of simvastatin with colchicine may induce acute myopathy. 
It is suggested that complete blood counts, platelet count, serum multiphasic analysis (i.e. tests of renal and hepatic function), and urinalysis be performed at least every 3 months. Monthly laboratory monitoring for the first few months of therapy is a reasonable protocol. Colchicine should not be used during pregnancy (risk of teratogenicity) 
Colchicine has many useful actions in dermatological disorders and is well tolerated. Although colchicine is not a first-line medication for any of the conditions mentioned, we are more likely to use it early in patients with leukocytoclastic vasculitis, Sweet′s syndrome, and aphthous ulcers. This medication is inexpensive and safe in moderate doses than most immunosuppressive agents.
BoDD (Botanical Dermatology Database) monographs (COLCHICACEAE) latest update:03 Jan 2009.[Google Scholar]
Surajana G, Bhattacharyya B. The colchicine -tubulin interaction: A review. Curr Sci 1997;73:1.[Google Scholar]
Pelletier PS, Caventon J. [Title unknown]. Ann Chim Phys 1820;14:69.[Google Scholar]
Davis S. Newer uses of older drugs -an update. In: Wolverton S, editor.Comprehensive dermatologic drug therapy. Indianapolis: WB Saunder; 2001. p. 426-44.[Google Scholar]
Cronstein BN, Molad Y, Reibman J, Balakhane E, Levin RI, Weissmann G. Colchicine alters the quatitative and qualitative display of selectins on endothelial cells and neutrophils. J Clin Invest 1995;96:994-1002.[Google Scholar]
Perico N, Ostermann D, Bontempeill M, Morigi M, Amuchastegui CS, Zoja C, et al. Colchicine interferes with L-selectin and leukocyte function-associated antigen-1 expression on human T lymphocytes and inhibits T cell activation. J Am Soc Nephrol 1996;7:594-601.[Google Scholar]
Sabroe R. Colchicine. In: Wakelin SH, Maibach HI, editors. Handbook of systemic drug treatment in dermatology. London: Manson; 2003. p.105.[Google Scholar]
Mekori YA, Baram D, Goldberg A, Klajman A. Inhibition of delayed hypersensitivity reactions in mice by colchicine. I. Mechanism of inhibition of contact sensitivity in vivo. Cell Immunol 1989;120:330-40.[Google Scholar]
Sullivan TP, King LE Jr, Boyd AS. Colchicine in dermatology. J Am Acad Dermatol 1998;39:993-9.[Google Scholar]
Sagorin C, Ertel NH, Wallace SL. Photoisomeration of colchicine. Loss of significant antimitotic activity in human lymphocytes. Arthritis Rheum 1972;15:213-7.[Google Scholar]
Simons RJ, Kingma DW. Fatal colchicine toxicity. Am J Med 1989;86:356-7.[Google Scholar]
Bonnel RA, Villalba ML, Karwoski CB, Beitz J. Deaths associated with inappropriate intravenous colchicine administration. J Emerg Med 2002;22:385-7.[Google Scholar]
Simmons JW, Harris WP, Koulisis CW, Kimmich SJ. Intravenous colchicine for low back pain: a double-blind study. Spine (Phila Pa 1976) 1990;15:716-7.[Google Scholar]
Nuki G. Colchicine: Its mechanism of action and efficacy in crystal-induced inflammation. Curr Rheumatol Rep 2008;10:218-27.[Google Scholar]
Wahba A, Cohen H. Therapeutics trials with oral colchicines in psoriasis. Acta Derm Venereol 1980;60:515-20.[Google Scholar]
Kaidbey KH, Petrozzi JW, Kligman AM. Topical colchicine therapy for recalcitrant psoriasis. Arch Dermatol 1975;111:33-6.[Google Scholar]
Seideman P, Fjellner B, Johannesson A. Psoriatic arthritis treated with oral colchicine. J Rheumatol 1987;14:777-9.[Google Scholar]
Horiguchi M, Takigawa M, Imamura S. Treatment of generalized pustular psoriasis with methotrexate and colchicine. Arch Dermatol 1981;117:760.[Google Scholar]
Zachariae H, Kragballe K, Herlin T. Colchicine in generalized pustular psoriasis: clinical response and antibody-dependent cytotoxicity by monocytes and neutrophils. Arch Dermatol Res 1982;274:327-33.[Google Scholar]
Mori S, Hino K, Izumi H, Hino H. Clinical manifestations and treatment of pustulosis palmaris et plantaris. J Dermatol 1976;86:671.[Google Scholar]
Katz J, Langevitz P, Shemer J, Barak S, Livneh A. Prevention of recurrent aphthous stomatitis with colchicine: an open trial. J Am Acad Dermatol 1994;31:459-61.[Google Scholar]
Mangelsdorf HC, White WL, Jorizzo JL. Behcet's disease. Report of 25 patients from the United States with prominent mucocutaneous involvement. J Am Acad Dermatol 1996;34:745-50.[Google Scholar]
Aktulga E, Altaç M, Müftüoglu A, Ozyazgan Y, Pazarli H, Tüzün Y, et al. A double blind study of colchicine in Behcet's disease. Haematologica 1980;65:399-402.[Google Scholar]
Sander HM, Randle HW. Use of colchicine in Behçet's syndrome. Cutis 1986;37:344-8.[Google Scholar]
Suehisa S, Tagami H. Treatment of acute febrile neutrophilic dermatosis (Sweet's syndrome) with colchicine. Br J Dermatol 1981;105:483.[Google Scholar]
Silvers DN, Juhlin EA, Berczeller PH, McSorley J. Treatment of dermatitis herpetiformis with colchicine. Arch Dermatol 1980;116:1373-4.[Google Scholar]
Aram H. Linear IgA bullous dermatosis: Successful treatment with colchicine. Arch Dermatol 1984;120:960-1.[Google Scholar]
Megahed M, Scharffetter-Kochanek K. Epidermolysis bullosa acquisita: Successful treatment with colchicine. Arch Dermatol Res 1994;286:35-46.[Google Scholar]
Zeharia A, Hodak E, Mukamel M, Danziger Y, Mimouni M. Successful treatment of chronic bullous dermatosis of childhood with colchicine. J Am Acad Dermatol 1994;30:660-1.[Google Scholar]
Wiles JC, Hansen RC, Lynch PJ. Urticarial vasculitis treated with colchicine. Arch Dermatol 1985;121:802-5.[Google Scholar]
Bibas R, Gaspar NK, Ramos-e-Silva M. Colchicine for dermatological diseases. J Drugs Dermatol 2005;4:196-204.[Google Scholar]
Zemer D, Pras M, Sohar E, Modan M, Cabili S, Gafni J. Colchicine in the prevention and treatment of the amyloidosis of familial Mediterranean fever. N Engl J Med 1986;314:1001-5.[Google Scholar]
Nath D. Probable mechanism of action of colchicine in macular and lichen amyloidosis. Indian J Dermatol Venereol Leprol 1999;65:48-9.[Google Scholar]
Chakravarty K, Chanda M. Role of colchicine in primary localised cutaneous amyloidosis. Indian J Dermatol Venereol Leprol 1995;61:268-9.[Google Scholar]
Kar HK, Roy RG. Comparison of colchicine and aspirin in the treatment of type 2 lepra reaction. Lepr Rev 1988;59:201-3.[Google Scholar]
Sarojini PA, Mshana RN. Use of colchicine in the management of erythema nodosum leprosum. Lepr Rev 1983;54:151-3.[Google Scholar]
Rampal P, Benzaken S, Schneider S, Hebuterne X. Colchicine in pyoderma gangrenosum. Lancet 1998;351:1134-5.[Google Scholar]
Jeong S, Lee CW. Acne conglobata: Treatment with isotretinoin, colchicine, and cyclosporin as compared with surgical intervention. Clin Exp Dermatol 1996;21:462-3.[Google Scholar]
Fuchs D, Fruchter L, Fishel B, Holtzman M, Yaron M. Colchicine suppression of local inflammation due to calcinosis in dermatomyositis and progressive systemic sclerosis. Clin Rheumatol 1986;5:527-30.[Google Scholar]
Von Krogh G. Topical treatment of penile condyloma acuminata with podophyllin, podophyllotoxin and colchicine. Acta Dermatol Venereol 1978;58:163-8.[Google Scholar]
Dominguez-Malagon HR, Alfeiran-Ruiz A, Chavarria-Xicotencatl P, Duran-Hernandez MS. Clinical and cellular effects of colchicine in fibromatosis. Cancer 1992;69:2478-83.[Google Scholar]
Eng AM, Reddy VB. Relapsing polychondritis responding to colchicine. Int J Dermatol 1994;33:448-9.[Google Scholar]
Braun RP, Borradori L, Chavaz P, Masouyé I, French L, Saurat JH. Treatment of primary anetoderma with colchine. J Am Acad Dermatol 1998;38:1002-3.[Google Scholar]
Pavithran K. Colchicine in the treatment of subcorneal pustular dermatosis. Indian J Dermatol Venereol Leprol 1995;61:56-7.[Google Scholar]
Wallace SL. Erythema nodosum treatment with colchicine. JAMA 1967;202:1056.[Google Scholar]
Gruson LM, Franks A Jr. Scleredema and diabetic sclerodactyly. Dermatol Online J 2005;11:3.[Google Scholar]
Grimaître M, Etienne A, Fathi M, Piletta PA, Saurat JH. Topical colchicine therapy for actinic keratoses. Dermatology 2000;200:346-8.[Google Scholar]
Merlin HE. Azoospermia caused by colchicine. A case report. Fertil Steril 1972;23:180-1.[Google Scholar]
Cabili S, Shemer Y, Revach M. Allergic reaction and desensitization of colchicine in familial Mediterranean fever. Rheumatologie 1982;12:207.[Google Scholar]
Arroyo MP, Sanders S, Yee H, Schwartz D, Kamino H, Strober BE. Toxic epidermal necrolysis-like reaction secondary to colchicine overdose. Br J Dermatol 2004;150:581-8.[Google Scholar]
Malkinson FD, Lynfield YL. Colchicine alopecia. J Invest Dermatol 1959;33:371-84.[Google Scholar]
Macleod JG, Phillips L. Hypersensitivity to colchicine. Ann Rheum Dis 1947;6:224-9.[Google Scholar]
Putterman C, Ben-Chetrit E, Caraco Y, Levy M. Colchicine intoxication:clinical pharmacology, risk factors, features and management. Semin Arthritis Rheum 1991;21:143-55.[Google Scholar]
Porter RS, editor. Colchicine drug information-2008. The merck manual's online medical library: Merck Research Laboratories: 2004.[Google Scholar]
Callen JP, af Ekenstam E. Cutaneous leukocytoclastic vasculitis: clinical experience in 44 patients. South Med J 1987;80:848-85.[Google Scholar]