NORD is very grateful to Mark Lebwohl, MD, Professor and Chairman, Department of Dermatology, The Mount Sinai School of Medicine, for assistance in the preparation of this report.
Synonyms of Pyoderma Gangrenosum
- No synonyms found.
- No subdivisions found.
Pyoderma gangrenosum (PG) is an inflammatory skin disorder that is characterized by small, red bumps or blisters (papules or nodules) that eventually erode to form swollen open sores (ulcerations). The size and depth of the ulcerations vary greatly, and they are often extremely painful. In approximately 50 percent of cases, PG occurs secondary to another disorder such as inflammatory bowel disease. The exact cause of PG is unknown (idiopathic). Some researchers believe it may be an autoimmune disorder.
Pyoderma gangrenosum often begins as small, quick-spreading reddish or purple colored bumps or blisters. These small growths eventually develop into swollen, open sores (ulcerations) with a well-defined blue or violet-colored border. The size and depth of ulcerations vary. Ulcerations may spread, widen and deepen and may become extremely painful. In individual cases, ulcerations may continue to spread, remain unchanged, or heal without treatment (spontaneously).
Ulcerations can affect any part of the body and have been classified into four variants: classic, atypical/bullous, pustular, and vegetative.
Classic pyoderma gangrenosum most often occurs on the legs and is characterized by deep ulcerations. These lesions often begin as small pus-filled bumps (pustules) that enlarge and spread rapidly. This form of the disease is often very painful and may also affect the trunk, penis, head and neck areas.
Classic PG also occurs near surgical openings (stoma sites) in the body. This condition is referred to as peristomal pyoderma gangrenosum.
Atypical or bullous pyoderma gangrenosum is characterized by superficial blisters (bullae). This form of the disease most often affects the hands and is often associated with an underlying disorder especially hematological malignancy such as leukemia. Some cases that have been called atypical pyoderma gangrenosum actually represent Sweet syndrome.
Classic pyoderma gangrenosum is often characterized by the presence of pus and can begin with pustules. Pustular pyoderma gangrenosum is characterized by painful bumps (pustules) most often found on the arms and legs. These lesions eventually develop into ulcerations. This form is often associated with inflammatory bowel disease.
Vegetative pyoderma gangrenosum is characterized by chronic ulcerations that are not usually painful.
Additional findings sometimes associated with PG include fever, localized tenderness, joint pain (arthralgia), and a general feeling of ill health (malaise). PG may occur as a secondary characteristic of another disorder, most oftenulcerative colitis or Crohn's disease.
The exact cause of pyoderma gangrenosum is unknown (idiopathic) although it is suspected to be an autoimmune disease. Autoimmune disorders are caused when the body's natural defenses (e.g., antibodies) against foreign or invading organisms begin to attack healthy tissue for unknown reasons.
Approximately 50 percent of cases of pyoderma gangrenosum are associated with other disorders, especially the inflammatory bowel diseases ulcerative colitis or Crohn's disease. Additional disorders associated with pyoderma gangrenosum include rheumatoid arthritis, acute and chronic myelogenous leukemia, myeloid metaplasia, and paraproteinemias.
In some cases the development of pyoderma gangrenosum follows surgery or trauma. This condition is known as pathergy.
Pyoderma gangrenosum affects women slightly more often than men. It occurs most often between the ages of 20 to 50 years. Infants or adolescents account for fewer than 4 percent of cases. One estimate places the incidence of PG at 1 in every 100,000 people in the United States.
Symptoms of the following disorders can be similar to those of pyoderma gangrenosum. Comparisons may be useful for a differential diagnosis:
Sweet syndrome is a rare skin disorder characterized by fever, inflammation of the joints (arthritis), and the sudden onset of a rash. The rash consists of bluish-red, tender papules that usually occur on the arms, legs, face or neck, most often on one side of the body (asymmetric). In many cases, Sweet syndrome occurs by itself for no known reason (idiopathic). In some cases, the disorder is associated with an underlying malignancy, usually a hematologic malignancy such as certain types of leukemia. The exact cause of Sweet syndrome is unknown. (For more information on this disorder, choose "Sweet" as your search term in the Rare Disease Database).
Cutaneous sporotrichosis is a chronic yeast infection under the skin (subcutaneous) spread by way of the lymph glands and caused by the bacteria known as Sporothrix Schenckii. The disease may remain localized or may become generalized, involving bones, joints, lungs, and the central nervous system. Lesions may be grainy, full of pus, ulcerative or draining.
The following disorders may precede the development of pyoderma gangrenosum. They can be useful in identifying an underlying cause of some forms of this disorder:
Ulcerative colitis is a non-specific inflammatory disease of the bowel characterized by chronic ulceration. The chief characteristic of this disorder is bloody diarrhea. This disease is of unknown cause. It generally begins in the area of the rectum, but may involve the entire large bowel. Ulcerative colitis is usually chronic, with acute inflammation of the colon. It is characterized by multiple, irregular superficial ulcerations, thickening of the wall of the colon with scar tissue, and polyps. (For more information on this disorder, choose "Ulcerative Colitis" as your search term in the Rare Disease Database.)
Crohn's disease is a form of inflammatory bowel disease, characterized by severe chronic inflammation of the wall of the small intestine, but it can involve any part of the gastrointestinal tract. The symptoms include fatigue, anorexia, weight loss, abdominal pain, and chronic diarrhea. Less commonly, there is inflammation of the mucosa of the mouth, the esophagus, or stomach. Regional lymph nodes can become involved. A solid mass may be felt in the abdomen during acute stages of the disease. (For more information on this disorder, choose "Crohn" as your search term in the Rare Disease Database.)
No specific diagnostic tests exist for pyoderma gangrenosum. Diagnosis is made by excluding similar disorders based upon a thorough clinical evaluation, a detailed a patient history and a variety of tests such as surgical removal and microscopic evaluation of affected tissue (biopsy).
Treatment of PG consists of open wet dressings on the ulcers and topical application of anti-inflammatory creams and ointments such as corticosteroids. The skin must be protected from any other injury that could result in development of additional ulcers. In some cases, the grafting of new skin to the wound may be recommended once the inflammation is controlled.
Additional treatment of PG includes the administration of corticosteroid drugs such as methylprednisolone and prednisone. Corticosteroids may be administered by intramuscular injection or orally or by intralesional injection directly into the pyoderma gangrenosum.
According to some researchers, individuals with a past history of PG should receive preventive (prophylactic) treatment with corticosteroids before undergoing surgery because surgery may cause a recurrence of the disorder.
Immunosuppressive therapies (drugs that suppress the immune system) are sometimes used to treat people with pyoderma gangrenosum. Cyclosporine is effective for many patients. Azathioprine and cyclophosphamide are also immunosuppressive drugs that have been used to treat PG. In recent years drugs known as tumor necrosis factor inhibitors have been used very successfully to treat pyoderma gangrenosum. Infliximab and adalimumab have been most successful.
Antibacterial agents such as Dapsone may also be administered. In some cases surgical treatment of the underlying disorder such as ulcerative colitis has alleviate symptoms of pyoderma gangrenosum.
Additional treatment is symptomatic and supportive.
Researchers are studying the use of the orphan drug thalidomide as a treatment for pyoderma gangrenosum. Thalidomide can have severe effects on a developing fetus and must be administered with extreme caution. More studies are needed to determine the long-term safety and effectiveness of this treatment. For more information, contact:
7 Powder Horn Drive
Warren, NJ 07059
Tollfree: (888) 423-5436
Thalidomide is available in England under special license from Penn Pharmaceuticals of South Tredegar, South Wales.
Additional drugs that have been explored as potential treatments for individuals with PG include tacrolimus, ustekinumab, chlorambucil, clofazimine, mycophenolate mofetil, and intravenous immune globulin. More research is necessary to determine the long-term safety and effectiveness of these treatments for individuals with PG.
Information on current clinical trials is posted on the Internet at www.clinicaltrials.gov. All studies receiving U.S. Government funding, and some supported by private industry, are posted on this government web site.
For information about clinical trials being conducted at the NIH Clinical Center in Bethesda, MD, contact the NIH Patient Recruitment Office:
Tollfree: (800) 411-1222
TTY: (866) 411-1010
For information about clinical trials sponsored by private sources, contact:
Pyoderma Gangrenosum Resources
NORD Member Organizations:
(To become a member of NORD, an organization must meet established criteria and be approved by the NORD Board of Directors. If you're interested in becoming a member, please contact Susan Olivo, Membership Manager, at firstname.lastname@example.org.)
Lebwohl MG, Gohara M. Pyoderma Gangrenosum. In: NORD Guide to Rare Disorders. Philadelphia, PA: Lippincott Williams & Wilkins; 2003:134-5.
Bennett JC, Plum F, eds. Cecil Textbook of Medicine. 20th ed. Philadelphia, PA: W.B. Saunders Co; 1996:2212.
Yamada T, et al., eds. Textbook of Gastroenterology. 2nd ed. Philadelphia, PA: J.B. Lippincott Company; 1995:955-56.
Champion RH, et al., eds. Textbook of Dermatology. 5th ed. Cambridge, MA: Blackwell Scientific Publications; 1992:1922-26.
Brooklyn TN, Dunnill GS. Shetty A, et al. Infliximab for the treatment of pyoderma gangrenosum: a randomized, double-blind placebo-controlled trial. Gut. 2006;55(4):505-9.
Vujnovich A. Clinical treatment options for peristomal pyoderma gangrenosum. Br J Nurs. 2005;14:S4-8.
Burton J. Case study: diagnosis and treatment of pyoderma gangrenosum. Br J Nurs. 2005;14:S10-3.
Reichrath J, Bens G, Bonowitz A, Tilgen W. Treatment recommendations for pyoderma gangrenosum: an evidence-based review of the literature based on more than 350 patients. J Am Acad Dermatol. 2005;53:273-83.
Nyback H, Olsen AG, Karlsmark T, Jemec GB. Topical therapy for peristomal pyoderma gangrenosum. J Cutan. Med Surg. 2004;8:220-3.
Hughes AP, et al. Clinical features and treatment of peristomal pyoderma gangrenosum. JAMA. 2000;284:1546-48.
Federman GL, et al. Recalcitrant pyoderma gangrenosum treated with thalidomide. Mayo Clin Proc. 2000;75:842-44.
Coors EA, et al. Pyoderma gangrenosum in a patient with autoimmune haemolytic anaemia and complement deficiency. Br J Dermatol. 2000;143:154-56.
MacKenzie D, et al. Pyoderma gangrenosum following breast reconstruction. Br J Plast Surg. 2000;53:441-43.
Hensley CD, et al. Neutrophilic dermatoses associated with hematologic disorders. Clin Dermatol. 2000;18:355-67.
Lyon CC, et al. Parastomal pyoderma gangrenosum: clinical features and management. J Am Acad Dermatol. 2000;42:992-1002.
Powell FC, et al. Pyoderma gangrenosum. Clin Dermatol. 2000;18:283-93.
Bennett ML, et al. Pyoderma gangrenosum. A comparison of typical and atypical forms with an emphasis on time to remission. Case review of 86 patients from 2 institutions. Medicine (Baltimore). 2000;79:37-46.
Hafner J, et al. Management of vasculitic leg ulcers and pyoderma gangrenosum. Curr Probl Dermatol. 1999;27:271-76.
V'lckova-Laskoska MT, Laskoski DS, Caca-Biljanovska NG, Darkoska JS. Pyoderma gangrenosum successfully treated with cyclosporin A. Adv Exp Med Biol. 1999;455:541-45.
Armstrong PM, et al. Pyoderma gangrenosum. A diagnosis not to be missed. J Bone Joint Surg Br. 1999;81:893-94.
von den Driesch P. Pyoderma gangrenosum: a report of 44 cases with follow-up. Br J Dermatol. 1997;137:1000-05.
Jackson JM. Pyoderma Gangrenosum. Emedicine. http://emedicine.medscape.com/article/1123821-overview. Updated March 23, 2010. Accessed March 2, 2012.
Wollina U. Pyoderma Gangrenosum. Oprhanet. http://www.orpha.net/data/patho/GB/uk-Pyoderma-Gangrenosum.pdf . Updated February 2005. Accessed March 2, 2012.
Wines N, Wines M, Ryman W. Understanding pyoderma gangrenosum: a review. Medscape General Medicine. 2001;3(2). http://www.medscape.com/viewarticle/408145. Accessed March 2, 2012.
The information in NORD’s Rare Disease Database is for educational purposes only. It should never be used for diagnostic or treatment purposes. If you have questions regarding a medical condition, always seek the advice of your physician or other qualified health professional. NORD’s reports provide a brief overview of rare diseases. For more specific information, we encourage you to contact your personal physician or the agencies listed as “Resources” on this report.
The National Organization for Rare Disorders (NORD) web site, its databases, and the contents thereof are copyrighted by NORD. No part of the NORD web site, databases, or the contents may be copied in any way, including but not limited to the following: electronically downloading, storing in a retrieval system, or redistributing for any commercial purposes without the express written permission of NORD. Permission is hereby granted to print one hard copy of the information on an individual disease for your personal use, provided that such content is in no way modified, and the credit for the source (NORD) and NORD’s copyright notice are included on the printed copy. Any other electronic reproduction or other printed versions is strictly prohibited.
Copyright ©1988, 1989, 1992, 1995, 1997, 1998, 2000, 2006, 2009, 2012
Report last updated: 2012/03/19 00:00:00 GMT+0
NORD's Rare Disease Information Database is copyrighted and may not be published without the written consent of NORD.