Erythema gyratum repens

WikiDoc Resources for Erythema gyratum repens
Articles
Most recent articles on Erythema gyratum repens Most cited articles on Erythema gyratum repens Review articles on Erythema gyratum repens Articles on Erythema gyratum repens in N Eng J Med, Lancet, BMJ
Media
Powerpoint slides on Erythema gyratum repens Images of Erythema gyratum repens Photos of Erythema gyratum repens Podcasts & MP3s on Erythema gyratum repens Videos on Erythema gyratum repens
Evidence Based Medicine
Cochrane Collaboration on Erythema gyratum repens Bandolier on Erythema gyratum repens TRIP on Erythema gyratum repens
Clinical Trials
Ongoing Trials on Erythema gyratum repens at Clinical Trials.gov Trial results on Erythema gyratum repens Clinical Trials on Erythema gyratum repens at Google
Guidelines / Policies / Govt
US National Guidelines Clearinghouse on Erythema gyratum repens NICE Guidance on Erythema gyratum repens NHS PRODIGY Guidance FDA on Erythema gyratum repens CDC on Erythema gyratum repens
Books
Books on Erythema gyratum repens
News
Erythema gyratum repens in the news Be alerted to news on Erythema gyratum repens News trends on Erythema gyratum repens
Commentary
Blogs on Erythema gyratum repens
Definitions
Definitions of Erythema gyratum repens
Patient Resources / Community
Patient resources on Erythema gyratum repens Discussion groups on Erythema gyratum repens Patient Handouts on Erythema gyratum repens Directions to Hospitals Treating Erythema gyratum repens Risk calculators and risk factors for Erythema gyratum repens
Healthcare Provider Resources
Symptoms of Erythema gyratum repens Causes & Risk Factors for Erythema gyratum repens Diagnostic studies for Erythema gyratum repens Treatment of Erythema gyratum repens
Continuing Medical Education (CME)
CME Programs on Erythema gyratum repens
International
Erythema gyratum repens en Espanol Erythema gyratum repens en Francais
Business
Erythema gyratum repens in the Marketplace Patents on Erythema gyratum repens
Experimental / Informatics
List of terms related to Erythema gyratum repens

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Synonyms and keywords: Gammel's disease.

Historical Perspective

• The association between cutaneous manifestations and systemic malignancies was first studied in 1925 by Rothman, the Hungarian investigative dermatologist, who wrote a comprehensive review on this subject and since then, cases were added to proof for the relationship between internal neoplasm and some skin lesions.
• Erythema gyratum repens was first described by Dr. John A Gammel, the dermatologist, who was trained to link bizarre or recalcitrant dermatoses to internal malignancy, In 1952, in a 55-year-old patient who had been complaining of pruritic scaly skin eruption and diagnosed nine months later with poorly differentiated adenocarcinoma of the breast with metastasis to axillary lymph nodes.
• In 1950, Dr. Gammel presented his case of Erythema gyratum repens before the Cleveland Dermatological Society as Erythema gyratum migrans then he changed the term to erythema gyratum repens because the eruption does not "migrate" from one place to another but "crawls" constantly in the areas involved, like "ants on an anthill".
• In 1973, 45 year old man was diagnosed with erythema gyratum repens associated with metastatic, undifferentiated adenocarcinoma which was removed following a right- sided craniotomy. The patient was misdiagnosed with erythema perstans and the malignancy was discovered after 8 months of the skin manifestations.
• Up to 1992, there were only 49 cases in the literature, 41 of which (84%) were associated with a neoplasm and that is why erythema gyratum repens has been considered as a paraneoplastic syndrome.
• Between 1990 and 2010, a literature review was done by collecting data from the medical records of patients form dermatology department in University of Genoa and from databases as pubmed and medline, to conclude that erythema gyratum repens is no longer considered as an obligate paraneoplastic syndrome. More than expected cases of EGR were found with no neoplasm association.

Classification

• Erythema gyratum repens has no established system for the classification. However, we can classify erythema gyratum repens based on its association with systemic malignancy as:
  • Paraneoplastic EGR
    • Erythema gyratum repens is associated with internal malignancy in 82% of cases.
  • Non-paraneoplastic EGR could be:
    • Idiopathic EGR
    • EGR-like eruptions (different dermatologic lesions that mimic EGR).
      • Can appear in various autoimmune conditions.
      • Characterized by annular lesions with expanding concentric pattern and coalescing to form a zebra-like pattern or grain of wood pattern.
      • EGR-like eruption in Sjögren syndrome (SS) is extremely rare.
    • EGR with concomitant skin disease as:
      • Pityriasis rubra pilaris, psoriasis, ichthyosis, CREST, rheumatoid arthritis, tuberculosis, bullous pemphigoid, linear IgA disease, and hypereosinophilic syndrome.
    • Drug-induced EGR examples are:
      • Azathioprine with type I autoimmune hepatitis.
      • Interferon given for hepatitis C virus–related chronic hepatitis.

• Erythema Gyratum Repens classification

Types of Erythema gyratum repens	Characterestics
Paraneoplastic EGR	Erythema gyratum repens is associated with internal malignancy in 82% of cases The most common neoplasms are: Lung/bronchogenic, esophageal, and breast cancer
Non-paraneoplastic EGR	Idiopathic EGR EGR-like eruptions EGR with concomittant skin disease Drug-induced EGR
Idiopathic EGR	EGR with no underlying malignancy, associated conditions, or precipitating cause
EGR-like eruptions	Can appear in various autoimmune conditions Characterized by annular lesions with expanding concentric pattern and coalescing to form a zebra-like pattern or grain of wood pattern EGR-like eruption in Sjögren syndrome (SS) is extremely rare
EGR with concomittant skin disease	Pityriasis rubra pilaris, psoriasis, ichthyosis, CREST, rheumatoid arthritis, tuberculosis, bullous pemphigoid, linear IgA disease, and hypereosinophilic syndrome
Drug-induced EGR	Azathioprine with type I autoimmune hepatitis Interferon given for hepatitis C virus–related chronic hepatitis

Pathophysiology

• The pathogenesis of erythema gyratum repens is unclear
• Many immunologic theories have been implicated in its pathogenesis.
• The immunologic mechanism theory is evidenced by the observed immunofluorescence patterns of IgG, C3, and C4 at the basement membrane:
  • Theory 1: the tumor induces antibodies that cross-react with the basement membrane of skin.
  • Theory 2: the tumor produces polypeptides that bind skin antigens and render them immunogenic. 
  • Theory 3: deposition of tumor antigen-antibody complexes onto the basement membrane causes reactive dermatitis seen in EGR.
• The gross appearance of the unique eruptions are:
  • Wavy erythematous concentric bands that can be figurate, gyrate, or annular
  • The bands are arranged in parallel rings and lined by a fine trailing edge of scales, a pattern often described as “wood grained”.
  • The distinctive woodgrain appearance of the eruption is pathognomonic.
  • The rash typically involves large areas of the body but tends to spare the face, hands, and feet and it can expand as fast as 1 cm a day.
  • Bullae can also form from within the areas of erythema.
• The microscopic histologic features of erythema gyratum repens are not characteristics but the following are the biopsy specimen findings that are compatible with the diagnosis:
  • The epidermis has thin atrophic patches with areas of acanthosis, focal parakeratotic horny layers, and spongiosis.
  • The dermis contains a moderate perivascular mononuclear, lymphocytic, and histiocytic infiltrate in the superficial plexus as well as mild focal spongiosis and parakeratosis.
  • Eosinophils and melanophages have also been reported in the dermal infiltrate.
  • Diffuse to moderate edema of the connective tissue can be seen.

Causes

• The exact cause of erythema gyratum repens is unknown.
• Various immunologic mechanisms suggest that erythema gyratum repens etiology is stemmed from an immunologic reaction.
• The association between erythema gyratum repens and systemic malignancy is evidenced by the disappearance of the pruritic eruptions after the treatment of the underlying neoplasm.
• The association doesn't necessarily mean causation.

Differentiating Erythema Gyratum Repens from Other Diseases

• EGR has a narrow differential diagnosis. It has to be differentiated from Reactive gyrate erythematous eruptions, such as:
  • Reactive (figurate or gyrate) erythemas that are associated with malignancy include:
    • Erythema annulare centrifugum (EAC)
    • Necrolytic migratory erythema (NME)
  • Reactive (figurate or gyrate) erythemas that are not associated with malignancy include:
    • Erythema marginatum rheumaticum
    • Erythema chronicum migrans   
    • Familial annular erythema
    • The carrier state of chronic granulomatous disease
    • Subacute cutaneous lupus erythematosus
    • Neonatal lupus erythematosus

• Reactive (figurate or gyrate) erythemas that are associated with malignancy include:
  

Disease	Erythema Characteristics	Signs and Symptoms	Associated Conditions	Histopathology	Lab finding & Other evaluation	prognosis
Erythema gyratum repens (EGR)	Migratory annular and configurate erythematous bands that form concentric rings Wood grain scaly appearance scales follows the leading edge of the bands Eruption migrates more rapidly, 1cm/d	Skin eruptions Severe Generalized itching (pruritus) Scaly erythematous patches over trunk and proximal extremities, sparing the hands, feet, and face, can eventually involve the face.    weight loss Malaise and fatigue fever anorexia Lymphadenopathy Headache and convulsion (intracranial metastasis) Shortness of breath (bronchogenic carcinoma)	Dermatologic conditions: Ichthyosis palmar/plantar hyperkeratosis Less frequently EGR copresent with: Pityriusis rubru piluris, bullous pemphigoid, pemphigus vulgaris, discoid lupus eythemutosus, psoriusiform lesions, and nonspecific vesicles and bullae Tuberculosis CREST syndrome (Calcinosis, Raynaud’s phenomenon, Esophageal Cysmotility, Sclerodactyly, and Telangiectasia)	The epidermis: Acanthosis Focal parakeratotosis and spongiosis The dermis: Mild focal spongiosis and parakeratosis Moderate perivascular mononuclear, lymphocytic, and histiocytic infiltrate Eosinophils and melanophages have also been reported in the infiltrate Diffuse to moderate edema of the connective tissue can be seen	There are no diagnostic laboratory findings associated with erythema gyratum repens Eosinophilia is observed in 60% of cases Decreased T lymphocytes and increased B lymphocytes observed in an EGR patient with increased luteinizing hormone and follicle-stimulating hormone Decreased serum levels of C3 Normal percentages of B and T lymphocytes and normal T-cell function were reported in an EGR patient without cancer	Skin manifestations can be improved within 48 hours of the resection of the underlying tumor with on of the following: Complete cure of the skin eruption and pruritus Temporary improvement then recurrence of the eruption (specially in cases of metastasis) No effect of the tumor treatment on the course of EGR Death can occur few weeks after the discovery of the malignancy, few months, or four years as in Gammel's patient.
Erythema annulare centrifugum (EAC)	Migratory annular and configurate erythematous or polycyclic lesions Urticarial in appearance, ringed, arcuate figures Eruption migrate at a slower rate (2 -3 mm/d) reaching up to 10 cm in diameter with central clearing Cover only a small percentage of the total body surface	Annular or polycyclic lesions which may begin as urticaria-like papule Eventually old lesions can spontaneously resolve in several days to a few weeks while new eruptions develop. The deep form of EAC has a firm, indurated border, is rarely pruritic, and has no scale The superficial type of EAC has an indistinct scaly border and is usually pruritic	Infections Allergic reactions to drugs	Deep form: Mononuclear, perivascular infiltrate in the middle and lower portions of the dermis (coat sleeve-like configuration) Infiltrate is primarily of lymphocytes, but eosinophils are occasionally presen Extravasation of erythrocytes is associated with endothelial swelling    No epidermal changes    Superficial: More non-specific Slight superficial perivascular lymphohistiocytic infiltrate    Focal parakeratosis and mild spongiosis with microvesiculation	No specific laboratory changes Eosinophilia of the peripheral blood, as well as tissue, can be observed in EAC associated with a drug reaction or parasitic infection    Evaluation for possible infection or drug reaction (prescribed and non-prescribed) complete blood count urinalysis Liver function tests Kidney function test	Lesions disappear after the underlying etiology is managed (allergy, infection, malignancy) if no underlying cause, lesions can recur after discontinuation of the supportive treatment
Necrolytic migratory erythema (NME)	Migratory circinate erythema/plaques with areas of necrosis and sloughing Crusted  Erythematous scaly plaques with centrifugal growth	Red erythematous scaly plaques over Perineum, distal extremities, lower abdomen, and face Spontaneous exacerbation and remission periods without knowing what the trigger is Weight loss Anemia Diabetes Diarrhea Stomatitis.	No other association Can be misdiagnosed as: Contact dermatitis Intertrigo Inverse psoriasis Zinc deficiency Other nutritional deficiencies	Paleness and spongiosis of the upper layer of the epidermis A perivascular lymphocytic and histiocytic infiltrate Necrotic keratinocytes are common and can lead to erosions, crusting and scaling	Increased glucagon level Evaluation of the associated tumor: CT or MRI abdomen * Selective visceral angiography to localize the tumor * Positron Emission tomography (PET) * Octreotide scintigraphy	Due to the difficulty of NME recognition, and its association with glucagonoma, diagnosis is usually delayed NME usually resolved after the resection and treatment of the pancreatic tumor, eg.10 days after tumor resection Early recognition is crucial for better diagnosis and prognosis

Epidemiology and Demographics

• EGR is a rare, characteristic, and paraneoplastic syndrome with the following demographics:

Age

• The average age of onset of EGR is in the seventh decade of life (65 years old).

Gender

• The male to female ratio is 2:1.

Race

• EGR commonly affects Caucasians.

Risk Factors

• There are no established risk factors for erythyma gyratum repens.
• Many patients with erythyma gyratum repens and malignancy had a history of tobacco smoking.
• Some patients with erythyma gyratum repens and malignancy have a family history of neoplasm.

Screening

• There are no screening tests for EGR.
• Screening for internal malignancy should be done immediately after EGR is diagnosed.

Natural History, Complications, and Prognosis

• The majority of patients with EGR presents with severely pruritic erythematous skin lesions that appear several months prior to the malignancy diagnosis
• If the underlying malignancy left untreated, the debilitating pruritus could persist until the patient dies
• Prognosis depends on the type of the underlying tumor and the probability of its treatment. It depends on the time of the EGR onset and the neoplasm discovery. The course and prognosis of EGR can be one of the following:
  • Complete cure of the skin eruption and pruritus after removal and treatment of the internal neoplasm.
  • Temporary improvement then recurrence of the eruption (specially in cases of metastasis).
  • No effect of the tumor treatment on the course of EGR.
  • Death can occur few weeks after the discovery of the malignancy, few months, or four years as in Gammel's patient.

Diagnosis

Diagnostic Study of Choice

• Erythyma gyratum repens is mainly diagnosed clinically by its characteristic skin lesions.
• It is considered as a cutaneous marker of malignancy with high specificity so physicians shouldn't miss its unique clinical skin presentation.

History and Symptoms

• The universal symptoms of erythema gyratum repens are:
  • Skin eruptions
  • Intense pruritus
• Other symptoms related to the associated internal malignancy may include:
  • Weight loss
  • Fatigue
  • Anorexia
  • Vomiting
  • Fever
  • Headache
  • Convulsion
  • Shortness of breath
  • Abdominal distention

Physical Examination

• Patients with erythyma gyratum repens usually are ill-appearing and lethargic
• Physical examination may be remarkable for:
  • Wood-grain erythematous scaly skin eruption.
  • Bullae can also form within the areas of erythema.
  • Typically involves large areas of the body but tends to spare the face, hands, and feet and it can expand as fast as 1 cm a day.
  • Signs of malignancy can be seen based on the neoplasm location such as:
    • Lymphadenopathy
    • Palpable mass
    • Abdominal ascites
    • Pleural effusion
    • Papilloedema

Laboratory Findings

• There are no diagnostic laboratory findings associated with erythema gyratum repens.
• Eosinophilia is observed in 60% of cases.
• Decreased T lymphocytes and increased B lymphocytes observed in an erythema gyratum repens patient with increased luteinizing hormone and follicle-stimulating hormone.
• Decreased serum levels of C3.
• Normal percentages of B and T lymphocytes and normal T-cell function were reported in an erythema gyratum repens patient without cancer.

Imaging Findings

• There are no imaging findings associated with erythyma gyratum repens.
• Imaging to look for systemic neoplasms are:
• * Computed tomography of the head, neck, chest, abdomen, and pelvis.
  • Positron emission tomography/computed tomography
  • Upper and lower gastrointestinal endoscopy
• The abnormal findings that heightened concern for systemic or widespread malignancy are:
  • Brain, chest, lung, abdominal, peritoneal, or pelvic mass.
  • Lymphadenopathy.
  • Enhanced bone lucencies suggestive of diffuse metastasis.

Other Diagnostic Studies

• The histopathologic features of EGR is non-specific.
• Biopsy specimens show the following:
  • Acanthosis, mild hyperkeratosis, focal parakeratosis, and spongiosis confined to the epidermis and superficial dermis
  • Mononuclear, lymphocytic, and histiocytic perivascular infiltrate in the superficial plexus can also be seen
  • Eosinophils and melanophages have also been reported in the dermal infiltrate
  • Diffuse to moderate edema of the connective tissue can be seen
  • Direct immunofluorescence can show patterns of IgG, C3, and C4 at the basement membrane
• Thorough paraneoplastic and systemic workup includes:
  • Computed tomography of head, neck, chest, abdomen, and pelvis.
  • Positron emission tomography/computed tomography.
  • Upper and lower gastrointestinal endoscopy.
  • Complete blood chemistry (CBC).
  • Comprehensive metabolic panel (CMP).
  • Urinanalysis.
  • Rapid plasma reagin test [to exclude syphilis].
  • Anti-nuclear antibody test [to exclude autoimmune disorders as systemic lupus erythematosus (SLE)].
  • Guaiac stool test.
  • Serum protein electrophoresis [to exclude cancers as multiple myeloma].
  • Lactate dehydrogenase [tissue damage, kidney disease, liver disease].
  • QuantiFERON [to exclude tuberculosis].
  • Tumor markers.

Treatment

Medical Therapy

• Treatment of erythema gyratum repens, and its associated intense pruritus depends on the recognition and treatment of the underlying malignancy
• Symptomatic management:
  • Hydroxyzine for itching, ibuprofen and oxycodone for pain, and triamcinolone 0.1% cream for the rash.
• Management of the neoplasm depends on its type, location, stage, and time of its discovery and on patient preference:
  • Surgical removal
  • Chemotherapy
  • Conservative palliative management
• Various dermatologic and immunosuppressive therapies have been used to treat EGR.
• Systemic steroids are frequently ineffective.
• Topical steroids, vitamin A, and azathioprine have also failed to relieve skin manifestations

Surgery

• Surgical resection of the discovered malignancy could be recommended as part of the management of Erythyma gyratum repens.

Prevention

• Primary prevention:
  • There are no primary preventive measures available for erythema gyratum repens
• Secondary Prevention:
  • If the thorough screening after Erythyma gyratum repens diagnosis detected the malignancy in its earliest stages.
• Tertiary prevention:
  • If the thorough screening after Erythyma gyratum repens diagnosis detected the malignancy in its late stages or with widespread metastasis.
  • Tertiary prevention aims to improve the quality of life and life expectancy.