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==Classification==
==Classification==
* There is no established system for the classification of EGR. However, we can classify EGR as:  
* There is no established system for the classification of EGR. However, we can classify EGR as:  
*Paraneoplastic EGR  
**Paraneoplastic EGR  
*Non-paraneoplastic EGR could be: <ref name="pmidPMID: 30345340">{{cite journal| author=Richey PM, Fairley JA, Stone MS| title=Transformation from pityriasis rubra pilaris to erythema gyratum repens-like eruption without associated malignancy: A report of 2 cases. | journal=JAAD Case Rep | year= 2018 | volume= 4 | issue= 9 | pages= 944-946 | pmid=PMID: 30345340 | doi=10.1016/j.jdcr.2018.07.009 | pmc=6191946 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=30345340  }} </ref>
**Non-paraneoplastic EGR could be: <ref name="pmidPMID: 30345340">{{cite journal| author=Richey PM, Fairley JA, Stone MS| title=Transformation from pityriasis rubra pilaris to erythema gyratum repens-like eruption without associated malignancy: A report of 2 cases. | journal=JAAD Case Rep | year= 2018 | volume= 4 | issue= 9 | pages= 944-946 | pmid=PMID: 30345340 | doi=10.1016/j.jdcr.2018.07.009 | pmc=6191946 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=30345340  }} </ref>
** Idiopathic EGR
*** Idiopathic EGR
** EGR-like eruptions (different dermatologic lesions that mimic EGR)
*** EGR-like eruptions (different dermatologic lesions that mimic EGR)
** EGR with concomittant skin disease as:
*** EGR with concomittant skin disease as:
*** pityriasis rubra pilaris, psoriasis, ichthyosis, CREST, rheumatoid arthritis, tuberculosis, bullous pemphigoid, linear IgA disease, and hypereosinophilic syndrome
**** pityriasis rubra pilaris, psoriasis, ichthyosis, CREST, rheumatoid arthritis, tuberculosis, bullous pemphigoid, linear IgA disease, and hypereosinophilic syndrome
** Drug-induced EGR examples are:
*** Drug-induced EGR examples are:
*** Azathioprine with type I autoimmune hepatitis
**** Azathioprine with type I autoimmune hepatitis
*** Interferon given for hepatitis C virus–related chronic hepatitis <ref name="pmidPMID: 30345340" />
**** Interferon given for hepatitis C virus–related chronic hepatitis <ref name="pmidPMID: 30345340" />


==Pathophysiology==
==Pathophysiology==

Revision as of 14:46, 24 June 2019

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

Synonyms and keywords: Gammel's disease.


Overview

Historical Perspective

  • In 1925 Rothman wrote a comprehensive review on the subject of cutaneous manifestations in patients with malignant tumors and since then cases were added to proof for the relationship between internal neoplasm and some skin lesions.
  • In 1953, the dermatologist, Dr. John A Gammel who was trained to link bizarre or recalcitrant dermatoses to internal diseases was the first one who described and labeled Erythema Granulatum Repens in a 55-year-old patient who had been complaining of pruritic scaly skin eruption and found few months later to have poorly differentiated adenocarcinoma
  • Up to 1992, there were only 49 cases in the literature, 41 of which (84%) were associated with a neoplasm
  • EGR is associated with internal malignancy in 82% of cases. However, between 1990 and 2010, data was collected from the medical records of patients form dermatology department in University of Genoa and from databases as pubmed and medline, the conclusion of this literature review was that EGR is no longer considered as an obligate paraneoplastic syndrome. More than expected cases of EGR were found with no neoplasm association

Classification

  • There is no established system for the classification of EGR. However, we can classify EGR as:
    • Paraneoplastic EGR
    • Non-paraneoplastic EGR could be: [1]
      • Idiopathic EGR
      • EGR-like eruptions (different dermatologic lesions that mimic EGR)
      • EGR with concomittant 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 [1]

Pathophysiology

  • The cause of EGR has not been identified.
  • Many theories suggest that EGR is due to immunologic mechanisms 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

Causes

  • The cause of erythema gyratum repens has not been identified.
  • Different theories suggest that EGR etiology is stemmed from an immunologic reaction
  • There is strong evidence of the association of EGR and systemic neoplasm proofed by the improvement of the skin lesions after the neoplasm treatment. however, that association doesn't 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
EGR EAC NME
Reactive erythema (figurate or Gyrate) Yes Yes Yes
Associated malignancy? more closely associated (84%) only a minority of patients     Mainly pancreatic neuroendocrine tumors (PNETs)


glucagonoma pancreatic neuroendocrine tumour.


NME can be the first clinical manifestation of the glucagonoma syndrome (1).

The presenting symptom in 70% of cases (2) the most specific feature


Obligatory paraneoplastic syndrome (2)

NME is the hallmark of gluconoma (3)

Most common associated neoplasm lung cancer    

esophageal cancer   

Breast cancer

metastatic cancer with an unknown origion

Cervical, stomach, and pharyngeal cancer (less common)

no particular type of cancer appears to predominate   

mutinous ovarian carcinoma   

bronchial carcinoma   

myeloma   

Other association tuberculosis

CREST syndrome (calcinosis, Raynaud’s phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia).

infections and allergic reactions to drugs  
Skin lesion description migratory annular and configurate erythematous bands

that form concentric rings  

Wood grain scaly appearance

scale follows the leading edge of the bands.

cover the trunk and proximal extremities, sparing the hands, feet, and face.   

Eruption migrates more rapidly, 1cm/d   

migratory annular and configurate

annular or polycyclic lesions which may begin as urticaria-like papules Urticarial in appearance

ringed, arcuate figures erythematous lesions   

cover only a small percentage of the total body surface  migrate at a slower rate (2 -3 mm/d) reaching up to 10 cm in diameter and resulting in central clearing.

circinate erythema with areas of necrosis and sloughing (3)


crusted  Erythematous scaly lesions/plaques with centrifugal growth


Perineum, distal extremities, lower abdomen, and face are the most commonly affected sites.


Spontaneous exacerbation and remission periods without knowing what the trigger is .

First named/described by Gammel in 1952     Darier 1916
Becker et al. in 1942 was the first to describe the association


Wilkinson in 1973 was the first who named it.

Incidence     Very rare uncommon but not rare Rare paraneoplastic dermatosis

Studies in the US showed only 2,705 cases of pancreatic neuroendocrine tumors in a period of 28 years, with glucagonomas in only 1.3% of these neoplasms


combined with glucagonoma syndrome, has an estimated global incidence of 1 case per 20 million people (3)

Demographics Caucasian

male: female ratio is 2: 1

average age was 62 years.

no tendency for EAC to favor any age, race, or sex.
Subgroups Deep: Firm border, rarely pruritic, no scales

Superficial: indistinct scaly border , usually pruritic,

Histopathology Nonspecific

moderate perivascular lymphohistiocytic infiltrate   

mild focal spongiosis

parakeratosis   

Eosinophils and melanophages have also been reported in the dermal infiltrate   

deep form

mononuclear, perivascular infiltrate is present in the middle and lower portions of the dermis (coat sleeve-like configuration)

infiltrate is usually composed primarily of lymphocytes, but eosinophils are occasionally present

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

paleness and spongiosis of the upper layer of the epidermis.


A perivascular lymphocytic and histiocytic infiltrate is also frequent.


Necrotic keratinocytes are common and can lead to erosions, crusting and scaling

Lab finding   


No specific laboratory changes are associated

Eosinophilia has been reported


Decreased T lymphocytes and increased B lymphocytes

were observed in an EGR patient with increased luteinizing hormone and follicle-stimulating hormone as well as 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. Therefore, it appears that any laboratory abnormality detected in patients with EAC or EGR would reflect the underlying etiology of the reactive erythema.


No specific laboratory changes are associated

Eosinophilia of the peripheral blood, as well as tissue, can be observed in EAC associated with a drug reaction or parasitic infection   

Decreased T lymphocytes and increased B lymphocytes   

increased glucagon level (3)


Extensive evaluation for possible cancer


EGR patients with underlying malignancies had cancers associated with tobacco abuse.

Evaluation for possible infection or drug reaction (prescribed and non-prescribed)

complete blood count, urinalysis, and routine serum liver and kidney function tests.

Evaluation of the associated tumor:

CT or MRI abdomen


Selective visceral angiography to localize the tumor


Positron Emission tomography (PET)


octreotide scintigraphy

Treatment   


identification and treatment of the underlying condition, as the course of either eruption usually parallels that of the underlying process.

identification and treatment of the underlying condition, as the course of either eruption usually parallels that of the underlying process.
Symptomatic therapy as antihistamine and corticosteroids systemic corticosteroids for the deep form and topical corticosteroids for the superficial form

Lesions of EAC, however, frequently recur following discontinuation of such treatment   

Pathogenesis Not fully clarified but attributed to zinc deficiency and hypoaminoacedemia

Increased glucagon increases gluconeogesis

clinical manifistation/symptoms weight loss, diabetes, diarrhea, and stomatitis.
Prognosis due to the difficulty of NME recognition, and its association with glaconoma, diagnosis is usually delayed(3)


NME usually resolved after the resection and treatment of the pancreatic tumor


Epidemiology and Demographics

  • EGR is a rare dermatologic disease, usually associated with paraneoplastic neoplasm

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 EGR

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

  • EGR 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 EGR are:
    • Skin eruptions
    • Intense pruritus
  • Other symptoms related to the associated internal malignancy are:
    • Weight loss
    • Anorexia
    • Fatigue
    • Fever
    • Many patients with EGR and malignancy had a history of tobacco smoking
    • some patients with EGR and malignancy have a family history of neoplasm

Physical Examination

  • Patients with EGR can be ill-appearing and lethargic
  • Thorough physical exam should be done to look for signs of malignancy as lymph node enlargements, mass, abdominal distension, shortness of breath, pleural effusion,or papilloedema.
  • The rash consisting of 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 scale, a pattern often described as “wood grained.
  • 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 a cm a day.
  • Bullae can also form from within the areas of erythema

Laboratory Findings

  • There are no diagnostic laboratory findings associated with EGR.
  • Eosinophilia is observed in 60% of cases [2]
  • Evaluation to exclude systemic involvement:
    • CBC, CMP, urine analysis, LFT, guaiac stool test, serum protein electrophoresis


Imaging Findings

  • There are no imaging findings associated with EGR.
  • Imaging of the chest and abdomen could show malignancy findings.

Other Diagnostic Studies

  • Direct immunofluorescence in some cases shows patterns of IgG, C3, and C4 at the basement membrane [2]
  • 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 [2]
  • Thorough paraneoplastic workup includes:
    • Computed tomography of thorax, abdomen, and pelvis
    • Positron emission tomography/computed tomography
    • Upper and lower gastrointestinal endoscopy
    • Tumor markers
    • Blood tests including lactate dehydrogenase and QuantiFERON to exclude tuberculosis.

Treatment

Medical Therapy

  • There is no treatment for EGR; the mainstay of therapy is supportive care and treating the underlying condition [2]
  • 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.
  • Improvement of EGR, and its associated intense pruritus depends on recognition and treatment of the underlying malignancy.
  • Chemotherapy can be used to treat the internal malignancy.

Surgery

  • Surgical resection of the internal tumor could be recommended as part of the management of EGR.

Prevention

  • There are no primary preventive measures available for [disease name].

References

Template:WikiDoc Sources

  1. 1.0 1.1 Richey PM, Fairley JA, Stone MS (2018). "Transformation from pityriasis rubra pilaris to erythema gyratum repens-like eruption without associated malignancy: A report of 2 cases". JAAD Case Rep. 4 (9): 944–946. doi:10.1016/j.jdcr.2018.07.009. PMC 6191946. PMID 30345340 PMID: 30345340 Check |pmid= value (help).
  2. 2.0 2.1 2.2 2.3 Gore M, Winters ME (2011). "Erythema gyratum repens: a rare paraneoplastic rash". West J Emerg Med. 12 (4): 556–8. doi:10.5811/westjem.2010.11.2090. PMC 3236141. PMID 22224159 PMID: 22224159 Check |pmid= value (help).