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| __NOTOC__
| | {{ACM}} {{SemRikken}} |
| {{SI}} | |
| {{CMG}} | |
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| {{SK}} Gammel's disease.
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|
| | | ''SANDBOX'' |
| Erythema gyratum repens is a rare highly specific and characteristic paraneoplastic syndrome that usually affect older people. It is characterized by wood-grain scaly skin eruption with intense pruritus. The cause of erythema gyratum repens is unknown but many theories suggest immunologic etiology or toxicologic products that are released by the associated tumor. The first case of erythema gyratum repens was described by a dermatologist named Gammel in the year 1952. For many years after erythema gyratum repens original description, there was little progress in defining the pathogenesis of erythema gyratum repens. Erythema gyratum repens has no specific classification but we can classify it based on its association with an internal malignancy into para-neoplastic and non-para-neoplastic erythema gyratum repens. The most common malignancies associated with erythema gyratum repens are lung or bronchogenic cancer, esophageal cancer, and breast cancer. Erythema gyratum repens can also be associated with non-neoplastic diseases such as tuberculosis, autoimmune disorders, or CREST syndrome. Erythema gyratum repens is characterized by its pathogonomic figurate, gyrate, or annular erythematous skin eruptions. The intense pruritus can be debilitating and usually urges the patient to go to the emergency department. The microscopic histopathological features of erythema gyratum repens consist of acanthosis, focal parakeratotic, and spongiosis of the epidermis with perivascular mononuclear, lymphocytic, and histiocytic infiltrate in the superficial plexus of the dermis. Erythema gyratum repens is very rare and it mainly affects people in their seventieth decade, the male to female ratio is 2:1. Erythema gyratum repens is diagnosed clinically by its characteristic skin eruption and an urgent thorough paraneoplastic workup should be initiated to look for internal malignancies. Patients with erythema gyratum repens presents with intensely pruritic, gradually progressive, skin lesions that crawl rather than migrate from one body region to the other. It can start in the upper trunk or upper back and extends to involve the extremities sparing the face. The mainstay of the treatment of erythema gyratum repens is finding and treating the underlying malignancy. Symptomatic treatment is not very effective in relieving the pruritus and its associated pain. The management can be surgical removal of the tumor, chemotherapy, or palliative conservative management. The skin eruptions can improve completely after the removal of the underlying tumor, or can recur especially if the tumor recurred or metastasized. Patients can live a few weeks, months or up to five years depending on when and at what stage the malignancy was detected.
| | [[File:Captura de Pantalla 2024-05-18 a la(s) 9.33.11 p.m..png]] |
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| 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.[1][2]
| |
| 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.[3][4]
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| 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".[3]
| |
| 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.[5]
| |
| 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.[6]
| |
| 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.[7]
| |
| | |
| ==Pathophysiology==
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| The pathogenesis of erythema gyratum repens is unclear[12][13]
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| Many immunologic theories have been implicated in its pathogenesis.
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| The immunologic mechanism theory is evidenced by the observed immunofluorescence patterns of IgG, C3, and C4 at the basement membrane: [13]
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| Theory 1: the tumor induces antibodies that cross-react with the basement membrane of skin.
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| Theory 2: the tumor produces polypeptides that bind skin antigens and render them immunogenic.
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| Theory 3: deposition of tumor antigen-antibody complexes onto the basement membrane causes reactive dermatitis seen in erythema gyratum repens.
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| The gross appearance of the unique eruptions are:
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| Wavy erythematous concentric bands that can be figurate, gyrate, or annular
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| The bands are arranged in parallel rings and lined by a fine trailing edge of scales, a pattern often described as “wood grained”.
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| The distinctive wood-grain appearance of the eruption is pathognomonic.
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| 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.
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| Bullae can also form from within the areas of erythema.
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| 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:[3][5][14]
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| The epidermis has thin atrophic patches with areas of acanthosis, focal parakeratotic horny layers, and spongiosis.
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| The dermis contains a moderate perivascular mononuclear, lymphocytic, and histiocytic infiltrate in the superficial plexus as well as mild focal spongiosis and parakeratosis.
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| Eosinophils and melanophages have also been reported in the dermal infiltrate.
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| Diffuse to moderate edema of the connective tissue can be seen.
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| | |
| ==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.[1][2]
| |
| 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.[3][4]
| |
| 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".[3]
| |
| 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.[5]
| |
| 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.[6]
| |
| 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.[7]
| |
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| ==Classification==
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| *There is no established system for the classification of EGR. However, we can classify EGR as:
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| **Paraneoplastic EGR
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| **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>
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| ***Idiopathic EGR
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| ***EGR-like eruptions (different dermatologic lesions that mimic EGR)
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| ***EGR with concomitant skin disease as:
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| ****pityriasis rubra pilaris, psoriasis, ichthyosis, CREST, rheumatoid arthritis, tuberculosis, bullous pemphigoid, linear IgA disease, and hyper eosinophilic syndrome
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| ***Drug-induced EGR examples are:
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| ****Azathioprine with type I autoimmune hepatitis
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| ****Interferon given for hepatitis C virus–related chronic hepatitis <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>
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| | |
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| ==Pathophysiology==
| |
| | |
| *The cause of EGR has not been identified.
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| *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: <ref name="pmidPMID: 22224159">{{cite journal| author=Gore M, Winters ME| title=Erythema gyratum repens: a rare paraneoplastic rash. | journal=West J Emerg Med | year= 2011 | volume= 12 | issue= 4 | pages= 556-8 | pmid=PMID: 22224159 | doi=10.5811/westjem.2010.11.2090 | pmc=3236141 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22224159 }} </ref>
| |
| **Theory 1 the tumor induces antibodies that cross-react with the basement membrane of skin
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| **Theory 2 the tumor produces polypeptides that bind skin antigens and render them immunogenic
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| **Theory 3 deposition of tumor antigen-antibody complexes onto the basement membrane causes reactive dermatitis seen in EGR
| |
| | |
| <ref name="pmidPMID: 22224159">{{cite journal| author=Gore M, Winters ME| title=Erythema gyratum repens: a rare paraneoplastic rash. | journal=West J Emerg Med | year= 2011 | volume= 12 | issue= 4 | pages= 556-8 | pmid=PMID: 22224159 | doi=10.5811/westjem.2010.11.2090 | pmc=3236141 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22224159 }} </ref>
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| ==Causes==
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| *The cause of erythema gyratum repens has not been identified.
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| *Different theories suggest that EGR etiology is stemmed from an immunologic reaction.
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| *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.
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| ==Differentiating Erythema Gyratum Repens from Other Diseases==
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| *EGR has a narrow differential diagnosis. It has to be differentiated from Reactive gyrate erythematous eruptions, such as: <ref name="pmidPMID: 22224159">{{cite journal| author=Gore M, Winters ME| title=Erythema gyratum repens: a rare paraneoplastic rash. | journal=West J Emerg Med | year= 2011 | volume= 12 | issue= 4 | pages= 556-8 | pmid=PMID: 22224159 | doi=10.5811/westjem.2010.11.2090 | pmc=3236141 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22224159 }} </ref>
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| **Reactive (figurate or gyrate) erythemas that are associated with malignancy include:
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| ***Erythema annulare centrifugum (EAC)
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| ***Necrolytic migratory erythema (NME)
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| **Reactive (figurate or gyrate) erythemas that are not associated with malignancy include:
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| ***Erythema marginatum rheumaticum <ref name="pmidhttps://doi.org/10.1002/1097-0142(19880801)62:3<54">{{cite journal| author=Schmoldt A, Benthe HF, Haberland G| title=Digitoxin metabolism by rat liver microsomes. | journal=Biochem Pharmacol | year= 1975 | volume= 24 | issue= 17 | pages= 1639-41 | pmid=https://doi.org/10.1002/1097-0142(19880801)62:3<54 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=10 }} </ref>
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| ***Erythema chronicum migrans
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| ***Familial annular erythema
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| ***The carrier state of chronic granulomatous disease
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| ***Subacute cutaneous lupus erythematosus
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| ***Neonatal lupus erythematosus
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| | |
| {| style="border: 0px; font-size: 90%; margin: 3px;" align="center"
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| ! rowspan="1" style="background: #4479BA; padding: 5px 5px;" |{{fontcolor|#FFFFFF| Disease}}
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| ! rowspan="1" style="background: #4479BA; padding: 5px 5px;" |{{fontcolor|#FFFFFF|Erythema Characteristics}}
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| ! colspan="1" style="background: #4479BA; padding: 5px 5px;" |{{fontcolor|#FFFFFF|Signs and Symptoms}}
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| ! rowspan="1" style="background: #4479BA; padding: 5px 5px;" |{{fontcolor|#FFFFFF|Associated Conditions}}
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| ! rowspan="1" style="background: #4479BA; padding: 5px 5px;" |{{fontcolor|#FFFFFF|Histopathology}}
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| ! colspan="1" style="background: #4479BA; padding: 5px 5px;" |{{fontcolor|#FFFFFF|Lab finding
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| &
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| Other evaluation}}
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| ! rowspan="1" style="background: #4479BA; padding: 5px 5px;" |{{fontcolor|#FFFFFF| prognosis}}
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| |-
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| | style="padding: 5px 5px; background: #DCDCDC;" |'''[[Erythema gyratum repens (EGR)]]'''
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| | style="padding: 5px 5px; background: #F5F5F5;" |
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| *Migratory annular and configurate erythematous bands that form concentric rings
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| *Wood grain scaly appearance
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| *scales follows the leading edge of the bands
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| *Eruption migrates more rapidly, 1cm/d<br />
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| | style="padding: 5px 5px; background: #F5F5F5;" |
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| *Skin eruptions
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| *severe Generalized itching (pruritus)
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| *scaly erythematous patches over trunk and proximal extremities, sparing the hands, feet, and face. Can eventually involve the face
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| *weight loss
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| *Malaise and fatigue
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| *fever
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| *anorexia
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| *Lymphadenopathy
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| *Headache and convulsion (intracranial metastasis)
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| *Shortness of breath (bronchogenic carcinoma)
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| | style="padding: 5px 5px; background: #F5F5F5;" |
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| *Dermatologic conditions: ichthyosis palmar/plantar hyperkeratosis
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| *Less frequently EGR copresent with:
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| **pityriusis rubru piluris, bullous pemphigoid, pemphigus vulgaris, discoid lupus eythemutosus, psoriusiform lesions, and nonspecific vesicles and bullae.
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| *Tuberculosis
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| *CREST syndrome
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| (calcinosis, Raynaud’s phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia).
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| | style="padding: 5px 5px; background: #F5F5F5;" |
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| *The epidermis:
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| **Acanthosis
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| **Focal parakeratotosis and spongiosis
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| *The dermis:
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| **Mild focal spongiosis and parakeratosis
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| **Moderate perivascular mononuclear, lymphocytic, and histiocytic infiltrate
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| **Eosinophils and melanophages have also been reported in the infiltrate
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| *Diffuse to moderate edema of the connective tissue can be seen
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| | style="padding: 5px 5px; background: #F5F5F5;" |
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| *No specific laboratory changes
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| *Eosinophilia has been reported
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| <br />
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| *Decreased T lymphocytes and increased B lymphocytes observed in an EGR patient with increased luteinizing hormone and follicle-stimulating hormone as well as decreased serum levels of C3
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| *Normal percentages of B and T lymphocytes and normal T-cell function were reported in an EGR patient without cancer
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| *Extensive evaluation for possible cancer
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| *CBC,CMP, imaging as CT chest or abdomen
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| <br />
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| | style="padding: 5px 5px; background: #F5F5F5;" |
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| *Skin manifestations can be improved within 48 hours of the resection of the underlying tumor
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| *The improvement sometimes can be temporary with recurrence of the skin lesions specially in cases of metastasis
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| *Death can occur any time depending on the type and location of tumor and the timing of its discovery
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| |-
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| | style="padding: 5px 5px; background: #DCDCDC;" |'''[[Erythema annulare centrifugum (EAC)]]'''
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| | style="padding: 5px 5px; background: #F5F5F5;" |
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| *Migratory annular and configurate erythematous
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| or polycyclic lesions
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| *Urticarial in appearance, ringed, arcuate figures
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| *Eruption migrate at a slower rate (2 -3 mm/d) reaching up to 10 cm in diameter with central clearing.
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| *Cover only a small percentage of the total body surface
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| | style="padding: 5px 5px; background: #F5F5F5;" |
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| *annular or polycyclic lesions which may begin as urticaria-like papules
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| *Eventually old lesions can spontaneously resolve in several days to a few weeks while new eruptions develop.
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| *The deep form of EAC has a firm, indurated border, is rarely pruritic, and has no scale.
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| *The superficial type of EAC has an indistinct scaly border and is usually pruritic
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| | style="padding: 5px 5px; background: #F5F5F5;" |
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| *Infections
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| *Allergic reactions to drugs
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| | style="padding: 5px 5px; background: #F5F5F5;" |
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| *Deep form:
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| **Mononuclear, perivascular infiltrate in the middle and lower portions of the dermis (coat sleeve-like configuration)
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| **Infiltrate is primarily of lymphocytes, but eosinophils are occasionally presen
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| **Extravasation of erythrocytes is associated with endothelial swelling
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| **No epidermal changes
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| *Superficial:
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| **more non-specific
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| **slight superficial perivascular lymphohistiocytic infiltrate
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| **Focal parakeratosis and mild spongiosis with microvesiculation
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| | style="padding: 5px 5px; background: #F5F5F5;" |
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| *No specific laboratory changes
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| *Eosinophilia of the peripheral blood, as well as tissue, can be observed in EAC associated with a drug reaction or parasitic infection
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| <br />
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| *Evaluation for possible infection or drug reaction (prescribed and non-prescribed)
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| *complete blood count, urinalysis, and routine serum liver and kidney function tests.
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| | style="padding: 5px 5px; background: #F5F5F5;" |
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| *Lesions disappears after the underlying etiology is managed (allergy, infection, malignancy)
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| *if no underlying cause, lesions can recur after discontinuation of the supportive treatment.
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| |-
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| | style="padding: 5px 5px; background: #DCDCDC;" |'''[[Necrolytic migratory erythema (NME)]]'''
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| | style="padding: 5px 5px; background: #F5F5F5;" |
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| *Migratory circinate erythema/plaques with areas of necrosis and sloughing (3)
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| *Crusted Erythematous scaly plaques with centrifugal growth
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| | |
| *
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| | style="padding: 5px 5px; background: #F5F5F5;" |
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| *Red erythematous scaly plaques over Perineum, distal extremities, lower abdomen, and face
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| *Spontaneous exacerbation and remission periods without knowing what the trigger is
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| *Weight loss
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| *anemia
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| *diabetes
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| *diarrhea
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| *stomatitis.
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| | style="padding: 5px 5px; background: #F5F5F5;" |
| |
| *No other association
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| *can be misdiagnosed as contact dermatitis
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| | |
| or intertrigo, inverse psoriasis, zinc deficiency, and other nutritional deficiencies
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| | style="padding: 5px 5px; background: #F5F5F5;" |
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| *Paleness and spongiosis of the upper layer of the epidermis.
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| | |
| *A perivascular lymphocytic and histiocytic infiltrate
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| | |
| *Necrotic keratinocytes are common and can lead to erosions, crusting and scaling
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| | style="padding: 5px 5px; background: #F5F5F5;" |
| |
| *Increased glucagon level (3)
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| | |
| *Evaluation of the associated tumor:
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| CT or MRI abdomen
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| *Selective visceral angiography to localize the tumor
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| | |
| *Positron Emission tomography (PET)
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| | |
| *Octreotide scintigraphy
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| | style="padding: 5px 5px; background: #F5F5F5;" |
| |
| *Due to the difficulty of NME recognition, and its association with glucagonoma, diagnosis is usually delayed(3)
| |
| | |
| *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 <br />
| |
| |-
| |
| |Erythema gyratum repens (Gammel's syndrome)
| |
| |The particularly typical eruption, mainly affecting the trunk.
| |
| |
| |
| *weight loss
| |
| | |
| *fatigue
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| | |
| *eruptive rash
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| | |
| *itching
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| | |
| *signs and symptoms of associated cancer
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| |Associated with a squamous cell carcinoma of the esophagus
| |
| |
| |
| |CBC gives eosiophilia
| |
| |The paraneoplastic dermatosis cleared after radiotherapy of the cancer.
| |
| |}
| |
| | |
| ==Epidemiology and Demographics==
| |
| | |
| *EGR is a rare dermatologic disease, usually associated with paraneoplastic neoplasm
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| | |
| '''Age'''
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| | |
| *The average age of onset of EGR is in the seventh decade of life (65 years old)
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| '''Gender'''
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| | |
| *The male to female ratio is 2:1
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| | |
| '''Race'''
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| | |
| *EGR commonly affects Caucasians
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| | |
| ==Risk Factors==
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| | |
| *There are no established risk factors for EGR
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| | |
| | |
| ==Screening==
| |
| | |
| *There are no screening tests for EGR.
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| *Screening for internal malignancy should be done immediately after EGR is diagnosed.
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| | |
| ==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 <ref name="pmidPMID: 22224159">{{cite journal| author=Gore M, Winters ME| title=Erythema gyratum repens: a rare paraneoplastic rash. | journal=West J Emerg Med | year= 2011 | volume= 12 | issue= 4 | pages= 556-8 | pmid=PMID: 22224159 | doi=10.5811/westjem.2010.11.2090 | pmc=3236141 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22224159 }} </ref>
| |
| *If the underlying malignancy left untreated, the debilitating pruritus could persist until the patient dies <ref name="pmidPMID: 22224159">{{cite journal| author=Gore M, Winters ME| title=Erythema gyratum repens: a rare paraneoplastic rash. | journal=West J Emerg Med | year= 2011 | volume= 12 | issue= 4 | pages= 556-8 | pmid=PMID: 22224159 | doi=10.5811/westjem.2010.11.2090 | pmc=3236141 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22224159 }} </ref>
| |
| *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 <ref name="pmidPMID: 22224159">{{cite journal| author=Gore M, Winters ME| title=Erythema gyratum repens: a rare paraneoplastic rash. | journal=West J Emerg Med | year= 2011 | volume= 12 | issue= 4 | pages= 556-8 | pmid=PMID: 22224159 | doi=10.5811/westjem.2010.11.2090 | pmc=3236141 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22224159 }} </ref>
| |
| | |
| ===Laboratory Findings===
| |
| | |
| *There are no diagnostic laboratory findings associated with EGR.
| |
| *Eosinophilia is observed in 60% of cases <ref name="pmidPMID: 22224159">{{cite journal| author=Gore M, Winters ME| title=Erythema gyratum repens: a rare paraneoplastic rash. | journal=West J Emerg Med | year= 2011 | volume= 12 | issue= 4 | pages= 556-8 | pmid=PMID: 22224159 | doi=10.5811/westjem.2010.11.2090 | pmc=3236141 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22224159 }} </ref>
| |
| *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 <ref name="pmidPMID: 22224159">{{cite journal| author=Gore M, Winters ME| title=Erythema gyratum repens: a rare paraneoplastic rash. | journal=West J Emerg Med | year= 2011 | volume= 12 | issue= 4 | pages= 556-8 | pmid=PMID: 22224159 | doi=10.5811/westjem.2010.11.2090 | pmc=3236141 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22224159 }} </ref>
| |
| *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 <ref name="pmidPMID: 22224159">{{cite journal| author=Gore M, Winters ME| title=Erythema gyratum repens: a rare paraneoplastic rash. | journal=West J Emerg Med | year= 2011 | volume= 12 | issue= 4 | pages= 556-8 | pmid=PMID: 22224159 | doi=10.5811/westjem.2010.11.2090 | pmc=3236141 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22224159 }} </ref>
| |
| *Thorough paraneoplastic workup includes: <ref name="pmidPMID: 31111084">{{cite journal| author=Ridge A, Tummon O, Laing M| title=Response to "Transformation from pityriasis rubra pilaris to erythema gyratum repens-like eruption without associated malignancy: A report of 2 cases". | journal=JAAD Case Rep | year= 2019 | volume= 5 | issue= 5 | pages= 461-462 | pmid=PMID: 31111084 | doi=10.1016/j.jdcr.2019.03.012 | pmc=6510971 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=31111084 }} </ref>
| |
| **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 <ref name="pmidPMID: 22224159">{{cite journal| author=Gore M, Winters ME| title=Erythema gyratum repens: a rare paraneoplastic rash. | journal=West J Emerg Med | year= 2011 | volume= 12 | issue= 4 | pages= 556-8 | pmid=PMID: 22224159 | doi=10.5811/westjem.2010.11.2090 | pmc=3236141 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22224159 }} </ref>
| |
| *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].
| |
| | |
| | |
| {| class="wikitable" style="width: 80%;"
| |
| |-
| |
| | colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]]
| |
| |-
| |
| | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.'''
| |
| |-
| |
| | bgcolor="LightGreen" |<nowiki>"</nowiki>'''2.'''
| |
| |}
| |
| | |
| | |
| {| class="wikitable" style="width: 80%;"
| |
| |-
| |
| | colspan="1" style="text-align:center; background:LightCoral" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class III: Harm]]
| |
| |-
| |
| | bgcolor="LightCoral" |<nowiki>"</nowiki>'''1.'''
| |
| |-
| |
| | bgcolor="LightCoral" |<nowiki>"</nowiki>'''2.'''
| |
| |}
| |
| | |
| {| class="wikitable" style="width: 80%;"
| |
| |-
| |
| | colspan="1" style="text-align:center; background:LemonChiffon" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIa/IIb]]
| |
| |-
| |
| | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: A]])''<nowiki>"</nowiki>
| |
| |-
| |
| | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''2.''' ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B]])''<nowiki>"</nowiki>
| |
| |}
| |
| | |
| ==References==
| |
| {{reflist}}
| |
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