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  1. Article ; Online: Do not forget about myasthenia gravis when performing botulinum toxin injections.

    Dell'Antonia, Massimo / Mugheddu, Cristina / Ferreli, Caterina / Atzori, Laura

    Journal of the European Academy of Dermatology and Venereology : JEADV

    2023  

    Language English
    Publishing date 2023-04-15
    Publishing country England
    Document type Letter
    ZDB-ID 1128828-0
    ISSN 1468-3083 ; 0926-9959
    ISSN (online) 1468-3083
    ISSN 0926-9959
    DOI 10.1111/jdv.19115
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    Zs.A 3492: Show issues Location:
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  2. Article ; Online: Erythema annulare centrifugum with perieccrine inflammation triggered by SARS-CoV-2 infection.

    Dell'antonia, Massimo / Pilloni, Luca / Ala, Lorenzo / Conti, Brunella / Ferreli, Caterina / Atzori, Laura

    Italian journal of dermatology and venereology

    2023  Volume 158, Issue 5, Page(s) 423–424

    MeSH term(s) Humans ; COVID-19/complications ; Erythema/etiology ; Inflammation ; SARS-CoV-2 ; Female ; Middle Aged
    Language English
    Publishing date 2023-08-04
    Publishing country Italy
    Document type Case Reports ; Journal Article
    ZDB-ID 3065415-4
    ISSN 2784-8450
    ISSN (online) 2784-8450
    DOI 10.23736/S2784-8671.23.07562-X
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  3. Article ; Online: Non-familial paraneoplastic pityriasis rotunda associated with chronic lymphocytic leukemia in a Sardinian patient.

    Dell'antonia, Massimo / Atzori, Laura / Pilloni, Luca / Ferreli, Caterina

    Italian journal of dermatology and venereology

    2022  Volume 157, Issue 4, Page(s) 375–376

    MeSH term(s) Autoantibodies ; Humans ; Keratosis/complications ; Leukemia, Lymphocytic, Chronic, B-Cell/complications ; Pityriasis/complications
    Chemical Substances Autoantibodies
    Language English
    Publishing date 2022-07-29
    Publishing country Italy
    Document type Journal Article
    ZDB-ID 3065415-4
    ISSN 2784-8450
    ISSN (online) 2784-8450
    DOI 10.23736/S2784-8671.21.07113-9
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    Zs.B 119: Show issues Location:
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  4. Article ; Online: Epidemiology, characteristics of disease and unmet needs of patients with generalized pustular psoriasis: a large Italian Delphi consensus.

    Prignano, Francesca / Atzori, Laura / Bellinato, Francesco / Damiani, Giovanni / Galeone, Carlotta / Mariani, Paolo / Potenza, Concetta / Scopinaro, Annalisa / Piaserico, Stefano / Fabbrocini, Gabriella

    Dermatology (Basel, Switzerland)

    2024  

    Abstract: Introduction: Generalized pustular psoriasis (GPP) is a rare and chronic, debilitating skin condition characterised, in its acute flare phase, by clinically severe and potentially life-threatening systemic manifestations. Data on GPP are still scanty, ... ...

    Abstract Introduction: Generalized pustular psoriasis (GPP) is a rare and chronic, debilitating skin condition characterised, in its acute flare phase, by clinically severe and potentially life-threatening systemic manifestations. Data on GPP are still scanty, particularly in Europe and at a national level. To provide expert indications on several disease-related and patient-related aspects of GPP, with specific focus to the Italian context.
    Methods: We conducted an iterative eDelphi study following the recommended criteria for reporting methods and results. After a thorough bibliographic review aimed to identify unknown or controversial issues in GPP, the following areas were investigated through a few specific questions/statements for each area: 1) disease epidemiology; 2) disease characteristics, with specific interest towards GPP flares; 3) diagnosis and diagnostic delay; 4) GPP treatment; 5) GPP patient journey and use of healthcare resources in Italy; 6) unmet needs and quality of life. An Executive Board of 9 principal investigators revised and approved the topics to be examined and overviewed the whole project. A total of 35 experts from different Italian areas, including 34 board-certified Italian dermatologists and one representative of patients' associations, took part in the study.
    Results: A high agreement in responses from Italian experts emerged during two eDelphi iterations on - among several other aspects - GPP prevalence and incidence in Italy, use of European Rare and Severe Psoriasis Expert Network diagnostic criteria, flare frequency and duration, best diagnostic and care pathway, and main unmet needs of Italian patients. On the other hand, a broad spectrum of treatments (of different drug classes) was reported both in the acute and chronic phases of GPP, and no consensus on the issue was thus achieved.
    Conclusions: Consensus findings from this Delphi study of GPP experts may be useful to fill gaps of knowledge and improve awareness of this rare disease, as well as to help clinical and public health management of GPP in Italy.
    Language English
    Publishing date 2024-03-17
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 1099692-8
    ISSN 1421-9832 ; 1018-8665
    ISSN (online) 1421-9832
    ISSN 1018-8665
    DOI 10.1159/000538072
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  5. Article ; Online: Safety of secukinumab treatment in COVID-19 affected psoriatic patients.

    Mugheddu, Cristina / Sanna, Silvia / Atzori, Laura / Rongioletti, Franco

    Dermatologic therapy

    2021  Volume 34, Issue 1, Page(s) e14710

    MeSH term(s) Antibodies, Monoclonal, Humanized/adverse effects ; Antibodies, Monoclonal, Humanized/therapeutic use ; Arthritis, Psoriatic/drug therapy ; COVID-19 ; Humans ; SARS-CoV-2
    Chemical Substances Antibodies, Monoclonal, Humanized ; secukinumab (DLG4EML025)
    Language English
    Publishing date 2021-01-03
    Publishing country United States
    Document type Letter
    ZDB-ID 1354801-3
    ISSN 1529-8019 ; 1396-0296
    ISSN (online) 1529-8019
    ISSN 1396-0296
    DOI 10.1111/dth.14710
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    Zs.A 5181: Show issues Location:
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  6. Article: Glomeruloid reactive angioendotheliomatosis in a woman with systemic lupus erythematosus and antiphospholipid syndrome mimicking reticular erythematous mucinosis.

    Ferreli, Caterina / Atzori, Laura / Rongioletti, Franco

    JAAD case reports

    2020  Volume 8, Page(s) 56–59

    Language English
    Publishing date 2020-12-17
    Publishing country United States
    Document type Case Reports
    ZDB-ID 2834220-3
    ISSN 2352-5126
    ISSN 2352-5126
    DOI 10.1016/j.jdcr.2020.12.012
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  7. Article ; Online: Erythema annulare centrifugum with anosmia and ageusia in a SARS-CoV-2 exposed patient successfully treated with doxycycline.

    Montinari, Martina / Atzori, Laura / Valdevit, Sefora / Rongioletti, Franco

    International journal of dermatology

    2020  Volume 60, Issue 3, Page(s) 384–386

    MeSH term(s) Adult ; Ageusia/diagnosis ; Ageusia/drug therapy ; Ageusia/immunology ; Anosmia/diagnosis ; Anosmia/drug therapy ; Anosmia/immunology ; Biopsy ; COVID-19/complications ; COVID-19/diagnosis ; COVID-19/immunology ; COVID-19/virology ; COVID-19 Serological Testing ; Doxycycline/therapeutic use ; Drug Repositioning ; Erythema/diagnosis ; Erythema/drug therapy ; Erythema/immunology ; Erythema/pathology ; Female ; Humans ; SARS-CoV-2/immunology ; SARS-CoV-2/isolation & purification ; Skin/immunology ; Skin/pathology ; Skin Diseases, Genetic/diagnosis ; Skin Diseases, Genetic/drug therapy ; Skin Diseases, Genetic/immunology ; Skin Diseases, Genetic/pathology ; Treatment Outcome
    Chemical Substances Doxycycline (N12000U13O)
    Language English
    Publishing date 2020-12-23
    Publishing country England
    Document type Case Reports ; Letter
    ZDB-ID 412254-9
    ISSN 1365-4632 ; 0011-9059 ; 1461-1244
    ISSN (online) 1365-4632
    ISSN 0011-9059 ; 1461-1244
    DOI 10.1111/ijd.15356
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    Ui VI Zs.189: Show issues Location:
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  8. Article ; Online: Pseudoxanthoma elasticum-like papillary dermal elastolysis: A mimicker of genetic pseudoxanthoma elasticum.

    Atzori, Laura / Ferreli, Caterina / Pilloni, Luca / Rongioletti, Franco

    Clinics in dermatology

    2020  Volume 39, Issue 2, Page(s) 206–210

    Abstract: Pseudoxanthoma elasticum (PXE)-like papillary dermal elastolysis (PDE) is an acquired, rare, elastic tissue disorder that presents with multiple asymptomatic, nonfollicular yellowish or normochromic papules, coalescing into symmetrical cobblestone ... ...

    Abstract Pseudoxanthoma elasticum (PXE)-like papillary dermal elastolysis (PDE) is an acquired, rare, elastic tissue disorder that presents with multiple asymptomatic, nonfollicular yellowish or normochromic papules, coalescing into symmetrical cobblestone plaques, with a predilection for the neck of postmenopausal women. The condition develops slowly, in months to years, and, although clinically similar to PXE, it is devoid of any systemic implication, being only of esthetic concern. The etiology is unknown, but it is speculated that there is a multifactorial pathogenesis, with the contribution of intrinsic aging, exposure to ultraviolet radiation, abnormal elastogenesis, and genetic factors. The diagnosis is confirmed by histopathology, with special stains specific for elastic fibers revealing loss of elastic plexus in the papillary dermis and the presence of melanophages. Its prevalence is probably underestimated, which reinforces the importance of better clinical and histologic identification to distinguish it from inherited PXE and to avoid extensive systemic investigations and unnecessary medical visits for the patient.
    MeSH term(s) Dermis ; Elastic Tissue ; Female ; Humans ; Pseudoxanthoma Elasticum/diagnosis ; Pseudoxanthoma Elasticum/genetics ; Rare Diseases ; Ultraviolet Rays
    Language English
    Publishing date 2020-10-16
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1064149-x
    ISSN 1879-1131 ; 0738-081X
    ISSN (online) 1879-1131
    ISSN 0738-081X
    DOI 10.1016/j.clindermatol.2020.10.018
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  9. Article ; Online: Acral persistent papular mucinosis.

    Rongioletti, Franco / Ferreli, Caterina / Atzori, Laura

    Clinics in dermatology

    2020  Volume 39, Issue 2, Page(s) 211–214

    Abstract: Acral persistent papular mucinosis (APPM) is a subtype of localized lichen myxedematosus (LM) characterized by the chronic development of white to skin-colored papules and limited to the extensor surfaces of the hands and distal part of forearms, in the ... ...

    Abstract Acral persistent papular mucinosis (APPM) is a subtype of localized lichen myxedematosus (LM) characterized by the chronic development of white to skin-colored papules and limited to the extensor surfaces of the hands and distal part of forearms, in the absence of systemic or laboratory manifestations. There is a strong predominance in women. Histopathology shows focal accumulation of mucin in the upper portion of the dermis sparing the grenz zone. The etiology is unknown. It is a benign condition, although dynamic changes occur with the progressive development of additional lesions. No specific treatment is required, and patients should be reassured about the prognosis.
    MeSH term(s) Female ; Humans ; Laboratories ; Scleromyxedema/diagnosis ; Skin Diseases
    Language English
    Publishing date 2020-10-16
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1064149-x
    ISSN 1879-1131 ; 0738-081X
    ISSN (online) 1879-1131
    ISSN 0738-081X
    DOI 10.1016/j.clindermatol.2020.10.001
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  10. Article ; Online: Aquagenic (pseudo) keratoderma (aquagenic palmoplantar keratoderma, aquagenic wrinkling of palms).

    Atzori, Laura / Ferreli, Caterina / Rongioletti, Franco

    Clinics in dermatology

    2020  Volume 39, Issue 2, Page(s) 256–260

    Abstract: Aquagenic palmoplantar keratoderma (APK) is an uncommon hereditary or sporadic condition that is characterized by edematous flat-topped papules appearing on palmar skin with wrinkling after brief water exposure. APK has been associated with cystic ... ...

    Abstract Aquagenic palmoplantar keratoderma (APK) is an uncommon hereditary or sporadic condition that is characterized by edematous flat-topped papules appearing on palmar skin with wrinkling after brief water exposure. APK has been associated with cystic fibrosis (CF), presenting with the same mutations found in CF (usually ΔF508 of the CFTR gene), either homozygous or heterozygous. APK may be idiopathic or drug-induced. The diagnosis is easily made if one is aware of this entity. Topical aluminum hydroxide and botulinum toxin injections are the most commonly used treatments. The sporadic form may have a shorter course compared with the hereditary one, resolving spontaneously after a few years. The condition should no longer be considered a true keratoderma but rather a pseudo keratoderma, and in spite of the many different names found in the literature, the term "aquagenic (pseudo) keratoderma" seems to be the most appropriate one.
    MeSH term(s) Heterozygote ; Humans ; Keratoderma, Palmoplantar/diagnosis ; Mutation ; Skin ; Skin Aging
    Language English
    Publishing date 2020-10-16
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1064149-x
    ISSN 1879-1131 ; 0738-081X
    ISSN (online) 1879-1131
    ISSN 0738-081X
    DOI 10.1016/j.clindermatol.2020.10.003
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