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  1. Article ; Online: New and emerging conditions of acquired cutaneous mucinoses in adults.

    Rongioletti, F

    Journal of the European Academy of Dermatology and Venereology : JEADV

    2022  Volume 36, Issue 7, Page(s) 1016–1024

    Abstract: Cutaneous mucinoses are a heterogenous group of conditions, characterized by the deposition of glycosaminoglycans (mucin) in the dermis, follicles, or in the epidermis. Major cutaneous mucinoses include lichen myxedematosus, scleredema, mucinoses ... ...

    Abstract Cutaneous mucinoses are a heterogenous group of conditions, characterized by the deposition of glycosaminoglycans (mucin) in the dermis, follicles, or in the epidermis. Major cutaneous mucinoses include lichen myxedematosus, scleredema, mucinoses associated with thyroid disease, reticular erythematous mucinosis, papulonodular mucinosis associated with connective tissue diseases, and cutaneous focal mucinosis. The aim of this review is to provide an update of what has currently been reported in the last 30-year literature about several new or emerging conditions of acquired cutaneous mucinoses in adults. Two new clinico-pathologic entities have been described: (i) Obesity-associated lymphedematous mucinosis and pretibial stasis mucinosis; (OACM) (ii) Nodular mucinosis of the breast (NMB). Two relatively new disease categories encompassing cutaneous mucinoses with a common pathogenetic mechanism have been identified: (i) Cutaneous mucinoses associated with drug exposure including biologic therapy, anti-colony-stimulating factor 1 receptor (CSF1R) and subcutaneous intralesional interferons (toxic dermal mucinoses); (ii) Cutaneous mucinosis following physical agents including mechanical traumas and after knee replacement.
    MeSH term(s) Adult ; Breast ; Connective Tissue Diseases ; Humans ; Mucinoses/etiology ; Mucinoses/pathology ; Scleredema Adultorum ; Scleromyxedema ; Skin Diseases/complications ; Skin Diseases/pathology
    Language English
    Publishing date 2022-02-17
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 1128828-0
    ISSN 1468-3083 ; 0926-9959
    ISSN (online) 1468-3083
    ISSN 0926-9959
    DOI 10.1111/jdv.17983
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  2. Article ; Online: Thirty years of new entities in inflammatory dermatology and dermatopathology.

    Rongioletti, F

    Journal of the European Academy of Dermatology and Venereology : JEADV

    2021  Volume 35, Issue 11, Page(s) 2121–2122

    MeSH term(s) Dermatology ; Humans
    Language English
    Publishing date 2021-10-14
    Publishing country England
    Document type Journal Article
    ZDB-ID 1128828-0
    ISSN 1468-3083 ; 0926-9959
    ISSN (online) 1468-3083
    ISSN 0926-9959
    DOI 10.1111/jdv.17653
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  3. Article ; Online: The crucial role of clinicopathological correlation in COVID-19-related cutaneous manifestations.

    Rongioletti, F

    Journal of the European Academy of Dermatology and Venereology : JEADV

    2021  Volume 35, Issue 9, Page(s) 1742–1743

    MeSH term(s) COVID-19 ; Humans ; Prognosis ; SARS-CoV-2 ; Skin Diseases/etiology
    Language English
    Publishing date 2021-08-18
    Publishing country England
    Document type Journal Article ; Comment
    ZDB-ID 1128828-0
    ISSN 1468-3083 ; 0926-9959
    ISSN (online) 1468-3083
    ISSN 0926-9959
    DOI 10.1111/jdv.17414
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  4. Article ; Online: Commentary: New, Emerging, and Revisited Entities in Dermatology.

    Rongioletti, Franco

    Clinics in dermatology

    2021  Volume 39, Issue 2, Page(s) 173–175

    MeSH term(s) Dermatology ; Humans
    Language English
    Publishing date 2021-06-23
    Publishing country United States
    Document type Editorial
    ZDB-ID 1064149-x
    ISSN 1879-1131 ; 0738-081X
    ISSN (online) 1879-1131
    ISSN 0738-081X
    DOI 10.1016/j.clindermatol.2021.06.001
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  5. Article ; Online: Frequency, risk factors and prognosis of systemic haematologic malignancies, cutaneous and other neoplasms in lymphomatoid papulosis: where are we now?

    Rongioletti, F

    Journal of the European Academy of Dermatology and Venereology : JEADV

    2020  Volume 34, Issue 2, Page(s) 216–217

    MeSH term(s) Hematologic Neoplasms ; Humans ; Lymphomatoid Papulosis ; Neoplasms ; Prognosis ; Risk Factors
    Language English
    Publishing date 2020-02-14
    Publishing country England
    Document type Journal Article ; Comment
    ZDB-ID 1128828-0
    ISSN 1468-3083 ; 0926-9959
    ISSN (online) 1468-3083
    ISSN 0926-9959
    DOI 10.1111/jdv.16157
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  6. Article ; Online: SARS-CoV, Mers-CoV and COVID-19: what differences from a dermatological viewpoint?

    Rongioletti, F

    Journal of the European Academy of Dermatology and Venereology : JEADV

    2020  Volume 34, Issue 10, Page(s) e581–e582

    MeSH term(s) Betacoronavirus ; COVID-19 ; Coronavirus Infections/complications ; Humans ; Middle East Respiratory Syndrome Coronavirus ; Pandemics ; Pneumonia, Viral/complications ; SARS Virus ; SARS-CoV-2 ; Skin Diseases/pathology ; Skin Diseases/therapy ; Skin Diseases/virology
    Keywords covid19
    Language English
    Publishing date 2020-07-02
    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.16738
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  7. Article ; Online: Actinic keratoses: what classification is useful to predict the risk of progression? PROs and cons.

    Rongioletti, F

    Journal of the European Academy of Dermatology and Venereology : JEADV

    2019  Volume 33, Issue 6, Page(s) 983–984

    MeSH term(s) Carcinogenesis ; Carcinoma, Squamous Cell/pathology ; Disease Progression ; Humans ; Keratosis, Actinic/classification ; Keratosis, Actinic/pathology ; Neoplasm Invasiveness ; Skin Neoplasms/pathology
    Language English
    Publishing date 2019-05-23
    Publishing country England
    Document type Journal Article
    ZDB-ID 1128828-0
    ISSN 1468-3083 ; 0926-9959
    ISSN (online) 1468-3083
    ISSN 0926-9959
    DOI 10.1111/jdv.15649
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  8. Article ; Online: Primary paediatric cutaneous mucinoses.

    Rongioletti, F

    The British journal of dermatology

    2019  Volume 182, Issue 1, Page(s) 29–38

    Abstract: Background: Primary cutaneous mucinoses are a heterogeneous group of diseases characterized by the abnormal deposition of glycosaminoglycans (mucin) in the skin. This is the main histopathological clue resulting in distinctive clinical presentations. ... ...

    Abstract Background: Primary cutaneous mucinoses are a heterogeneous group of diseases characterized by the abnormal deposition of glycosaminoglycans (mucin) in the skin. This is the main histopathological clue resulting in distinctive clinical presentations. They are usually diseases of adult age and are uncommon in children, in whom diagnosis and management are difficult tasks. In particular, the classification of primary cutaneous mucinoses occurring in childhood is a difficult and confusing challenge because of the very limited number of described cases and overlaps in their clinicopathological features in the absence of reports of homogeneous case series.
    Objectives: The aim of this review is to help dermatologists and paediatricians to identify patients with cutaneous mucinoses at a paediatric age and to enable institution of appropriate management. A classification of primary paediatric cutaneous mucinoses is also proposed.
    Results: New investigations have yielded significant insights into a classification of paediatric cutaneous mucinoses.
    Conclusions: The current update tries to offer a more meaningful guide to the diagnosis and treatment of these rare diseases in paediatric patients. What's already known about this topic? The nosography of primary cutaneous mucinoses occurring in childhood is confusing because of the very limited number of cases and overlaps in their clinicopathological features in the absence of homogeneous case series. The diagnosis and management of paediatric patients with cutaneous mucinoses are also difficult as these diseases are rarely seen in children. What does this study add? New investigations have yielded significant insights into a classification of paediatric cutaneous mucinoses. The current update tries to offer a more meaningful guide to diagnosis and treatment of these rare diseases in patients of paediatric age.
    MeSH term(s) Administration, Cutaneous ; Adult ; Child ; Glycosaminoglycans ; Humans ; Mucinoses/diagnosis ; Mucinoses/therapy ; Skin
    Chemical Substances Glycosaminoglycans
    Language English
    Publishing date 2019-07-15
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 80076-4
    ISSN 1365-2133 ; 0007-0963
    ISSN (online) 1365-2133
    ISSN 0007-0963
    DOI 10.1111/bjd.18004
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  9. Article ; Online: Annular dermatoses with rheumatologic implications.

    Paolino, Giovanni / Rongioletti, Franco

    Clinics in dermatology

    2023  Volume 41, Issue 3, Page(s) 376–381

    Abstract: A wide variety of cutaneous disorders present with annular (ringlike) skin lesions, and some of them carry rheumatologic implications because they may involve the joints or belong to the spectrum of connective tissue diseases. The diagnosis of an annular ...

    Abstract A wide variety of cutaneous disorders present with annular (ringlike) skin lesions, and some of them carry rheumatologic implications because they may involve the joints or belong to the spectrum of connective tissue diseases. The diagnosis of an annular rheumatologic skin disease is possible with a correct clinicopathologic correlation, with a correct anamnesis of the patient, with the evaluation of systemic symptoms, laboratory and instrumental investigations, and finally with a cutaneous biopsy.
    MeSH term(s) Humans ; Skin Diseases/diagnosis ; Skin Diseases/etiology ; Skin Diseases/pathology ; Skin/pathology ; Connective Tissue Diseases/complications ; Connective Tissue Diseases/diagnosis ; Connective Tissue Diseases/pathology ; Arthritis, Rheumatoid/complications
    Language English
    Publishing date 2023-07-11
    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.2023.07.006
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Nodular-Type Lichen Myxedematosus: A Rare Variant With Exclusive Involvement of the Hands-Report of Two Cases With a Comprehensive Review of the Literature.

    Cerroni, Lorenzo / Rongioletti, Franco

    The American Journal of dermatopathology

    2023  Volume 46, Issue 1, Page(s) 36–39

    Abstract: Abstract: Lichen myxedematosus (LM) is an uncommon cutaneous mucinosis characterized by the deposition of mucin and fibroblast proliferation in the dermis. This condition can be classified into 2 forms: a diffuse/generalized LM, also known as ... ...

    Abstract Abstract: Lichen myxedematosus (LM) is an uncommon cutaneous mucinosis characterized by the deposition of mucin and fibroblast proliferation in the dermis. This condition can be classified into 2 forms: a diffuse/generalized LM, also known as scleromyxedema, associated with monoclonal gammopathy and systemic implications, and a localized form, primarily affecting the skin. Within the localized form, nodular-type LM is a rare variant presenting as firm, skin-colored to pinkish mucinous nodules. In this article, we report 2 new cases of nodular-type LM with exclusive involvement of the hands and provide a comprehensive review of the diagnosis, histopathological aspects, and therapeutic considerations of this rare condition.
    MeSH term(s) Humans ; Scleromyxedema/diagnosis ; Scleromyxedema/pathology ; Skin/pathology ; Skin Diseases/pathology ; Hand/pathology ; Upper Extremity/pathology
    Language English
    Publishing date 2023-11-20
    Publishing country United States
    Document type Review ; Case Reports ; Journal Article
    ZDB-ID 448469-1
    ISSN 1533-0311 ; 0193-1091
    ISSN (online) 1533-0311
    ISSN 0193-1091
    DOI 10.1097/DAD.0000000000002589
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