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  1. Book ; Online ; E-Book: Neutrophilic dermatoses

    Wallach, David / Vignon-Pennamen, Marie-Dominique / Valerio, Marzano Angelo

    2018  

    Author's details Daniel Wallach, Marie-Dominique Vignon-Pennamen, Angelo Valerio Marzano editors
    Keywords Medicine ; Immunology ; Dermatology ; Rheumatology
    Subject code 616.5
    Language English
    Size 1 Online-Ressource (ix, 334 Seiten), Illustrationen
    Publisher Springer
    Publishing place Cham
    Publishing country Switzerland
    Document type Book ; Online ; E-Book
    Remark Zugriff für angemeldete ZB MED-Nutzerinnen und -Nutzer
    HBZ-ID HT019744050
    ISBN 978-3-319-72649-6 ; 9783319726489 ; 3-319-72649-8 ; 331972648X
    DOI 10.1007/978-3-319-72649-6
    Database ZB MED Catalogue: Medicine, Health, Nutrition, Environment, Agriculture

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  2. Article ; Online: From Histiocytoid Sweet Syndrome to Myelodysplasia Cutis: History and Perspectives.

    Vignon-Pennamen, Marie-Dominique / Battistella, Maxime

    Dermatologic clinics

    2023  Volume 42, Issue 2, Page(s) 209–217

    Abstract: In 2005, a new histologic variant of Sweet syndrome (SS) has been described and termed histiocytoid SS (HSS). Clinically, patients had a typical SS, but on skin biopsy, the infiltrates were composed of immature nonblast myeloid cells. Nearly 50% of ... ...

    Abstract In 2005, a new histologic variant of Sweet syndrome (SS) has been described and termed histiocytoid SS (HSS). Clinically, patients had a typical SS, but on skin biopsy, the infiltrates were composed of immature nonblast myeloid cells. Nearly 50% of patients with HSS have myelodysplastic syndrome (MDS). HSS may be the first manifestation leading to the diagnosis of MDS. In 2015, a new category of myeloid dermatosis has been proposed, called myelodysplasia cutis, describing the specific skin infiltration by myelodysplastic cells in patients with MDS.
    MeSH term(s) Humans ; Sweet Syndrome/diagnosis ; Skin/pathology ; Myelodysplastic Syndromes/complications ; Myelodysplastic Syndromes/diagnosis ; Myelodysplastic Syndromes/pathology ; Biopsy
    Language English
    Publishing date 2023-09-11
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 82798-8
    ISSN 1558-0520 ; 0733-8635
    ISSN (online) 1558-0520
    ISSN 0733-8635
    DOI 10.1016/j.det.2023.08.004
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Clinical and histological features of histiocytoid Sweet syndrome associated with VEXAS syndrome.

    Lecoeuvre, Hortense / Le Gall, Franҫois / Le Naoures, Cécile / Vignon-Pennamen, Marie-Dominique / Lamaison, Claire / Kammerer-Jacquet, Solène-Florence / Lescoat, Alain / Oger, Emmanuel / Pastoret, Cédric / Dupuy, Alain

    Clinical and experimental dermatology

    2024  

    Abstract: Background: "Vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic" (VEXAS) syndrome is caused by acquired somatic mutations in the ubiquitin-activating enzyme 1 (UBA1) gene. Sweet-syndrome-like skin disorders (and especially histiocytoid Sweet ... ...

    Abstract Background: "Vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic" (VEXAS) syndrome is caused by acquired somatic mutations in the ubiquitin-activating enzyme 1 (UBA1) gene. Sweet-syndrome-like skin disorders (and especially histiocytoid Sweet syndrome (HSS)) may be associated with VEXAS syndrome.
    Objective: To characterize the clinical and histopathological features of HSS in patients with VEXAS syndrome.
    Methods: The skin biopsies with a histological diagnosis of HSS had been collected at Rennes University Medical Center (Rennes, France) between October 2011 and January 2022. Sanger sequencing and digital PCR were used to screen skin, blood, and bone marrow samples for UBA1 variants, and thus classify patients as having VEXAS syndrome or not. We evaluated the clinical, histological, and molecular (UBA1) characteristics of patients with or without VEXAS syndrome.
    Results: We compared 15 skin biopsies from seven patients found to have VEXAS syndrome and 19 skin biopsies from 15 patients without VEXAS syndrome. Persistent inflammatory syndrome, macrocytosis, anemia, and hematological malignancies were more prevalent in patients with VEXAS syndrome (86%, 86%, 100%, and 86%, respectively) than in patients without (36%, 40%, 53%, and 53%, respectively). These features sometimes appeared after the first skin manifestations, and a UBA1 mutation was found in the skin of five patients with VEXAS syndrome. Dermal infiltration by myeloperoxidase-positive, CD163-positive, reniform histiocytoid cells and a periadnexal distribution were more frequently observed in VEXAS syndrome biopsies (100% and 20% respectively, vs. 58% and 0% in non-VEXAS syndrome biopsies, respectively).
    Conclusion: Our findings might help the pathologist to consider a diagnosis of VEXAS syndrome and to initiate early genetic testing.
    Language English
    Publishing date 2024-02-16
    Publishing country England
    Document type Journal Article
    ZDB-ID 195504-4
    ISSN 1365-2230 ; 0307-6938
    ISSN (online) 1365-2230
    ISSN 0307-6938
    DOI 10.1093/ced/llae015
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  4. Article ; Online: Periorbital erythema and oedema revealing angioimmunoblastic T cell lymphoma.

    De Clippele, Donatienne / Frumholtz, Laure / Vignon-Pennamen, Marie-Dominique / Molina, Thierry / Moatti, Hannah / Battistella, Maxime / Ochmann, Marlène / Ram-Wolff, Caroline / Petit, Antoine / Bagot, Martine / De Masson, Adèle

    European journal of dermatology : EJD

    2023  Volume 33, Issue 1, Page(s) 58–59

    MeSH term(s) Humans ; Immunoblastic Lymphadenopathy/complications ; Immunoblastic Lymphadenopathy/diagnosis ; Immunoblastic Lymphadenopathy/pathology ; Lymphoma, T-Cell, Peripheral/pathology ; Erythema/etiology ; Edema/etiology
    Language English
    Publishing date 2023-06-01
    Publishing country France
    Document type Journal Article
    ZDB-ID 1128666-0
    ISSN 1952-4013 ; 1167-1122
    ISSN (online) 1952-4013
    ISSN 1167-1122
    DOI 10.1684/ejd.2023.4426
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Histiocytoid Sweet Syndrome and Myelodysplastic Syndrome.

    Vignon-Pennamen, Marie Dominique / Osio, Amélie / Battistella, Maxime

    JAMA dermatology

    2017  Volume 153, Issue 8, Page(s) 835–836

    MeSH term(s) Humans ; Myelodysplastic Syndromes ; Sweet Syndrome
    Language English
    Publishing date 2017-06-12
    Publishing country United States
    Document type Journal Article ; Comment
    ZDB-ID 2701761-8
    ISSN 2168-6084 ; 2168-6068
    ISSN (online) 2168-6084
    ISSN 2168-6068
    DOI 10.1001/jamadermatol.2017.1669
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Two cases of dupilumab-responsive Kimura disease.

    Battesti, Gilles / Jachiet, Marie / Lepelletier, Clémence / Petit, Antoine / Vignon-Pennamen, Marie-Dominique / Cassius, Charles / de Masson, Adèle / Battistella, Maxime / Bagot, Martine / Bouaziz, Jean David / Mahévas, Thibault

    Clinical and experimental dermatology

    2023  Volume 49, Issue 5, Page(s) 502–506

    Abstract: Kimura disease (KD) is a rare, chronic angiolymphoproliferative inflammatory disease appearing to be mostly restricted to the skin and soft tissue. Cutaneous involvement of KD includes head and/or neck nodules showing suggestive histological features, ... ...

    Abstract Kimura disease (KD) is a rare, chronic angiolymphoproliferative inflammatory disease appearing to be mostly restricted to the skin and soft tissue. Cutaneous involvement of KD includes head and/or neck nodules showing suggestive histological features, frequently associated with an atopic dermatitis-like or prurigo-like presentation. KD is challenging to treat, with high rate of recurrence using current therapeutic strategies. Evidence for involvement of a T-helper type 2 (Th2) immune response in KD pathogenesis has been found in previous studies. Consequently, this study aimed to determine the efficacy and safety of dupilumab, a human monoclonal antibody that inhibits signalling of key Th2 cytokines, interleukin (IL)-4 and IL-13, within a single-centre cohort of patients with cutaneous KD. Two adults with a diagnosis of refractory (failure of at least one treatment line) cutaneous-restricted KD based on clinical, biological, histological, molecular and imaging findings received dupilumab for KD, and showed dramatic response with a good safety profile.
    MeSH term(s) Humans ; Antibodies, Monoclonal, Humanized/therapeutic use ; Male ; Adult ; Kimura Disease/drug therapy ; Kimura Disease/pathology ; Middle Aged ; Female ; Treatment Outcome ; Interleukin-4 ; Interleukin-13/antagonists & inhibitors
    Chemical Substances Antibodies, Monoclonal, Humanized ; dupilumab (420K487FSG) ; Interleukin-4 (207137-56-2) ; Interleukin-13
    Language English
    Publishing date 2023-12-27
    Publishing country England
    Document type Journal Article ; Case Reports
    ZDB-ID 195504-4
    ISSN 1365-2230 ; 0307-6938
    ISSN (online) 1365-2230
    ISSN 0307-6938
    DOI 10.1093/ced/llad455
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  7. Article ; Online: Multicentric reticulohistiocytosis associated with organizing pneumonia.

    Nguyen, Yann / Huynh, Sandra / de Clippele, Donatienne / Vignon-Pennamen, Marie-Dominique / Petit, Antoine / Frumholtz, Laure

    Joint bone spine

    2021  Volume 88, Issue 5, Page(s) 105192

    MeSH term(s) Arthritis ; Histiocytosis, Non-Langerhans-Cell/complications ; Histiocytosis, Non-Langerhans-Cell/diagnosis ; Histiocytosis, Non-Langerhans-Cell/drug therapy ; Humans ; Pneumonia
    Language English
    Publishing date 2021-04-20
    Publishing country France
    Document type Letter
    ZDB-ID 2020487-5
    ISSN 1778-7254 ; 1297-319X
    ISSN (online) 1778-7254
    ISSN 1297-319X
    DOI 10.1016/j.jbspin.2021.105192
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  8. Article ; Online: Possible Paradoxical Photosensitive Psoriasis Induced by Tumour Necrosis Factor-alpha Inhibitors.

    Bataille, Pauline / Masson, Adèle De / Vignon-Pennamen, Marie-Dominique / Bouaziz, Jean-David / Gornet, Jean-Marc

    Acta dermato-venereologica

    2019  Volume 99, Issue 13, Page(s) 1293–1294

    MeSH term(s) Administration, Topical ; Biopsy, Needle ; Blood Chemical Analysis ; Crohn Disease/diagnosis ; Crohn Disease/drug therapy ; Facial Dermatoses/diagnosis ; Facial Dermatoses/etiology ; Follow-Up Studies ; Humans ; Immunohistochemistry ; Infliximab/adverse effects ; Infliximab/therapeutic use ; Male ; Photosensitivity Disorders/chemically induced ; Photosensitivity Disorders/drug therapy ; Photosensitivity Disorders/pathology ; Psoriasis/chemically induced ; Psoriasis/pathology ; Risk Assessment ; Tacrolimus/therapeutic use ; Treatment Outcome ; Tumor Necrosis Factor-alpha/adverse effects ; Tumor Necrosis Factor-alpha/antagonists & inhibitors ; Young Adult
    Chemical Substances Tumor Necrosis Factor-alpha ; Infliximab (B72HH48FLU) ; Tacrolimus (WM0HAQ4WNM)
    Language English
    Publishing date 2019-10-03
    Publishing country Sweden
    Document type Case Reports ; Journal Article ; Review
    ZDB-ID 80007-7
    ISSN 1651-2057 ; 0001-5555
    ISSN (online) 1651-2057
    ISSN 0001-5555
    DOI 10.2340/00015555-3330
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Cutaneous clonal mature plasmacytoid dendritic cell dermatosis in patients with myeloid neoplasms.

    Mahévas, Thibault / Osio, Amélie / Larcher, Lise / Clappier, Emmanuelle / Kempf, Werner / Adès, Lionel / Fenaux, Pierre / Sébert, Marie / Delaleu, Jérémie / Jachiet, Marie / Cordoliani, Florence / Charvet, Estelle / Carpentier, Olivier / Itzykson, Raphaël A / Weinborn, Marie / Mardare, Nicoleta / Marco-Bonnet, Joséfina / de Masson, Adèle / Duployez, Nicolas /
    Huynh, Tony / Bouaziz, Jean-David / Vignon-Pennamen, Marie-Dominique / Battistella, Maxime

    Blood advances

    2024  

    Language English
    Publishing date 2024-04-12
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2915908-8
    ISSN 2473-9537 ; 2473-9529
    ISSN (online) 2473-9537
    ISSN 2473-9529
    DOI 10.1182/bloodadvances.2023012489
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  10. Article ; Online: Toxic epidermal necrolysis possibly associated with mogamulizumab in a patient with Sézary syndrome.

    Lazaridou, Ingrid / Calvani, Julien / Annabi, Elissa / Moins-Teisserenc, Hélène / Ta, Van Anh / Rivet, Jacqueline / Ram-Wolff, Caroline / Dumont, Maëlle / Mahevas, Thibault / Vignon-Pennamen, Marie-Dominique / Mourah, Samia / Bouaziz, Jean-David / Louveau, Baptiste / Bagot, Martine / Battistella, Maxime / de Masson, Adèle

    Journal of the European Academy of Dermatology and Venereology : JEADV

    2023  Volume 37, Issue 6, Page(s) e715–e717

    MeSH term(s) Humans ; Sezary Syndrome/drug therapy ; Stevens-Johnson Syndrome/etiology ; Antibodies, Monoclonal, Humanized/adverse effects ; Skin Neoplasms/drug therapy
    Chemical Substances mogamulizumab (YI437801BE) ; Antibodies, Monoclonal, Humanized
    Language English
    Publishing date 2023-01-21
    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.18868
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