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    Complete resolution of febrile ulceronecrotic Mucha-Habermann disease following infliximab therapy.
    J Dtsch Dermatol Ges 2016 Feb 20;14(2):184-6. Epub 2016 Jan 20.
    Department of Dermatology, Venereology, and Allergology, HELIOS St. Elisabeth Hospital, Oberhausen. Germany.

    Similar Publications

    [Febrile ulceronecrotic Mucha-Habermann disease].
    Rev Med Chil 2016 Sep;144(9):1214-1217
    Anatomía Patológica, Hospital Clínico San Borja Arriarán, Universidad de Chile, Santiago, Chile.
    Pityriasis lichenoides et varioliformis acuta (PLEVA), pityriasis lichenoides chronica (PLC) and febrile ulceronecrotic Mucha-Habermann disease (FUMHD) are considered different manifestations of the same disease. Febrile ulceronecrotic Mucha-Habermann disease is a rare, and potentially lethal illness which is characterized by fast progression of numerous papules that converge, ulcerate and form a plaque with a necrotic center, together with hemorrhagic vesicles and pustules that are associated with high fever and variable systemic symptoms. We report a 16 years old male presenting with erythematous papules with crusts and fever. Read More
    Febrile ulceronecrotic Mucha-Habermann disease in adult patient successfully treated with systemic corticosteroid.
    An Bras Dermatol 2010 Nov-Dec;85(6):891-4
    Lauro de Souza Lima Institute , Bauru, SP, Brasil.
    The Febrile Ulceronecrotic Mucha-Habermann (FUMHD) disease is a rare variant of pityriasis lichenoides et varioliformis acuta (PLEVA). Its etiology still remains unknown and it is characterized by a sudden onset of ulceronecrotic skin lesions associated with systemic symptoms. It is reported here the case of a male patient with a sudden and acute evolution of macules and papules, ulceronecrotic and vesicle-bullous lesions associated with systemic symptoms. Read More
    Febrile ulceronecrotic Mucha-Habermann disease with central nervous system vasculitis.
    Pediatr Dermatol 2013 Jan-Feb;30(1):90-3. Epub 2012 Jan 26.
    Division of Dermatology, Department of Internal Medicine, School of Medicine Washington University, and St. Louis Children's Hospital, St. Louis, Missouri 63110, USA.
    Febrile ulceronecrotic Mucha-Habermann disease (FUMHD) is a severe variant of pityriasis lichenoides et varioliformis acuta (PLEVA). We report a case of FUMHD in an 11-year-old boy who subsequently developed neurologic symptoms and was found to have necrotizing vasculitis on brain biopsy. Over 5 years of follow-up, he had one biopsy-proven recurrence of his skin lesions and continued rehabilitation and treatment for residual neurologic complications. Read More
    Febrile ulceronecrotic Mucha-Habermann disease: a case report and review of the literature.
    Acta Derm Venereol 2008 ;88(4):350-5
    First Dermatologic Clinic, Aristotle University of Thessaloniki, Greece.
    Febrile ulceronecrotic Mucha-Habermann disease is a severe variant of pityriasis lichenoides et varioliformis acuta characterized by the sudden onset of ulceronecrotic skin lesions and associated with high fever and systemic symptoms. We report here a case of a 20-year-old woman in whom the disease started as pityriasis lichenoides et varioliformis acuta and evolved to febrile ulceronecrotic Mucha-Habermann disease. Almost 90% of the body surface was involved, together with high fever and malaise. Read More