Results 81 to 90 of about 12,179 (241)
Case Reports in Medicine, 2015 The pathogenesis of mastocytosis is not well defined and thus treatment remains challenging and remains on a palliative basis. We present two cases (a 48-year-old woman and a 57-year-old man) with indolent systemic mastocytosis in whom omalizumab (anti ...
Sofie Lieberoth, Simon Francis Thomsen
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Mastocytosis: One Word for Different Diseases
Oncology and Therapy, 2018 Mastocytosis is a neoplastic disease originating from tissue infiltration by transformed mast cells. The diagnosis requires a high grade of suspicion due to the large variety of presenting symptoms. The World Health Organization classification recognizes
Marianna Criscuolo +3 more
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Allergen-specific immunotherapy of Hymenoptera venom allergy:also a matter of diagnosis [PDF]
, 2015 Stings of hymenoptera can induce IgE-mediated hypersensitivity reactions in venom-allergic patients, ranging from local up to severe systemic reactions and even fatal anaphylaxis.
Schiener, Maximilian +4 more
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Neurological manifestations of chronic graft versus host disease
Internal Medicine Journal, Volume 55, Issue 10, Page 1639-1646, October 2025.Abstract Introduction Allogeneic haemopoietic stem cell transplant (allo‐HSCT) is an established therapy for many malignant and non‐malignant conditions, with an increasing number of uses and indications in recent decades. Complications including graft versus host disease (GvHD) carry significant morbidity and mortality.
Tal Koren +7 more
wiley +1 more source
Mastocitose bolhosa na criança: relato de caso Bullous mastocytosis in child: case report
Anais Brasileiros de Dermatologia, 2005 A mastocitose é doença rara, definida como a infiltração desordenada de mastócitos em vários tecidos. Compreende diferentes quadros clínicos, variando de formas cutâneas indolentes a condições sistêmicas e malignas. O termo mastocitose bolhosa descreve a
Ana Lúcia França da Costa +2 more
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Systemic Mastocytosis - a Diagnostic Challenge [PDF]
, 2014 Mastocytosis refers to a group of disorders characterized by the infiltration of clonally derived mast cells to the skin or extracutaneous tissues resulting in a heterogeneous clinical picture. It is a rare hematologic disorder in all its forms.
Galzerano, A +3 more
core
American Journal of Hematology, Volume 100, Issue 9, Page 1566-1576, September 2025.Overall survival data among 910 Mayo Clinic patients with systemic mastocytosis stratified by the International Consensus Classification (ICC) and the Mayo Alliance Prognostic Scoring System (MAPS). ABSTRACT The current study includes 910 patients with systemic mastocytosis (SM) seen at the Mayo Clinic from 1968 to 2024.
Fnu Aperna +13 more
wiley +1 more source
Pruritic Plaque on the Right Lower Limb: A Rare Case of Kimura Disease and Literature Review
Clinical Case Reports, Volume 13, Issue 9, September 2025.ABSTRACT Kimura disease, though rare in adolescents, should be considered in cases of persistent itchy nodules. Histopathology confirms diagnosis. Surgical excision is effective for localized lesions, with favorable outcomes. Early recognition prevents misdiagnosis and unnecessary treatments.
Xiaoxiao Liu, Xiaolan Zhang
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Neonatal Epidermolytic Ichthyosis Caused by a KRT10 Mutation (c.467G>A, p.Arg156His): A Case Report
Clinical Case Reports, Volume 13, Issue 8, August 2025.ABSTRACT We present a neonatal case of skin blisters and erythema. While epidermolysis bullosa was initially suspected, immunofluorescence antigen mapping and genetic testing confirmed epidermolytic ichthyosis, with a heterozygous pathogenic variant in the KRT10 gene (c.467G>A, p.Arg156His).
Elke Smits +4 more
wiley +1 more source