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| http://dx.doi.org/10.1016/j.jaip.2022.02.043 | DOI Listing |
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Systematic Review of Granulomatous Invasive Fungal Sinusitis Management.
Laryngoscope Investig Otolaryngol
February 2025
Otolaryngology-Head & Neck Surgery Department, College of Medicine King Saud University Riyadh Saudi Arabia.
Objectives: Granulomatous invasive fungal sinusitis (GIFS) affects immunocompetent individuals. There is ongoing debate over whether surgery, antifungal medication, or a combined approach is the best treatment. This article summarizes reports about GIFS and its management.
View Article and Find Full Text PDFUnusually indolent CML: a stable non-responder without complete cytogenetic remission for 30 years including 17 years on tyrosine kinase inhibitor therapy.
Leuk Lymphoma
January 2025
Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Sequential Occurrence of Eosinophilic Gastrointestinal Disease in a Case of Waldenström's Macroglobulinemia in Remission: An Unusual Report with Review.
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October 2024
Apollo CBCC Cancer Care, Ahmedabad, Gujarat, India.
Waldenström macroglobulinemia (WM) is a rare lymphoproliferative malignancy presenting with para-proteinemia. The symptoms are attributable to both lymphoproliferation and IgM flare. Gastrointestinal manifestations are not uncommon.
View Article and Find Full Text PDFClinical and histopathological characteristics of atrophic pigmented dermatofibrosarcoma protuberans: A retrospective study of 14 cases.
Heliyon
November 2024
Department of Dermatology, The Second Affiliated Hospital of Xi'an Jiaotong University, Shaanxi, China.
Article Synopsis
- Dermatofibrosarcoma protuberans (DFSP) with atrophic and pigmentary features (AP-DFSP) is a rare skin condition characterized by lesions mainly on the trunk and limbs, often presenting as depressed, colored plaques.
- This study analyzed 14 cases of AP-DFSP to determine clinical features, treatment responses, and prognostic outcomes, finding that patients had a mean age of 25 years and most cases were successfully treated with complete surgical excision.
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Complete skin remission of Sneddon-Wilkinson disease with acalabrutinib.
Australas J Dermatol
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Sir Peter McCallum Department of Oncology, University of Melbourne, Melbourne, Victoria, Australia.
Sneddon-Wilkinson (SW) disease is rare condition which typically occurs in the context of a monoclonal immunoglobulin and treatment options have not been well studied. Here we present a case of a 65-year-old female with SW with underlying, otherwise indolent, lymphoplasmacytic lymphoma (LPL) with an IgA paraprotein, who achieved a complete skin remission with the administration of the Bruton Tyrosine Kinase inhibitor (BTKi), acalabrutinib.
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