Results 41 to 50 of about 66,314 (265)

Mast Cell Sarcoma of the Retroperitoneum With Concurrent Systemic Mastocytosis and an Undisclosed Associated Hematologic Neoplasm: A Case Report

Clinical Pathology, 2022
Mastocytosis is a rare disorder affecting both children and adults by gathering of functionally defective mast cells in the body’s tissues. The World Health Organization (WHO) classified mastocytosis into cutaneous mastocytosis, systemic mastocytosis (SM)
Ing Chen, Jia-Bin Liao, Jung-Chia Lin, Pin-Pen Hsieh, Ming-Yun Hsieh   +4 more
doaj   +1 more source

Diffuse large B cell lymphoma coexistence with systemic mastocytosis

Journal of Cancer Research and Practice, 2016
Systemic mastocytosis is a rare disease and characterized by excessive mast cell accumulation in one or multiple organs. One subtype of systemic mastocytosis is systemic mastocytosis-associated clonal hematological non-mast cell lineage disease (SM-AHMND)
Sheng-Hsuan Chien, Yao-Chung Liu, Ying-Chung Hong, Ching-Fen Yang, Chun-Yu Liu, Tzeon-Jye Chiou, Cheng-Hwai Tzeng, Jin-Hwang Liu, Jyh-Pyng Gau   +8 more
doaj   +1 more source

Klinikai tapasztalataink cutan mastocytosisban. [PDF]

, 2013
Introduction: Mastocytosis is a clonal mast cell proliferative disease, devided into cutaneous and systemic forms. The characteristic symptoms are caused by neoplastic mast cell infiltrations in different organs and/or the release of mediators.
Csomor, Judit, Hidvégi, Bernadett, Hársing, Judit, Kovalszky, Ilona, Kárpáti, Sarolta, Marschalkó, Márta, Mihalik, Noémi, Várkonyi, Judit   +7 more
core   +1 more source

SYSTEMIC MASTOCYTOSIS: RADIOLOGICAL POINT OF VIEW

Mediterranean Journal of Hematology and Infectious Diseases, 2021
Radiological diagnosis of systemic mastocytosis (SM) can be hard to establish. This is mainly due to the variable radiological features involving many organ systems (e.g., respiratory, cardiovascular, lympho-reticular, digestive systems, and most commonly skin), and the broad spectrum of skeletal findings, in particular.
Daniele Perla, Giulia D'Ambra, Giuseppe Veltri, Antonio Maria Leone, Silvia Macagnino   +4 more
openaire   +5 more sources

Solitary mastocytoma presenting in an adult: report and literature review of adult-onset solitary cutaneous mastocytoma with recommendations for evaluation and treatment

Dermatology Practical & Conceptual, 2016
Background: Mastocytosis is either cutaneous (with skin-limited proliferation of mast cells) or systemic (with mast cells in extracutaneous sites). The onset of solitary mastocytoma in an adult is rare.
Philip R. Cohen
doaj   +1 more source

An intriguing coexistence of cutaneous and systemic mastocytosis with atypical chronic myeloid leukemia: An associated hematologic neoplasm (SM-AHN)

Journal of Applied Hematology, 2021
Systemic mastocytosis (SM) characterized by focal or diffuse infiltrates of neoplastic mast cells can range from indolent cutaneous disease to aggressive systemic disease.
B R Rajalakshmi, Vijaya Basavaraj
doaj   +1 more source

Comparative analysis of IL6 and IL6 receptor gene polymorphisms in mastocytosis [PDF]

, 2013
Mastocytosis is a rare disease with reported high interleukin-6 (IL6) levels influencing disease severity. The present study investigated polymorphisms within the genes that encode IL6 and its receptor (IL6R) in relation to mastocytosis development in a ...
Aladzsity István, Csomor Judit, Falus András, Hidvégi Bernadett, Kokai Márta, Lange M, Lautner-Csorba Orsolya, Marschalkó Márta, Nedoszytko B, Niedoszytko M, Rausz Eszter Zsófia, Szakonyi József, Szilágyi Ágnes, Valent P, Várkonyi Judit   +14 more
core   +1 more source

Epidemiology of systemic mastocytosis in Denmark [PDF]

British Journal of Haematology, 2014
SummaryMastocytosis is a heterogeneous group of diseases characterized by abnormal proliferation of mast cells. Systemic mastocytosis (SM), in which abnormal mast cells are present in tissues beyond the skin, is divided into seven subcategories with varying degrees of severity and prognosis.
Cohen, Sarah, Hoffmann, Stine Skovbo, Vestergaard, Hanne, Kielsgaard Kristensen, Thomas, Bindslev-Jensen, Carsten, Møller, Michael Boe, Broesby-Olsen, Sigurd, P. Fryzek, Jon   +7 more
openaire   +4 more sources

Splenomegaly, elevated alkaline phosphatase and mutations in the SRSF2/ASXL1/RUNX1 gene panel are strong adverse prognostic markers in patients with systemic mastocytosis [PDF]

, 2016
We evaluated the impact of clinical and molecular characteristics on overall survival (OS) in 108 patients with indolent (n=41) and advanced SM (advSM, n=67).
Clemens, J., Cross, N.C.P., Fabarius, A., Hausmann, D., Henzler, T., Hofmann, W.-K., Horny, H.-P., Jawhar, M., Metzgeroth, G., Naumann, N., Reiter, A., Schoenberg, S.O., Schwaab, J., Sotlar, K., Valent, P.   +14 more
core   +1 more source

The Basophil Activation Test Is Not a Useful Screening Tool for Hymenoptera Venom-Related Anaphylaxis in Patients with Systemic Mastocytosis [PDF]

, 2016
Background: Systemic mastocytosis (SM) patients are at a high risk for anaphylaxis, with Hymenoptera as the main culprit. A screening instrument to identify which patients are sensitized to Hymenoptera before they experience anaphylaxis would therefore ...
Daele, P.L.A. (Paul) van, Gerth van Wijk, R. (Roy), Hermans, M.A.W. (Maud A.W.), Rietveld, M.J.A. (Mark J.A.), Schreurs, M.W.J. (Marco)   +4 more
core   +1 more source