Results 31 to 40 of about 869 (178)
Mast cell activation syndrome. About a clinical case
Background: Monoclonal mast cell activation syndrome is included in mast cell activation disorders in which, after a diagnostic process, it is not possible to meet the required criteria for a diagnosis of systemic mastocytosis.
Ricardo Cardona +4 more
doaj +1 more source
Mast cell-related disorders presenting with Kounis syndrome [PDF]
Letter to the Editor.-- et al.Peer ...
Escribano, Luis +9 more
core +1 more source
Mastocitosis Cutánea y Urticaria Pigmentosa: Estudio de Casos y Actualización Terapéutica [PDF]
Cutaneous mastocytosis is a rare disease with a good prognosis. It is characterized by the invasion of mast cells, in abnormal amount, in the skin.
Burgos Iturra , Guillermo
core +2 more sources
Definitions, Criteria and Global Classification of Mast Cell Disorders with Special Reference to Mast Cell Activation Syndromes: A Consensus Proposal [PDF]
Activation of tissue mast cells (MCs) and their abnormal growth and accumulation in various organs are typically found in primary MC disorders also referred to as mastocytosis.
Akin C +73 more
core +1 more source
Background: Hearing loss and blindness are seldom encountered as primary manifestations in patients with chronic myeloid leukemia. Chronic myeloid leukemia (CML) commonly presents with weakness, dysphagia, abdominal distension and pain and rarely constitutional symptoms.
S., S. Tandon, R. Gupta, S. Nityanand
wiley +1 more source
Mastocitosis sistémica: Revisión sistemática [PDF]
La mastocitosis es una enfermedad definida por un crecimiento anormal y por la acumulación de mastocitos. En la clasificación de consenso de la OMS del 2001, se distinguió entre procesos bien limitados a piel (mastocitosis cutánea) o bien acumulados a nivel de otros tejidos: médula ósea y/u otros órganos extracutáneos (mastocitosis sistémica) como ...
Molina-Garrido, M.J. +6 more
openaire +3 more sources
Background: Myelodysplastic syndrome (MDS) is a heterogeneous group of diseases characterized by ineffective erythropoiesis and dysplasia. MDS and its subtype CMML is highly associated with chronic inflammatory and autoimmune diseases; however the combination of MDS with other bone marrow neoplasms is not a common entity. Only few cases of MDS combined
A. Sevoyan, A. Sevoyan
wiley +1 more source
Mastocitoma solitario. Comunicación de un caso
Antecedentes: El mastocitoma solitario es una variante de mastocitosis cutánea de buen pronóstico, congénita, que aparece durante las primeras semanas de vida.
Camila Delgadillo Jordán
doaj +1 more source
How patients remember when they were given the diagnosis. About fifteen testimonies related to rare diseases [PDF]
Doctor-patient communication has led, in recent years, great interest among the health community. Communicating the diagnosis is one of the key moments for people suffering an illness.
Arcos Urrutia, Juan Manuel +2 more
core +2 more sources
Background: We present here the case of a 52 year old male patient who was diagnosed of D816 V + indolent systemic mastocytosis in 2006. The patient received only symptomatic treatment with fexofenadine, sodium cromoglycate, and ranitidine. In November 7th 2016, mild leukocytosis was detected in one of the screenings.
A. Savchuk +8 more
wiley +1 more source

