Results 171 to 180 of about 68,714 (217)
Some of the next articles are maybe not open access.
Annual Review of Medicine, 2004
Systemic mastocytosis is a clonal disorder of the mast cell and its progenitor. The symptoms of systemic mastocytosis are due to the pathologic accumulation and activation of mast cells in various tissues such as bone marrow, skin, gastrointestinal tract, liver, and spleen.
Cem, Akin, Dean D, Metcalfe
openaire +2 more sources
Systemic mastocytosis is a clonal disorder of the mast cell and its progenitor. The symptoms of systemic mastocytosis are due to the pathologic accumulation and activation of mast cells in various tissues such as bone marrow, skin, gastrointestinal tract, liver, and spleen.
Cem, Akin, Dean D, Metcalfe
openaire +2 more sources
The American Journal of Surgical Pathology, 1983
The clinical, radiologic, ultrastructural, and histopathologic findings in 14 patients with systemic mastocytosis were evaluated. Seven patients had evidence of urticaria pigmentosa (UP) and seven patients presented with no recognizable cutaneous lesions.
R D, Brunning +4 more
openaire +2 more sources
The clinical, radiologic, ultrastructural, and histopathologic findings in 14 patients with systemic mastocytosis were evaluated. Seven patients had evidence of urticaria pigmentosa (UP) and seven patients presented with no recognizable cutaneous lesions.
R D, Brunning +4 more
openaire +2 more sources
Aggressive systemic mastocytosis
Joint Bone Spine, 2003Systemic mastocytosis is a rare and occasionally aggressive condition that raises major diagnostic challenges. We report a case in a 72-year-old patient in whom the diagnosis of malignant mastocytosis required two bone marrow smears and three bone marrow biopsies examined using specific staining techniques.
Rachida, Inaoui +4 more
openaire +2 more sources
Systemic Mastocytosis and the Mastocytosis Syndrome
Journal of Cutaneous Pathology, 1979A patient with extensive systemic mastocytosis and the mastocytosis syndrome was studied by light and electron microscopy. Mast cell proliferation was found in the bone marrow, the liver, spleen and lymph node. In addition, the patient had telangiectasia macularis eruptiva perstans and elevated histamine levels.
G D, Monheit, T, Murad, M, Conrad
openaire +2 more sources
MALIGNANT SYSTEMIC MASTOCYTOSIS
Australian and New Zealand Journal of Medicine, 1988Abstract:Malignant systemic mastocytosis is a rare disorder, a subgroup of the mast cell neoplasms. Its clinical and histological diagnosis is often difficult, especially in patients without cutaneous involvement. We report an unsuspected case who underwent laparotomy complicated by life‐threatening hypotension consistent with vasoactive mediator ...
S M, Jane, R, Sutherland, H H, Salem
openaire +2 more sources
2006
Systemic mastocytosis is a fascinating disease with diverse clinical features. There have been numerous advances in understanding the basis of clinical manifestations of this disease and of its molecular pathogenesis in the last several decades. The development of methods to study mast cell biology using cell culture and murine models has proven ...
Jamie, Robyn, Dean D, Metcalfe
openaire +2 more sources
Systemic mastocytosis is a fascinating disease with diverse clinical features. There have been numerous advances in understanding the basis of clinical manifestations of this disease and of its molecular pathogenesis in the last several decades. The development of methods to study mast cell biology using cell culture and murine models has proven ...
Jamie, Robyn, Dean D, Metcalfe
openaire +2 more sources
DeckerMed Gastroenterology, Hepatology and Endoscopy, 2018
Systemic mastocytosis (SM) is a disease characterized by an abnormal proliferation and accumulation of a clonal population of mast cells in the tissues including the bone marrow, gastrointestinal tract, and skin. In the most common form, indolent mastocytosis, the symptoms are most often due to the consequences of mast cell activation and include ...
Andrew Kuykendall, Kenneth Zuckerman
+4 more sources
Systemic mastocytosis (SM) is a disease characterized by an abnormal proliferation and accumulation of a clonal population of mast cells in the tissues including the bone marrow, gastrointestinal tract, and skin. In the most common form, indolent mastocytosis, the symptoms are most often due to the consequences of mast cell activation and include ...
Andrew Kuykendall, Kenneth Zuckerman
+4 more sources
[Systemic mastocytosis and malignant mastocytosis].
Presse medicale (Paris, France : 1983), 1990Systemic mastocytosis is a rare, often undiagnosed disease characterized by the proliferation of mast cells in several tissues. The clinical symptoms are related to the mast cell infiltrates, but also to the release of numerous mediators. Malignant mastocytosis is a term that refers to two different entities: aggressive mastocytosis, where the outcome ...
O, Lortholary +4 more
openaire +1 more source
2016
Clinical History Image Findings Discussion Find Diagnosis Differential ...
openaire +1 more source
Clinical History Image Findings Discussion Find Diagnosis Differential ...
openaire +1 more source

