Detailed Information on Publication Record
2022
Aggressive systemic mastocytosis with diffuse bone marrow (18) F-FDG uptake
KOUKALOVÁ, Renata, Jiří VAŠINA, Jiří ŠTIKA, Michael DOUBEK, Petr SZTURZ et. al.Basic information
Original name
Aggressive systemic mastocytosis with diffuse bone marrow (18) F-FDG uptake
Authors
KOUKALOVÁ, Renata (203 Czech Republic, belonging to the institution), Jiří VAŠINA (203 Czech Republic, belonging to the institution), Jiří ŠTIKA (203 Czech Republic, belonging to the institution), Michael DOUBEK (203 Czech Republic, belonging to the institution) and Petr SZTURZ (203 Czech Republic, guarantor)
Edition
Nuklearmedizin-Nuclear Medicine, Stuttgart, Schattauer GmbH-Verlag Medizin Naturwissenschaften, 2022, 0029-5566
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30224 Radiology, nuclear medicine and medical imaging
Country of publisher
Germany
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 1.500
RIV identification code
RIV/00216224:14110/22:00125372
Organization unit
Faculty of Medicine
UT WoS
000715521100001
Keywords in English
mastocytosis; positron emission tomography; computed tomography; KIT D816V mutation; osteopenia; osteosclerosis
Tags
International impact, Reviewed
Změněno: 19/2/2024 11:10, Mgr. Tereza Miškechová
Abstract
V originále
Mastocytosis is a clonal hematopoietic disorder characterized by proliferation of abnormal mast cells in various organs including the skin, digestive system, lymph nodes, and bone marrow. We report on a 75-year-old woman presenting with abdominal pain, vomiting, diarrhoea, myalgia, and weight loss. Abdominal CT showed hepatosplenomegaly with heterogeneous splenic parenchyma, lymphadenopathy, and osteopenia with areas of osteosclerosis but no primary tumour. An 18F-FDG PET/CT revealed an overall low metabolic activity of the lesions with a diffuse bone marrow involvement raising suspicion of a haematological neoplasm. Subsequently, bone marrow and peripheral blood examinations confirmed the diagnosis of aggressive systemic mastocytosis.