2014, Number 4
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An Med Asoc Med Hosp ABC 2014; 59 (4)
Mediastinal Castleman’s disease evaluated by 18F-FDG PET/CT
Olarte CMÁ, Padilla RÁ, García OJR, Martínez MR
Language: Spanish
References: 34
Page: 279-284
PDF size: 349.46 Kb.
ABSTRACT
Castleman’s disease or angiofollicular hyperplasia is an atypical lymphoproliferative disorder. First described in 1956 by Benjamin Castleman, it is considered a heterogeneous disease that can be classified in two clinical groups: unicentric or localized, and multicentric or systemic. Histologically, there are three variants: hyaline vascular, plasma cell, and a mix of both. Its etiology remains unknown, but it is related with a chronic antigenic stimulation caused by viral infections, which determines the reactive lymphoid hyperplasia that distinguishes this entity. Approximately 70% of these tumors grow in the mediastinum. Castleman’s disease does not have demonstrable characteristics by imagenological studies, so biopsy provides the accurate diagnosis. Due to the fact that
18F-FDG PET/CT (positron emission tomography/computed tomography) allows an anatomical and metabolic evaluation, especially for lymphoproliferative disorders, it is an excellent diagnostic tool to determine the location and extension of Castleman’s disease, as well as to identify the optimal site for biopsy and thereby reduce the morbidity associated with improperly performed biopsies. In the same way, this modality enables to adequately stage the patient prior to making a therapeutic decision, and also allows to evaluate the response to treatment and to follow up the disease.
Objective: is to identify the metabolic behavior of mediastinal Castleman’s disease and evaluate the usefulness of
18F-FDG PET/CT as a tool to identify the lesion and the extent of disease, and in assessing response to treatment.
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