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1.
Am J Case Rep ; 25: e943275, 2024 Apr 22.
Article in English | MEDLINE | ID: mdl-38644602

ABSTRACT

BACKGROUND Marginal zone lymphoma is a low-grade, B-cell, non-Hodgkin lymphoma. Bone marrow involvement (BMI) of leukemia or lymphoma can usually be displayed in fluorine-18-fluorodeoxyglucose positron emission tomography/computed tomography (¹8F-FDG PET/CT) with high standardized uptake values (SUV), while diffuse homogeneous ¹8F-FDG bone marrow uptake (BMU) in PET/CT primarily reflects hyperplastic bone marrow status. This report is of a 74-year-old man presenting with anemia and a diagnosis of recurrent marginal zone lymphoma with bone marrow involvement identified with 18F-FDG PET/CT imaging and biopsy. CASE REPORT A 64-year-old man with severe anemia and body weight loss of 7 kg in 1 month was diagnosed with marginal zone lymphoma, stage III, in July 2011. He went into complete remission in April 2012 after 6 cycles of chemotherapy, with Hb restored. Anemia and diffuse homogeneous ¹8F-FDG BMU in PET/CT were then noted during a routine check-up in October 2021, and recurrent disease was established through positive biopsy of subcutaneous nodules and bone marrow. Subsequent complete remission after 6 cycles of combination therapy was validated with pathologically negative BMI, the resolution of the slightly enhanced ¹8F-FDG BMU in PET/CT, and restored hemoglobin. CONCLUSIONS This report has highlighted the importance of follow-up for patients with lymphoma and supports the diagnostic role of ¹8F-FDG PET/CT imaging and the pathological verification in identifying malignant involvement in bone marrow.


Subject(s)
Bone Marrow , Fluorodeoxyglucose F18 , Lymphoma, B-Cell, Marginal Zone , Positron Emission Tomography Computed Tomography , Radiopharmaceuticals , Humans , Male , Aged , Lymphoma, B-Cell, Marginal Zone/diagnostic imaging , Lymphoma, B-Cell, Marginal Zone/pathology , Bone Marrow/pathology , Bone Marrow/diagnostic imaging , Neoplasm Recurrence, Local/diagnostic imaging , Biopsy , Antineoplastic Combined Chemotherapy Protocols/therapeutic use
2.
Fish Physiol Biochem ; 40(5): 1587-99, 2014 Oct.
Article in English | MEDLINE | ID: mdl-24894980

ABSTRACT

The aims of the present study are to determine whether triiodothyronine (T3) and/or thyroxine (T4) in tilapia larvae is gifted through the mother, and to investigate the change profiles of thyrotropin (TSH), thyroid follicular cells and type I deiodinase (D1) gene expression following larval development. T3 and T4 contents were measured using radioimmunoassay, thyrotropin was observed using immunocytochemistry, and the D1 gene was cloned and measured using real-time PCR. Results indicated that the ß-TSH-immunoreactive cells (thyrotropin ICC) signals were detected at 9 dph (i.e., 9 days of post-hatching). Thyroid follicular cells were observed first at 3 dph, while the T3 contents of the whole body gradually decreased before 11 dph. T4 contents were detected until 13 dph, with higher secretion during 19-21 dph. In addition, the T3 synthesis was not inhibited by thiourea (TU) before 13 dph, but the TU response in the larvae appeared after 13 dph. Type I deiodinase (D1: GenBank accession number KC591724) was found to contain 2444 bases and encoded 248 amino acids. The D1 mRNA expression began to increase at 13 dph, with a higher expression during 15-19 dph. These results suggested that the T3 contents were maternally derived before 13 dph. Both thyroid hormonal changes and some parameters related to thyroid hormone synthesis in ontogenetic tilapia are discussed.


Subject(s)
Gene Expression Regulation, Developmental/physiology , Iodide Peroxidase/genetics , Thyrotropin/metabolism , Thyroxine/metabolism , Tilapia/growth & development , Triiodothyronine/metabolism , Analysis of Variance , Animals , Base Sequence , Cloning, Molecular , DNA Primers/genetics , Immunohistochemistry/veterinary , Larva/growth & development , Larva/metabolism , Molecular Sequence Data , Radioimmunoassay/veterinary , Real-Time Polymerase Chain Reaction , Sequence Analysis, DNA , Tilapia/metabolism
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