ABSTRACT
ABSTRACT: We describe a 57-year-old man with prostate cancer. A radical prostatectomy with a pelvic lymphadenectomy was performed. After 2 years, a mild swelling of the lower extremities appeared, and the patient was referred for lower-limb lymphoscintigraphy. A lymphoscintigraphy of the superficial lymphatic system in the limbs showed prominent, dermal backflow in the area of the right hypogastrium. Lymphoscintigraphy of the deep lymphatic system showed reflux in the left hypogastrium. This discrepancy between the findings in the superficial and deep lower-limb lymphatic systems was explained by asymmetric sampling of the lymph nodes during the lymphadenectomy.
Subject(s)
Lower Extremity , Lymphatic System , Lymphoscintigraphy , Humans , Male , Middle Aged , Lymphatic System/diagnostic imaging , Lymphatic System/physiopathology , Lower Extremity/diagnostic imaging , Prostatectomy , Prostatic Neoplasms , Lymph Nodes , Pelvis/diagnostic imagingABSTRACT
We present the case of a 26-year-old man with congenital primary lymphedema. A lymphedema of the right upper limb appeared at the age of 2 years, followed by edemas of the right lower limb and of the right part of the head and neck. A lymphedema of the left lower limb began 5 years ago, and finally an edema of the external genitalia began 2 years ago. Lymphoscintigraphy of the lower limbs and pelvic/abdominal region (including SPECT/ldCT) revealed interesting abnormalities.
Subject(s)
Lymphedema/diagnostic imaging , Lymphoscintigraphy , Single Photon Emission Computed Tomography Computed Tomography , Adult , Humans , Lower Extremity/diagnostic imaging , Male , Pelvis/diagnostic imagingABSTRACT
A 7-year-old girl had been followed up for persistent conjugated hyperbilirubinemia since birth. Alanine aminotransferase, aspartate aminotransferase and γ-glutamyl transpeptidase activity was within the normal range, and liver protein synthesis had always been normal. Infectious etiology of jaundice, autoimmune diseases, drug-induced liver injury, hemolytic anemia, α-1 anti-trypsin deficiency, Wilson disease and Gilbert syndrome were ruled out. At the age of 8 years the patient underwent radionuclide dynamic cholescintigraphy, indicating poor accumulation of the radiotracer in the liver on one hand, and severe retention of the radiopharmaceutical in the blood pool (including the heart) on the other hand. Rotor syndrome was suspected and finally confirmed on molecular analysis. This case represents the first cholescintigraphy report in a pediatric patient with genetically proven Rotor syndrome.
Subject(s)
Cholecystography/methods , Gallbladder/diagnostic imaging , Hyperbilirubinemia, Hereditary/diagnosis , Jaundice/etiology , Radionuclide Imaging/methods , Child , Diagnosis, Differential , Female , Humans , Hyperbilirubinemia, Hereditary/complications , Jaundice/diagnosisABSTRACT
A male patient had undergone total thyroidectomy for thyroid papillary carcinoma. He was administered thyroablation activity of radioiodine. Whole body imaging after diagnostic activity of 131-I demonstrated intense radioiodine uptake in the right side of the upper abdominal region. The serum thyroglobulin level was low. Ultrasonography demonstrated a large irregular anechoic structure in the centre of the right kidney--a cyst in the parapelvic region. Renal cysts can lead to erroneous interpretation of radioiodine scintigraphy.
