scholarly journals Renal arteriography with endovascular ultrasound for the management of renal infarction patients

2020 ◽  
Vol 21 (1) ◽  
Author(s):  
Fabrice Ivanes ◽  
Jean Dewaele ◽  
Caroline Touboul ◽  
Philippe Gatault ◽  
Bénédicte Sautenet ◽  
...  
Radiology ◽  
1966 ◽  
Vol 86 (1) ◽  
pp. 52-56 ◽  
Author(s):  
H. Rodney Hartmann ◽  
Allan W. Newcomb ◽  
Asa Barnes ◽  
Robert M. Lowman

1968 ◽  
Vol 99 (5) ◽  
pp. 506-512 ◽  
Author(s):  
Erich K. Lang ◽  
J.H.O. Mertz ◽  
Myron Nourse

1978 ◽  
Vol 14 (2) ◽  
pp. 332
Author(s):  
BT Kim ◽  
YH Lee ◽  
KK Oh ◽  
KO Choi ◽  
BS Choi

1982 ◽  
Vol 18 (3) ◽  
pp. 411
Author(s):  
M C Han ◽  
B I Choi ◽  
J H Park ◽  
S W Ha ◽  
K H Chang

2020 ◽  
Vol 1 (1) ◽  
Author(s):  
Mounia Bendari ◽  
Nouama Bouanani ◽  
Mohamed Amine Khalfaoui ◽  
Maryam Ahnach ◽  
Aziza Laaraj ◽  
...  

The myelodysplastic syndrome-myeloproliferative neoplasms (MDS/MPNs) are defined by a group of heterogeneous hematological malignancies resulting from stem cell−driven clonal growth of pathological hematopoietic progenitors and ineffective hematopoiesis, they are characterized concomitant myelodysplastic and myeloproliferative signs. Myelodysplastic/myeloproliferative disorders have been considered to have a higher risk of thrombus formation.We report a rare case about a 64 years old Moroccan woman, experienced renal infarction (RI) associated with pulmonary embolism as a complication of a myelodysplastic/myeloproliferative disorder.The patient complained of acute-onset severe left flank pain, a contrast-enhanced computed tomography (CT) of the chest and abdomen revealed RI by a large wedge-shaped defect in the right kidney with pulmonary embolism.Biological exam showed deep anemia, the bone marrow aspiration found myelodysplasia.the bone biopsy showed signs of myeloproliferatif disease. The karyotype was normal, BCR-ABL, JAK2, CALR mutations were absents, and MPL mutation was positive. The International Prognostic Scoring System (IPSS-R) was 0, and the patient was included to the low risk group.Anticoagulation therapy was initiated with heparin to treat RI and pulmonary embolism. Three months later, pulmonary embolism had resolved without the appearance of additional peripheral infarction.This case emphasizes the need to consider myelodysplastic/myeloproliferative disorders as a cause of infraction renal and pulmonary embolism.


2021 ◽  
Vol 17 (1) ◽  
Author(s):  
Silvia Pavone ◽  
Roberto Rinoldo ◽  
Elisa Albini ◽  
Alessandro Fiorucci ◽  
Biagio Caponi ◽  
...  

Abstract Background Comamonas kerstersii is rarely associated with infections in humans and has never been reported in animals until now. Case presentation Herein, we describe a case of urinary tract infection caused by C. kerstersii in a young goat. A seven-month-old male goat showed lethargy, generalised weakness and anorexia and in the last hours before its death, severe depression, slight abdominal distention, ruminal stasis, and sternal recumbency. Grossly, multifocal haemorrhages in different organs and tissues, subcutaneous oedema and hydrocele, serous fluid with scattered fibrin deposition on the serosa of the abdominal organs and severe pyelonephritis with multifocal renal infarction were detected. Histopathological examination confirmed severe chronic active pyelonephritis with renal infarcts, multi-organ vasculitis and thrombosis suggestive of an infectious diseases of bacterial origin. The bacterium was identified using routine methods, matrix assisted laser desorption/ionisation time-of-flight mass spectrometry (MALDI-TOF-MS), and sequencing of the gyrB gene. Conclusions To the best of our knowledge, this is the first report of C. kerstersii infection in animals (goat). Our findings support the possibility of C. kerstersii isolation from extraintestinal sites and suggest this organism as a possible cause of urinary tract infection.


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