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1.
Gynecol Obstet Fertil Senol ; 49(9): 677-683, 2021 Sep.
Article in French | MEDLINE | ID: mdl-33484900

ABSTRACT

INTRODUCTION: Current guidelines (ASCO, ESTRO, and ESGO) recommend para-aortic lymphadenectomy (PAL) for lymph node staging in patients with a negative initial PET-CT in locally advanced cervical cancer (LACC), with the aim to determine the radiation fields for radiochemotherapy. The main goal of this study was to compare overall survival (OS) in two groups, which differed according to the para-aortic lymph node staging technique used: imaging alone versus imaging and PAL. Secondary objectives were to determine recurrence-free survival (RFS), the proportion of false negatives on PET-CT, and surgery-related complications. METHODS: We conducted a retrospective, observational study on data from the Côte d'Or gynaecological cancer registry collected from 2003 to 2016, and compared two groups of LACC with different techniques for staging para-aortic lymph nodes: PET-CT alone (iN group) (n=99) and PET-CT associated with PAL (pN group) (n=35) for a total of 134 patients. RESULTS: OS (HR=1.04 (95% CI: 0.53-2.03); P=0.9) and RFS (HR=0.65 (95% CI: 0.29-1.45); P=0.29) were similar in both groups. There were 11.4% of false negatives in PET-CT, and 2.9% of patients who underwent PAL experienced complications. The staging method, iN or pN, had no impact on the time to the implementation of concomitant radiochemotherapy. CONCLUSION: For lymph node staging in LACC, PAL after a PET-CT as compared with PET-CT staging alone, had no significant impact on OS or RFS.


Subject(s)
Uterine Cervical Neoplasms , Female , Fluorodeoxyglucose F18 , Humans , Lymph Node Excision , Lymph Nodes/diagnostic imaging , Lymph Nodes/pathology , Lymphatic Metastasis , Neoplasm Staging , Positron Emission Tomography Computed Tomography , Registries , Retrospective Studies , Uterine Cervical Neoplasms/diagnostic imaging , Uterine Cervical Neoplasms/pathology , Uterine Cervical Neoplasms/therapy
2.
Presse Med ; 36(5 Pt 1): 804-7, 2007 May.
Article in French | MEDLINE | ID: mdl-17329067

ABSTRACT

INTRODUCTION: We present a typical case of adult respiratory distress syndrome (ARDS) occurring during infection with Plasmodium falciparum, in a nonimmune adult. The patient recovered after treatment. CASE: A 63-year-old man who had traveled in Kenya without malaria prophylaxis came to the hospital after 72 hours of fever on his return. On admission, the blood smear revealed severe P. falciparum parasitemia (45%), thrombopenia (4000/mm3), disseminated intravascular coagulation, and hepatic dysfunction. He was treated with intravenous quinine, and the initial course was favorable. On day 4, his parasitemia resolved, but he developed dyspnea with hypoxemia and required mechanical ventilation. Chest radiography showed bilateral diffuse infiltrate. Low central venous and pulmonary artery occlusion pressure confirmed ARDS. Bacteriological testing remained negative. Secondary course was favorable: he was extubated on day 10 and discharged on day 13. DISCUSSION: During the first five days of treatment for severe or multisystemic P. falciparum malaria, patients have a substantial risk of ARDS. This case illustrates the principal predisposing factors: severe parasitemia, hypoalbuminemia and fluid overload; hypoglycemia and lactic acidosis are also common. CONCLUSION: Physicians caring for patients with malaria must anticipate the possible onset of complications, including ARDS.


Subject(s)
Malaria, Falciparum/complications , Respiratory Distress Syndrome/etiology , Anti-Bacterial Agents/administration & dosage , Anti-Bacterial Agents/therapeutic use , Antimalarials/administration & dosage , Antimalarials/therapeutic use , Cephalosporins/administration & dosage , Cephalosporins/therapeutic use , Drug Therapy, Combination , Follow-Up Studies , Hospitalization , Humans , Macrolides/administration & dosage , Macrolides/therapeutic use , Malaria, Falciparum/diagnosis , Malaria, Falciparum/drug therapy , Male , Middle Aged , Quinine/administration & dosage , Quinine/therapeutic use , Radiography, Thoracic , Respiration, Artificial , Respiratory Distress Syndrome/diagnosis , Respiratory Distress Syndrome/diagnostic imaging , Respiratory Distress Syndrome/therapy , Time Factors , Travel , Treatment Outcome
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